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#700 From: MRomaniec@...
Date: Tue Jun 7, 2005 9:17 pm
Subject: Rare form of Alzheimers strikes family
mromaniec123
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Updated: 11:41 AM EDT
Rare Form of Alzheimer's Disease Strikes Family

FARGO, N.D. (June 7) - For 16 years, Dean DeMoe watched Alzheimer's disease change his father, who died at age 58. Now, two of his brothers, both in their 40s, struggle with the disease.

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Dean himself, was diagnosed with the disease in February, though he does not yet display symptoms. Alzheimer's, an incurable neurological disease, devastates a person's memory and brain functions.

The entire DeMoe family, including six siblings and their 12 children, has been hit hard by a rare form of Alzheimer's disease that is hereditary and strikes early. They are taking part in research and trying to find hope.

Of the six DeMoe siblings, four have gone through genetic testing, including 42-year-old Dean, 44-year-old Doug and 49-year-old Brian.

Brother Jamie DeMoe, 33, of Williston, and sister Lori McIntyre, 45, of Alpine, Texas, have not been tested.

A November diagnosis brought relief to their sister, Karla Hornstein, 47, of Fargo, who learned she will not develop the disease. Hornstein's co-workers at Concordia College in Moorhead, Minn., had a cake made for her. "Now your only excuse is you're blond," it read.

"My children, they are free and clear," Hornstein said, talking about 21-year-old Cole and 20-year-old Amber. "They have been given a clean bill of health.

"Then I switch to, I've been given a gift that I will use to help my siblings to make sure they get the quality of life they deserve," she said.

Hornstein grasps onto any piece of information she can find on familial Alzheimer's disease. She has files on each of the siblings, federal legislation, as well as research studies.

"If you're involved in something, you feel like there's hope," Hornstein said.

Brian, Doug, Dean and Karla spent a week at the National Institute of Mental Health in Bethesda, Md., for a family study.

They have sent blood samples and medical records to a national repository in Indiana.

Next, they will travel to the University of Pittsburgh Medical Center for research on familial Alzheimer's. They will be injected with radioactive material so the plaque in their brains can be observed.

"This family is just a Petri dish of information," said Dr. Bret Haake, a neurologist with Fargo's MeritCare Hospital, where Doug and Brian were diagnosed in March 2004.

In his 10 years at MeritCare, he said, the DeMoe family was the first case of familial Alzheimer's he had seen.

Dean DeMoe and Hornstein were tested for the mutation in Bethesda last August.

"The thinking and worrying and wondering just drives you crazy," Dean said.

His 9-year-old daughter, McKenna, sometimes forgets things on purpose to make him feel better.

Older children must choose whether they want to know their fate.

Kassie Kinvig of Dickinson, Brian's 26-year-old daughter, decided she will be tested. She wants to have children but doesn't want to pass along the disease if she has it.

At the same time, she is thinking about her own mortality, and her father's shortened lifespan.

"I kind of feel like I'm getting the chance to get to know him, but I'll ever really get the chance to know who he is because this disease affects his personality," she said.

She said her father is now childlike. He likes to laugh and play pranks.

"In some ways, I think he doesn't realize he has it," she said.

Other times, it seems like he knows. He tells her in his own way.

Dean DeMoe and Hornstein have power of attorney for Brian and Doug. They think about when to take away their driver's licenses, when to put them in nursing homes. They've chosen a facility in Kenmare.

The family members have formed their own support group, Kinvig said.

"Even though it's a devastating disease, we've all become stronger as a family because of it," she said.

"I just take it day by day," Dean said. "What's handed to you is handed to you."

06-07-05 11:27 EDT

Copyright 2005 The Associated Press. The information contained in the AP news report may not be published, broadcast, rewritten or otherwise distributed without the prior written authority of The Associated Press. All active hyperlinks have been inserted by AOL


#701 From: MRomaniec@...
Date: Mon Jun 20, 2005 11:09 pm
Subject: Two experimental therapies for Alzheimers
mromaniec123
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Many of you may have seen this news article about the two types of medicines currently showing promise in the fight against Alzheimers.  One of them is IVIG, an expensive treatment that uses human immune globulin to boost the fragile immune system.  This allows the body to heal, the central nervous system to heal and the brain. 

Why I know a bit about IVIG is that it is the treatment that saved my son after he was diagnosed with autism.  The research scientist who pioneered this method to treat autism is a world reknowed immunologist in California. 

Many researchers have begun to realize Alzheimers and autism may be related in varying degrees.  The belief by some researchers is both are caused by oxidative stress.  And what causes oxidative stress is mercury exposure (think flu vaccines and amalgams). 

Passing this along in case you find this of interest.  Just a footnote on IVIG, it is VERY expensive!!  And most insurance companies will not pay for it unless a true immune dysfunction is diagnosed.

Mary

Two experimental therapies show promise at preventing a sticky gunk from clogging up the brains of Alzheimer's (search) patients, a buildup called amyloid that is the newest focus in the fight against the disease.

One, an experimental drug called Flurizan (search), has begun late-stage testing to see if it at least helps slow Alzheimer's inevitable worsening. Government-funded researchers are planning a large study of the second approach, a therapy called intravenous immune globulin (search), or IVIG.

"Most scientists think if you get rid of amyloid (search), it'll moderate the disease," explained William Thies, scientific director of the Alzheimer's Association.

About 4.5 million Americans have Alzheimer's, a creeping brain degeneration that slowly robs its victims of memory and the ability to reason, communicate and care for themselves. With the aging population, a staggering 14 million may have it by 2050.

No one knows what causes Alzheimer's. But the leading theory is that something spurs abnormal production of a protein called beta-amyloid, which forms clumps that coat and then kill brain cells — plaque that is the disease's trademark.

Healthy people's immune systems produce antibodies that can get rid of at least some of the beta-amyloid that floats in everyone's bodies. But older people produce one-third fewer antibodies against the protein than younger people do, said Dr. Marc Weksler of the Weill Medical College of Cornell University.

Immune globulin is a cocktail of antibodies culled from blood donors and given intravenously to treat a variety of immune-related diseases. The question is whether giving IVIG to Alzheimer's patients might act as a sponge to soak up extra beta-amyloid.

Weksler gave eight people with mild to moderate Alzheimer's six months of IVIG therapy. The amount of beta-amyloid in their cerebral spinal fluid — a measure of how much reaches the brain — dropped about 45 percent. Cognitive tests suggest the patients may have stabilized during treatment, although Weksler stressed that it's impossible to tell from such a small study that had no comparison group.

"I'm encouraged but not convinced," Weksler cautioned at an Alzheimer's Association conference on preventing the disease. "We don't want people to go out and buy this and treat themselves."

But Weksler's is the second small study to suggest IVIG may help Alzheimer's. Now other researchers are working with the National Institutes of Health and manufacturer Baxter Pharmaceuticals, which helped fund Weksler's work, to plan a larger study.

Myriad Genetics Inc. already has begun a large study of Flurizan, a revamped version of an old painkiller called flurbiprofen.

In Phase 2 testing of 128 people with mild Alzheimer's, treated patients didn't worsen as quickly as those given a placebo, with few side effects, said Dr. Gordon Wilcock of Britain's University of Bristol. It didn't work as well in patients with moderate-stage disease.

"If it really does work, what this drug does is reduce the rate at which beta-amyloid is made," Wilcock said. That suggests the sooner in illness it's used, the better.


#702 From: "Sally Rugh" <sal5371@...>
Date: Tue Jun 21, 2005 3:53 am
Subject: Re: Two experimental therapies for Alzheimers
sally195371
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What do you mean by it saved your son with Autism? The reason I ask is because I have an 11 year old with high functioning Autism ( Aspergers) I really don't think that it was cased by Mercury.
Sally
----- Original Message -----
Sent: Monday, June 20, 2005 11:09 PM
Subject: [alzheimers_support] Two experimental therapies for Alzheimers

Many of you may have seen this news article about the two types of medicines currently showing promise in the fight against Alzheimers.  One of them is IVIG, an expensive treatment that uses human immune globulin to boost the fragile immune system.  This allows the body to heal, the central nervous system to heal and the brain. 

Why I know a bit about IVIG is that it is the treatment that saved my son after he was diagnosed with autism.  The research scientist who pioneered this method to treat autism is a world reknowed immunologist in California. 

Many researchers have begun to realize Alzheimers and autism may be related in varying degrees.  The belief by some researchers is both are caused by oxidative stress.  And what causes oxidative stress is mercury exposure (think flu vaccines and amalgams). 

Passing this along in case you find this of interest.  Just a footnote on IVIG, it is VERY expensive!!  And most insurance companies will not pay for it unless a true immune dysfunction is diagnosed.

Mary

Two experimental therapies show promise at preventing a sticky gunk from clogging up the brains of Alzheimer's (search) patients, a buildup called amyloid that is the newest focus in the fight against the disease.

One, an experimental drug called Flurizan (search), has begun late-stage testing to see if it at least helps slow Alzheimer's inevitable worsening. Government-funded researchers are planning a large study of the second approach, a therapy called intravenous immune globulin (search), or IVIG.

"Most scientists think if you get rid of amyloid (search), it'll moderate the disease," explained William Thies, scientific director of the Alzheimer's Association.

About 4.5 million Americans have Alzheimer's, a creeping brain degeneration that slowly robs its victims of memory and the ability to reason, communicate and care for themselves. With the aging population, a staggering 14 million may have it by 2050.

No one knows what causes Alzheimer's. But the leading theory is that something spurs abnormal production of a protein called beta-amyloid, which forms clumps that coat and then kill brain cells — plaque that is the disease's trademark.

Healthy people's immune systems produce antibodies that can get rid of at least some of the beta-amyloid that floats in everyone's bodies. But older people produce one-third fewer antibodies against the protein than younger people do, said Dr. Marc Weksler of the Weill Medical College of Cornell University.

Immune globulin is a cocktail of antibodies culled from blood donors and given intravenously to treat a variety of immune-related diseases. The question is whether giving IVIG to Alzheimer's patients might act as a sponge to soak up extra beta-amyloid.

Weksler gave eight people with mild to moderate Alzheimer's six months of IVIG therapy. The amount of beta-amyloid in their cerebral spinal fluid — a measure of how much reaches the brain — dropped about 45 percent. Cognitive tests suggest the patients may have stabilized during treatment, although Weksler stressed that it's impossible to tell from such a small study that had no comparison group.

"I'm encouraged but not convinced," Weksler cautioned at an Alzheimer's Association conference on preventing the disease. "We don't want people to go out and buy this and treat themselves."

But Weksler's is the second small study to suggest IVIG may help Alzheimer's. Now other researchers are working with the National Institutes of Health and manufacturer Baxter Pharmaceuticals, which helped fund Weksler's work, to plan a larger study.

Myriad Genetics Inc. already has begun a large study of Flurizan, a revamped version of an old painkiller called flurbiprofen.

In Phase 2 testing of 128 people with mild Alzheimer's, treated patients didn't worsen as quickly as those given a placebo, with few side effects, said Dr. Gordon Wilcock of Britain's University of Bristol. It didn't work as well in patients with moderate-stage disease.

"If it really does work, what this drug does is reduce the rate at which beta-amyloid is made," Wilcock said. That suggests the sooner in illness it's used, the better.


#703 From: MRomaniec@...
Date: Tue Jun 21, 2005 11:56 am
Subject: Re: Two experimental therapies for Alzheimers
mromaniec123
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Sally,
 
My son is considered "recovered" from autism.  He was written about in Mothering Magazine last year. I speak at conferences, seminars and radio programs about our experiences with my son.  What helped us was dietary intervention, IVIG and behavior therapies.  He went from being totally non verbal to full sentences within four months of IVIG.  By his 12th infusion his immunologist declared him to be a recovery kid.  By the 18th infusion his pediatrician declared he could no longer see any traces of autism in him and considered it remarkable. 
 
Our experiences with my son's recovery (and the recovery of other children I know) tells me Alzheimers answers are out there.  We were told "NO HOPE, NO CURE" for my son when he was diagnosed.  We proved them wrong.  I have already told my husband that if he showed the slightest symptoms I would do for him much of what we did for my son. 
 
That is why I wonder why there is not more emphasis placed on this awareness.
 
Mary

#704 From: "Sally Rugh" <sal5371@...>
Date: Tue Jun 21, 2005 8:15 pm
Subject: Re: Two experimental therapies for Alzheimers
sally195371
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Wow Mary,
That is great! My Mom has Alzheimers, it is a terrible thing. I will have to look into all this. Maybe I can help my son and my mother at the same time.
Thanks,
Sally
----- Original Message -----
Sent: Tuesday, June 21, 2005 11:56 AM
Subject: Re: [alzheimers_support] Two experimental therapies for Alzheimers

Sally,
 
My son is considered "recovered" from autism.  He was written about in Mothering Magazine last year. I speak at conferences, seminars and radio programs about our experiences with my son.  What helped us was dietary intervention, IVIG and behavior therapies.  He went from being totally non verbal to full sentences within four months of IVIG.  By his 12th infusion his immunologist declared him to be a recovery kid.  By the 18th infusion his pediatrician declared he could no longer see any traces of autism in him and considered it remarkable. 
 
Our experiences with my son's recovery (and the recovery of other children I know) tells me Alzheimers answers are out there.  We were told "NO HOPE, NO CURE" for my son when he was diagnosed.  We proved them wrong.  I have already told my husband that if he showed the slightest symptoms I would do for him much of what we did for my son. 
 
That is why I wonder why there is not more emphasis placed on this awareness.
 
Mary

#705 From: "Diane(Dee)" <runspencer4@...>
Date: Mon Jul 4, 2005 11:10 pm
Subject: Hi I'm new...
runspencer4
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Hello. I hope this post finds everyone safe on this 4th of July. My
name is Dee. My Mother-in-law has the late stages of Alzheimer's and
my hubby will not join any support group. He jsut keeps it locked up
inside. I met my hubby in 1999(my second marriage) and also first met
his Mom then. In these past yrs she has declined terribly to the point
of being placed in a "home" just about 6 months ago. We live about 600
miles from her, so hubby visits about 4-5 times a yr. The last visit
was the one he dreaded most. He met her wandering the halls that day
he arrived and walked and talked with her for 30 minutes and she never
even knew it was her son! He just kept walking and talking and never
said anything ti her about being her son. He asked her what her name
was and he said his name to her, and she replied, "ohhhh, I have a
brother by that name". (she doesn't) I feel so bad for him and don't
know how to help him. He's one of those very big hearted "tough"
guys..tattoos and all, but never lets his true feelings show. He
believes she is fading quickly and even pre paid the funeral and
arrangements are made by him and his sister."Mom" doesn't know that,
of course.
I just needed to come here and "vent" and maybe find advice from you
experiences.
Thanks for listening..and bless you all.
Dee

#706 From: "pjb12345uk" <pho@...>
Date: Sat Jul 9, 2005 7:53 am
Subject: Re: Hi I'm new...
pjb12345uk
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---and maybe find advice from you
experiences.

try
Spiritual Healing /Reiki healing

Spiritual healing/ reiki to many people conjures up so many images
and meanings, for those who do not know what it is all about, all
that I would ask is that you approach the subject with an open
unprejudiced mind and with a wish to explore and evaluate the
evidence carefully and properly. It is hoped with such an attitude
truth will prevail and misconceptions from misguided people will be
put in their rightful place.

From the outset it must be clearly understood that we live on a
planet of causes and effects, every thing seen on this planet has a
cause and an effect. We live in and are surrounded by all sorts of
effects like wind blowing from the north or a light shining from a
star or a leaf growing on a tree or wealth,
health,suffering,Happiness,Love,Sound,lightning,Music in fact
everything we see, feel, touch, smell, all have causes. Magic is the
name simply applied to happenings where no obvious cause can be
seen, at least to some of those witnessing it.As you can easily
appreciate no effect is without a cause.


We are know witnessing one of the great turnings in our century
where old healing practises are re-emerging such as Reiki healing,
Colour healing, Seichim, Spiritual healing, Osteopathy, Massage and
many others. Some of these are thousands of years old, Spiritual
healing/reiki  is one of those. It is exactly the same kind of
energy used by Jesus in so many of his healings.


Put simply Spiritual Healing/Reiki is the transference of certain
energies through a channel which could be a person or an animal or
even the planet, the wavelengths of this healing energy are well
outside the limits of most scientific equipment but a lot of people
can feel this energy .

The energy in my experience has been very uplifting and beautiful
which can touch and vastly influence parts of us such as the spirit
or soul or our mental selves and our physical selves. It can bring a
steadiness and balance and sense of well-being second to none .Its
limits as to its use are in the realms of the infinite.

A very simplistic analogy would be to liken it to a massive energy
reservoir which can be tapped into by people and animals which act
as the conduits of this energy and like wires of electricity some of
which are bigger than others and so therefore big wires can transmit
more energy than smaller wires. Bearing this point in mind the
reader can soon appreciate that going to one spiritual healer ,
Reiki healer can be vastly different than going to another as it is
with so many things whether it be dentists, doctors, policeman or
what have you.

Spiritual Healing, Reiki is natural healing energy, which is present
in this universe. Spiritual healers and Reiki work in many different
ways to some it is the laying on of hands onto a person or animal,
to others it can be sent through the power of thought. To be even in
the presence of some healers can have a profound and beneficial
effect on people and one wishes that there were more people giving
off just as beautiful vibrations as these people were this world
would truly transform it.


Everyone needs healing, because there is not a single person which
on some part of their being does not require healing. I will clarify
that point further because some people are so physically orientated
they perceive people and their suffering on a basis of you look OK
you must be OK.

  This perception can be likened to looking at a puddle of water and
because it looks all right and then assuming that because the rest
of the ocean is made of the same kind of stuff it must be the same,
being absolutely oblivious to the rest of the entire ocean.

  We are a very complicated beings comprising of many different parts
some of which are the mental self, the subconscious, the Physical
self and the spiritual self. I will leave it up to the reader to
discover the parts of themselves and their true importance to their
well beings.
During the healing process as a general rule people should simply
relax, all sorts of sensations may be felt typically heat, cold,
energy, sometimes even noises from your body.

Who is suitable for healing? All people at all stages of their life
especially the terminally ill;Animals even plants seem to respond.
Will one session be enough? Sometimes but probably a series may be
the answer.
Will healing cure me? All healing from all sources be it Doctor,
drugs, etc comes under the law of Karma.

There are no guarantees that healing from any source may give the
effect which the Desiree wishes.

  However it has been my experience that even if you do not get the
effect you desire, on some part of your being you most very probably
will receive some healing, even it is just upliftment. Which can be
extremely valuable


Harry Edwards was one such channel who was told to concentrate on
the next person he hears about who is sick. A case arrived one who
had TB who was dying .He concentrated on that person with his mind
and within 24 hrs the bleeding had stopped the pain had stopped and
the temperature had come down to almost normal. The Doctors
attending were amazed, the man returned to work in a short time.
More cases followed, people came with Cancer, Consumption and other
blights. Of notable healing was a boy with Spinal Meningitis and who
was dying. Harry sought healing for the boy and within a short
period of time the boy's parents were astonished to find their boy
sitting up in bed, the doctors looking on in amazement. A growing
queue was starting to form at his house and mail started to arrive.
But what truly amazed harry was the use of Absent healing where the
healing was sent by thought, the patient was not even present but it
seemed even more effective.

  To cope with the growing demands of his work he set up a healing
sanctuary at Burrows lea in surrey and his secretaries started
answering the hundreds of letters which came each day. He was in
constant demand to give talks all over England. Then on one day he
had the great urge to demonstrate what he could do before an
audience ``is there anyone suffering from Arthritis''? he asked.
Hands shot up from all over the auditorium, which started off the
public healing. The demonstrations grew, a thousand people attended
a demonstration at Croydon and typically Harry would treat
Arthritis, Spinal curvature, Deafness and poor sight. One lady who
had not been able to walk for three years was given healing, after a
few minutes of healing she walked down the aisle much to the
audience's delight. A child of six had her spinal curvature
straightened much to people's amazement.

Gradually over the years of healing he drew together the letters and
testimonials and presented them in an incredible book called The
evidence for Spiritual Healing which contained ten thousand cures,
yes that's right ten thousand .

Newspapers captured the signs with headlines like `'Sight restored
after seventeen years'' `'the Deaf hear'' `'After healing the
cripple danced'' `'Paralysed children walk off the stage
unaided''and so on.

  He would make the point quite clear that Spiritual Healing was not
faith healing and if it were so young babies and mental cases with
no comprehension about faith would not even respond.

  On another occasion Harry was called before a panel of Doctors who
presented him with their very own patients. The first patient had
Disseminated Sclerosis and came in with two helpers. On the first
treatment mobility was restored to the spastic spine then co-
ordination of the leg movements followed, she responded well and
started to walk, the session ended with the Doctors asking for
healing for their own personal troubles. Then royalty sought him out
Princess Marie Louise granddaughter of Queen Victoria sought healing
for Arthritis and she was instrumental in the royals attending the
sanctuary.

In less than five years Harry had received no less than one million
letters and in less than seven years over forty thousand people
attended the sanctuary.

In the thirty years from the time he moved to Burrows lea up to his
passing in 1976 he received an average of 9000 letters a week .In
over thirty years he received over 14 million letters from patients.

Harry passed to the other side of life in 1976 but not before
teaching Ray and Joan branch how to continue with the good work at
Burrows lea where they still are today.

Happily now Spiritual healers are used quite extensively in the
N.H.S, in fact they are in over 1500 hospitals and at long last a
lot of churches have finally complied with what the master told them
to do two thousand years ago and that is to go forth and heal the
sick. In the year 2000 even our prince Charles published a report
stating that spiritual healers should be extensively available
throughout the entire NHS. Over 7000 healers are now registered to
treat patients in the health system. I know of no cases where
spiritual healing when given by a trained healer has been
detrimental in any way, I know of no side effects except better
health.


Just a few reports –"When I had finished treating him, it was a real
delight to see how wonderfully glad he was to be able to use his
legs, feet, arms and hands again... and then he told me: "When I
came here, I was convinced no one could help me, and I came only to
please my Aunt, who brought me."

You worked a miracle with his father when he was very ill 1983-84
when I wrote to you, but you will be pleased to know he is now
working for the Council and lives a fairly normal life.
"You and the late Harry Edwards helped me so often and indeed I am
still pressing on 18 years after I was expected to die from my last
bout of cancer."

"On behalf of my mother, daughter and myself may I thank you for the
lovely day at your Sanctuary last Tuesday. My mother is so much
better it is truly amazing. She can stretch out her arms and even
raise them to her head and her walking is much stronger. My daughter
was very impressed, too."
My condition improved in as much as I now have much more self-
confidence and ability to deal with my everyday life.

Reiki,
Millions of people are aware of this fantastic healing energy and
there are literally thousands of healers [channels for this energy].

The word Reiki is made of two Japanese words - Rei which
means "God's Wisdom or the Higher Power" and Ki which is "life force
energy". So Reiki is actually "spiritually guided life force
energy."

A treatment feels like a wonderful glowing radiance that flows
through and around you. Reiki treats the person including body,
emotions, mind and spirit and creates many beneficial effects
including relaxation and feelings of peace, security and well being.
Many have reported miraculous results.

Reiki is a simple, natural and safe method of spiritual healing and
self-improvement that a lot of people can use. It has been effective
in helping virtually every known illness and malady and can create a
very beneficial effect. It also works in conjunction with all other
medical or therapeutic techniques sometimes to relieve side effects
and promote recovery.

An amazingly simple technique to learn, the ability to use Reiki is
not taught in the usual sense, but is transferred to the student
during a Reiki class. This ability is passed on during
an "attunement" given by a Reiki master and allows the student to
tap into an unlimited supply of "life force energy" to improve one's
health and enhance the quality of life.

It has been successfully taught to thousands of people of all ages
and backgrounds.
The Reiki system of healing is a technique for transmitting this
subtle energy to yourself and others. Reiki can restore energy
balance and vitality by relieving the physical and emotional effects
of unreleased stress. It can gently and effectively open blocked
meridians, nadas and chakras, and clears the energy bodies, leaving
one feeling relaxed and at peace.

Reiki can accelerate healing. Assist the body in cleansing toxins.
Balance the flow of subtle energy by releasing blockages. Help the
client contact the 'healer within.'
A treatment feels like warm, gentle sunshine, which flows through
you, surrounds you and comforts you. Reiki treats the person's body,
emotions, mind and spirit as a whole. Reiki is a simple, natural and
safe method of spiritual healing and self-improvement that most
people can use. Reiki is powerful, yet wonderfully gentle and
nurturing.

  During a treatment, the clients usually remain fully clothed. Reiki
is an effective alternative, or complement to massage therapy. Reiki
can support any medical or supplemental healing methods a client may
be using and is of growing interest to chiropractors, medical
doctors, physiotherapists, psychotherapists, psychologists and
hypnotherapists. In fact it is in use by quite a few doctors.


A Brief History of Reiki.
The history of Reiki, like all other histories, is tainted with
different views of the one event.
Reiki is seemingly an ancient form of healing that was lost and then
rediscovered, during a mystical experience, by Dr. Mikao Usui who
was a Japanese psychic. In 1922 Dr. Usui started a healing society
in Japan. He created three degrees (or levels) for Reiki healing and
initiated a small number of followers. One of his followers, Dr.
Hayashi, a retired naval officer, was charged with preserving Reiki.
He did this and further developed the Usui system.

  He gave the knowledge to his wife and to Mrs. Hawayo Takata. Mrs.
Takata practiced Reiki healing and initiated twenty-two people into
Reiki mastership Today, Reiki is known and practiced in many parts
of the world and is increasing in popularity and acceptance.

  One problem a student might have in learning Reiki is the existence
of different Reiki schools, giving different attitudes and different
symbols by different teachers.
  All that is required is a genuine desire for spiritual growth and
an open mind.


Reiki Research
There are now quite a few experiments that validate the usefulness
of Reiki and other vibrational healing techniques. The following are
few of the more interesting experiments.
A registered nurse describes a Reiki experiment she conducted in her
paper, "Reiki Healing: A Physiologic Perspective." In her study,
forty-eight people made up the experimental group while 10 made up a
control group. Both groups had blood samples taken at the beginning
and at the end of the experiment. The experimental group received
First Degree Reiki training. The control group was not involved in
the Reiki training.


The blood samples were measured for hemoglobin and hematocrit
values. Hemoglobin is the part of red blood cells that carry oxygen.
Hematocrit is the ratio of red blood cells to total blood volume.
The people in the experimental group who received Reiki training
experienced a significant change in these values with 28 percent
experiencing an increase and the remainder experiencing a decrease.
The people in the control group who did not receive Reiki training
experienced no significant change.

  It is thought that changes, whether an increase or decrease are
consistent with the purpose of Reiki which is to bring balance on an
individual basis.
One individual experienced a 20% increase in these values. She
continued to treat herself with Reiki daily and after three months,
her increase had been maintained and in fact had continued to
improve. This improvement was appropriate for her as she had been
experiencing iron deficiency anemia.

Another experiment using a Reiki like technique has also
demonstrated its ability to increase hemoglobin values. A medical
doctor conducted an experiment with a group of 79 sick patients.
Together the patients had a wide range of diagnosed illnesses
including pancreatitis, brain tumor, emphysema, multiple endocrine
disorders, rheumatoid arthritis, and congestive heart failure.
Laying-on hands treatments were given to 46 patients with 33 as
controls. The treated patients showed significant increases in
hemoglobin values.

  The effect was so pronounced that even cancer patients who were
being treated with bone marrow-suppressive agents which predictably
induce decreases in hemoglobin values showed an increase. The
majority of patients also reported improvement or complete
disappearance of symptoms. Both this experiment and the one above,
demonstrate that healers are able to induce actual biological
improvements in the patients they treat rather than simply create a
feeling of well being.

Laying-on hands healing has been validated by experiments carried
out at St. Vincent's medical Center in New York. The experiment was
carried out by Janet Quinn, assistant director of nursing at the
University of South Carolina. The design of this experiment tends to
rule out the placebo effect. Thirty heart patients were given a 20
question psychological test to determine their level of anxiety.
Then they were treated by a group trained in laying-on hands
healing. A control group of patients were also treated by sham
healers who imitated the same positions as those who had training.
Anxiety levels dropped 17 percent after only five minutes treatment
by trained practitioners, but those who were only imitating a
treatment created no effect.

Daniel Wirth of Healing Sciences International in Orinda, California
conducted a tightly controlled experiment involving a Reiki-like
healing technique.

Forty-four male college students received identical minor wounds
deliberately inflicted by a doctor in the right or left shoulder.
Twenty-three then received a Reiki like healing and the other twenty-
one did not. The treatments were given in such a way that the
possibility of a placebo effect was ruled out. All forty-four
students extend their arms though a hole in the wall. In the other
room, a trained healer was present for those who received healing
and administered healing from a distance without touching.

For those who did not receive healing, no one was present in the
room. Both the students and the doctor who administered the wounds
and later also evaluated their healing rate had been told that the
experiment was about the electrical conductivity of the body.
Neither knew that the experiment was about healing. Eight and
sixteen day follow-up measurements of the rate of wound healing were
done.

After eight days, the treated groups wounds had shrunk 93.5 percent
compared with 67.3 percent for those not treated. After sixteen
days, the figures were 99.3 and 90.9. After debriefing, the students
stated they did not know the true nature of the experiment and had
felt no contact with the healer. The possibility that expectations
of the students caused the healing was ruled out.
Dr. John Zimmerman of the University of Colorado using a SQUID
(Superconducting Quantum Interference Device) has discovered that
magnetic fields several hundred times stronger than background noise
are created around the hands of trained healers when doing healing
work on patients.

No such fields are created by sham' healers making the same
movements indicating something special is happening with the trained
healers. The frequencies of the magnetic fields surrounding the
hands of the trained healers were of the alpha and theta wave range
similar to those seen in the brain of meditators.


Dr. Barnard Grad of McGill University in Montreal, used barley seeds
to test the effect of psychic healing energies on plants. The seeds
were planted in pots and watered with a saline solution, which is
known to retard their sprouting and growth. With elaborate double-
blind conditions set-up, one group of seeds were watered with saline
solution that had been treated by a psychic healer.




Dr. Grad carried out similar experiments involving tap water and
plants. Sealed containers of water were given to a psychic healer to
hold and others were given to a severely depressed patient to hold.
The plants watered with the healer-held water had an increased
growth rate and those watered with the water held by the severely
depressed patient had a decrease in growth rate compared to
controls.
These experiments involving plants, in addition to confirming the
non-placebo nature of psychic healing, scientifically confirm the
ancient metaphysical understanding that healing energies can be
stored in water for future use.


In another experiment involving psychic healer Olga Worrall, Dr.
Robert Miller used an electromechanical transducer to measure the
microscopic growth rate of rye grass. The device used has an
accuracy of one thousandth of an inch per hour. Dr. Miller set-up
the experiment in his laboratory and then left, locking the door
behind him to eliminate any unnecessary disturbance. Olga, located
over 600 miles away was asked to pray for the test plant at exactly
9 PM that evening.

When Dr. Miller returned to the laboratory the next day, the test
equipment had recorded normal continuous growth of 6.25 thousandths
of an inch per hour up to 9 PM. At that time, the record began to
deviate upward and had risen to 52.5 thousands of an inch per hour
which was an increase of 840 percent! This increased growth rate
remained till morning when it decreased but never to its original
level.

The Spindrift group has done extensive research involving prayer and
plants. Their results indicate that prayed for plants always grow
faster and are healthier than non-prayed for plants even though the
conditions are equal for both groups of plants and those doing the
praying are miles away. These results were consistent regardless of
the distance involved and occurred over and over. They are described
by Robert Owen in his book, "Qualitative Research: The early years":

One of the interesting results of their research work is that they
were best when the prayer was non-directional, that is when the
prayer was simply for the plants general well-being, rather than for
a specific result, such as a certain growth rate or overall height.
More experiments are being done and scientific theories are being
developed to describe Reiki and Reiki like healing techniques. As we
continue into the millennium, increasing interest along with more
sensitive equipment will allow science to more completely
understand, validate, and accept the reality of Reiki. As this
happens, we will see increasing use of Reiki and other laying-on
hands healing coming into common use by individuals for themselves
and family along with its use in hospitals and doctors offices.

The deeper understanding about the nature of health and the unity of
all life this re-discovered age old wisdom will provide will reduce
suffering and make earth a more worthwhile place to live. With this
in mind, let us be encouraged to continue in the spirit of Reiki to
help others and to heal the planet.

Practitioners have some real interesting stories. Reiki can also
enhances natural abilities. If you are an artist, it can help
develop your artistic expression. If you have an intuitive sense,
Reiki can heighten that. If you have a business head, Reiki can
enhance that as well. In the practice of Reiki, working with energy
helps you to connect with your path, your skills, and develop your
senses. But it takes practice and trusting what you feel.

Reiki is also present in some hospitals.
Reiki has been applied to these conditions and more with very
beneficial results. There are a lot more applications of Reiki – see
there web site for more information.
http://www.reikimedresearch.com/

ADDICTIONS (drugs and alcohol)
Addictions and suicidal behavior
Appendicitis
Arthritis (osteo-, rheumatoid)
Add/adhd
Aids /HIV
Burns
Cancer all types
Cervical dysphasia
Childbirth
Chronic fatigue syndrome & fibromyalgia
Coma –phenomenal result
Croons
Depression
Diabetes
Dyslexia
Eye sight
Endometriosis
Heart conditions -saved surgery
Hypothyroidism
Insomnia –results good
Leukemia -recovered
Lupus-improvements
Mole – fell off
Migraine- pain free
Multiple sclerosis – beneficial results
Neuropathy
Pagets - beneficial results
Pain relief – very beneficial
Paralysis- beneficial results recovered
Polyps –surgery cancelled
Prenatal condition- child born healthy
Psoriasis 70% cleared
Seizure beneficial
Shingles- patient in remission


Karuna Reiki
Laura gifford gives some interesting differences between reiki and
Karuna Reiki and says that Reiki increases the awareness of the way
God works in life. Usui Reiki, is the connection to the highest and
most holy spiritual energies. Usui Reiki is unconditional Love. Usui
Reiki is gentle and peaceful, but very powerful. Usui Reiki is a
conduit for Karuna Reiki® to flow through.
When receiving Karuna:

Karuna Reiki® is very serious, let's get down to business energy.
Karuna Reiki® energy goes very deep, gently, but quickly. She
describes vibrating at a rapidly increasing rate, feeling like more
light than I am flesh. The first few times she received a Karuna
treatment she describes rising out of her body, and was taken into
the symbols used. One repeated occurrence has been that she has seen
flashes of traumatic experiences in this life, and from other times.
They appeared as if I am looking through a picture window.

The image briefly comes into focus so she was clear on what she was
seeing, and then a beam of white and gold light pierces the images
and shatters them into zillions of pieces, which immediately become
pure light. When she had these experiences she also felt and at
times saw physical releases within my body. She experienced deep
physical and emotional healing.

She describes Karuna being profoundly transformational for her as
Usui Reiki and she felt that it had come into her life to assist her
in her growth. She says how multi-dimensional Karuna feels to her.
She felt it working simultaneously on the emotional, mental and
physical bodies, and it has her me layers in her energy field and
within her consciousness that go beyond anything she can
intellectually comprehend. Karuna Reiki® takes her to that space
beyond form, color, time and sound that just cannot be described
within the constraints of words except perhaps, the purest sense of
peace, and total love she have ever felt.

Those words don't even do it justice.
She also had sensations of Karuna Reiki® reaching into other times,
connecting with karmic issues, and flashing through incarnations
linking them and bringing the related lessons to her conscious
awareness, and offering her the opportunity to transmute it in the
moment. So in this sense, she felt it very gracefully transcends
time and space on many levels simultaneously. She also used Karuna
Reiki® to do spirit release work with others.

phil







  In alzheimers_support@yahoogroups.com, "Diane(Dee)"
<runspencer4@c...> wrote:
> Hello. I hope this post finds everyone safe on this 4th of July.
My
> name is Dee. My Mother-in-law has the late stages of Alzheimer's
and
> my hubby will not join any support group. He jsut keeps it locked
up
> inside. I met my hubby in 1999(my second marriage) and also first
met
> his Mom then. In these past yrs she has declined terribly to the
point
> of being placed in a "home" just about 6 months ago. We live about
600
> miles from her, so hubby visits about 4-5 times a yr. The last
visit
> was the one he dreaded most. He met her wandering the halls that
day
> he arrived and walked and talked with her for 30 minutes and she
never
> even knew it was her son! He just kept walking and talking and
never
> said anything ti her about being her son. He asked her what her
name
> was and he said his name to her, and she replied, "ohhhh, I have a
> brother by that name". (she doesn't) I feel so bad for him and
don't
> know how to help him. He's one of those very big hearted "tough"
> guys..tattoos and all, but never lets his true feelings show. He
> believes she is fading quickly and even pre paid the funeral and
> arrangements are made by him and his sister."Mom" doesn't know
that,
> of course.
> I just needed to come here and "vent" and maybe find advice from
you
> experiences.
> Thanks for listening..and bless you all.
> Dee

#707 From: "Diane(Dee)" <runspencer4@...>
Date: Sat Jul 9, 2005 1:39 pm
Subject: Phil
runspencer4
Send Email Send Email
 
Thank you so much for the valuable, yet, overwhelming amount of
information you shared with me in the previous post.Thanks you for
allowing me to post. I have a lot of researching to do, don't I?

I will contue to read the posts here and try me best to support my
husband.
Thanks again
Dee

#708 From: cad721@...
Date: Sun Jul 10, 2005 2:00 pm
Subject: To dee
cadonn721
Send Email Send Email
 

Dee,

I am a little confused as to what the post from Phil had to do with your problem....I hope that it did not scare you away, I don't believe it belongs here...

My mother who will be 58 this month suffers from Alzheimers and is in the mid-late stages.  My father has a care taker at home full time to help him take care of her.  She is pacing the house constantly....talks to herself and does not remember most family member, she hasn't said my name in over a year.  I just gave birth to her first grandchild...Kieran, and some days she thinks he is a girl.  It breaks my heart.  There are some wonderful people that are on this site that have experienced this disease.  There are also other groups on Yahoo that are more active, this one is not very active.  I found "Dementiarescue" on yahoo groups that is a very active site for family and the patients suffering from dementia diseases.  I do not really know what to tell you, Alz. is so painful and it is so hard to see the mother we knew fade away and this disease take over.  And if your husband sdoesn't visit her ofter the changes will be very sign ificant.  I can understand why she was wandering the halls....my mom wanders the house all day, we try to get her to sit, watch tv, play a puzzle, it works only for a few minutes...

I really recommend that you look for the group I  mentioned above, it is very active.  I hope this helps a bit.

Cheryl


#709 From: "Diane(Dee)" <runspencer4@...>
Date: Sun Jul 10, 2005 3:51 pm
Subject: Cheryl
runspencer4
Send Email Send Email
 
Thanks for the post and the info. I will look the group up.
I must say I was confused, but not put off by Phil'd post. I know many
folks believe in theories ans methods that he mentioned and I am
willing able to read and try to apply anything that a person suggests.
I usually takw out what applies to me and "file away" the rest. I
don't ever want  to be rude to anyone who has taken their time to post.
Thanks again, Cheryl
I look forward to hearing from you again.
Dee

#710 From: "terry" <terry1953@...>
Date: Sun Jul 10, 2005 3:33 pm
Subject: Re: To dee
terry120953
Send Email Send Email
 

My mother who will be 58 this month suffers from Alzheimers and is in the mid-late stages.  My father has a care taker at home full time to help him take care of her.  She is pacing the house constantly....talks to herself and does not remember most family member, she hasn't said my name in over a year.  I just gave birth to her first grandchild...Kieran, and some days she thinks he is a girl.  It breaks my heart.  There are some wonderful people that are on this site that have experienced this disease.  There are also other groups on Yahoo that are more active, this one is not very active.  I found "Dementiarescue" on yahoo groups that is a very active site for family and the patients suffering from dementia diseases.  I do not really know what to tell you, Alz. is so painful and it is so hard to see the mother we knew fade away and this disease take over.  And if your husband sdoesn't visit her ofter the changes will be very sign ificant.  I can understand why she was wandering the halls....my mom wanders the house all day, we try to get her to sit, watch tv, play a puzzle, it works only for a few minutes...

That is so sad, Im so sorry. So young she is. I am 51, and I do repeat myself a lot and forget, but this all pretty much began when I started perimenopause last August. I hope it goes away. Unfortunately the gene is on my mom's side of the family, so I don't know. I never knew it affected people so young. My mom seems to be staying the same. Right now its just short term memory and some forgetfulness. A litle combative at times from what my dad says. I am grateful to have 81 healthy years with them. I appreciate all the warm welcomes...thank you. Terry

 


#711 From: Judie <jhensel@...>
Date: Sat Jul 16, 2005 8:44 pm
Subject: CBS News | Protein Key In Alzheimer's Fight? | July 15, 2005 12:00:16
deenaborracc...
Send Email Send Email
 
#712 From: "smoothshirley12" <smoothshirley12@...>
Date: Wed Jul 13, 2005 3:01 pm
Subject: Mail
smoothshirley12
Send Email Send Email
 
I had to change my user name and now am getting no posts.How can i
receive messages again?

#713 From: "hdscotland" <hdscotland@...>
Date: Mon Jul 18, 2005 11:04 am
Subject: stem cell research
hdscotland
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a story about stem cells is a story about hope. which my dictionary
tells me is to cherish a desire. for paul gallagher a 26 year old
from edinburgh he found out 5 years ago he had huntington's disease.
huntington's is a genetic condition that attacks nerve cells in the
brain. usually sufferers find out between the ages of 30 and 50 that
they have been given a death sentence. but dispite being so young
paul is already showing some of the classic signs of huntington's.
uncontrollable twitches and forgetfulness. huntington's has plagued
pauls family for generations. he was 8 when his mum hellen first
found out she had inherited huntington's from her father.for more
than 10 years paul helped nurse his mother through the condition. his
mum was only 42 when she died just a couple of months later pauls
uncle who also had huntington's died too.the symptoms can vary but
usually sufferers only have around 15 to 20 years to live after
diagnosis. pauls sister has just had the test to see if she has the
hd gene and it was very sad news for her and her  family. she had it
too.but dispite lots of research into the condition there still no
sign of a cure.however a private american foundation (the high q
foundation) dicided to sponsor the huntington's project with over
$57.000.000. the euro-hd network aims to provide a platform for
professionals and people affected by h.d to assist working together
throughout europe. it aims to facilitate natural history studies and
interventional trials meeting high standards thus helping on the road
towards a cure for h.d. paul is among the first in scotland to
registar for euro hd this month.but i think stem cells will bring
hope and not only to people with hd. if debilitating illness can be
conquered with stem cell therapy why is it so controversial. isn't it
a medical miracle to be celebrated ? yes and no. though we stand on
the threshold of the realm of possibility we are not yet inside it.
the door opened by science include one marked moral dilemma. many
scientists believe that stem cells from human embryos offer even more
hope for cures than the ones found in bonemarrow. yet to destroy
embryos to create stem cell therapies is an unforgivable obstacle for
many people.hope must break through the rhetoric. my own hope the
disire i cherish is that we can freely discuss the complex sometimes
uncomfortable,friction between science and ethics. that is what this
stem cell story is about. http://groups.msn.com/scottishhuntingtons

#714 From: Feather Forestwalker <feather@...>
Date: Wed Jul 20, 2005 6:15 am
Subject: Just a LOT of venting. . .combined e mails to family
featherbirdlady
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What I sent to the niece of my client, on June 26th, before her appointment at a memory center almost 200 miles away on June 30th):

1). How would certain anti-depressants interfere, if at all, with my client's current medications, currently at 10 mg SID Aricept and 10 mg BID Namenda?

2). She is currently taking "Calms Forte" to keep her from having outbursts.

3). Outbursts: at times my client gets extremely confused. This has led to extreme expressions of anger - which in turn has at times become violent. She has shoved, pushed, attempted to punch/slap me, and has thrown objects around. The first time was when she threw a book at me. I simply but firmly told her she couldn't be throwing things at me; she became a bit more angry, so I asked her if she wanted me to call a friend or her brother. I ended up calling her brother and he was able to calm her down. This was before I started actually working with my client. (I had been writing in the journal and reading it so I could get a better understanding of what people had been doing with her before taking on the job). The Calms Forte so far (since early June) has seemed to be working, but there are times she gets a little drowsy in the Day Program at the Alzheimer's/Senior Center. (This is new - since she's been off the Doxepin [for nervous scratching, which made her break out in rashes]- as, when she went off the Doxepin, she wasn't falling asleep in the Day Program. Now she is dozing during some of the activities and sometimes right before lunch).

4). How much longer will it be before she gets really lost when wandering? A few times, before I came on board, she would wander and the police would bring her back. Since I've been working with her, she's only had one incident where she got angry with me, threw an object on my porch into the parking lot, and stomped off in a huff. From there she ended up about two blocks away, flagging down cars, etc. Finally a CHP officer saw her and called the local PD. They picked her up and brought her to the hospital but refused to release her to me - pending the arrival of Adult Protective Services (APS). When APS arrived we talked, then they released her to them, and she came home. Later, I went over to fix dinner and it was as if nothing had happened; she was completely relaxed and smiling. Since then, she hasn't had a single violent outburst. It's been a couple of months - since after her brother and niece left in April (it was, I believe, approximately two weeks after their departure that this happened).

5). My client has slowly but surely deteriorated to such a degree that she needs help in figuring out her socks, bathing, dressing and after-toilet wiping. All her meals are made for her, but she occasionally gets into the refrigerator and finds things to eat. She of course leaves things lying around in odd places, but it's easy to pick up after her without being demeaning. :)

6). Another concern is that since she has been off the Doxepin, there have been some minor skin eruptions and she picks, occasionally, at these eruptions. We use Neosporin and after her showers she gets powder and Neosporin (the Retin A has stopped because it's $110.00 per tube and her insurance doesn't cover it).

Here is something from an online group (alzheimers@yahoogroups.com) that I am a member of. I never use her name, nor do I give away other personal details:

My client is always saying she wants to go "home," and I was reading in one of the many books I've read on Alz. Disease that it's usually a reference to a deep inner longing for something "familiar." Whenever she says this to me, I say, "I know, sweetie, let's take a look at this," and I pull out one of many photo albums she has. We start looking through them and she calms down. Other times I tell her, "Yes, I know - you want something familiar, right?" And she gets a relieved look on her face and nods emphatically, saying, "YES, I DO." So, we start again to look though photo albums, or I remind her of a trip she's taking in August, then show her the calendar and how far away August is. That gets her to calm down a lot. Sometimes it doesn't work.

In a nursing home situation, it must be harder for caregivers and family members to know exactly what to say when the patient says they want to go home. *sigh* All I can suggest is perhaps lying, saying something like what was already suggested regarding having tests done first, etc. Something else that might work is whenever you visit, if you have time, to take her or him on a day tip if they are mobile enough. A picnic, a walk in a park, etc. if they liked animals before, maybe a quiet trip to a zoo or a farm. If they liked flowers and gardening, a botanical garden or the local nursery. If they love little kids, a trip to a daycare center. . .something to distract from the webs of confusion going on inside of their heads. And at the return trip, lots of calm reassurance that you WILL be back and that you WILL be bringing them home as soon as the remodeling is done, or as soon as the hospital tests are done, or as soon as the new room is ready; whatever the lie, it's serving one purpose and one purpose only: it's keeping your relative calm and reassured under all circumstances.

One of the tricks I've learned with my client, who lives very close by so I can keep an eye on her, (she's an EOAD case), is that she cannot read numbers anymore. . .numerical forms confuse her. So, I've taken to writing out the date: example: Today is June Twenty-sixth instead of June 26th. She doesn't get the numbers at all, but is reasonably reassured when her calendar actually spells it out for her. So, each new day that I go in to feed breakfast and give meds is combined with the routine of writing on her erase-board the fact that: "Today is Sunday, June Twenty-sixth," and writing the word "Today" on the calendar she carries around with her. . .and another thing I've noticed with her is that she gets extremely confused the closer we get to the end of the month; she's not sure whether she should turn the page to the next month and even got so upset in March that she ripped out April's page entirely and tore it to shreds before anyone could see it.

=======

If there are more specific areas you need information in,  please let me know. Also, I trust you won't let my client read any of this. . .it may cause her to become agitated and angry. . .

Thanks,

Feather

=========================

Written June 27th:

Question for the doctor at the memory clinic:

Would my client benefit from the drug Exelon?

http://www.exelon.com/index.jsp?checked=y

Dear Niece,

My stepfather is taking this for his symptoms of dementia, which no one wants to diagnose as Alzheimers (he sure acts like he has it, though). . .

My mom says that so far, he's showing some minor improvements of symptoms.

Hope you're having a great day,

Feather

======================

My response to her response of my e mail about a new test I found on one of these lists:

Dated July 6th:

The niece wrote:

Hello Feather,
How is your client doing?


A bit disoriented after this last trip - she hasn't been this confused since her brother and other niece were here. It's no one's fault; it's just a fact of the situation - every time she has a lengthy visit or time away, she gets more confused.

Has she started the Seroquel yet?


Yes - we are starting the double-pill dose this evening. She so far is doing OK with it, but with the added confusion about everything that's happening (she asks "what's happening," a lot) it will be hard to tell until she settles back into the routine we have here. . .*if* she settles back in. You know how unpredictable this disease can get. . .and I am not totally sure, but I wonder if she's slipped further as a result of the disruption, or if she actually will eventually settle down? She did after the April visit, so who knows for sure? Certainly not I. I will keep observing, of course.


Let me know how she is doing --- I need to know if she can make the trip to her home state in August; the tentative dates are 8/8 to 8/13.  I asked Dr. * about the Alzemed study, and he said we should try to get her in.  The problem we might anticipate is that the study will probably want someone early in the course of the disease.  The way they identify these prospective patients is with a MMSE --- a mini-mental status exam.  The study will probably want a score of 15 or better, and, sadly, your client scores around an 8.

She scored around 4 with one of the aides at the Resource Center a couple of weeks ago. . .and before that, with someone from Community Care, she got around an 8 - but that was in her home and not at the center. . .or in an office. I wonder if that has anything to do with it?

She refused to take the exam with the doctor at the memory clinic.  I do not notice any specific change in your client's condition since last I saw her, but I would like to try for the study.

I would too. Problem would also be getting her there.

Question: is there any reason she cannot be on the new Exelon?

I did notice your client's myxedema in her legs, particularly the right side; can you mention that to the Physician's Assistant at your client's next appointment?

I most certainly will. The PA thought it might have been due to the Doxepin? She's been off that since March, I believe.

I believe it is worse at the end of the day after her legs have been dependent for a while.


OK, I will keep an eye on that.

Also, the doctor at the memory clinic stated that the oral Lamisil for your client's fungus infection would interact with her Alzheimer's meds.

Yes, that's what the PA said, too, if I remember correctly.

That nail is dead, so can you also ask the PA to remove it, and we will try to keep the fungus away by conscientious cleaning.

She is very good about cleaning. . .washing her feet and everything when I give her the wash cloth.  .I always remind her if she forgets. . .she sometimes gets confused in the shower, but with step-by-step reminders ("here comes the shampoo, rub that into your hair." "Good." "Now rinse." "Good." "OK, here comes the conditioner", etc and so forth), she handles it pretty well.

Thanks again, Feather, for all of your patience and hard work.

You're welcome; I would want this for me, know what I mean? If something ever happened to me like that, I would want to be helped, too. . .and when I was recovering from my surgery. . .I did get a lot of help. . .so I have been on both sides of this fence, up to a point. . .

I will leave a check for your week in your client's apartment if it turns out we are going to her home state.


No worries. I was talking to one of her friends and she said something about my client's Auntie coming? She thought it would be good if both you and her auntie were with my client on the flight to sort of box her in without making her *feel* boxed in. . .and to alert the airline staff that there's an EOAD person coming aboard on the day of her flight. . .to be alert for some minor episodes of confusion. . .that sort of thing, so that people don't panic. Just some ideas. . .

Hope you are well!

 

Feather

===================

(Written July 11th)

My client has been extremely agitated and depressed ever since returning from
a memory clinic on June 30th.

 I am wondering if it's just that she needs to get used to the
Seroquel, combined with the unavoidable disruption to her routine? What
do you think?

She's been crying, runs out to my van whenever she see's me arriving
home from somewhere, is hard to calm down, says, "I want to go HOME,"
and "I want ME back," and "I want my people," quite often. Last evening,
when a friend was scheduled to come take her out to dinner, she was
at my door every two to five minutes in the space of less than a half an
hour to ask what was happening. When her friend finally arrived, she
practically jumped into her car. . .and that threw the friend off a bit; she
almost forgot to get my client's  meds. Her friend took her to Mass, then to
dinner at a Pub down the coast. On their way home, just before
a bridge that leads into town, my client started freaking out - saying she didn't want to do
this anymore - saying she wanted herself back - saying she hates this town. . .when one of the other caregivers had her down the coast a while ago, he noticed
the same thing, and so did the new caregiver for weekends. (I
cannot take her down the coast because my vehicle won't make it that far
without overheating. I have to get a mechanic to look at the van to see
what needs fixing, then get an estimate to give to my mother, who is
going to either pay for it to be fixed, or send me the money to look
into buying a better vehicle).

Meantime, I believe (unless it's the Seroquel just needing to be in her
system for a while), that my client is slipping fast. She is more anxious
than ever about what's happening at any given moment, because she
doesn't remember what just happened. . .such as, she did not remember
this morning that she went out with her friend last night. She did not
remember anything of her trip with her niece to the memory clinic; she doesn't
remember freaking out at the day program last week and my having to
chase her down before she got hit by a car (I took her to the horse
ranch to calm her down and that worked for that moment, anyway). She
really needs more than what three daytime folks can give her. I think we
need to seriously start looking again for a live-in.

Barring that, we need to maybe look into a care facility. I personally
wouldn't recommend anything local - one local nursing home, in my not-so-humble
opinion, bites.  The one I would have thought would have been good for
my client has closed down, and even they were too close to the highway .

Here's a link to something that might help us find the right solution
for her:

http://www.calregistry.com/housing/res_care.htm

This site has a  number to call to get a list of good Residential Care
homes (like the other care facility locally, used to be). I worked for a short time at
there, and in terms of it being a homey environment with good
care, it was excellent. The owners lived in a smaller house behind the
facility and had hired help to work in the home doing meds and meals,
cleaning and personal care of the clientele, which numbered anywhere
from six to nine clients at a given time.

I am sure you've seen some of these kinds of facilities. I will get back
in touch with the neighbor upstairs from me, who said she'd
found an excellent Alzheimer's care facility.

It's coming down to the wire, the more confused and agitated she gets.
This is reminding me of when she was first coming to me asking for help,
when it seemed as if no one was caring for her. When I asked her today
if she wanted a shower, she refused, and I wasn't about to force it. It
took me about a half an hour after her return from down the coast last night
to calm her down. Usually, she just goes inside, smiling and happy, and
this friend sits with her for a while. She has forgotten how to get herself
ready for bed. So last night I sat with her, talking, made her some tea
and then helped her get ready for bed. She was so drowsy that she
eventually just teetered off into sleep, saying, "I don't want to do
this anymore. . ."

I hope that this hasn't been too unsettling for you.

(remember, this was written to her family member and one other very close friend).

It very well could be that she needs to adjust to the Seroquel - but for
now, it seems to be making her seem more confused and agitated.

Right now she is out with the weekend caregiver, which is the only reason I could sit
down and write this. Prior to this she was in and out of the apartment,
looking very scared and confused. I left for a meeting at around 3:15
and when I returned at around 5 PM, my son said that she had come by
crying and saying she didn't want to "do this, I want to be down THERE,"
more than likely indicating a town down the coast from here, because whenever I ask her if
that's what she means lately, that's when she nods her head. . .if we
could find a caregiver to live in with her in that town, that would be
excellent. She really doesn't like this town. . .*sigh* Her moments of
clarity combined with her moments of confusion and agitation are wearing
her out. She's exhausted, the poor thing. And more aware of what's wrong
than ever.

I will keep working for her of course, until such time as my services
are no longer needed.

==========================

What I wrote on July 13th to the relative:

Last evening, about 45 minutes after my client received her evening meds, I
was in the back bedroom at my apartment, going through my closet.
Apparently, she had been walking back and forth between my apartment
and hers, looking for me. She went back to her place and started
slamming her door, over and over again (nothing new; it's just been a
while since she's done this). Her neighbor in another apartment,
above and to the left of my client's apartment, heard the noises and came
downstairs to try and calm her down. She wasn't to be calmed by this neighbor,
and apparently (allegedly) grabbed her arm and dug her fingernail
into her hand, drawing blood. The neighbor went up to her apartment then and
called the police (!).

About five seconds afterwards, I was out in my livingroom and heard my client
at my window. So, I went over to her apartment with her. She had gotten
dressed again in her regular clothes, (I had gotten her into a
nightshirt shortly before dark), and seemed scared and also angry. It
surprised me, because she was almost docile when I'd left her earlier.
While I was getting my client settled on the couch with a blanket and her
cocoa, the neighbor came pounding on my client's door when she heard my voice and
told me what had happened. I was shocked, and said to her that calling
the police in that situation wasn't appropriate. She got angry with me
and my client slammed the door in her face. A picture of a woman with a
horse fell off the wall and the glass broke. (The male caregiver and I are going to
get rid of all glass inside frames at this point). I cleaned up the
glass, got my client re-settled on the couch and went outside to find the neighbor.

She was up at the head of the parking lot telling two little girls (!)
what had happened. Sheesh. So, when the officers arrived (Officers
"X" and "O"), they very quickly and efficiently assessed the
situation and told the neighbor that the next time something like this happens
with my client slamming doors, to call ME and NOT intervene again, for "your
own protection." This neighbor is the type of person who is rather loud and
completely oblivious of a person's personal space. She's definitely got
a mental condition, so I cannot totally blame her, but the police
officers were very accomodating to my client and when my client came out in her
nightshirt I quietly guided her back to her apartment with promises of
another very close friend coming (which she is today at noon) and promises that if we
keep ourselves very calm, that her auntie and niece are going
to bring her to her home state in a month. She calmed down and after I finished
giving the police my information and returned to my apartment to call
Adult Protective Services to let them know what happened, I went back over. My client was very
thankful and finally beginning to calm down. It was about 9:30 PM when I
left her. . .

This morning she was smiling and happy to see me. . .and I got her
cleaned up (the blister on the bottom of her foot is healing, but she
has a new one on the top of the same foot that she let me pop and put
Neosporin on after her shower. Then a bandaid, clean socks and shoes. .
.she's definitely ready to go somewhere with her other friend when she gets here.

I am letting you (remember, I am writing to her niece here,) know that this happened because I think the neighbor may complain to the owner of the building about my client. The cops
didn't really take the neighbor too seriously, but she is a reactionary kind of
person and I am afraid, that since she's the oldest tenant in this
building, that she might use that as some kind of leverage against my client.
You might want to call him (gave numbers to both the owner and the assistant manager at this point).

Feather
===============================
July 17th:

These last few days have been more peaceful; my client is decidedly *less* agitated and confused, though depression seems stronger - she was weepy and teary-eyed today, for example.

I calmed her down with the thoughts that I have calls in to various people. She's especially *keen* lately, on going "home," and wants to hear fromher auntie. She has managed to connect Auntie and Niece with her home state and "home," but more often than not when I ask her if she just wants something more familiar, she nods her head and says "YES!" most emphatically.

Her walking in an agitated manner has decreased. (Partly due to blisters and pains in her legs, for which I have gotten some physical therapy prescribed, to begin on July 19th, 2 X per week for 4 weeks).

She is sundowning a little bit less now, too.

I do find that now I have to help her get into bed at night; she seems to really appreciate the extra attention. She will put on pajamas for me, whereas before she would refuse, most vehemently. She retires earlier; around 8 PM instead of 9 PM.

The Calms Forte are better for calming her down than the Seroquel was, that's for sure.

I was reading about Vitamin B deficiency and Alzheimer's:

http://www.google.com/search?hl=en&q=Alzheimer%27s+Disease+and+Vitamin+B&btnG=Google+Search

That's the search results, and since Vitamin B is great for warding off depression, I wondered if it would be OK to get her on a Vitamin B Complex capsule or tablet, and which type would you recommend?

Again, I think a trip to her home state to see her family would be good for her - IF her auntie can be involved in the process (provided she wants to?). She is calming down enough now to be easier to talk to, though of course I also think that the changes to her routine would be a bit disruptive.

So, with that in mind, here's what usually happens when I am there:

8 AM, I go over, crack some jokes and start breakfast. Sometimes I act really goofy as I am cooking (i.e., faking crying over spilt milk should I happen to dribble a bit on the counter, for example - for some reason that really makes her laugh). She is seated and eating at the table with a bowl of cereal with a teaspoon of goat's whey sprinkled over it before the main part of her breakfast. Orange juice and Think O-2 tea with a teaspoon of honey are given also. As she begins her main course, she gets her meds. She will hold out her hand and I dump them into the palm of her hand and then mimic popping them into my mouth as she watches and copies what I do. If I DON'T pretend to take them, she will dump them in her juice (oops). So, that's the method I've developed to get her to take them on her own. There are times when she remembers and just does it without any prompting, but these are becoming fewer and farther between. Then I wash the dishes as she finishes eating and she always brings me her dishes.  Then we head into the bedroom to have her remove her clothes for a shower.

Once in the shower, she rinses her hair on her own. Then I mix shampoo and conditioner into the palm of my hand, and when her hair is wet, I say, "OK, now I am putting the shampoo into your hair." She vigorously massages that combo into her hair and then just as vigorously rinses it out. While she is doing that, I get her washcloth damp, and then pour some Aveeno scrub into it, lathering it up. When she's done rinsing out her hair, I tell her to "Wash your body off now," and make sure she gets those "hard to reach areas." Often, I wash her back while she is rinsing out the shampoo-conditioner. . .she really relaxes when she's done with her shower.

I set out clothes prior to the shower, with her approval. This has gotten easier. She appreciates the two or three newer pairs of pants she's gotten, and has figured out how to wear the drawstring pants that her friend got her: she removed the drawstring! :)

Before using lotion, I have her use baby powder between her legs and under her breasts. This is corn starch type, not talcum - it's better for her. It lessens the chafing that comes at her upper thighs. Then she dresses and I have to show her to put the socks on each foot, or she will put two socks on one foot and NO sock on the other. She remembers to put her shoes on correctly, though. Then we go in, brush her teeth and then out to the kitchen to blow dry and brush her hair, which she loves.  Inevitably, if we aren't planning a trip to the Day Program, she will start asking me lots of questions about "going down THERE now," and about going "home" and the like. This to me, is showing her anxiety over the fact that I have to leave. If, for example, the shower and stuff are on a Monday (I do showers for her every other day, sometimes every day, if she's had a particularly trying day walking, for example, and gets all sweaty - on those occasions, she will have a shower each day), and I have to leave and the male caregiver is coming a little bit later, she will start getting a bit anxious. That's when I tell her that we're working on stuff and that it's all good; lately this calms her down.

Lunchtime is variable: the male caregiver does lunch Mon Wed Fri, and I take her to the day program for lunch on Tue and Thur. The weekend caregiver does lunch on Sat / Sun, and sometimes a friend will come and take her for lunch. These variables in her routine do not seem to bother her.

Dinner is usually at 5 or 6 PM - sometimes later if a friend is coming, and this variation in her routine does seem to bother her a bit. I will make the dinner and make the "good tea" (Think O 2) and a cup of hot cocoa. For dessert lately, it's been light icecream. (The weekend caregiver made her an apple cobbler yesterday, tho). I give her the meds in the same fashion as breakfast. She spit them out at the weekend caregiver last weekend, but took them for me. . .depends on whether she's been upset or not, I guess.

I took her friend's advice and am going over every night before bedtime to make sure she's settled in for the night. She appreciates that, and I can tuck her into bed and turn off all the lights so she gets a full night's sleep. She's very good with me about that now. AND, I am LOCKING the door at night just to be safe. That way no one can just walk in there when she's asleep.

Again, my client is calming down and taking things with better humor than before. She is, however, somewhat depressed. She *does* know that something's wrong with her and will sometimes mention it. But she manages the best she can.

God bless,

Feather

===============================

What I wrote to the niece and her friend on July 18th:

The door experiment's a definite wash. After bed last night, my client decided to go out and walk. . .she was depressed and sad, but not too agitated. She did knock some stuff off the shelf on my porch in her angst, but it's nothing I can't replace. She's more sad than angry.

Took about a half an hour to calm her down and get her to sleep; reminded me of the times I had to calm my kids down after a nightmare, she is that childlike when tired. By 9:30 PM she was happily tucked away into bed. So, of course, I decided to keep the door locked.

This morning she awoke early and again locked herself out. The apartment manager called me at about 6:30 AM to let me know that she needed to be let back in. So, I went over and again, it took half an hour to calm her down; by 7 AM, after much weeping and saying "I want to go HOME," I got her to eat breakfast and take her meds. She wouldn't eat dinner last night for the weekend caregiver, but I managed to get something into her simply by telling her she didn't have to eat it if she didn't want to.

I really would like to see her get on Vitamin B Complex, but want her niece's input before I go forward with having the male caregiver pick some up.

Hope you're both well,

Feather

=======================

Finally, THIS morning, July 19th:

Hi, Niece,

Today my client is *VERY* depressed. She's been crying off and on for *days* and was agitated this morning at the Senior Center to the point of storming out. When I got outside, I called her name, and she turned around with that all-too-familiar glare in her eyes.

She'd started getting agitated and very quiet right after her shower this morning. This was shortly after forgetting how to use the wash cloth, how to shampoo her hair and how to dress herself - it's getting to the point where she needs help with each step, even more than before. "The sock goes on THAT foot," for example, whenever she attempted to put the sock on the same foot she's just put a sock on. (I suppose that when she's alone and putting them on, that's how it goes, but usually when I am there, she gets it just RIGHT. Today she didn't.) She forgets how to put the toothpaste on the brush and I have to do it for her or show her to remind her. She almost forgot to spit the water in her mouth out into the sink after brushing; something she NEVER forgets usually.

Finally, as she forgot each step, she said, "I don't know what I'm DOING." And I said, "That's OK, that's why I am here, to help you stay focused." It seemed to relieve her temporarily, but as each thing slips and she's more aware that it is slipping, she becomes more depressed and agitated. The agitation today had the potential to turn into something bad physically, so we walked it off. During the walk, she was not interested *at all* in flowers or gorgeous houses, as is usually the case. The *only* thing that *temporarily* calmed her down was playing with some friends dogs for a few moments.

Nothing I did would calm her completely down. She remains depressed, even after talking with one of her best friends, which never fails to calm her down. NOTHING her friend could say would work - my client says "I want to go HOME," a lot and is *very* confused about nearly everything.

I finally left her with the television turned to I LOVE LUCY and later, she was out walking, slowly walking. . .then she went back home. I am heading over in a few to do lunch and then take her to a physical therapist who she has been assigned to to get some mild exercises for her back and legs, which seem to be bothering her even more.

We need to get her on an antidepressant that won't interfere with her meds and that won't make her memory worse. (I read that Paxil can make memory problems worse, but have yet to verify that with any documentation that I can research online, so perhaps you can find out more than I at this point).

Please let me know what the doctor at the memory clinic says about vitamin B complex in the interim, and let's get her on some antidepressants ASAP. . .for now, at least, the depression is calm, but she cries so often it breaks my heart.

Thanks in advance,

Feather

=================

OK, those of you who have actually managed to read this far, THANK YOU.

Please let me know if you think there is anything I can do to make this better?

I have yet to hear back from the niece on most of the topics. . .she is a nurse, in case you were wondering.

Thanks in advance,

Feather, who is exhausted, but glad that tonight, her client was happy. .




#715 From: "jd_1951_54" <jd_1951_54@...>
Date: Wed Jul 27, 2005 11:01 pm
Subject: Re: Just a LOT of venting. . .combined e mails to family
jd_1951_54
Send Email Send Email
 
--- In alzheimers_support@yahoogroups.com, Feather Forestwalker
<feather@e...> wrote:
> Hi Feather, "I want to go HOME"...I truly believe "Home is where
the heart is"...a place of comfort that doesn't exist anymore for
her. Takes alot of work to try and recreate that special place we all
desire.

You Wrote: It very well could be that she needs to adjust to the
Seroquel - but for
now, it seems to be making her seem more confused and agitated.

Reply:BRAND NAME(S):
Seroquel
View images

WARNING:
Learn more

USAGE:
This medication is used for the treatment of certain mental
conditions (e.g., schizophrenia, the manic stage of bipolar disorder).


Warning on Drugs for Elderly Behavioral Issues

FDA Orders Warning Labels After More Deaths Seen in Elderly Patients
With Dementia

By Miranda Hitti
WebMD Medical News Reviewed By Michael  Smith, MD
on Monday, April 11, 2005

April 11, 2005 -- The FDA has issued a public health advisory about
certain drugs used to treat behavioral problems in elderly patients
with dementia.

That's an unapproved use of the drugs, called antipsychotic drugs,
which include:

Abilify
Zyprexa
Seroquel
Risperdal
Clozaril
Geodon
Symbyax, which is approved for treating depressive episodes
associated with bipolar disorder.
The FDA's warning does not extend to people who are taking the drugs
for the approved uses - treating schizophrenia and mania.

These drugs are sometimes used to treat agitation and other behavior
disturbances in elderly patients with dementia, such as Alzheimer's
disease. Doctors should review treatment for elderly patients with
dementia who are taking the drugs for behavioral problems, says the
FDA's advisory.

More Deaths

The FDA's decision was based on 17 studies of four of the drugs
(Zyprexa, Abilify, Risperdal, and Seroquel) in elderly patients with
dementia and behavioral disorders.

In those studies, the death rate was about 1.6 to 1.7 times higher
for elderly patients with dementia than for those taking a placebo.

The causes of death varied. Most seemed to be either heart-related
(such as heart failure or sudden death) or from infections (mostly
pneumonia), says the FDA.

Atypical antipsychotic drugs fall into three categories based on
their chemical structure. Because the increased death rate was seen
with drugs from all three classes, the FDA concluded that the effect
is probably related to common effects of all such drugs, including
those drugs that haven't been studied in people with dementia.

New Warning Labels

The FDA has asked the drugs' makers to add a boxed warning to the
drugs' labels describing the risk. The label will also note that the
drugs are not approved for the treatment of behavioral symptoms in
elderly patients with dementia.

The FDA says it's considering adding a similar warning to the
labeling of older antipsychotic medications, such as Haldol, because
limited data also suggest a similar increase in deaths for these
drugs. However, the FDA's review of data on those older drugs isn't
done yet, says an FDA news release.


----------------------------------------------------------------------
----------

SOURCE: FDA Public Health Advisory, "Deaths with Antipsychotics in
Elderly Patients with Behavioral Disturbances." News release, FDA.

Feather, your observations I beleive are correct. The info above came
from WebMDHealth.com (Drugs & Herbs) it's a good site for checking
out meds.

It takes alot of tender loving care Feather. I've been caring for my
wife now, by myself, for 10 years. It's sad what happens to people
with Alzheimer's. They need special care 24/7 that most will never
receive because there is no one willing to go the distance. Sometimes
I don't know if I can. I'm 54 years old. I whole life is now
dedicated to taking care of my wife 24/7. Neither of us has any
family willing to help. You are a very caring person I can tell. God
Bless you Feather....he knows you are doing the best you can for this
lady and then some.....I don't feel or believe that more drugs are
the answer....... Jd

#716 From: "baymarekz" <baymarekz@...>
Date: Tue Aug 2, 2005 12:12 pm
Subject: Re: Just a LOT of venting. . .combined e mails to family
baymarekz
Send Email Send Email
 
You have to watch the side effects of these drugs. My Mom really had
trouble swallowing after taking Zyprexa and Risperdal, but she did
very well on Seroquel.Almost all of the drugs lost effectiveness
after about 6 months of use. Don't know if this is typical for
Alzheimers sufferers but it seemed like we needed to switch at the 6
month mark. Now that she is beyond the point of needing these drugs
she is only on Ativan to control muscle twitches.

KZ

--- In alzheimers_support@yahoogroups.com, "jd_1951_54"
<jd_1951_54@y...> wrote:
> --- In alzheimers_support@yahoogroups.com, Feather Forestwalker
> <feather@e...> wrote:
> > Hi Feather, "I want to go HOME"...I truly believe "Home is where
> the heart is"...a place of comfort that doesn't exist anymore for
> her. Takes alot of work to try and recreate that special place we
all
> desire.
>
> You Wrote: It very well could be that she needs to adjust to the
> Seroquel - but for
> now, it seems to be making her seem more confused and agitated.
>
> Reply:BRAND NAME(S):
> Seroquel
> View images
>
> WARNING:
> Learn more
>
> USAGE:
> This medication is used for the treatment of certain mental
> conditions (e.g., schizophrenia, the manic stage of bipolar
disorder).
>
>
> Warning on Drugs for Elderly Behavioral Issues
>
> FDA Orders Warning Labels After More Deaths Seen in Elderly
Patients
> With Dementia
>
> By Miranda Hitti
> WebMD Medical News Reviewed By Michael  Smith, MD
> on Monday, April 11, 2005
>
> April 11, 2005 -- The FDA has issued a public health advisory about
> certain drugs used to treat behavioral problems in elderly patients
> with dementia.
>
> That's an unapproved use of the drugs, called antipsychotic drugs,
> which include:
>
> Abilify
> Zyprexa
> Seroquel
> Risperdal
> Clozaril
> Geodon
> Symbyax, which is approved for treating depressive episodes
> associated with bipolar disorder.
> The FDA's warning does not extend to people who are taking the
drugs
> for the approved uses - treating schizophrenia and mania.
>
> These drugs are sometimes used to treat agitation and other
behavior
> disturbances in elderly patients with dementia, such as Alzheimer's
> disease. Doctors should review treatment for elderly patients with
> dementia who are taking the drugs for behavioral problems, says the
> FDA's advisory.
>
> More Deaths
>
> The FDA's decision was based on 17 studies of four of the drugs
> (Zyprexa, Abilify, Risperdal, and Seroquel) in elderly patients
with
> dementia and behavioral disorders.
>
> In those studies, the death rate was about 1.6 to 1.7 times higher
> for elderly patients with dementia than for those taking a placebo.
>
> The causes of death varied. Most seemed to be either heart-related
> (such as heart failure or sudden death) or from infections (mostly
> pneumonia), says the FDA.
>
> Atypical antipsychotic drugs fall into three categories based on
> their chemical structure. Because the increased death rate was seen
> with drugs from all three classes, the FDA concluded that the
effect
> is probably related to common effects of all such drugs, including
> those drugs that haven't been studied in people with dementia.
>
> New Warning Labels
>
> The FDA has asked the drugs' makers to add a boxed warning to the
> drugs' labels describing the risk. The label will also note that
the
> drugs are not approved for the treatment of behavioral symptoms in
> elderly patients with dementia.
>
> The FDA says it's considering adding a similar warning to the
> labeling of older antipsychotic medications, such as Haldol,
because
> limited data also suggest a similar increase in deaths for these
> drugs. However, the FDA's review of data on those older drugs isn't
> done yet, says an FDA news release.
>
>
> --------------------------------------------------------------------
--
> ----------
>
> SOURCE: FDA Public Health Advisory, "Deaths with Antipsychotics in
> Elderly Patients with Behavioral Disturbances." News release, FDA.
>
> Feather, your observations I beleive are correct. The info above
came
> from WebMDHealth.com (Drugs & Herbs) it's a good site for checking
> out meds.
>
> It takes alot of tender loving care Feather. I've been caring for
my
> wife now, by myself, for 10 years. It's sad what happens to people
> with Alzheimer's. They need special care 24/7 that most will never
> receive because there is no one willing to go the distance.
Sometimes
> I don't know if I can. I'm 54 years old. I whole life is now
> dedicated to taking care of my wife 24/7. Neither of us has any
> family willing to help. You are a very caring person I can tell.
God
> Bless you Feather....he knows you are doing the best you can for
this
> lady and then some.....I don't feel or believe that more drugs are
> the answer....... Jd

#717 From: "rouxlily1968" <rouxlily1968@...>
Date: Tue Aug 2, 2005 2:25 pm
Subject: I feel like I am losing my mind too
rouxlily1968
Send Email Send Email
 
I am not only child whose mother has alzheimer's.  I did not realize
how much it had progressed with her until she recently had knee
surgery and I had to stay with her.  I am currently looking to move
her closer to me. Does anyone have any suggestions to make this an
easier process?

I am very stressed out which is not good for me either.  I have a
seizure disorder which is often triggered by stress..HELP!!!

#718 From: "JD" <jd_1951_54@...>
Date: Wed Aug 3, 2005 8:46 pm
Subject: Re: I feel like I am losing my mind too
jd_1951_54
Send Email Send Email
 
--- In alzheimers_support@yahoogroups.com, "rouxlily1968"
<rouxlily1968@y...> wrote:
> I am not only child whose mother has alzheimer's.  I did not realize
> how much it had progressed with her until she recently had knee
> surgery and I had to stay with her.  I am currently looking to move
> her closer to me. Does anyone have any suggestions to make this an
> easier process?
>
> I am very stressed out which is not good for me either.  I have a
> seizure disorder which is often triggered by stress..HELP!!!

Reply: It may be the extra medication shes taking for pain, etc.,
making thing harder for her and you. You say move her closer to you?
Are you going to move her in with you? Now might be the time to look
for a long term placement unless you want to take care of her yourself
which is a life long commitment. Lots to consider. Be careful about
Assisted Living Facilities unless they have a very good Alzheimer's
Unit....Please feel free to email me....Jd

#719 From: "JD" <jd_1951_54@...>
Date: Thu Aug 4, 2005 12:57 pm
Subject: Re: CBS News | Protein Key In Alzheimer's Fight? | July 15, 2005 12:00:16
jd_1951_54
Send Email Send Email
 
Thanks for posting this very interesting and important information. We
need all the "HOPE" we can get. I saved the link and will follow up on
the research.....Ibthere....Jd


--- In alzheimers_support@yahoogroups.com, Judie <jhensel@c...> wrote:
>
> <http://www.cbsnews.com/stories/2005/07/15/health/main709348.shtml?
cmp=EM8707>

#720 From: "Telitha" <telitha@...>
Date: Thu Aug 4, 2005 6:29 pm
Subject: Re: I feel like I am losing my mind too
telithaaw
Send Email Send Email
 
Keep everything you can in her bedroom the same as it was in her home. This will make her feel more secure.
Alzheimer's patients get lost in strange surroundings. Even changing bedspreads and curtains can be a dramatic change for them.
 
If at all possible put her own things in her bedroom so she can tell that is her home.
 
Hang in there. You will find this group and Alzheimer'sCaregiving@yahoogroups.com will be a lifesaver as you travel this unfamiliar road. We have been there, are there or will be there. We are here for you. The beauty of the e-mail groups is you can write when you can and read when you can.
 
My Husband had Alzheimer's for 12 years. He went to Heaven March 22, 2005. He was able to stay here at home and knew everyone of us all the way to the end.
 
Let me know any time I can help.
 
Forever Friends, Telitha
----- Original Message -----
Sent: Tuesday, August 02, 2005 9:25 AM
Subject: [alzheimers_support] I feel like I am losing my mind too

I am not only child whose mother has alzheimer's.  I did not realize
how much it had progressed with her until she recently had knee
surgery and I had to stay with her.  I am currently looking to move
her closer to me. Does anyone have any suggestions to make this an
easier process?

I am very stressed out which is not good for me either.  I have a
seizure disorder which is often triggered by stress..HELP!!!






#721 From: "angela147g" <angela147g@...>
Date: Sun Aug 7, 2005 5:06 am
Subject: Feel like I cant take it anymore
angela147g
Send Email Send Email
 
Hi everyone. If anyone has any suggestions please tell me because I
feel like i'm going crazy.
  I take care of my 84 y old aunt who has ad. She lives with me and
my husband and has for the last two years. She is in late middle
stage.
  We just returned from a three week trip visiting my mom (who is her
sister) who she is and has always been very close to, so she was
very happy to be going to see her.
  Well, as it turned out, I think the trip might have been a hugh
mistake.
  Needless to say, the traveling part was a trip in itself. She was
completely disoriented and confussed the entire time. She had no
idea where she was, couldnt understand that this was at my mothers
house and it was not ours. Could not remember or understand that we
did not live there etc.
   Now that we left and are home, she is constantly looking for my
mom, thinking that my mom lives here, forgot that we went there and
were there for the all that time and is constantly asking if and
when can we go to see her. This is constantly, when  I tell her that
we just came back and that we cant go again for a while, (if ever,
<I dont tell her that ofcourse) but when I tell her that she cant
understand and gets very depressed. I dont know how to handle
this , I need help, advice or suggestions of what to tell her when
she looks for my mom or asks when can we go see her etc. I call mom
on the phone so she can talk to her but then in 5 mins she forgets
that she spoke to her and starts the whole thing all over again .
What should I do ?  Should I try to explain that we were just there
and that she lives very far away and that we can not go there for a
while etc, or should I tell her something else? Anyone have any
simular sitation or any suggestions please ? I feel like I dont know
how to handle this problem and need help.
I hope someone can lend some advice, any , I will truely appreciate
Thanks for listeing and I will be looking for your suggestions and
help. I dont know where to turn for help other then here. Thanks
again

#722 From: "pjb12345uk" <pho@...>
Date: Sun Aug 7, 2005 7:18 am
Subject: Re: Feel like I cant take it anymore
pjb12345uk
Send Email Send Email
 
---the power of prayer can help and despite what some other rude and
ignorant people on the group think
spiritual and or reiki healing can help too
see my other posts for more info
p

  In alzheimers_support@yahoogroups.com, "angela147g"
<angela147g@y...> wrote:
> Hi everyone. If anyone has any suggestions please tell me because
I
> feel like i'm going crazy.
>  I take care of my 84 y old aunt who has ad. She lives with me and
> my husband and has for the last two years. She is in late middle
> stage.
>  We just returned from a three week trip visiting my mom (who is
her
> sister) who she is and has always been very close to, so she was
> very happy to be going to see her.
>  Well, as it turned out, I think the trip might have been a hugh
> mistake.
>  Needless to say, the traveling part was a trip in itself. She was
> completely disoriented and confussed the entire time. She had no
> idea where she was, couldnt understand that this was at my mothers
> house and it was not ours. Could not remember or understand that
we
> did not live there etc.
>   Now that we left and are home, she is constantly looking for my
> mom, thinking that my mom lives here, forgot that we went there
and
> were there for the all that time and is constantly asking if and
> when can we go to see her. This is constantly, when  I tell her
that
> we just came back and that we cant go again for a while, (if ever,
> <I dont tell her that ofcourse) but when I tell her that she cant
> understand and gets very depressed. I dont know how to handle
> this , I need help, advice or suggestions of what to tell her when
> she looks for my mom or asks when can we go see her etc. I call
mom
> on the phone so she can talk to her but then in 5 mins she forgets
> that she spoke to her and starts the whole thing all over again .
> What should I do ?  Should I try to explain that we were just
there
> and that she lives very far away and that we can not go there for
a
> while etc, or should I tell her something else? Anyone have any
> simular sitation or any suggestions please ? I feel like I dont
know
> how to handle this problem and need help.
> I hope someone can lend some advice, any , I will truely
appreciate
> Thanks for listeing and I will be looking for your suggestions and
> help. I dont know where to turn for help other then here. Thanks
> again

#723 From: Feather Forestwalker <feather@...>
Date: Sun Aug 7, 2005 3:55 pm
Subject: Re: Feel like I cant take it anymore
featherbirdlady
Send Email Send Email
 
angela147g wrote:

>Hi everyone. If anyone has any suggestions please tell me because I
>feel like i'm going crazy.
> I take care of my 84 y old aunt who has ad. She lives with me and
>my husband and has for the last two years. She is in late middle
>stage.
> We just returned from a three week trip visiting my mom (who is her
>sister) who she is and has always been very close to, so she was
>very happy to be going to see her.
> Well, as it turned out, I think the trip might have been a hugh
>mistake.
> Needless to say, the traveling part was a trip in itself. She was
>completely disoriented and confussed the entire time. She had no
>idea where she was, couldnt understand that this was at my mothers
>house and it was not ours. Could not remember or understand that we
>did not live there etc.
>  Now that we left and are home, she is constantly looking for my
>mom, thinking that my mom lives here, forgot that we went there and
>were there for the all that time and is constantly asking if and
>when can we go to see her. This is constantly, when  I tell her that
>we just came back and that we cant go again for a while, (if ever,
><I dont tell her that ofcourse) but when I tell her that she cant
>understand and gets very depressed. I dont know how to handle
>this , I need help, advice or suggestions of what to tell her when
>she looks for my mom or asks when can we go see her etc. I call mom
>on the phone so she can talk to her but then in 5 mins she forgets
>that she spoke to her and starts the whole thing all over again .
>What should I do ?  Should I try to explain that we were just there
>and that she lives very far away and that we can not go there for a
>while etc, or should I tell her something else? Anyone have any
>simular sitation or any suggestions please ? I feel like I dont know
>how to handle this problem and need help.
>I hope someone can lend some advice, any , I will truely appreciate
>Thanks for listeing and I will be looking for your suggestions and
>help. I dont know where to turn for help other then here. Thanks
>again
>
>

I have similar troubles with my early-onset client.

What I have done is simply, lie to her.

Since she forgets stuff in five minutes anyway, the lie that her
friend/relative/ will be coming to see *her* (especially after she's
been gone on a long visit to see *them*), seems to calm her down. After
several repetitions of this in the most reassuring tone I can muster,
she eventually calms down.

My client is also on Lexapro for depression, now at 10 mg per night. In
addition, she's on Namenda, one 10 mg tab in the morning, one at night,
and Aricept, one ten mg tab in the morning. She also takes flax seed
capsules three times a day, vitamin E, a multi-vitamin, some fiber,
folic acid, and Calms Forte, two tabs, three times a day (breakfast,
lunch and dinner). It works to keep her calm.

What I suggest to people who've seen me working with her and are amazed,
is to find what works for them. What works for me may not work with
others, see, even those who are working with her on a regular basis as I
do.While *my* lie might work, other people may not be able to use the
same lie. So they have to find whatever works.

I would recommend that you find a calm place to go to regroup - you may
need a small vacation. And you may need to call someone to come sit with
her while you take a mini-vacation which can be anything from a walk, to
a trip to the library alone - whatever *you* need to do to take this
respite for yourself will be important for your abilities to care for
your aunt on a day-to-day basis. It's NOT easy - and please forgive me
if I seem presumptuous here. . .

I hope you feel comfortable venting in this format; I wrote a
several-page long "venting" post to some other Alzheimer's groups a few
weeks ago; that helped me a lot, just to get stuff off my chest.

Meantime, find your lie. I know that sounds weird, but find it and just
go along with her delusions and the like; it will be a lot easier than
fighting and correcting, and easier than trying to explain that she's
already been there. IF you have photos of the trip, you might try
showing them to her and explain *then* that she has already been there.
IF, however, this does nothing but confuse her more, put the photos away
and go back to lying that your mom is coming to see her very soon.

Wishing you the very best,

Feather

#724 From: DON BURZEN <donburzen@...>
Date: Sun Aug 7, 2005 7:40 pm
Subject: Re: Feel like I cant take it anymore
isitstress
Send Email Send Email
 
Thank you, Feather, for being so blunt; as I do agree with you.
 
My wife has a harder time dealing with my mother's Alzheimer's than I do, because she wants to always tell the absolute truth.  While that is certainly the right way to deal with most of life's situations, this is not one of them.  The priority in cases like this is to calm the patient; and if stretching the truth is what it takes to do so, I feel the end justifies the means.
 
Angela, I get through these situations thinking more of telling "a story", rather than a "lie".  (Same reality; but easier to accept personally.)
 
As Feather says, our relatives who are at this stage will not come back and question later on whether our response actually came true.  However, if we try to get him or her to understand the real situation, we are in for nothing but frustration...on both sides of the discussion.
 
There are no easy answers for all situations, but trying to make someone with this dread disease understand the true facts is often a no-win situation for everyone concerned.
 
Good luck, and all the best,
 
Don
 


Feather Forestwalker <feather@...> wrote:
angela147g wrote:

>Hi everyone. If anyone has any suggestions please tell me because I
>feel like i'm going crazy.
> I take care of my 84 y old aunt who has ad. She lives with me and
>my husband and has for the last two years. She is in late middle
>stage.
> We just returned from a three week trip visiting my mom (who is her
>sister) who she is and has always been very close to, so she was
>very happy to be going to see her.
> Well, as it turned out, I think the trip might have been a hugh
>mistake.
> Needless to say, the traveling part was a trip in itself. She was
>completely disoriented and confussed the entire time. She had no
>idea where she was, couldnt understand that this was at my mothers
>house and it was not ours. Could not remember or understand that we
>did not live there etc.
>  Now that we left and are home, she is constantly looking for my
>mom, thinking that my mom lives here, forgot that we went there and
>were there for the all that time and is constantly asking if and
>when can we go to see her. This is constantly, when  I tell her that
>we just came back and that we cant go again for a while, (if ever,
><I dont tell her that ofcourse) but when I tell her that she cant
>understand and gets very depressed. I dont know how to handle 
>this , I need help, advice or suggestions of what to tell her when
>she looks for my mom or asks when can we go see her etc. I call mom
>on the phone so she can talk to her but then in 5 mins she forgets
>that she spoke to her and starts the whole thing all over again .
>What should I do ?  Should I try to explain that we were just there
>and that she lives very far away and that we can not go there for a
>while etc, or should I tell her something else? Anyone have any
>simular sitation or any suggestions please ? I feel like I dont know
>how to handle this problem and need help.
>I hope someone can lend some advice, any , I will truely appreciate
>Thanks for listeing and I will be looking for your suggestions and
>help. I dont know where to turn for help other then here. Thanks
>again

>

I have similar troubles with my early-onset client.

What I have done is simply, lie to her.

Since she forgets stuff in five minutes anyway, the lie that her
friend/relative/ will be coming to see *her* (especially after she's
been gone on a long visit to see *them*), seems to calm her down. After
several repetitions of this in the most reassuring tone I can muster,
she eventually calms down.

My client is also on Lexapro for depression, now at 10 mg per night. In
addition, she's on Namenda, one 10 mg tab in the morning, one at night,
and Aricept, one ten mg tab in the morning. She also takes flax seed
capsules three times a day, vitamin E, a multi-vitamin, some fiber,
folic acid, and Calms Forte, two tabs, three times a day (breakfast,
lunch and dinner). It works to keep her calm.

What I suggest to people who've seen me working with her and are amazed,
is to find what works for them. What works for me may not work with
others, see, even those who are working with her on a regular basis as I
do.While *my* lie might work, other people may not be able to use the
same lie. So they have to find whatever works.

I would recommend that you find a calm place to go to regroup - you may
need a small vacation. And you may need to call someone to come sit with
her while you take a mini-vacation which can be anything from a walk, to
a trip to the library alone - whatever *you* need to do to take this
respite for yourself will be important for your abilities to care for
your aunt on a day-to-day basis. It's NOT easy - and please forgive me
if I seem presumptuous here. . .

I hope you feel comfortable venting in this format; I wrote a
several-page long "venting" post to some other Alzheimer's groups a few
weeks ago; that helped me a lot, just to get stuff off my chest.

Meantime, find your lie. I know that sounds weird, but find it and just
go along with her delusions and the like; it will be a lot easier than
fighting and correcting, and easier than trying to explain that she's
already been there. IF you have photos of the trip, you might try
showing them to her and explain *then* that she has already been there.
IF, however, this does nothing but confuse her more, put the photos away
and go back to lying that your mom is coming to see her very soon.

Wishing you the very best,

Feather


YAHOO! GROUPS LINKS





#725 From: "angela147g" <angela147g@...>
Date: Sun Aug 7, 2005 8:20 pm
Subject: wanting to thank you
angela147g
Send Email Send Email
 
I want to say thank you to Don and to Feather for the advice. I am
going to try this new approach, and try to keep a positive attitude,
and keep my fingers crossed. Thank you so much .
Also, I want to thank "pjb12345uk also. I too believe in the power of
prayer. Thank's to all.
Angela

#726 From: Feather Forestwalker <feather@...>
Date: Sun Aug 7, 2005 9:56 pm
Subject: Re: wanting to thank you
featherbirdlady
Send Email Send Email
 
angela147g wrote:

>I want to say thank you to Don and to Feather for the advice. I am
>going to try this new approach, and try to keep a positive attitude,
>and keep my fingers crossed. Thank you so much .
>Also, I want to thank "pjb12345uk also. I too believe in the power of
>prayer. Thank's to all.
>Angela
>
>
>

Angela,

It's hard to gain perspective, especially when the person is close to
you. *sigh*

I appreciate your dilemma so much. . .and have often wondered how it is
that I am so deeply entrenched in the care of my neighbor. . .she came
to me last year and that's when I was hired. It's taken a lot of reading
(The 36-Hour Day comes to mind, along with Lenore Rowland's book called
Alzheimer's). There's a lot of good material out there that has helped
me tremendously in dealing with my client.

When she says over and over again that she wants to go home, I've told
her everything from "Your friends are working on it," to "You ARE home."
Some days one works, some days, the other. What she is really looking
for, however, is a sense of familiarity; a time when everything made
sense and she was feeling more useful.

It's a tough row to hoe. . .and yes prayer is very important.

God bless,

Feather

#727 From: cad721@...
Date: Mon Aug 8, 2005 1:19 am
Subject: To P
cadonn721
Send Email Send Email
 

This is not a prayer group.  We are here to help each other deal with the devastating disease of Alzheimers.  I am the one who found your long and unrelated post a few weeks ago to be inappropriate for this website.  To call me rude and ignorant is so uncalled for.  I am a very educated and well rounded individual who visits this group to find some answers on how to deal with my 56 year old mom's disease.  If I were looking for a prayer group I would have found one.  I do not know if I am the only one that feels this way, but to push your religous feelings here is not appropriate.  Prayer is not going to make my mother better, I do believe in God and am Catholic, I am just not happy with him lately.

Cheryl

 


#728 From: "Sally Rugh" <sal5371@...>
Date: Mon Aug 8, 2005 4:18 am
Subject: Re: To P
sally195371
Send Email Send Email
 
Prayer should be one of the most important things in your life. God created us and he will take us away. He does answer prayer, maybe not the way you want it answered but it does get answered. We should all be on our knees asking for peace for our dear ones.
That is the biggest downfall of the USA right now. This country was founded under GOD. Know one seems to remember that or they don't want to.
I praise the Lord everyday for getting me this far in life and I praise him for my Mother's long life. I ask him to comfort her in times of despair and I know that he does.
 
Sally in PA
----- Original Message -----
From: cad721@...
Sent: Sunday, August 07, 2005 9:19 PM
Subject: [alzheimers_support] To P

This is not a prayer group.  We are here to help each other deal with the devastating disease of Alzheimers.  I am the one who found your long and unrelated post a few weeks ago to be inappropriate for this website.  To call me rude and ignorant is so uncalled for.  I am a very educated and well rounded individual who visits this group to find some answers on how to deal with my 56 year old mom's disease.  If I were looking for a prayer group I would have found one.  I do not know if I am the only one that feels this way, but to push your religous feelings here is not appropriate.  Prayer is not going to make my mother better, I do believe in God and am Catholic, I am just not happy with him lately.

Cheryl

 


#729 From: "J.D." <jd_1951_54@...>
Date: Mon Aug 8, 2005 11:20 am
Subject: Re: To P
jd_1951_54
Send Email Send Email
 
You are wrong to a point Sally....You Wrote: We should all be on our knees asking for peace for our dear ones......We should be on our knees "BEGGING" God, not just asking. I agree with you, but I also understand where Cheryl is coming from and she has the right to express her feelings also. That's called "FREEDOM"....you are both right......Ibthere......Jd
 
PS: May God Bless You Both.....and he will.

Sally Rugh <sal5371@...> wrote:
Prayer should be one of the most important things in your life. God created us and he will take us away. He does answer prayer, maybe not the way you want it answered but it does get answered. We should all be on our knees asking for peace for our dear ones.
That is the biggest downfall of the USA right now. This country was founded under GOD. Know one seems to remember that or they don't want to.
I praise the Lord everyday for getting me this far in life and I praise him for my Mother's long life. I ask him to comfort her in times of despair and I know that he does.
 
Sally in PA
----- Original Message -----
From: cad721@...
Sent: Sunday, August 07, 2005 9:19 PM
Subject: [alzheimers_support] To P

This is not a prayer group.  We are here to help each other deal with the devastating disease of Alzheimers.  I am the one who found your long and unrelated post a few weeks ago to be inappropriate for this website.  To call me rude and ignorant is so uncalled for.  I am a very educated and well rounded individual who visits this group to find some answers on how to deal with my 56 year old mom's disease.  If I were looking for a prayer group I would have found one.  I do not know if I am the only one that feels this way, but to push your religous feelings here is not appropriate.  Prayer is not going to make my mother better, I do believe in God and am Catholic, I am just not happy with him lately.

Cheryl

 


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