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AUTISM FIRST STEPS
AUTISM DAILY NEWSLETTER    
Thursday, November 22, 2001 
Happy Thanksgiving!


INDEX:
My Story: Discovering Nolan’s Abilities
A Thanksgiving Message
IDEA: Speak Your Mind::Speak Now VIA KIDS_Advocate
Some Programs Available at UCSD
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COMMUNICATION MADE EASY ©
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Talking To Your Pediatrician
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My Story: Discovering Nolan’s Abilities


As parents of children with learning differences, we know we have our work cut out for us. Raising confident, responsible kids often seems impossible as we wipe away their tears of frustration while they stand on the sidelines watching their peers accomplish goals seemingly unattainable to them. Helping My Son ManageMy eight-year-old son Nolan is dyslexic. It’s difficult to watch him struggle because he always tries his best. As I think back on my own childhood, I remember being very much like him. Maybe that’s why I put so much effort into finding ways to buffer the challenges he encounters. I try to show Nolan (a born pessimist) the positive side of every situation. For example, I’ll say:
“You didn’t get three words wrong on your test -- you got ten correct,” or
“The beginning of the school year isn’t the end of the world or the end of fun activities. It’s a new season of fun! Think about Halloween, fall camping, and the holidays.” I also find timing is of the essence. If Nolan isn’t attentive, we set his work aside until he’s more “on the mark.” Nolan is talkative, over-sensitive, and has a difficult time adjusting to change because he’s very anxious. Although tall for his age, Nolan is immature socially and physically. This zaps his confidence. However, these traits don’t detract from his outstanding work ethic and creativity. Encouraging His InterestsWe allow Nolan “space” to entertain his interests. Right now it’s plumbing -- you read it right -- plumbing! He spends countless hours digging up the yard and installing copper pipes in every direction. He loves it, and he’s proud to impress his friends with his endless knowledge of plumbing supplies. My husband Kevin is a pipe fitter, so Nolan’s interest has a family connection. On weekends, they review Nolan’s hand-drawn blueprints. They solder and install pipes, then they test the final job. Our home is usually in disarray, but allowing Nolan to succeed at anything is well worth the small inconvenience. I believe he enjoys plumbing because no one judges his work. After all, don’t we all need a little of that freedom? Enjoying Family ActivitiesNolan prefers his father’s company when they’re fishing or tackling a job around the house. But I’m Nolan’s companion of choice when it’s time to do homework or if we just need quiet time. He tags along with his older brother, Drew, but also enjoys the company of his younger cousins.You don’t need to spend a fortune to entertain your kids. During the winter we’re outside as much as possible enjoying physical activities like sledding, hiking, and ice-fishing. Warm weather brings opportunities to camp, swim, or float down a nearby river. I believe keeping active reduces stress levels and teaches the importance of healthy living. Our entire family enjoys “down time” spent outdoors. And for Nolan, it’s a needed respite from the effort he puts into his schoolwork. Nolan loves to explore the outdoors. In fact, he often entertains his classmates and teachers with stories about his “finds,” such as an old fishing lure, a snail shell, or a sighting of a migratory bird.Keeping a Healthy PerspectiveI realize Nolan’s education is important. It can’t be the sole focus, though. If it were, we’d all be depressed. A friend of mine who also has a son with a learning difference keeps asking herself, “Why did this happen to my son?” My response is, “If you truly feel that way, think about how a parent of a child with leukemia or cerebral palsy feels.” Having a learning difference is life-changing, not life-threatening. When I reach the end of my rope, I try to consider things may not be as bad as they appear at the moment. Nolan’s struggle may last a lifetime. It’s important to take things day-by-day and not become overwhelmed by thoughts of his future.
About the AuthorAnn Hansen is a graphic designer who left her career to stay at home with her two sons and has never regretted it. She’s highly involved with volunteer efforts in her Pennsylvania borough and local schools. For Ann, life’s greatest pleasures include enjoying good food and exploring new areas with her family.
©Schwab Learning 2001  
Created: 11/19/2001
http://www.schwablearning.org/Articles.asp?r=381&g=3&d=3
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A Thanksgiving Message

 

Author Unknown


"WHAT AM I GRATEFUL FOR?" People in stores who don't stare or question my child's behavior. Families members who understand and support myself and my child. The wonderful people who provide respite care so that families like ourscan regroup and find the strength to endure another day. Professionals who go the extra mile to supply us with help and resourcesand understand the stress of having a child with a disability, and do notjust give us another label or say, I don't know what to tell you, I havenever seen a child like this before and than say, "...that will be $200.00,please pay the receptionist and out the door we go with nothing. Educators, who are willing to learn and understand about our child'sdisability.  Anyone can attend a conference or a workshop, but how lucky aparent is for those educator's and community agencies who can bring thatknowledge back to the table and classrooms and apply it. A team that can park their ego's at the door and roll up their sleeves andsay, "how can we BEST serve this child?"  In a perfect world, programs aredesigned for the "individual" child and families, not the other wayaround.  Services should be available to "all" families of children withdisabilities and "not" just the one's that are lucky enough to have parentswho can afford to provide attorney's or scream the loudest. Friends who are "always" there for us and not just in the good times. Pityparties are fun, but when you lose all the battles and "win" the war, thatis when you really need your friends to celebrate in your triumph.  Whenyour child eats from a spoon for the first time, or says a word, orcompletes a sentence or goes to the bathroom for the first time ... theseare "major" accomplishments for families like ours, as some of our childrenacquire these skills many years later, some before milestones and somenever will.  THANK GOD for "our" friends that our always there for us. Most importantly?  Thank God for the opportunity to have a support grouplike this that reaches so many families. To the Universities, Hospitals, Foundations, Society's and most of all toall of you "parents" who have supported us. have always been there for meand eachother. To all the families and victims of September 11th you will "never" beforgotten worldwide.  Let us remember what makes us strong and not dividesus and "what" we have to continue to be thankful for. So to all of "us" .....
HAPPY THANKSGIVING

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IDEA: Speak Your Mind::Speak Now VIA KIDS_Advocate


Citizenship and patriotism are more than just flying flags. They
demand participation.  The war on terrorism is also about  protecting
our right to participate in our civic affairs.  We have a
responsibility to make our opinions known and to voice our concerns.

IDEA, the Individuals with Disabilities Education Act, is in the
process of reauthorization.  The Federal Department of Education is
asking parents for their input.  This is your chance to be heard.

I am urging everyone to complete the e-mail form at
http://www.specialkidsla.com/ideareauthorization.htm.
  No one has
nothing to say. 

-if you feel it is working and you like it the way it is, please tell
them. 
-if your child has been helped by IDEA, please thank them. 
-if you have suggestions on how it could be improved, please give
them your ideas.
-if you feel it is burdensome, please let them know.

Our children's right to a free, appropriate, public education is
governed by this law.  Parent participation in the IEP process was
strengthened in the 1997 reauthorization, as was access to the
general curriculum.  What will the 2002 reauthorization include?

Education Secretary Rod Paige is in favor of more funding for IDEA,
but first he feels it must be fixed.  Researchers at Harvard have
testified to Congress that too many minorities are being classified
as having learning disabilities.  Various members of Congress want to
make it easier to suspend or expel kids for discipline issues. 

Numbers count.  It is important that the Dept of Education hear from
as many parents as possible.  Everyone has something to say.  The
letter is preformatted to make responding as easy as possible.

Mike Savory

AWAK(e)A  (c) 2001
"Advocacy With Abundant Keys to
Excellence and Access" 
Offering Advocacy in: Community Service,
Student Advocacy, Facilitation & Mediation
(Volunteer)

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Some Programs Available at UCSD


Treatment of Echolalia Study
This research project offers assessment and treatment for children with autism who use immediate echolalia.  Immediate echolalia is when a child repeats something that someone else just said.  Children participating will be assessed to identify situations in which they currently use echolalia.  An individualized treatment for echolalia will then be developed based on assessment information, in which children will be trained to use appropriate language in place of echolalia.  Participants will come to the laboratory for two 2-hour visits per week for approx. four months.
To participate, children must:
*have a diagnosis of autism
*use immediate echolalia in at least 25% of speech
*be between the ages of 4 and 6 years
Contact: Michelle Sullivan at sullivan@psy.ucsd.edu

Imitation and Play Training
This research project is designed to assess the efficacy of an imitation training program and its effect on language, play and peer interaction skills.  Participation in this study will include child training in imitation, language, and play using both discrete train and pivotal response training.  Treatment does not require parent participation.  The children are required to come to the laboratory three times per week for 1.5 hours.  This program will run approximately 20-30 weeks.
To participate, children must:
*be between the ages of 2 and 4 years
*have a diagnosis of autism
*have difficulty with imitation
*not have a diagnosis of severe or profound mental retardation
Contact Brooke Ingersoll at bingerso@ucsd.edu

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COMMUNICATION MADE EASY ©

HAVE YOU EVER BEEN FRUSTRATED WITH MISPLACED OR DISORGANIZED PICTURES FOR YOUR COMMUNICATION SYSTEM?
You and your child need a user-friendly, easy to use communication binder that is organized to make communicating fast and fun! BENEFITS OF HAVING AN EASY AND ORGANIZED BINDER INCLUDE:
Pictures are always located in the same place which eliminates frustration while searching for "words".
It is easier to recognize when pictures are lost or need to be replaced.
Categories and colours make finding and putting pictures away much easier than in the past!
Sentence strip is located on the front of the binder for easy access.
Binder is small therefore portable.

You can use a number of different sizes and types of pictures
COMMUNICATION MADE EASY ©
supports many types of picture communication systems. PCS ~ Boardmaker Picture
This CD ROMs
Your own PhotographsCommunication Made Easy
©
will transfer the picture communication system of your choice, put it into a Fitzgerald Key and add to your very own binder. Pages will be totally organized by skill.
Customizable: we will be happy to look at incorporating other types of pictures into your child's binder. We will also customize the size of binder. Coming soon...Themed Binders: Going to School, Going to a Restaurant, Going to Grandma's.To read more about the Fitzgerald Key, go
to this page: http://www.bbbautism.com/pecs_fitzgerald_key.htm.
For more information, contact Dawn GutowskiCell
# 905-868-2282
Phone # 905-868-8370

E-mail: dawngutowski@hotmail.com
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Talking To Your Pediatrician
Make the most of your time with your doctor
From About Pediatrics

In medical school, doctors learn how to 'present' their patients as they tell more senior doctors what is wrong with the patient. This usually begins with a chief complaint, or the main reason that you came to the doctor, such as my 'child has a fever ' or 'he has a bad cough.' The chief complaint is followed by the 'history of present illness,' which includes what other symptoms he has, when they began, and what makes the symptoms better or worse.If you learn to 'present' your child to your Pediatrician at the beginning of the visit, then that will leave more time for your doctor to ask some follow up questions, examine your child, and then discuss what is wrong and what the treatment should be.
Read this helpful article here: http://pediatrics.about.com/library/weekly/aa110701a.htm
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Autism Awakening, Autism FIrst Steps Newsletter, or any staff do not endorse any individuals, groups or programs.  References regarding programs, meetings, resources, research, opinions, treatment, etc., should not be interpreted as an indication of endorsement.  They are provided for informational purposes only. This is an attempt to keep the nation advised to all diagnostic, treatment, therapy, educational,
options available as well as legislative autism updates and more.



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ALL INFORMATION, DATA, AND MATERIAL CONTAINED, PRESENTED, OR PROVIDED HERE IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT TO BE CONSTRUED AS REFLECTING THE KNOWLEDGE OR OPINIONS OF THE PUBLISHER, AND IS NOT TO BE CONSTRUED OR INTENDED AS PROVIDING MEDICAL OR LEGAL ADVICE.  THE DECISION WHETHER OR NOT TO VACCINATE IS AN IMPORTANT AND COMPLEX ISSUE AND SHOULD BE MADE BY YOU, AND YOU ALONE, IN CONSULTATION WITH YOUR HEALTH CARE PROVIDER.