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...
Read you loud and clear, Blain! I was able to contact Sara through email and we're thinking of having a face to face meeting sometime in January. What do you...
Hi Sue, this be Blain. I just emailed you on the idea of having a face to face meeting in January, and I think it would be a good idea. A man just moved into...
Yes, I remember Ben and his dad! I hope Ben is doing well and can join us for the meeting. I'll get with Sara, we'll figure out a couple of dates and scan...
Good job Lynn. It just takes a bit of figuring out sometimes.Knew you could do it :). Maraika Cent_Wa_Epilepsy_Support@yahoogroups.com wrote: There is 1...
Hi everyone, Epilepsy Foundation America's media relations team has worked for weeks to help USAToday with two stories that are featured in today’s paper....
Yes, this be Blain. I believe in the story that not being able to drive, do to epilepsy, is a disorder in it's self. I have not been able to drive in over 6...
Hey Blain, I couldn't get either article to open...but I do work for the City, and if their transit isn't serving the citizens, then you need to let them...
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