This group is dedicated to parents or family members of someone with Autism and Epilepsy or Developmentally Delayed Individuals.
Location: Palos Park, Illinois
Members: 33
Latest Activity: Apr 19
Started by Amie Gaines. Last reply by D Graham Mar 14. 1 Reply 0 Likes
I am a single parent who lives with my boyfriend because he was kind enough to take us in resulting from me not being able to financially take care of myself and my daughter. I have three older…Continue
Started by Candy Hester. Last reply by Jennifer Taylor Jan 30. 1 Reply 0 Likes
My son is 11 years old and on an IEP. He has a brother diagnosed with Aspergers and the school has asked that he now be tested also. Of course I've battled who is responsible for testing and his…Continue
Started by cathy castille. Last reply by Jennifer Taylor Nov 1, 2012. 2 Replies 0 Likes
Hello, I was wondering what any of you have taken for your seizures during pregnancy. I took trilleptal for both my pregnancies. I have an 8 yr old boy and a 4 yr old girl both were healthy and fine…Continue
Started by LizaCallahan. Last reply by Jennifer Taylor Nov 1, 2012. 2 Replies 1 Like
We hear so much about autism awareness but so little about epilepsy awareness -which is weird because epilepsy is so common among people with autism. I just finished writing a book about my…Continue
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Comment by Jennifer Taylor on September 30, 2012 at 12:41pm My 15 yr old daughter has tonic-clonic seizures and was just diagnosed with Asperger's Syndrome a few days ago. I'm still trying to process it all.
We're still battling the system (and Medicaid)! J's neuro still asks me if he has "autism behaviors"! Well, duh, he has autism so he has autism behaviors. He stims, he has OCD spots, he has learning disabilities, he has speech problems, he's very SPD, he gets violent with anxiety. Autism is something you don't grow out of or get cured from (unless God grants you a miracle with a new brain wave pattern). High functioning PPD's/Aspies can learn to overcome many of their issues. But they still have the issues, just have learned to appear NT.
It's pretty common sense - if your brain is misfunctioning enough to have one disorder, it's probably going to have other disorders or issues. Epilepsy damages brain cells and changes neuron pathways, therefore it disrupts the normal ability to process logic in a normal way. It's just that each person is impacted in a different way, to a different level, depending on many factors. I guess it all depends on what is causing the brains disruption in normal functioning.
Hope you all find the right help you need. HUGS
Comment by sandra acre on September 27, 2012 at 10:27pm When my daughter (Now 19) had intractable Infantile Spasms we took her to Canada for a PET scan and a doctor who specialized in IS. He told us that over 90% of kids with IS also have Autism so get her evaluated. He told us one doesn't cause the other, but the underlying damage (wherever it is hidden) causes both. Indeed we got her evaluated and into an Early Intervention program, but the neurologists at our regular hospital did not seem to want to connect epilepsy and "behavior," which is how I think they viewed autism at the time. They were brain doctors, and as far as they were concerned the seizures had to stop and who cares what else you work on. Thank God for good social workers and second/third/fourth opinions!
Comment by Melissa Smith on May 31, 2012 at 12:30pm It's strange how nobody in the public believes autism & epilepsy are related because not only can children born with autism have higher brain stimulation that puts them at risk for brain damage. Having Epilepsy will cause them to keep to them selves, people rarely talk to a person with seizures, & the same amount of discrimination and can cause epileptics to develope autistic symptoms over time.
Although the public is starting to pay closer attention to autism. It just isn't right that they ignore the need of epileptics.
Comment by Beth Baker on February 23, 2012 at 10:03pm Hi Kathy,
I am sorry you've worked so hard and now are combating Epilepsy as well. If the Keppra isn't cutting it, there could be some other medication out there that could, don't give up! If your son does well with dietary changes, and medication does not work, the Ketogenic diet is an option. Check out the website: charliefoundation.org or there are links to it on my website through my blog: www.calebsmom.com Best wishes to you and your family for answers and solutions.
Hi Kathy-I have a 36 year old daughter who had her first tonic clonic seizure at age 32 and after drug interactions with Depakote and/or Zyprexa she ended up bedridden for almost a year and finally after a few hospitalizations she remains on dilantin and seroquel(she became very manic)she needed 24/7 care but did regain her ability to walk,feed herself,etc. but we parents had to make a very hard decision to place her in a carehome(excellent though). It is very scary when you have never used any meds like us all through their lives and then those tonic clonic seizures start. I pray you get some help,answers,but just keep loving your son and know you will just keep doing your best,sincerely Maureen
Hello
I have a 16 year old son who has recovered from Autism all thru diet and supplements along with therapy. Last August he had a grand mal seizure out of no where and is diagnosed with Epilespy. I have been working with him since the age of 2 to get him healed from Autism and now this. He has grand mal seizure and takes 4000 mg. of keppra a day. He still has been having seizures about every 4 weeks. I hate this because he has never been sick or took medicine until now. Anyone else going through this. We live in Kansas City Missouri.
Comment by LizaCallahan on June 24, 2011 at 11:19am We have updated our Terms of Service for eCommunities Groups.
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