MY DAUGHTER HAS HAD SO MANY PROBLEMS WITH HER MEDS. AND NOW WE ARE GETTING READY TO CHANGE THEM AGIAN DOSE ANYONE KNOW IF KEPPRA IS A GOOD MED. WITH FEW SIDE...
My daughter takes 2000 per day. She has no side effects, but others have reported mood problems and tiredness. She's 12. By the way, I'm headed out of ...
Hello, Just a note to let you know that The Neurological Resource Center (TNRC) will be holding a seminar titled "The Bill of Rights for People with Epilepsy"....
When my daughter was three when she was diagnosed with epilepsy. Now that she is eight it is getting hard for her to understand why she has seizures and why...
Just recieved this from TNRC regarding the upcoming seminar: Larry (TNRC) One note of change; because we are expecting quite a large crowd, lunch will not be...
I sure know how you feel! My daughter's 12, and we're walking a really tight rope. Though she continues to have several seizures a year, she hasn't had one...
Sue, Thank you so much for telling me your story. I completely understand your daughters feelings. It sounds like they have a lot in common. Take care....
As un-luck would have it...my daughter had a grand mal seizure today. She had one about 2 months ago, one a couple of weeks before that, and then she hadn't...
I am sorry to hear that your daughter is going through such a tough time. Did you recently change her meds or is it time for an increase? My daughter usually...
Hi Becky, Thanks for the kind thoughts. When Chelsi had seizures a couple of months ago, she was in a weird transition with her drugs. She now takes Keppra...
Hello there! I'd like to say that this is a great way to feel better about my epilepsy: knowing that there are others out there like me. I had my first seizure...
Hello again! I see you found the list. Welcome! It's been a little quiet here lately, but hopefully you'll find someone to talk to. I don't have epilepsy,...
Hi everyone, I don't have epilepsy, but my husband does. He was diagnosed 3 years ago when we were trying to find out where his seizures were coming from. In...
Hi Sue, Thanks for your response! So the Lamictal really can have side effects...I thought I was going crazy. I'm still taking it but it's making me...
Hi Emily, I don't have seizures but my 20 year old son does and before he was diagnosed I know that he was really depressed. He was having them at night so we...
Hi Emily, We tried Lamictal twice. Granted - my daughter was only 4 at the time, and 8 the second time. Can't really tell you if she had less seizures with...
Hi Sam & Everyone, Since my daughter (Chelsi) is 12, I think we're just starting the "I feel different because I have seizures" thing. I don't know how to...
Hello all We are pleased to let you know that our new updated Epilepsy Website is available for viewing. www.2betrhealth.com We hope you like the new look. In...
Hello my Name is Heidi, im 26, I was born with Epilepsy, I have myoclonic tonic nocturnal juvinelle epilepsy. I am trying to find info on 2 things... #1 trying...
Heidi: You can find some scholarship information here; Search for "epiepsy scholarship" in any search engine to get more (many are local and may not apply to...
Hi, Is anyone interested in coming to this conference? It is free of charge, and travel assistance is available for those with limited resources. Please ...
Hi Sue. I am sure that we mentioned this fact in our Triggers List. You do have it don't you? Under Hormonal changes. If you want some more info on this I will...
Hi Sue, Thank you for the welcome. =) I honestly dont remember if the two came at the same time, mine were very spiratic, just like you described nothing for a...
Thanks Heidi! Sorry it's taken so long to respond, but I've been a bit under the weather myself. Take care, Sue In a message dated 10/30/2006 8:33:34 A.M....
"The Bill of Rights for People Living with Epilepsy" will be Held Friday November 10. 06 at the Richland Community Center, 500 Amon Park Drive in Richland, WA....
Hello, Just a note to let you know that The Neurological Resource Center (TNRC) will be holding a seminar titled "The Bill of Rights for People Living with...
Hello... My name is Lynn. I'm new to this site. I was reading your post and I understand how you feel...at least I think I do. I was finally diagnosed in...
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