Guest guest Posted October 4, 2005 Report Share Posted October 4, 2005 http://www.pecanbread.com/seizures.html SCD for Seizure Control http://www.breakingtheviciouscycle.info/autism/autism_with_no_gi_problems.htm I was afraid of how it would interfere with her seizure meds http://www.breakingtheviciouscycle.info/testimonies/rachael_recovers_fron_siezur\ es.htm recovers fron Siezures ________________________________________ Loving Care, Grammy E-mail: Grammy_Bauer@... FAX: 1- IN *My Web Site: http://www.SCDiet.net/ Contact: hebegb70@... *Put in Subject: SCDiet SCD PALS, Please *** Or I may not see your post to me. ALSO: *** *FOR SCD-Friendly Doctor; help, Compunding Pharmacy, and Vacation area, please ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ *LIST OF SCD FOODS: E-mail to scdiet@... SCDiet.com will provide this at no charge. In the subject put CARD REQUEST Give your name and address to get it snail mail. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Active Parenting Today Online Groups [parenting classes from the comfort of home] Join: *http://www.activeparenting.com/aptog.htm THERE IS A LIFE AFTER IBD! --------------------------------- Yahoo! for Good Click here to donate to the Hurricane Katrina relief effort. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 4, 2005 Report Share Posted October 4, 2005 Thank you all for your responses & emails. The information has been very helpful. I have forwarded all the information and hope that she will give SCD a try. She is very encouraged by the progress my son has made on SCD. Thanks again, > > > > There is a 2.5 yr girl that goes to the same speech thearpy as my ASD > >son. > > > > She is not autistic, but has seizure disorder. She has been taking > >meds to > > > > control the seizures for the past year + > > > > > > > > Once she goes off the meds, she regresses and the seizures come back. > >I > > > > recommened SCD to her mother, but I'm not sure it will help her. Does > >anyone > > > > have any advice for me to give. I don't feel the meds will help her in > >the > >long > > > > term, something more can be done. > > > > > > > > Thank you, > > > > > > > > > > A former member of this list, Patty Dubrovic used a Ketogenic Diet for > >her > >child Katera > > > who had a seizure disorder. I believe she had the child on SCD at some > >point. Perhaps Jody > > > will be able to recall the details > > > > > > Carol F. > > > SCD 5 years, celiac > > > > > > > > > > > > > > > > > > > > > For information on the Specific Carbohydrate Diet, please read the book > >_Breaking the Vicious Cycle_ by Elaine Gottschall and read the following > >websites: > > > http://www.breakingtheviciouscycle.info > > > and > > > http://www.pecanbread.com > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2005 Report Share Posted October 5, 2005 > hi > > my point of epilepsy is this, epilepsy, autistis spectrum disorders and migraine all run along the same bio-chemical pathway > > Dr Reichelt based in oslo university norway did a study on people with schizophrenia and epilepsy and found that by removing wheat and dairy, their symptoms either decreased so dramatically that they no longer required medication or required very little > > hth Dr. R. likes GFCF. Carol F. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2005 Report Share Posted October 5, 2005 Before starting SCD, especially since this is a seizure disorder/epilepsy concern... Make certain the pediatric neurologist and pediatrician are well aware of the dietary changes contemplated because my understanding is that such dietary changes can change the medication levels found in the blood. This means, if on Trileptal for example (a widely used anticonvulsant drug), the simple blood test to check Trileptal level would probably be increased to watch for sudden increase within the bloodstream (there are known risk factors to having too much Trileptal in the system). I'm not against SCD by any means, but playing around with diet while on anticonvulsants is something that needs doctor supervision as well. Good luck... Here's a link describing epilepsy and seizure disorders: http://www.epilepsyfoundation.org/answerplace/faq.cfm seizures are one " symptom " of epilepsy, but seizures do not equal epilepsy diagnosis. Granted, ASD and Epilepsy are in the same realm. My best recommendation would be talk with your ped. neuro. and pediatrician FIRST... A diet change for a child w/ epilepsy is NOT something that should be done without Dr consultation (and constant monitoring). Best wishes, Carol Mom of 4; 5 yr old daughter has childhood epilepsy and 3.5 year old son has regressive autism > > > There is a 2.5 yr girl that goes to the same speech thearpy as my ASD > son. > > > She is not autistic, but has seizure disorder. She has been taking meds to > > > control the seizures for the past year + > > > > > > Once she goes off the meds, she regresses and the seizures come back. I > > > recommened SCD to her mother, but I'm not sure it will help her. Does > anyone > > > have any advice for me to give. I don't feel the meds will help her in the > long > > > term, something more can be done. > > > > > > Thank you, > > > > > > > A former member of this list, Patty Dubrovic used a Ketogenic Diet for her > child Katera > > who had a seizure disorder. I believe she had the child on SCD at some > point. Perhaps Jody > > will be able to recall the details > > > > Carol F. > > SCD 5 years, celiac > > > > > > > > > > > > > > For information on the Specific Carbohydrate Diet, please read the book > _Breaking the Vicious Cycle_ by Elaine Gottschall and read the following > websites: > > http://www.breakingtheviciouscycle.info > > and > > http://www.pecanbread.com > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2005 Report Share Posted October 5, 2005 > There is a 2.5 yr girl that goes to the same speech > thearpy as my ASD son. > She is not autistic, but has seizure disorder. She > has been taking meds to > control the seizures for the past year + > > Once she goes off the meds, she regresses and the > seizures come back. I > recommened SCD to her mother, but I'm not sure it > will help her. Does anyone > have any advice for me to give. I don't feel the > meds will help her in the long > term, something more can be done. > Hi , my 7 year old son Hudson has now been seizure free for just over a year, he started SCD for his gut condition in August last year and his last major status sseizure was two weeks after that, none since, major celebrations here since he was having to go to hospital every5-6 weeks to stop the seizures and having many small ones each day. SCD is the only thing that could have changed this. He's also medication free, we had to change meds just before we started so asked his neuro if we could go med free for a while, give it a few weeks before starting a new med and started SCD right then, never needed another medication. Hudson has cerebral palsy, we have many friends with epilepsy and though every sees the changes with their own eyes not one has wanted to try the diet- so by all means recommend the diet but don't put a friendship on the line, so many people believe their neuro's that the epilepsy is intractible and only the right combination of medication will help, nothing else can because it's the brain that is damaged and nothing will change that. We no longer bother to see our neuro since he would never recommend the diet or even acknowledge that the diet is the only factor that could cause the seizures to stop, they think it's just a pause in his epilepsy and we'll be back- hahahaha!! I'm happy for anyone to give my email address to anyone who wants more details on his epilepsy, Chris in New Zealand. Send instant messages to your online friends http://au.messenger.yahoo.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2005 Report Share Posted October 5, 2005 Wow, your story is an inspiration. I'm glad your son is doing so well on SCD and med-free. I will forward your information to my friend. And you're absolutely right about recommending the diet. I've given her all the information and responses I received from this list, and I hope she gives it a try. I think she has some doubts. She has seen the progress my son has made on SCD and legal supplements…I really hope she gives it a try. Nothing to lose, right? Best, > > > > There is a 2.5 yr girl that goes to the same speech > > thearpy as my ASD son. > > She is not autistic, but has seizure disorder. She > > has been taking meds to > > control the seizures for the past year + > > > > Once she goes off the meds, she regresses and the > > seizures come back. I > > recommened SCD to her mother, but I'm not sure it > > will help her. Does anyone > > have any advice for me to give. I don't feel the > > meds will help her in the long > > term, something more can be done. > > > Hi , my 7 year old son Hudson has now been > seizure free for just over a year, he started SCD for > his gut condition in August last year and his last > major status sseizure was two weeks after that, none > since, major celebrations here since he was having to > go to hospital every5-6 weeks to stop the seizures and > having many small ones each day. SCD is the only thing > that could have changed this. He's also medication > free, we had to change meds just before we started so > asked his neuro if we could go med free for a while, > give it a few weeks before starting a new med and > started SCD right then, never needed another > medication. > Hudson has cerebral palsy, we have many friends with > epilepsy and though every sees the changes with their > own eyes not one has wanted to try the diet- so by all > means recommend the diet but don't put a friendship on > the line, so many people believe their neuro's that > the epilepsy is intractible and only the right > combination of medication will help, nothing else can > because it's the brain that is damaged and nothing > will change that. We no longer bother to see our neuro > since he would never recommend the diet or even > acknowledge that the diet is the only factor that > could cause the seizures to stop, they think it's just > a pause in his epilepsy and we'll be back- hahahaha!! > I'm happy for anyone to give my email address to > anyone who wants more details on his epilepsy, Chris > in New Zealand. > > Send instant messages to your online friends http:// au.messenger.yahoo.com Quote Link to comment Share on other sites More sharing options...
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