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Reply | Forward Message #324 of 612 |
Re: Anybody out there?

Dear Cheri,<br><br>I lost my mother to this
horrible disease on January 27th of this year. My mother
was a hard workingwomen her entire life and had to in
addition deal with the stress of raising three kids as a
single mother. She would periodically complain about not
feeling well, but doctors always diagnosed her with
overworked and being depressed. But about three going on
four years ago, my mother had a mammogram. Two day's
latter she developed a rash under her armpit. This was
diagnosed as shingles. Although the singles didn't spread
very far, she became very ill. I can say that my
mother was never the same active women as of this time.
Her symptoms become more and more painful. A doctor
along with tow ortho surgeon diagnosed her with carpal
tunnel. Her symptoms increased. Still no diagnosis. A
friend of mine told me my mother may be suffering from
Lupus and that I show demand a ref to specialist. My
mother was diagnosed Wednesday November 27th. She was
given two to three years to live. This was based on the
history of how she progressed over the last three years.
Needless to say I was divested. I never told my mother. I
was determined to learn as much about this condition
as possible. I read the Scleroderma Book in one day
and now knew what my mother and I would be dealing
with. The book gave me some hope. I was determined to
try new treatments for my mother. I had an
appointment at a center of reum in Redlands Calif. where they
have treated the disease with antibiotics. My mother
suffered a heart attack Dec 25th and never left the
hospital. She was only 55 years old. I have many of issues
I must learn to deal with. I try to stay focus and
think about helping others and raising public
awareness. This is really hard to do when I am feeling so
much emotional pain. I remember not like things about
my life, wanting to change this or that. Now I wish
I could be who I was. I will never be happy again.
I will never be loved so unconditionally again. She
is gone and I am left alone. Alone to look out for
my daughter and my husband with no one to share my
failures and glory's with. I hate this disease, it has
destroyed my life. I may not have scleroderma today (maybe
I never will) but it has destroyed me. It's rocked
my faith, it's robbed me of my happiness, it made me
insecure of my daughters health in the future, my health
in the future, as well as my sibling health. This
disease took my dreams, my plans for growing old with my
mother. My mother was a great woman. I am sad and I am
angry and those two emotions are not letting me be. I
feel good writing this. I feel good crying. It helps
me feel empty. Oh, I will fill up again. I am sorry
to hear you also lost your mother to this disease.
Truly I am sorry. Cheri how old was your mother? I am
33 years old and live in Woodland Hills, CA. I am
going to be the support group leader for the
scleroderma foundation in the west valley area starting Jan
2001. I will continue to educate myself on this disease
and work on healing my pain on a daily basis. If you
would like to e-mail me I have to
addresses:<br><br>annette@... (that
work)<br>anet_90065@...<br><br>I hope
you are doing well and may god bless
you.<br><br>Thanks for listening.<br><br>Sincerely<br>Anet




Thu Aug 2, 2001 6:37 am

anet_90065
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Message #324 of 612 |
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Hi Cheri<br><br>Well My Mum was diagnosed with SD about 4 years, it is really taken its toll and the affects it has on my Mum is on the increase. She is also ...
kentishlad_1999
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Jul 31, 2001
4:51 am

Dear Cheri,<br><br>I lost my mother to this horrible disease on January 27th of this year. My mother was a hard workingwomen her entire life and had to in ...
anet_90065
Offline Send Email
Aug 2, 2001
6:37 am

Hi Anet<br><br>Firstly I am so very sorry to hear of you loss, this disease is horrible.<br><br>My Mum was diagnosed with SD about 4 years ago, this was after...
kentishlad_1999
Offline Send Email
Aug 2, 2001
7:04 am

sorry i have been mia...things have been crazy on this end! busy, busy, busy! Glad to see so many of you posting!<br><br>Hope everyone is doing well...i keep...
blue-eyes-1012
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Aug 2, 2001
3:39 pm

hi...how is everyone surviving the heat wave...looks like it's almost over here in ny state...
blue-eyes-1012
Offline Send Email
Aug 10, 2001
4:27 pm

You are right, I also live in NY and I'm so glad it is over. I couldn't resist the heat and had to stayed home under AC all day. I hope the Electricity bill...
yobeca
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Aug 12, 2001
11:02 pm

Hi Chereller,<br><br>I'm not a Doctor or stocks holder of the company, only a scleroderma patient. I'm taking this medication for over eight months and it had ...
yobeca
Offline Send Email
Aug 12, 2001
11:41 pm

My sister was diagnosed w/raynauds syndrom about 10 years ago,scleroderma later.She's never been one to talk when things get tough in her life(which is really...
oz4glinda
Offline Send Email
Aug 13, 2001
1:42 am

Hi Lynne<br><br>I really do sympathise with you, my mother was diagnosed about 3 years with sceleraderma, this after many visits to the hospital to find out...
kentishlad_1999
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Aug 13, 2001
6:49 pm

My mother took a dose of the above back in march of this year I personally feel that it did not do anything noticeably better and in fact a few weeks after my...
kentishlad_1999
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Aug 13, 2001
6:57 pm

It was probably used to dilate blood vessels - is your mom having problems with finger ulcers or other affects from Raynaud's? Iloprost was shown to work well ...
alby40
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Aug 13, 2001
11:01 pm

I found a cool decal on this site. I thought I would share this with my buddy's!<br> Love,Tzeme2000...
tzeme2000
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Aug 14, 2001
3:54 pm

Dear Lynn,<br>My husband was diagnosed with scleroderma almost 2 yrs ago. 4 the 15 yrs we have been married he has been the picture of health. When he got sick...
dance_2168
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Aug 15, 2001
4:14 am

hi guys....just let me know if there is ever a color you don't like, that makes it hard to see or whatever ok....was just playing around with some ...
blue-eyes-1012
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Aug 16, 2001
1:53 am

just learned form the other SD yahoo club....<br><br>on the Lifetime channel <br>"Strong Medicine", on Sunday, Aug. 18 will feature a story about someone with ...
blue-eyes-1012
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Aug 16, 2001
12:42 pm

I just checked it online and Strong Medicine is on Sunday, the 19th.<br><br>Cheri...
cheri_dorwart
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Aug 16, 2001
2:31 pm

Do all Scleroderma Patience have to be on oxygen?<br>Are their some that are on oxygen,and some that are not,and if yes can someone explain this process and...
flflow1
Offline Send Email
Aug 16, 2001
11:56 pm

My husband doesn't have 2 b on oxygen and hasn't yet. I don't understand that. Has it affected the lungs? This is interesting 2 me. Let me know what u find...
dance_2168
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Aug 17, 2001
3:22 am

Hi! I was diagnosed with SD about 4 years ago, and I have lung involvement. I am on home oxygen as needed. Not every case requires oxygen, and not every SD ...
mycoloredcoat
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Aug 17, 2001
5:49 am

Thank you for the correction! You friends and family know about us patients and our brain-fog - that was a prime example! Almost as good as the time after ...
alby40
Offline Send Email
Aug 19, 2001
12:29 am

hey alby40,<br><br>yes my brain is in a fog. what are you talking about? sorry i am new to this computer stuff. what is the correction? don't understand. ...
DPettengill84
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Aug 19, 2001
5:16 am

sorry alby40,<br><br>just figured out i should have went to the home page first. oxygen problems i do not have yet. have a wonderful day....
DPettengill84
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Aug 19, 2001
5:23 am

my husband filed for divorce 7 months ago because of my sd. we were together 15 years. as anyone with sd knows stress is not good for the condition. how...
DPettengill84
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Aug 19, 2001
5:32 am

Hi well not too sure if I can tell how to deal with this, I have never been divorced myself. I would say that SD causes alot of fraustration, my mum suffers...
kentishlad_1999
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Aug 19, 2001
7:45 am

&lt;my husband filed for divorce 7 months ago because of my sd. we were together 15 years. as anyone with sd knows stress is not good for the condition. how...
alby40
Offline Send Email
Aug 19, 2001
1:29 pm

The movie on lifetime about SD is on at 8 PM on <br>Sunday, 8/19/01....
cheri_dorwart
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Aug 19, 2001
3:21 pm

Yes I am on Oxygen, been on it for ten years,been on it for 24 hrs 6 years.Would like to know other symptons of SD if possible,I am losing my eye sight and ...
flflow1
Offline Send Email
Aug 21, 2001
5:56 pm

Hi My sister/n/law is having it rough latley,wondering if she really does have SD.<br>She can't believe that she is going blind and all the test results have ...
flflow1
Offline Send Email
Aug 21, 2001
6:10 pm

What did you think of the movie? I found the show to be kind of hokey, and the SD patient not accurately portrayed....
lhodgins_1
Offline Send Email
Aug 22, 2001
2:13 am

was wondering that myself...what you all thought...i was away for the weekend, and was unable to watch it...set the VCR, adn there was a thunderstom that...
blue-eyes-1012
Offline Send Email
Aug 24, 2001
1:10 pm
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