Here's some info on sibling support that I found on ASA's site. I am looking up the ARC's Sib Shop Info.
My daughter is already saying that we should have a group that meets each month, and the kids can come up with a group name and plan activities and yes, she says t-shirts!
Sibling Issues
Raising a child with autism places some extraordinary demands on parents as individuals and on the family as a whole. Prime among these demands is the lack of enough hours in the day to do all one wishes. The time involved in meeting the needs of a family member with autism may leave parents with little time for their other children.
Many parents indicate that even as they do all they can for their child with autism, they are always struggling with how best to respond to the needs of the family as a whole. They say that although their own life as an individual may be put "on hold" and a couple may share an understanding of the need to make sacrifices on behalf of their child with autism, few parents are willing to make that same demand of other children in the family. As a result, there is a continual tension between the needs of the child with autism and the other children.
This section offers suggestions to parents about ways to help the other children in the family cope gracefully and effectively with the experience of having a brother or sister with autism. Research indicates that the majority of brothers and sisters of children with autism cope well with their experiences. That does not mean, however, that they do not encounter special challenges in learning how to deal with a sibling who has autism or a related disorder.
There are special demands on siblings, and learning how to manage these demands will make their childhood easier and will teach them skills that will make them more effective and resilient adults. The most important teachers of these coping skills are a child's mother and father. The gifts you give to your youngsters in childhood will serve them immediately, and in all the years ahead.
Many of the suggestions provided here are things that parents can do within the family to help a child understand what autism is all about, to improve the interactions among the children in the family, and to ensure that brothers and sisters grow up feeling they have benefited from the love and attention we all so much need.
Explaining Autism to Children
Common sense tells us and research supports the idea that children need to understand what autism is all about. The rule of thumb: Do it early and do it often! It is important that your children know about autism and that the information you give them is appropriate for their developmental age. From early childhood, they need explanations that help them understand the behaviors that are of concern to them. For the preschool, child this may be as simple as "Rick doesn't know how to talk," while for the adolescent, it may involve a conversation about the possible genetics of autism.
The key is to remember to adjust your information to your child's age and understanding. For example, very young children are mostly concerned about unusual behaviors that may frighten or puzzle them. An older child will have concerns of a more interpersonal nature, such as how to explain autism to his or her friends. For the adolescent, these concerns may shift to the long-range needs of their sibling with autism and the role they will play in future care. Every age has its needs, and your task is to listen carefully to your child's immediate concerns.
Another key to success is to remember that children need to be told about autism again and again as they grow up. Young children may use the words they hear us use, but not understand the full meaning of those words until they are much older. Don't be mislead by a young child's vocabulary of words like "autism" or "discrete trial." That does not mean the terms have real meaning for him or her. Just as you would not expect an early conversation about the obvious physical differences between boys and girls to constitute a sufficient sex education for children five years or 10 years later, similarly, you must explain again and again, in increasingly mature terms, what autism is all about.
Helping Your Children Form a Relationship
Because of the nature of autism, it is usually difficult for a young child to form a satisfying relationship with a brother or sister who has the disorder. For example, your child's attempts to play with his/her brother are probably rebuffed by his ignoring her, fall flat because of his lack of play skills, or end abruptly because his tantrums are frightening. How many of us would keep trying to form a friendship with someone who turned her back when we spoke to her, or, even worse, seemed angry when we approached?
It is not surprising that young children may become discouraged by the reactions they encounter and seek their playmates elsewhere.
The good news is that young children can be taught simple skills that will enable them to engage their brother or sister in playful interactions. Research has shown that siblings can learn basic teaching strategies to engage their brother or sister with autism. These skills included things like making sure they had their brother's attention, giving simple instructions, and praising good play. One research study showed that videotapes made before and after the children learned these skills showed in a very touching manner that, after training, they played together more and seemed much happier than they had been prior to training.
Special Times
Along with ensuring that the child with autism is a fully integrated member of the family; it is important to remember that other children in a family need their times to be special. Families are often urged to find some regular, separate time for the children in their family who do not have autism. It may be one evening a week, a Saturday morning, or even a few minutes at bedtime each night. If your child with autism has a home-based program or exhibits serious management problems, you will have neither the stamina nor the energy to give your other child exactly the same amount of attention. It is not necessary that everything in childhood be exactly the same. What is important is the opportunity to feel special to your parents and to feel that there is an overall atmosphere of equity in your home.
Not Everything as a Family
There are activities that should be shared by all the family and times that should not. Along with having regularly scheduled special times for each child, it is also important to remember that there will be some events when one child in the family deserves to be the focus of everyone's attention. Children have told us that it is sometimes frustrating to have to do everything with their brother or sister with autism. In fact, there may be times when it may not be fair to insist that he or she be included. For example, if your child with autism cannot sit still for a school play, then it may be better if he or she stayed home when your other child performs.
Adult Siblings
Being the brother or sister of a person with autism does not end with childhood. These are lifetime relationships that mature and grow over the years. The concerns of an adult sibling will be different from those of children. For the young adult, questions may focus on their own plans to have children and concern about whether there is a genetic component in the autism of their sibling. In some cases, young adults may also feel a keen sense of responsibility for their brother or sister with autism that makes it difficult for them to leave home and begin an independent life.
It is important that parents discuss with their adult children the expectations they have in caring for the person with autism, as well as reassuring them about the legitimacy of their assuming their own role as adults.
The questions of the role of the adult child become most acute as parents age and begin to anticipate the point when they will no longer have the stamina to continue to care for their child with autism. If the person with autism is not already living outside of the home, this may be a time when placement in a group home or supervised apartment become important. In those families where such care is necessary, adult children and parents must together address the question of who will assume guardianship for the person with autism when the parents die.
It is not easy for any of us to talk about our own death, and both you and your child may shy away from the conversation. Nonetheless, your adult children need to understand the financial plans you have made, the care arrangements in place, and your own expectations for them. Having these difficult conversations will ultimately be a gift to your adult children who will know that they can honor your wishes.
Sibling Groups and Other Resources
A problem frequently reported to clinicians by siblings is a sense of isolation. An ideal means of combating this isolation is to help the sibling connect with other siblings of children with autism. Peer support groups for siblings of children with autism and related disorders are becoming more available.
The Sibling Support Project of The Arc of the United States, based in Seattle, Washington, is one example. They offer a range of information on siblings of children with disabilities, including: reading lists for children and adults, information on local sibling group meetings, information on facilitating sibling discussion groups, or online resources. Their Web site address is: http://www.siblingsupport.org/
The New Jersey Center for Outreach and Services for the Autism Community (COSAC) matches siblings with pen pals around the country as well as internationally. Online resources are also available. For example, a chat room for siblings of children with disabilities, called "SibChat," meets periodically. A final resource to consider for siblings, particularly for those who are experiencing difficulty in adapting to the disability, would be individual counseling.
Most Siblings Cope Very Well
While growing up as the sibling of someone with autism can certainly be trying, most siblings cope very well. It is important to remember that while having a sibling with autism or any other disability is a challenge to a child, it is not an insurmountable obstacle. Most children handle the challenge effectively, and many of them respond with love, grace and humor far beyond their years.
Note: The previous section was provided by Sandra Harris, Ph.D.,professor and dean at the Graduate School of Applied and Professional Psychology and Executive Director of the Douglass Developmental Disabilities Center at Rutgers University.
Dr. Lauren Snyder in Ship Bottom on Long BEach Island
does this I believe.
Karen P. Schwing
Frederic A. Priff School
139 Wells Mills Road
Waretown, NJ 08758
609-693-0545
Karen_Schwing@...
________________________________________________________________________________\
____
Have a burning question?
Go to www.Answers.yahoo.com and get answers from real people who know.
Good Morning:
Looking for a Developmental Optometrist who specializes in reading
disabilities (vision therapy).
Any information is greatly appreciated.
Thanks!
Just wanted to know when the next Faces meeting is in Cape May
County...I know they are usually the 1st Monday of the month, but I
wanted to see if there was one for January....or when the next one
would be...Thanks
I was hoping to hear from one of the families in Southern Ocean County this month regarding the child care situation.
Unfortunately, this leaves me no other choice but to no longer offer these services during the monthly meetings. Effective Janaury 26th, there will be no child care available in Manahawkin.
We offer this service free of charge, and only need someone to coordinate the babysitters and FACES pays them for their time. I am not able to make it to all of the meetings to manage child care services since I do not live in Ocean County, and currently coordinate meetings in Atlantic and Cape May. You are welcome to attend those meetings, where we will continue to offer child care.
If there is a family who would be able to arrange for two babysitters at each meeting, we can resume business as usual. Please call me at 412-3750, if you would like to see this courtesy service continue in Manahawkin. I can give you many ideas on resources for child care in your area. Thank you for your concern and cooperation in this matter.
This workshop will focus on relationship-based intervention for children with autism and other disorders of relating and communicating. An understanding will be gained in the basic principals and philosophy of the DIR model. Relationships and their role in development will be discussed and DIR strategies will be given for use at home and in the community.
Speaker: Cheryl Lees, M.Ed., CCC-SLP
Cheryl Lees is a speech therapist for the Cape MayCountySpecialServicesSchool District.She has thirty years experience in working with children of all ages with disabilities.Cheryl is also a DIR candidate and working towards her certification.
COST:The fee for each workshop is a $5 donation for FACES members and a $10 donation for non-members. There is no charge for LinwoodSchool's staff members.
vOpen to all teachers, paraprofessionals, therapists and caregivers
vCEUs are available for educators upon request
vLight refreshments will be served
vTo register or for more information, please contact Jennifer atfaceseducation@yahoo.comor 609-927-2825 by February 2nd
FACES Autism Education Series Presents:
DR. STANLEY GREENSPAN¡¦S
¡§FLOORTIME¡¨ - the DIR
approach
Location:
Belhaven Avenue School
51 Belhaven Ave.
(off Patcong Ave.) Linwood, NJ (Atlantic County, NJ)
For school directions: 609-926-6700
Date:
Tuesday, Feb. 6, 2007
Time:
6:00pm to 9:00pm
This workshop will focus on relationship-based intervention for
children with autism and other disorders of relating and
communicating. An understanding will be gained in the basic
principals and philosophy of the DIR model. Relationships and their
role in development will be discussed and DIR strategies will be
given for use at home and in the community.
Speaker: Cheryl Lees, M.Ed., CCC-SLP
Cheryl Lees is a speech therapist for the Cape May County Special
Services School District. She has thirty years experience in working
with children of all ages with disabilities.
COST: The fee for each workshop is a $5 donation for FACES members
and a $10 donation for non-members.
**There is no charge for Linwood School¡¦s staff members. **
ľ Open to all teachers, paraprofessionals, therapists and caregivers
ľ CEUs are available for educators upon request
ľ Light refreshments will be served
ľ To register please contact Jennifer at faceseducation@... or
609-927-2825 by February 2nd. Please leave a message spelling your
last name & whether or not you would like CEU's.
Hi Everyone,
To find the pdf brochure for the Possibilities Conference, please use
box on the left and click on files, then click on the Special Events
Folder. The last post contains a broken link to the document.
NJ TASH, SPAN, ASPEN, 21 DOWN and FACES Present
2007 South Jersey
Possibilities Conference
on Autism and Developmental Disabilities
Saturday, February 24, 2007
8:30AM-4:30PM
Atlantic Cape Community College Theater
Mays Landing, NJ
Open to Families, Friends and Professionals
Registration costs $40 member/ $45 non-member /$50 Professional
*Free Session to ACCC Students and Faculty with Valid ID*
Explore topics such as: Changes to the Administrative Code, Diffusing
Anxiety, Fears and Phobias, Expanding Writing and Learning for
Struggling Students and much more.
Registration includes continental breakfast and box lunch.
Please take a moment to read Robin's comments, and this article by David Kirby.
It is amazing that all these intelligent people cannot agree that it is the family of autism which suffers, and they need support.
This is not a disease, it is a condition of the family which must be addressed with education, caring and funding for services. I am preaching to the choir again, huh?
Isabelle
FACES Autism Support Groups
Subject: HeARTs for Autism - the name game epidemic
Hello friends and families of HeARTs for Autism! Happy New Year!
Below is an article surfing around the autism community which is interesting. In years of youth ministry, I often heard "What's wrong with these kids today!?" The adults questioning often did so without the realization that the generation above them wondered the same thing. Today, there are many people asking the question of ASD and ADD and ADHD types - and many professionals who are quick to cite a "gene" as the cause, in hopes that failed medical, environmental and educational systems will be exonerated.
In pastoral care, we have a saying "naming is claiming", meaning if you can name what ails you or what demons haunt you, then it can be claimed and worked on and maybe even rid of. The hot potato of who and what causes autism, and if it even is a problem to be solved, might make an interesting cocktail conversation, but for kids and parents living with the frustration of it all, we need to move on. Yes there is an epidemic of "something". Yes some survive and even thrive despite it all.
My hope for 2007 is the potato gets dropped and the ASD person gets serious attention...that the families get the integrated, holistic services they need...that the profit lines yield to the needs...that politicians give early intervention agencies and school districts ample resources...that the quest for research dollars doesn't turn autism into the new cancer, where millions of dollars are used to raise funds for administrative persons to raise money for research which trickles ever so slowly if a patent or profit stream can't be secured. Ultimately, my hope is this is the year where Community on every level sees how to come together and work well together for the benefit of the Spectrum person and family.
Take care and may this be a fruitful year for all!
by David Kirby, Huffington Post http://www.huffingtonpost.com/david-kirby/there-is-no-autism-epidem_b_37647.html
It's been nearly two years since the release of my book, "Evidence of Harm, Mercury in Vaccines and the Autism Epidemic - A Medical Controversy," and I continue to be vilified by critics who insist that mercury does not cause autism, that autism is a stable genetic condition, and that it cannot be an "epidemic."
I am going to declare a New Year's truce, and announce that my critics are 100 percent correct.
This year, I hope we can ALL agree on one thing: There is no autism epidemic.
Among my most spirited and articulate detractors is a group of adults with autism who belong to a movement that refers to itself as the "neurodiversity" community.
These adults argue passionately that autism is neither a disease nor a disorder, but rather a natural and special variation of the chance genetic imprint left upon human behavior. Most of them, I believe, have what science calls "Asperger's Syndrome," or very high functioning autism.
From their eloquent and well reasoned point of view, autism has no "cause," and it certainly requires no "cure." To suggest otherwise is to brand these adults with the stigma of disease and disability, which is patently absurd given their educational and intellectual achievements.
It's like saying that left-handers or gays are deviant and need treatment - something that reasonable people stopped doing years ago.
So maybe autism really is just an odd genetic peculiarity that yields atypical people whose own set of talents and gifts can lead to perfectly happy and fulfilled lives, with little or no dependence on others for their survival.
If that's the case, then autism has always been with us at some steady, but largely overlooked rate. Growing awareness and better diagnostics have certainly helped us identify and count more people with the condition, who might have been mislabeled as "quirky" or "nerdy" a decade ago.
But if that's autism, then the kids that I have met suffer from some other condition entirely. When I talk about "curing" autism, I am not talking about curing the "neurodiverse."
I am talking about kids who begin talking and then, suddenly, never say another word.
I'm talking about kids who may never learn to read, write, tie their shoes or fall in love.
I'm talking about kids who sometimes wail in torture at three in the morning because something inside them hurts like a burning coal, but they can't say what or where it is.
I'm talking about kids who can barely keep food in their inflamed, distressed guts, and when they do, it winds up in rivers of diarrhea or swirls of feces spread on a favorite carpet or pet (no one said this kind of "autism" was pretty).
I'm talking about kids who escape from their home in a blaze of alarms, only to be found hours later, freezing, alone and wandering the Interstate.
I'm talking about kids who have bitten their mother so hard and so often, they are on a first name basis at the emergency room.
I'm talking about kids who spin like fireworks until they fall and crack their heads, kids who will play with a pencil but not with their sister, kids who stare at nothing and scream at everything and don't even realize it when their dad comes home from work.
These are the kids I want to see cured. And I don't believe they have "autism."
Scientists tell us that 1-in-104 American boys are currently diagnosed with some form of autism spectrum disorder. But the mildest, "high functioning" forms of autism have seemingly little in common with the most severe or even moderate cases.
My hunch (and yes, that is all it is) is that most of these kids do not have "autism" at all, and it's probably time we started calling it something else.
American kids are in huge trouble. One in six has a learning disability. Asthma, diabetes, allergies and arthritis are ravaging their bodies in growing numbers. And little of this is due to "better diagnostics" or "greater awareness."
It can only be attributed to radical changes in our environment over the last 10-20 years. There is something, or more likely some things in our modern air, water, food and drugs that are making genetically susceptible children sick, and we need to find out what they are.
Mercury remains a logical candidate for contributing to "autism spectrum disorders," either alone or in combination with other environmental insults. Mercury exposure can kill brain cells. It can cause loss of speech and eye contact, digestive and immune dysfunction, social withdrawal and anxiety, and repetitive and self-injurious behaviors.
So maybe we should leave the autistics in peace and focus on these environmentally toxic kids and what it is that ails them.
Maybe what these kids have is not autism, but something like, say, "Environmentally-acquired Neuroimmune Disorder," which we could call E.N.D. (Great slogan: "Let's End E.N.D.).
Maybe that would explain why a recent CDC-funded study of the San Francisco Bay Area showed that kids with "autism" were 50% more likely to be born in neighborhoods with high levels of airborne toxins, especially mercury. If a second study underway in Baltimore yields similar data, it will be that much harder to defend the "better diagnosis" argument, (other studies have shown an association between autism rates and proximity to coal-fired power plants).
So maybe what we have here is just a semantic failure to communicate. Columbus thought he had met "Indians," and we only recently began to use the term "Native American."
Columbus was not in the Indies, mercury doesn't cause autism, and there is no autism epidemic.
Do you need a respite program for your teen with autism?
Russ Berger from Autism Family Services is looking for DDD teens with
autism, (ages 13 to 25) for the Sat. afternoon drop-off program at the
JCC in Margate. Call your child's DDD case manager to sign up.
Isabelle Mosca
Hi Francine,
Barbara Strate of MOSAIC does a great presentation on Disney World with
Special Needs. She will be presenting at the Possibilities Conference on
February 24th at ACCC. I have attached a copy of the brochure and will post
one in the files at facesautism's website:
http://health.groups.yahoo.com/group/facesautism/.
I used many of her suggestions on our first trip this past October with our
twins, age seven. It really made the trip easier than it would've been.
Many may not agree with this, but my personal opinion is that Disney is hard
for anyone, but special needs families just need to plan out their
spontaneity. Meltdowns are eminent around every corner, but we found that
the typical child (AND PARENTS) had many more!
Isabelle
We have decided to venture off to Disney World this spring. Any
suggestions from anyone who has dealt with Disney and autism before??
This will be our 3rd time going, but this is the first time I plan to
bring a doc's note for my son's autism & epilepsy. What can I expect?
Thanks!
--Francine
Happy New Year to All of our FACES families and friends.
May we all discover new methods of engagement for our children with
autism, new ways for their siblings to establish a positive identity,
and may we, as parents and grandparents, develop those patience skills
and find friends to share their ideas of hope.
Look for programs to help us all meet these goals in 2007.
Isabelle and the FACES Team
I know you are looking for a non-fiction book on Asperger’s,
but I highly recommend you read for yourself The Curious Incident of the Dog in
the Night-Time by Mark Haddon. It’s a very fast read and gives an
unusual insight into the Aspie mind, as the main character is a 15-year-old boy
with Asperger’s. I don’t know how old your son is, but my son is
10 years old and high functioning and throughout the book I could see my son in
the main character. It was getting a unique view into my own son’s
brain. Very cool!
If your son is younger, I recommend a book for him called
When My Autism Gets Too Big. My son reads that book often. We never filled it
in when he first got it so now when we read it together, it’s interesting
to see how he answers the questions differently as he grows up. It’s
good for him to understand himself and for me to get a glimpse of what’s
going on inside him.
Can anyone recommend a good book on Asperger's Syndrome? My son was
recently diagnosed, and I'd like to find a reliable book on it. If
anyone's interested, I found "Children with Autism--A Parent's Guide"
to be an excellent book. I'm just looking for something more
specifically geared toward Asperger's. Thank you for your help.
Penny
T'was the night before Christmas..
The dinner is burned, the smoke alarm is buzzing,
your kids unwrapped ALL the gifts, but thanks to Chris and Mary,
your child with autism's good sensory diet has enabled him to
withstand it all with flying colors!
Share a dye-free candy cane, or stevia sweetened organic lemonade and
relax! Your gift has arrived!
There is PEACE in your house right now. I wish you all a moment of
peace, and a night out on Dec. 28th to the Children's Museum. We will
be there for all the families who need to escape from the relatives!
Come share your stories of fun and furor! We need a good laugh every
now and then.
Let us give thanks for all the gifts of love our families offer us
with each new day. I would not trade them for the world.
Here's to a great new year for all of us.
Hope you enjoy your holidays from all of us at FACES:
Isabelle, Trish, Mary Ann, Wanda, Beth, Kelly, Michele, Jennifer,
Kristen, Cindy, Susan, Chris,and Cheech
Our FACES Autism Education Series e-mail address will be changing
today. If you would like to continue receiving e-mails about future
FACES Autism Education workshops please e-mail us at our new address
at http://faceseducation@yahoo.com You will only receive updates from
FACES if you e-mail us at this new address..
As a reminder:
Schedule for FACES Autism Education Series at the
Belhaven Middle School in Linwood
Atlantic County)
6-9pm
Feb. 6 Cheryl Lees, ST- "DIR" Approach/Stanley Greenspan's "Floor
time"
March 6 Megann Czekalski, BCABA- Social Skills & Behavior Management
April 3 Pam Modugno, OTR- Brain gym, YOGA & Sensory Integration
Dysfunction
May 8 – To be determined
FACES Education Series is free of charge to any Linwood school
district educator
CEU's are provided upon request at registration
HAPPY HOLIDAYS to all & we look forward to seeing you in 2007!
Sincerely,
Jennifer Dowdell
FACES volunteer & coordinator of the 2006-2007 Autism Education Series
Sadly, I am embarrassed to say that before Autism touched my life all
I knew about the disorder came from watching the character played by
Dustin Hoffman in the film "Rainman".
Experts who I turned to help me understand autism did little to
explain to me about the options available and when I asked them about
special classes and treatment options - well let's just say they were
not very helpful.
So, I searched high and low for good books on Autism, but struggled
to find anything useful. The few that I did find were either poorly
written, written for doctors or medical practitioners, contained out-
of-date information or only part of the information that I needed. I
am sure you have found the same...
So, I searched high and low for good books on Autism, but struggled
to find anything useful. The few that I did find were either poorly
written, written for doctors or medical practitioners, contained out-
of-date information or only part of the information that I needed. I
am sure you have found the same...
So, the only option available was to find the answers myself...
And so, I spent many hours, days, weeks researching proven techniques
to diagnose and manage Autism, and they have been compiled into a
comprehensive, but easy to understand ebook for anyone looking for
answers...
http://autismres.blogspot.com/#
Since 1987, THE CAMP EXPERTS & TEEN SUMMERS has helped thousands of
families find quality overnight camps, teen travel, specialty camps,
sports camps, outdoor adventure programs, community service programs,
special needs camps and more – all with a personal touch.
Through our relationships with more than 900 programs, we help you
select the most appropriate program for the individual child.
Throughout the year, I am in contact with program directors to stay
abreast of the newest advances in program planning, facility
improvements and other updates. Every summer, I travel and view more
than 100 programs in action through first-hand, personal tours and
meetings with program directors for up-to-date information.
I interview parents by telephone so that I may learn about the
children's interests, strengths and personality in order to find
quality programs that best fit the children, in the right location,
for the right amount of time and for the right price.
I look forward to hearing from you!
Your Personal Summer Program Advisor,
Beth
THE CAMP EXPERTS & TEEN SUMMERS
BETH GOLDSTEIN / Joanne Paltrowitz
PHONE: 610-658-0744
FAX: 610-658-1947
beth@...
www.campexperts.com
Traveling with multiple children that can dart off in different
directions can be challenging. Ever since my kids were little
babies, I have dressed them in matching bright shirt colors so that
I can keep track of them as we navigate crowded airports, amusement
parks or even the zoo. Our brand new UA shirts are great for any
outing whether you are going far from home or just to the mall.
They are bright orange, not because it is our favorite color but
because it is easy to spot and people don't wear it often!
We have found it helpful in the past when traveling especially for
Liam to wear some article of clothing that says autism. When he is
talking to new people we come in contact with, it helps them
understand him more readily, increases their level of patience and
understanding which in turn helps him feel more confident in his
communication skills!
There are tons of other gift ideas and things on SALE from t-shirts
to bracelets and more! Make great presents for teachers and
therapists as well!
All orders placed by Midnight, Sunday, December 17th will be shipped
out via USPS Priority mail on Monday, December 18th.
Visit www.unlockingautism.org today!
THANKS FOR YOUR SUPPORT!!!!
Shelley Hendrix Reynolds
Unlocking Autism
PS: University of Tennessee, University of Florida and University of
Texas fans, people attending the Orange Bowl this year, etc., do not
need to send me emails telling me how much you like orange....we are
in the SEC conference down here...we know, we know!!!!
Please read and contact Kara Pothier DIRECTLY if youâ?Tre
interested, as I
have no other information:
kara.pothier@... or 609-279-0863.
Kara is a coordinating producer for Nick News with Linda Ellerbee.
Thank you.
Chris Walsh
From Kara Pothier:
>
I am working on a half-hour program for Nick News that will be all
about
Autism Related Disorders. Our goal is to explain to 12-15 year olds
what Autism is and what other disorders are related to it, what it
is
like to be a kid with a disability, and what other kids can learn
from
kids with Autism their and families.
>
For the show, we are looking for kids and families who may be
willing
to tell their stories about growing up with Autism and/or
Aspergers. I
assure you all kids/families will be featured in a positive light.
Nick News has been on the air for over 15 years now, and is highly
respected not only in the tv field, but also by parent and teacher
groups.
>
I am in the early stages of research/production, but I hope to start
talking to some families by phone in the next couple of weeks.
>
In general, we would like to feature the following on our show:
>
*A kid between the ages of 12-15 who has Aspergers who could talk
about what his/her life is like.â?
>
*A kid between the ages of 12-15 who has high functioning autism and
who may be able to explain in their own words what autism is and
what
their life is like.â?
>
*A kid between the ages of 12-15 who has a sibling with autism (more
severe) who would be willing to talk about how having a sibling
with a
disability has affected their lives.â?
>
*A kid between the ages of 12-15 who has an autism related disorder
and who is in a good example of an inclusive classroom. (We would
like
to interview classmates/friends if possible.)
We live in Barnegat, which doesn't have an autism program in its
school. However, Waretown does, so we want our son to go there. Should
we hire an attorney to help "persuade" Barnegat to let us put him into
the Waretown school district when we go to the IEP meeting? I hear
that it's difficult otherwise. Has anyone else faced this problem?
Thanks,
Penny
Read this, and you will understand the motivation of a parent whose child has autism. In fact, it applies to any compassionate heart. This woman has my respect and praise. Happy Holidays to you all.
Join our Yahoo group at: http://groups.yahoo.com/facesautism/ Please note: The information provided by FACES is for informational purposes and is not an endorsement or recommendation for treatment. We embrace all possibilities for a cure to autism spectrum disorders explored by families, but we are not intended to be a replacement for services or legal advice.
A motion from new justice: She praises her autistic son
Helen Hoens takes heartfelt oath of office
Friday, December 01, 2006
BY KATE COSCARELLI
Star-Ledger Staff
On a day when the state's legal luminaries took turns praising her, the newest justice of the state Supreme Court honored her son.
At her ceremonial swearing-in to the state's highest court yesterday, Justice Helen Hoens said her autistic son, Charles, is the one who "taught me everything I really needed to know to become an associate justice."
Hoens then took the oath of office, administered by a choked-up Chief Justice James Zazzali, with her hand placed on her son's Bible as he stood by her side before a crowd of about 200 people at the Masonic Temple in Trenton. They were joined by her husband, Robert Schwaneberg, a reporter for The Star-Ledger.
Hoens, a 52-year-old Republican from Basking Ridge, joined the Superior Court bench in 1994 and sat in Somerville. She was appointed to the Appellate Division four years ago. She joined the high court about a month ago, after the Senate unanimously approved her nomination.
Wayne Positan, president of the New Jersey State Bar Association and a former law partner of Hoens, said the day was "another chapter of excellence in her distinguished life. ... It is a great day not only for Helen, it is a great day for the justice system, for the court and for the people of New Jersey."
Several speakers said Hoens is smart and passionate about the law, but also stressed her compassion. John Gibbons, the retired chief judge of the U.S. Third Circuit Court of Appeals, said as a young law clerk for him, Hoens showed she could look beyond legal arguments and see that people were involved in every case.
"She will become a great justice," Gibbons said.
In an emotional and personal speech, Hoens said she wanted to thank her son even though he didn't understand what she was saying. She said having an autistic son was not what she planned, that he will never be independent or take care of her in her old age.
Hoens said Charles is one of the people "who lives in the shadows of life," and to be his parent "is to live in the shadows yourself."
"But it's not all bad because you learn things in the shadows," she said. "All around us are people who reach out and touch lives for the better."
Saying most people spend their life "in a hurry," Hoens encouraged those in the audience, when they next encounter someone like her son, to fight the urge to brush past and instead to stop and think and "dig deep down into the reservoir of compassion and kindness."
When she concluded her remarks, Hoens asked her son to stand at his place in the audience. The crowd rose to its feet and gave them both a standing ovation.
Kate Coscarelli covers the Supreme Court and legal issues. She may be reached at (973) 392-4147 or kcoscarelli@....