The Never Ending Autism Study. But, it is all good!!

Here is the info on what we did via the NESCA website



Children's Hospital Boston Research on Autism Spectrum Disorders

Children's Hospital Boston has asked our help in recruiting families to participate in their ongoing research study of possible genetic and environmental factors in the causation of autism spectrum disorders (ASD).

Participation will ordinarily require two hospital visits, the first generally lasting 4 - 5 hours and the second, about two hours, although these are estimates. Families may also choose to complete their involvement in a single, full-day appointment, from 9:00am - 4:00pm. Children's Hospital will validate parking for all participants, and families opting for the full day will also receive cafeteria meal vouchers.

Here's their information:

Autism Spectrum Disorder (ASD)
Study at Children’s Hospital Boston

· Who we are

We are a group of doctors and researchers from the Developmental Medicine Center, the Division of Genetics, the Department of Neurology, and the Program in Genomics at Children’s Hospital Boston.

· What we study and its importance

We are studying ASD and related disorders in order to better understand why they occur, increase our ability for early identification, and find improved treatments and an eventual cure. Specifically, we collect information on children aged 18 months and up who are diagnosed with ASD and their families.

· Your involvement

Participation in this study involves two research visits at Children’s Hospital Boston. We interview all immediate family members, including the individual diagnosed with ASD. The data we collect includes general facts about developmental history, family history, and environmental information. We also collect genetic material from a blood or saliva sample in order to look for possible gene changes that may be related to ASD.

Shortly after the visits, families receive a research report of our observations that includes developmental, cognitive, behavioral and social findings.

If you are interested in participating or would like more information, please contact us at 1-866-982-5826 (toll-free) or 617-355-9152. You can also email us at ASDResearch@childrens.harvard.edu.

We were also sent home with homework and $120 worth of American Express gift cheques. $40 per kid.


And a little homework. These envelopes were stuffed full of info on all five of us. Asking questions on behavior and communication over and over again in different ways. Making sure we answered the question the same way every time.  This took about 2 hours.

I also got a one hour follow up call this week filling in any questions that were unanswered and agreed to do a 2 hour over the phone interview/ research study to help them come up with a form to better identify children with autism at regular pediatricians visits.

I have a feeling I will be asked to do more.  But, the more we can do as a family, the further I hope we can get the information we need to help identify and find treatments or cures for Autism.

Plus they have to tell us anything they find in our gene pool that is treatable. This is for our entire lives. We gave them permission to use our blood for any research studies they would like. We can either decide to participate in interviews/paperwork (or not) that are associated with new studies.


This was well worth it for our family in more ways than one and probably will not end for a long time.

Autism, Epilepsy and Type 1 Diabetes Blaaahhhh

     Sometimes Type 1 Diabetes gets in the way of Autism and Autism gets in the way of Type 1 Diabetes. Today, Epilepsy took center stage. I try to keep things in little buckets and only think about one thing at a time, but occasionally that does not work.
 
     Like today. Keira had a Neurologists appointment at 10:30 and Kailyn had a Diabetes Appointment at 11:30. Then, Keira has her ABA teacher come to the house every day at 12 noon.  I had to choose and Autism/Epilepsy won by default.  Kailyn has NEVER needed a referral to the Endocrinologist nor have we had to pay a copay, but apparently we now do. I learned this when I opened a bill from her last visit on Saturday. Maybe too many children with Type 1 Diabetes are going to the Doctor so they can get their medicine and supplies to LIVE.  So, they decided to crack down on that. I mean really, a documented Type 1 Diabetic NEEDS a referral to get info on how to live and prescriptions to keep her alive? SERIOUSLY?

     The Neurologist appointment was normal. We talked about her seizures, looked at a recent video I took and talked about medication to keep the seizure monsters out of her brain.  Then came the news that her genetic deletion has now been linked to Epilepsy. She is no longer considered a Child with Benign Epilepsy. Now, she is considered to have Early Onset Epilepsy. All because of this gene mutation. I have to admit, I am taking it hard. Benign means she would outgrow it. Early onset means it is with her for life. I can't find much info on it either, which is frustrating.

     However, I am trying to take it with a grain of salt knowing that the research on the deletion is in its early stages.  And frankly, Doctors DO NOT know everything. It is a science. If they knew everything they would be able to tell us what the heck was going on! In my opinion, she has a form of Developmental Delay/Epilepsy that does not have a name yet. We go to Children's Hospital Boston in April (I have had this appointment since December) for a second opinion from an Epileptimologist that specializes in child development. They are ranked #1 in the nation. She may say the same thing, she may not. But, at least we are doing all we can to help our child meet her fullest potential in life.

Boston Trip: Children's Hospital Boston Research, Raincoat Cafe and Build a Bear.

We got up at 5am in hopes of leaving by 6am. We left at 6:10. We were going to Children's Hospital Boston to participate in a comprehensive study on Autism. Having two children on the spectrum and Keira with a special gene deletion associated with Autism made them especially interested in us. I swear the genetic researcher was bouncing up and down in her seat when I mentioned the deletion even though she already knew about it before we got there.

      A team of researchers from the Developmental Medicine Center greeted us on the 6th floor. Some Geneticists, a Psychologist, a Neurologist and a bunch of Post Docs were there to greet us. I think there were around eight of them. We checked in and they whisked us off to sign consent forms. After we got through all the paperwork we were all brought to separate rooms to be tested and interviewed for 3.5 hours. Everyone was fine with this part except Sam. At this point, I think he wished he had gone to school instead.  :) We got through the morning and then went down to the seriously busy cafeteria with vouchers in hand and a wide array of things to select from. One of Kailyn's favorite things about Hospitals is cafeterias. This one did not disappoint.

     Afterwards, we went back upstairs and they did a few more things with the kids while I was interviewed for another 3 hours. While I finished up interviewing, they took every one's blood except for Sam. We were waiting to do him last and did not tell him until the last minute because he would freak out. He did. He did not want what he called "a point" put in him even though they gave them numbing cream. We had to pin him down, but once he figured out it did not hurt he relaxed and watched the TV until his three vials were drawn. It was funny listening to them in the car talk about the blood draw. Kailyn swore that she had 5 vials taken and Sam said he had 4. Everyone in the family had three. I talked about both Sam and Keira for 6 hours yesterday. My face was bright red by the end of the day and my brain was fried. I still have a ton of homework to do that they sent home with me and more interviewing to do over the phone. They usually do the research in two trips, but since we were coming from so far we did it in one.

 This is them playing and being entertained while we waited for blood draws and for me to finish up interviewing.

 The Musical Stairs were a huge hit on our way out. We have been here a couple times and I never noticed this before.

Then off to Burlington and the Rainforest Cafe for a reward. (Or Raincoat Cafe as Kailyn enthusiastically shouted out to the researchers when we first got there) They were very good research participants. It was a long day of cognitive tests etc...and they did wonderful. Even Sam, who I hope won't be completely scarred for life about hospitals.

 In front of the fish tanks and rain.

 Sam and Keira both touching the rain. They inspected every inch of the restaurant and we survived two thunderstorms while we were there. There was a ginormous gorilla right next to our table. I thought it would freak Keira out, but no. Sam was the one that was scared and had to be convinced that it was not real. Kailyn wanted to get up and touch all of the animals.

 Type 1 Diabetes nightmare.

 Volcano cake for dessert. HUGE and thrilling for the kids. Never have had anything like it. Although, it could easily be recreated for a birthday party. ;) Keira loved playing with the top of it.

Then we went to the Lego Store and Build A Bear to get the rest of their rewards. All of them got bears. This was Keira's first bear and I named her Dreamy. She can't name things herself at this point. So, I named her this. I have big dreams and aspirations for Keira.

 The Bear Helper really made them work to put their hearts into their bears.Then, we finally left the mall. We basically closed it at 9pm. We headed home and they passed out on the way. First, Keira about 15 minutes after we got on the highway with Dreamy.

 Then Kailyn with Diabetes Bear and Candy.

 And finally Sam at 10pm, who usually goes to bed around 7:30, with Beary and Armyman Bear.

New and old Bears to cuddle with.

Keira woke up early, but Sam and Kailyn are still fast asleep. I will bring them to school when they wake up.(If they ever do) 

     Hopefully, we were helpful and will continue to be helpful in research for years to come. They will store our blood/DNA for years too and study it as needed. Our names are not on it. Just a number. However, if something major should ever come up they will track our names down and let us know. This also will help save us money on testing they wanted to do on Keira as well.