The Epilepsy Foundation of America has created a little bear that will be journeying the world to visit all epileptics of all ages. His mission is to help aid...
Hello all, My name is Tina and I have a 15 month old boy named Ryan. He has PVL, Spastic Quad CP, Mickey button, Absence siezures and Infantile Spasms. We...
Hi Tina, Welcome to this inactive group. When my son started the diet he was having around 30 drop seizures a day. For one month we noticed NO change at all,...
Hi Tina, and welcome. My son is on the keto diet - since June 01. He is 5 yrs old. It took months for the diet to kick in for my son, about 3 months to...
Hi Jenn, Thank you for the response. Ryan fasted before he started the diet. He was in large Ketones after 27 hours. He still had over a hundred seizures...
Hi to all my name is Linn.My 11yr old son Daniel was diagnosed with epilepsy in July.He has had 15 Grand mals since that time and according to his EEG he also...
Hi everyone, I have a seven year old with autism who experiences absence seizures. I first heard about the ketogenic diet when researching treatment options...
Hi i am new here. my name is john, i am 15 wiht epilepsy. My doctor is about to put me on VNS. it seesms that everyone here is partial to the diet, but do...
... A 15 year old just posted on the other ketogenic list about the VNS she had recently got. Her name was Ann. Sign up to the ketogenic list on yahoo and ask....
rose thanks for the reply.... it sounds like the vns was very successful for your son... that is really encouraging... thanks for the info... i really like...
hi everyone, i am new here. my name is susan, i have a 13 year old son with epilepsy. i have been researcing alternative treatments because he is not...
Hi Susan, I dont have too much info on the VNS - from what I have heard, it works for some and doesnt for some. There is alot of info on the internet - a good...
Susan, Hi, I am Rose Homuth. I have two sons. One that is 28 and one that is 14. Both have siezure disorders. The oldest has the vns, and the younger is on the...
Hi, I was very happy with the diet, it worked relly well for my daughter, puberty might be tougher because hormones set off seizures for my daughter. I...
Hello! This is David Rank. You may already know about our long journey with our daughter, Sarah Dudley, and our life with a brain tumor. We are inviting you to...
Susan, i have been researching VNS very extensively for my son Mike. After consultations wiht doctors and representatives at cyberonics, we have decided to get...
ok so this site may be dead, but i am going to write this any way. We have finaly gotten everything taken care of for mike and the VNS. he is getting it next...
Hi If anyone has any suggestions please mail me My daughter has been on the diet for about 18 months We have been very happy with it. She was losing way too...
Hi, My name is Tammy and I have a son who is 7yrs old....with Severe Intractable Epilepsy. There is no more medications to try.... and he is not a canidate for...
Tammy, Why don't you join the "ketogenic" list at yahoo groups as well? There are lots of families that have been in the same position as you have. There's a ...
Tammy, I am sorry to hear about your troubles... We have all been through what you are going through, so we understand. My son mike, got the VNS implant about...
My daughter Taylor is 2 1/2, she suffers from Lennox Gastaut syndrome. She has hundreds of violent seizures a day (mostly drop attacks that occur in clusters)....
Hi, my advice is to give the diet plenty of time. I'd say at least two months. When my son started on the diet we did not notice any improvement at all for a...
Jana - Thanks for the encouragement, I know it will be tough to get the hang of, but it is all worth it. I'll keep you posted. Thanks Again ... From:...
Hi my name is jaime and my 18 month old was diag. with infantile spasm in may. we have tried acth and depakote with no success. now i am deciding whether to go...
