Archive for the ‘Diagnosis’ Topic

Autism: Year 10 in Review

Sunday, January 1st, 2012

2011 was a good year. Connor, now ten and a half years old, is becoming quite the accomplished young gentleman. He attended fifth grade in a general ed classroom without a para or teacher’s assistant. He completed an etiquette class, joined the cross-country team and learned to swim. He began taking responsibility by completing his first job (assembling ornaments for USO fundraiser), writing and presenting to the school district CFO a right-sizing proposal, hosting two groups of state legislators, and assisting in the training of local area doctors on ADOS testing. He was honored as a Hopes and Dreams Child for our local Children’s Hospital, traveled overseas, and sang twice in front of an audience. His interests are varied and extensive — he earned all about US Presidents and their families, 70s/80s/90s rock bands, the history of British monarchs, Greek mythology and Egyptian pharaohs.

Was he perfect? Heck, no. He still needs extra help via tutoring and in-classroom prompts by his teacher. He came in next to last place in his cross-country race. His singing was way off key. He is still a picky eater, and he still seems to find his way back to our bed every night. He still cannot read for more than 10-15 minutes at a time, and he bombs all standardized tests. He has two or three friends at school, but he still prefers the company of adults. Noise and large groups still bother him, and he still cannot ride a bike, his gross motor delays make sports difficult for him, and even though he is left-handed, he still can’t decide which side he prefers for throwing and kicking.

The good news? Connor no longer has those dreadful allergies, ear, strep and sinus infections that plagued him for the first six years of his little life. He is feeling much better and he is getting physically stronger. His expressive language skills, reading comprehension, social skills, executive functioning and the desire to participate in group activities have come a looooooong way.

We did have a few setbacks this year. We experienced bullying for the first time. A student had been stealing Connor’s snack from his backpack for weeks before anyone noticed, especially since Connor still doesn’t tell us what he does at school nor talks about any of his classmates. The school was extremely responsive, and fortunately, we haven’t had any other incidences.

We also found that Connor had developed an adverse reaction to the various ADHD medications we tried, so he is flying sans-med, and that is taking his grades down from As and Bs to Bs and Cs. The intolerance to medication led us to pursue additional diagnostics which showed that Connor has a duplication in one of his gene sequences which is so rare that there is no comparable case in any genomic database, and there is no syndrome associated with it. We now need to have Connor take a nonverbal language test to see what Connor’s capabilities truly are, and an MRI to rule out any other issues.

As parents, Steve and I have also made progress. We are much more accepting of Connor’s differences. We are not the soccer/baseball family, but we do hike, travel and participate in Connor’s interests in politics and music. We are now investigating private school placement for middle school, because the public school district’s middle schools have well-over 1000 students, and Connor does better in a small group environment.

What to Expect from an Autism Center Evaluation – Part II

Saturday, August 15th, 2009

After our first visit to our new Autism Center (see What to Expect from an Autism Center Evaluation Part I), we returned a month later to regroup with the psychologist and a developmental pediatrician (OD).  The OD gave our son a neurological evaluation and observed his language, social skills and behaviors.

After the neurological evaluation, a office nurse played with our son in another room while the psychologist and the OD  reviewed all of the test results to date and collaborated with us on recommended next steps. As it turned out, my son’s original PDD-NOS diagnosis was updated to high functioning autism with an attention deficit disorder.  The topics we covered in the post-evaluation results conference were comprehensive and included: (more…)

What to Expect from an Autism Center Evaluation-Part I

Sunday, July 5th, 2009

I would gladly donate every penny of the gas money I’ve spent driving my son from one diagnostic center to another if I could  find a single, one-stop shop for autism screening!  My dream is to have all  of the tests and questionnaires completed in a single trip – preferably riding up an escalator or a moving sidewalk.  Can you imagine it? I could hold my son’s hand while we shared  ice cream cones or s’mores (it’s a dream, remember?).  As we  passed each diagnostic station– neurology, speech/language, sleep, nutrition, gastroenterology, ENT, fine motor, gross motor, etc –different specialists would take x-rays by digital camera and saliva samples by offering a cherry lollipop.  We’d then smile and move serenely from one specialist to the next, until we came to the end of the ride, where a cheerful uber-doctor would tell us in plain language what specifically we needed to do to help our child realize his potential.

The dream isn’t far off. 

Thanks to government grants, comprehensive development centers with specialties in autism spectrum disorders are springing up around the country.  And, after three months on a waiting list, we were ready to give our local autism center, located at our town’s most-respected children’s hospital,  a try.  We were particularly looking for an updated medical perspective.  Here’s a description of  our experience: (more…)

Trust Your Instincts! New Study Reveals Gap Between Possible and Actual Autism Diagnosis

Monday, May 11th, 2009

A study by Washington University professor Paul Shattuck, Ph.D. reveals that the average age of a child diagnosed with autism is six years old — that’s three to four years after a diagnosis is possible. Dr. Shattuck asks parents to trust their instincts, and follow up with any developmental concerns immediately. Closing the diagnosis gap will ensure that a child obtains the proper therapy and treatment as early as possible.

A note from Mae: Can you imagine the number of children who are mislabeled and misunderstood during those three to four years? Or those parents who blame themselves or their children for behavioral issues and delays?

See below to view the entire article or go directly to the Washington University website at http://news-info.wustl.edu/tips/page/normal/14077.html (more…)

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We  don’t assume these products will work for everyone–that’s why we ended the title with the parenthetical (for us). But if you are looking for new things to try, please read the accompanying blogs to view our experiences with these products. 

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L. Mae Wilkinson:

National Examiner for Autism and Education

National Public Policy Examiner

St. Louis Examiner for Autism and Parenting

Co-moderator, The Coffee Klatch blog talk radio and tweetchat 

Reporter,  Autism Hangout 

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