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        <![CDATA[Latest posts for the topic "epilepsy and autism" recent IAN discussions]]>
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		<description><![CDATA[Latest messages posted in the topic "epilepsy and autism"]]></description>
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				<title>epilepsy and autism</title>
				<description><![CDATA[ Despite the statistic that approximately 30% of individuals with autism will also have epilespy, I have not read much about epilepsy concurrent with autism. My adult child has intractable epilepsy and I am interested in talking to parents and professionals that have had experience dealing with both. The autism has been difficult, but the epilepsy has been much more difficult.]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#141</guid>
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				<pubDate><![CDATA[Sat, April 7, 2007]]> GMT</pubDate>
				<author><![CDATA[ angie young]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Thank you so much for your post.  

One question we are asking in the IAN Research questionnaires is about seizures and epilepsy.  As the data comes in, it will be important to find out how many parents are coping with this issue, and how it relates to other issues.]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#159</guid>
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				<pubDate><![CDATA[Tue, April 10, 2007]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ My son is 2 years old and has been taking zonegran (zonisamide) to help control his partial seizures.  Luckily with the help of this medication we have seen that the seizures are almost undetectable now.  At about 15 months we began noticing the seizures.  They started out as more staring seizures and once we put him on Keppra they began getting worse.  This is about the same time we really began noticing the "red flags" of autism.  I was really afraid the seizures would be a huge issue, as they were at first.  Now my son's Autism is more in the fore front than the seizures themselves.  ]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#170</guid>
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				<pubDate><![CDATA[Sat, April 14, 2007]]> GMT</pubDate>
				<author><![CDATA[ indianamomof2]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ My husband had intractable complex partial epilepsy and L anterior temporal lobectomy in 2001. I wondered if some of our sons behaviors could of been seizure disorder, but his 24 hr EEG showed no epileptiform activity. So we are back to the AS diagnosis.]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#171</guid>
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				<pubDate><![CDATA[Sat, April 14, 2007]]> GMT</pubDate>
				<author><![CDATA[ Cmom]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ My son just turned three, he was diagnosed with Autism just after he turned 2 and he was diagnosed with Epilepsy in October, six months after we started seeing the seizures, his stupid neurologist who is no longer his neurologist completely fixated on the fact that he had Autism and said what we were seeing was behavioral, it took my son having a seizure in his pediatricians office for it to be taken seriously, now he has been on meds since October, he had his last seizure the day he started his meds, he started off on tegratol and has recently switched to Trileptal which is known to have less serious side effects.
Tania
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				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#188</guid>
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				<pubDate><![CDATA[Tue, April 17, 2007]]> GMT</pubDate>
				<author><![CDATA[ justaboatguyswife]]></author>
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				<title>"K-9s for Autism/Seizures"</title>
				<description><![CDATA[ We are "The UNITED STATES K-9 Academy", which does an extensive amount of work and support for individuals with Autism/Seizures, nationwide. Take a look at our website (www.US-K9.com), which will give you more helpful information. Thank you, David Caylor Vice-President US-K9 davidcaylor@US-K9.com (760) 965-9763 ]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#219</guid>
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				<pubDate><![CDATA[Sat, April 28, 2007]]> GMT</pubDate>
				<author><![CDATA[ "K-9s for Autism/Seizures"]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ I was just looking over some of the research results and read that epilepsy in autism occurs most often in children with mental retardation. I would be very interested in more information about this.  My five year old son was diagnosed with seizure disorder at 10 months old and autism at 18 months.  Though he has not been diagnosed with mental retardation, he is not progressing as quickly as we had hoped and fights repeated periods of regression.  Can anyone direct me to more information on these issues?  And, how deeply will the IAN research delve into this particular issue?

Thanks,
Ivy]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#241</guid>
				<link>http://kki.qorvis.com/forum/posts/list/54.page#241</link>
				<pubDate><![CDATA[Sat, May 5, 2007]]> GMT</pubDate>
				<author><![CDATA[ Ivy]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hi Ivy.  I'm so sorry to hear that you and your son have had to cope with seizures in addition to an ASD.  :( 

I am not an expert in this specific area, but I will try to answer your question.  From looking at the scientific literature, it is clear we still don't know exactly why there is a connection between the Autism Spectrum Disorders and epilepsy, although there certainly is one.  The percentage of children with ASDs who also have epilepsy varies widely in studies --from 5 to 38%-- partly because children of different ages and different diagnoses (only autism, mixed ASDs) are being considered.  (Looking at only younger children will minimize the number because a large number of individuals only develop epilepsy after age 10 or even further into adolescence.)  

In one study, the risk of epilepsy "rose with both age and presumed diffuseness of the underlying brain dysfunction as shown by the severity of the cognitive deficit and the presence of cerebral palsy or other overt motor deficits." Children with normal or near-normal intelligence and no other risk factors (like cerebral palsy) had a very low rate of occurrence of epilepsy. (See "Epilepsy in Autism" by Tuchman and Rapin in <i>The Lancet Neurology </i>October 2002, Vol. 1, Issue 6.)

If you would like to dig deep yourself into the medical literature, the article cited above would be a good start.  (Articles have references to other articles, and you can quickly generate an entire stack on any topic to study.) Abstracts (which are quick summaries) are available to the public for free at www.pubmed.gov; to get full articles you might have to pay for them or make a trip to a medical library. Tips on how to evaluate the scientific articles you read can be found in "A Uniform Framework for Evaluating Research Studies" here: http://www.iancommunity.org/cs/understanding_research/oar_uniform_framework_for_eval_research

In truth, we do not yet have complete answers on the link between epilepsy and autism.  IAN will be able to play a role in future studies by providing data not on just a few, but on thousands of children, to researchers investigating this issue, as well as many others.

In addition, just by your post here, your views and priorities will be included when we at IAN meet with researchers.  We will be providing feedback and input from the Community, including these messageboards, to help make parents' voices heard.
]]></description>
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				<pubDate><![CDATA[Mon, May 7, 2007]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ That is wonderful to hear Connie, that IAN will be helping compile new statistics about Autism and Seizure disorder.  I too think there is some connection, too many children are affected by both things for there to be just a casual connection.

I will be very glad to see that part of the findings being compiled into stats.  It's very exciting to be part of this project, as a parent I want to thank you all for all the hard work you've put into this project and I have very high hopes for IAN, and will help any way I can. :)

]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#251</guid>
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				<pubDate><![CDATA[Tue, May 8, 2007]]> GMT</pubDate>
				<author><![CDATA[ Pamster]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Thank you for your encouraging words, Pamster.  :D 

In truth, it is we at IAN who must thank every parent who sits down in front of their PC and takes the time to share their information, not to mention all the people out spreading the word about IAN so that parents will know about us.  Our deepest thanks to all of YOU!]]></description>
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				<pubDate><![CDATA[Wed, May 9, 2007]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hi,

I have twin boys, 11 yrs old, both on the Spectrum.  One twin, Baby A, is easier to manage than the other, and is currently diagnosed with Aspergers.  This is the one who did have gran mal seizures earlier in life.  He was on phenobarbital for over a year, starting when he was 25 months old.  

He is also the one who didn't verbalize until 23 months, and then at age 3 began needing speech therapy for severe stuttering. 

He no longer has the seizures or the stuttering.  8)
]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#267</guid>
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				<pubDate><![CDATA[Thu, May 10, 2007]]> GMT</pubDate>
				<author><![CDATA[ With2ontheSpectrum]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ My son is 7 years old and has ASD.  He to is having seizers but only when he gets sick like a cold.  But this last time he had a seizer but he wasn't sick, when he has them its only when he sick, I took him to a new place and he got scared.  The next morning he had a seizer.  The neurologist said his brain overloads and that's why he has them.  His seizers consist of drooling, blank stare, teeth clenched, and limp then he goes to sleep.  It scares me when he has them.  The doctor won't do tests because he would have to put him to sleep and there is a risk.  He said they are on-set seizers what is the difference between the seizers and is it a form of epilepsy?]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#388</guid>
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				<pubDate><![CDATA[Thu, June 28, 2007]]> GMT</pubDate>
				<author><![CDATA[ bearsmiss]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hi, bearsmiss!  :-) 

I am so sorry to hear that your young son with ASD also has to struggle with seizures --those can be very scary and upsetting for both parent and child.  Your local physicians will have to decide exactly what type of seizures, and how to treat them, but I can provide some general information.

Epilepsy is defined as two unprovoked seizures.  So if a person has had more than one unprovoked seizure, you could say they have epilepsy.  In people with autism, seizures often occur either before 5 years of age or after 10 years of age, but they may begin at any time.  

We're not sure how many children with ASDs also have seizures.  Various studies have placed it somewhere between 20 and 33%. So far, 8% of children with ASDs taking part in our IAN Research study have reported seizures. That number goes up to 12% if we look only at children age 10 and over. (Since some children don't develop seizures until later, it is more accurate to look at older kids to get your percentage.) 

For many parents, it is difficult to get the information they need during hurried and stressed medical appointments.  Still, I would urge you to ask your doctor to explain exactly what he means by "on-set seizures" and anything else you want to understand better.  You might start by saying, "Doctor, it's very important for me to understand what is happening with my son.  What do you mean by 'onset seizure'?"  (or whatever your question is).  If you ask clearly, showing how important the information is, and the doctor does NOT provide a good, patient answer, you may want to consider finding a doctor who will communicate better with you. 

Sometimes it helps to go to the appointment with your questions written down, so you can hand it to the doctor and he or she can see the list.  It also gives you somewhere to write down the doctor's answers to help you remember what he or she said later.

My best wishes to you and your son.

]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#390</guid>
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				<pubDate><![CDATA[Thu, June 28, 2007]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ My 15 yr old son with Aspergers recently had two seizures.  He was seen by 3 Neurologists, who all agreed that the root cause of his seizures was not due to classic epilepsy.  They all agreed due to my description of the events that led to and his activity during the seizures had to be Cardiac in nature.  We are fortunate enough to live in the Philadelphia area, and had the correct testing and knowledgable physician to prove that the seizures were due to a vaso-vagal response to severe orthostatic hypotension. 
I am not sure if it is just due to his tall thin physic or his hypotonia due to his ASD.  He has been a beta blocker and no further seizures and a well adjusted blood pressure and heart rate.  I am wondering if orthostatic hypotension is common among children with ASD.
 
]]></description>
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				<pubDate><![CDATA[Mon, September 17, 2007]]> GMT</pubDate>
				<author><![CDATA[ Tkasp]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hi Tkasp.  :-) 

I have been unable to find anything in the medical literature relating orthostatic hypotension (more commonly referred to as a "head rush" or "dizzy spell") and autism spectrum disorders.  Hypotonia --that is, low muscle tone-- is quite common, however, and is likely part of the reason for the motor issues experienced by so many children with ASDs. (About 50% of the children with ASDs taking part in IAN Research have been diagnosed with a motor delay of some kind.)

If other parents have noticed that their child with ASD has also experienced orthostatic hypotension, I hope they will comment!]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#515</guid>
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				<pubDate><![CDATA[Tue, September 18, 2007]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Thanks, Connie!]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#526</guid>
				<link>http://kki.qorvis.com/forum/posts/list/54.page#526</link>
				<pubDate><![CDATA[Sun, September 23, 2007]]> GMT</pubDate>
				<author><![CDATA[ Tkasp]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Tkasp, you're welcome! Thanks for your post. :D ]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#527</guid>
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				<pubDate><![CDATA[Mon, September 24, 2007]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Seizures and autism may go together, but in my family it's in two different children.  My older daughter has autism.  My younger daughter has a mitochondrial disease that manifests with seizures, which we have only partially controlled.  :shock: Things are a little complicated at my house sometimes.]]></description>
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				<pubDate><![CDATA[Mon, October 8, 2007]]> GMT</pubDate>
				<author><![CDATA[ RevJJ]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ My son has been diagnosed with Autism and Landau Kleffner Syndrome..I often wonder if he only has Autism with seizures and not the L.K.S. He was delayed in being diagnosed with Autism, that is why they are thinking L.K.S., but, he doesn't have night seizures, only day time ones and it seems like the meds are constantly cycling. He will go 5 weeks without one, then start right back up again. He is LOADED with meds right now and I hate it.
Anyone have any thoughts??
Amanda]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#947</guid>
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				<pubDate><![CDATA[Fri, July 4, 2008]]> GMT</pubDate>
				<author><![CDATA[ Boog's Mom]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hi Boog's Mom. :) I'm so sorry to hear about all the difficulties you and your son are going through right now.

Just to let you know, it definitely takes experts to distinguish Landau-Kleffner syndrome from autism. Shinnar et al. describe it in their 2001 <i>Pediatric Neurology </i>article, "Language Regression in Childhood,":

<i>"The Landau-Kleffner syndrome or acquired epileptic aphasia is a childhood epilepsy syndrome in which children with previously acquired language undergo a regression of language in association with either clinical seizures or an epileptiform EEG or both."</i>

Autism can also involve loss of language skills and/or seizures. What is most important as you work with the team evaluating your child is to ask questions. Sometimes professionals forget to slow down and share their reasoning with you - how did they come to a certain diagnosis? What was their own mental process, as they looked at your child's profile and behaviors? You should definitely feel empowered to ask them to slow down and explain what they saw and why it led them to make the diagnosis they did, as well as how they then went on to propose a certain treatment.

Another thing to keep in mind whenever you deal with medical or mental health professionals is what specific field they are in. Each discipline has its own "lens." That is, a neurologist may approach a problem from one angle (maybe focusing on the child's EEG), a psychiatrist from another (maybe focusing on the child's behavior). Autism is so complex, in all its aspects, it almost forces parents to be able to shift their own perspectives, trying to see what's going on from all of these angles at once, and to encourage the professionals working with them to do the same.

]]></description>
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				<pubDate><![CDATA[Tue, July 8, 2008]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ It seems as if it's been a while since anyone posted on this topic. I have only recently found this very promising site. 

We discovered our son having a grand mal seizure upon waking when he was 17. He's 19 now and we have been seeing a biomed expert recommended by our internist. We have also seen an epileptologist and 2 nuerologists who seem to know very little about an autism/epilepsy connection. Since the first seizure he had a few more and then, after switching to a slightly different supplement protocol he began having a nocturnal seizure every 6 or 8 weeks. He has very low zinc and pyruvate levels and it seems to be tied in with glutamate (the first two seemed connected to having eaten food with msg).

He is mildly on the spectrum, maybe aspergers, very bright and the biomed protocol has done wonders for the spectrum issues but I'm fearing it's not enough for the seizures. How i wish there were a source of information that brought these two areas together in a more meaningful way. It's frustrating and the anxiety is overwhelming. We are thinking of putting him on lamictal but I'm very nervous about that. If autism is in part an inability to detox i cant see how putting such strong pharmaceuticals into his already taxed system could be a good thing. 

I'd greatly appreciate any advice, encouragement or direction.

Worn out,
F.]]></description>
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				<pubDate><![CDATA[Wed, February 18, 2009]]> GMT</pubDate>
				<author><![CDATA[ FrancineL]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hi FrancineL, and welcome to IAN. :)

I'm so sorry to hear that your son and family must cope not just with an autism spectrum disorder, but with seizures as well.

It has long been known that epilepsy (which is defined as two unprovoked seizures) occurs with greater frequency in individuals on the autism spectrum than in the general population. Researchers continue to explore the connection. A new article, "The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders," discusses this. The authors say it is long past time there was more treatment guidance, and propose a research agenda.

See: http://www.ncbi.nlm.nih.gov/pubmed/19218886?dopt=abstract

Of course, the frustrating thing is having to make decisions in the here and now before research has provided more guidance. (That is a frustration very familiar to any parent of a child on the autism spectrum, and is one reason IAN exists: to accelerate deperately needed research.)

The authors of the paper above said, with regard to treatment: <i>"Treatment of children with autism and epilepsy is guided by the principles of treating childhood epilepsy. Anti-epileptic drugs (AEDs) are chosen based on seizure type and clinicians strive for maximum seizure control with minimum side effects. The practicalities of certain treatment choices are very important in ASD. Factors such as available formulations (liquid vs. tablets vs. capsules), dosing schedules, need for blood monitoring, and, most importantly, behavioral side effects must be considered. It is important to note that treating epilepsy does not usually have a major impact on the autism symptomatology. Some children may show improvements in cognition, communication, or behavior, but the autism diagnosis does not change."</i>

The good news there is that they are not reporting that autism symptoms worsen as a result of treatments provided for epilepsy. 

As for whether medications may help...it is possible that they might. Parents are often reluctant to give their child medications, understandably, and that seems even more so for anything that effects the brain, from anti-seizure meds to antidepressants. One thing it is important to remember is that you can always try a medication and then stop it if you observe any negative side-effects. It is also important to keep in mind that there is some trial and error involved to find what works best, as un-fun as that process may be. Ultimately, you will need to consult with your medical team to decide if, when, and what to try. If you do decide to try medication, what may be most important is having a team that you know will be available if you have any concerns at all during the process.]]></description>
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				<pubDate><![CDATA[Wed, February 18, 2009]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ I had a few siezures as a child.  My mother has diagnosed epilepsy, her sister (my maternal aunt) has medication controlled epilepsy, and I have a 1st cousin on my mother's side of the family who has had seizures as an adult.  There is definately a trend toward epilepsy on my mother's side of the family.

I'd like to see the research eligibility on IAN extended to biological grandparents as well.  Having biological footprint over more than one generation is important in the medical history questionaires used on IAN, to get a better overall perspective of the family medical history.]]></description>
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				<pubDate><![CDATA[Thu, March 12, 2009]]> GMT</pubDate>
				<author><![CDATA[ MarineMom02]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ MarineMom02, we so agree! We have wanted to extend IAN Research to include another generation: grandparents. We are unfortunately not able to fund doing that in IAN Research at the moment because it would require a huge software overhaul. For now, we are working on a "Grandparents of Children with Autism Spectrum Disorders" survey that will appear on IAN Community, separate from IAN Research. This is a way we hope to give grandparents a voice even if we can't include them in IAN Research right now. I hope this will be ready by the summer of 2009. We have been working on it for over a year. :)]]></description>
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				<pubDate><![CDATA[Thu, March 12, 2009]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ I understand the large software and server issues that adding another generation would create.  Perhaps consider including a Family History questionaire that could be answered by the biological parent that looks at a variety of medical history of the family, not just psychological illnesses.

Most of us know our family history for genetically predisposed conditions so maybe just adding that as a survey, could assist until the funding is available to include them in the study.

A good idea to include it on the community site, but even better to be able to tie that history to children who we are completing research for onsite. ]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#1479</guid>
				<link>http://kki.qorvis.com/forum/posts/list/54.page#1479</link>
				<pubDate><![CDATA[Tue, March 17, 2009]]> GMT</pubDate>
				<author><![CDATA[ MarineMom02]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hello,
I have just discovered IAN, what an incredible resource/initiative! My son is 14 and has autism and epilepsy.  MRI scans of his brain have identified a damaged area(caused at birth due to asphyxia) which appears responsible for the complex partial seizures he experiences.  He also has occasional generalised seizures and lots of partial seizures (aura's).  He is currently on Tegretol (carbamazepine) and Topamax (topirimate) - not sure if these are the same drug names used in USA ?(We're in Australia). He's been on Tegretol for some years and has had no side affects.  He commenced Topamax about 18 months ago and initially experienced very heightened anxiety and increased stuttering/word loss.  This went on for about 5 months and I wanted to stop this AED but was encouraged to persist by my son's neurologist and paediatrician.  The symptoms have now settled and the combination of the two drugs are providing fairly good seizure control. I have often wondered about the autism/epilepsy diagnosis and whether there was a link.  I have also been interested to read other posts regarding nocturnal seizures.  My son has always woken through the night, appearing confused and not responsive.  We've never been quite sure if this is seizure activity or the after-effects of a dream (and so far have not pursued a sleeping EEG although this is still being considered.)  My son also has an intellectual disability (in the moderate range) and mild cerebral palsy. Anyhow, I look forward to reading further posts on this wonderful site.  
]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#1488</guid>
				<link>http://kki.qorvis.com/forum/posts/list/54.page#1488</link>
				<pubDate><![CDATA[Fri, March 20, 2009]]> GMT</pubDate>
				<author><![CDATA[ Tranquility]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hi Tranquility, and welcome to IAN. :)

So many families are coping with seizures in addition to autism spectrum disorders (ASDs). There is so much more we need to know about them and how they are related. One thing we hope to do at IAN is include seizures/epilepsy in an extensive "comorbidities" survey. This survey will ask about a long list of issues or conditions that frequently co-occur with ASD.  Our intent is to help researchers gain insight into which conditions occur how often...and in what type of individuals. Are there variations based on type of ASD (autism, Asperger's), developmental history, or any other factors? Do certain co-occurring conditions seem more frequent in certain "subtypes" of ASD? What clues does that knoweledge provide about causation, or potential ideal treatments?

(We are in the process of applying for a grant to fund the comorbidities survey right now.)]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#1492</guid>
				<link>http://kki.qorvis.com/forum/posts/list/54.page#1492</link>
				<pubDate><![CDATA[Fri, March 20, 2009]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ My 17 month old grandaughter bangs her head on the mattress constantly as she sleeps.  This can go on for hours, almost all night.  Her pediatrician says, it is normal.??????]]></description>
				<guid isPermaLink="true">http://kki.qorvis.com/forum/posts/list/54.page#1739</guid>
				<link>http://kki.qorvis.com/forum/posts/list/54.page#1739</link>
				<pubDate><![CDATA[Wed, September 16, 2009]]> GMT</pubDate>
				<author><![CDATA[ mcuebas]]></author>
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				<title>Re:epilepsy and autism</title>
				<description><![CDATA[ Hi mcuebas, and welcome to IAN. :)

I'm so sorry to hear about your family's worries about your granddaughter.

In the past, pediatricians have mostly advised parents not to worry, because all children do develop differently, and some are slower than others. However, they are now being urged to take a family's concerns more seriously - not to dismiss them, but to ask questions -- or so said the president-elect of the American Academy of Pediatrics (AAP) at the recent Autism Society of America (ASA) family conference. 

Of course, I do not know the exact situation for your family, but I can say in general: It is OK to go back to the pediatrician and say again, "We feel something is not right here. How many other children do this?" It is also OK to say, "We really will not be at peace until our child is seen by a specialist, such as a developmental pediatrician." One thing it might help to do is be ready with answers to other questions the pediatrician might have. For example, if there are concerns about autism, you might look at the "first signs" listed on the website by the same name, and be ready to discuss these with the doctor. If the head banging is the only issue, the doctor might counsel one thing. If there are other signs that are also worrisome, he might counsel something else.

You can find the First Signs site here: http://www.firstsigns.org/

I hope very much that your granddaughter is just displaying a little quirkiness, and that further discussion or evaluation will show no need for concern. If there is any concern, however, please do know that there are many resources to help your family, and many other families walking the same road.]]></description>
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				<link>http://kki.qorvis.com/forum/posts/list/54.page#1740</link>
				<pubDate><![CDATA[Wed, September 16, 2009]]> GMT</pubDate>
				<author><![CDATA[ Connie (IAN Staff)]]></author>
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