Community Forum Archive

The Epilepsy Community Forums are closed, and the information is archived. The content in this section may not be current or apply to all situations. In addition, forum questions and responses include information and content that has been generated by epilepsy community members. This content is not moderated. The information on these pages should not be substituted for medical advice from a healthcare provider. Experiences with epilepsy can vary greatly on an individual basis. Please contact your doctor or medical team if you have any questions about your situation. For more information, learn about epilepsy or visit our resources section.

Juvenile Myoclonic Epilepsy

Mon, 03/20/2006 - 12:45
Hello, Please excuse me if I sound like I don't know what I'm talking about. I don't. The possibility of epilepsy in our family has just very recently been brought up. Specifically -- juvenile myoclonic epilepsy. Perhaps not coincidentally our oldest son and I both have a history of unexplained "twitches" or spasms which last only a second or two. In both cases, we started noticing them sometime in our mid-teens. We don't lose consciousness. We are currently waiting for the results of our son's EEG. Does juvenile myoclonic epilepsy itself have any aftereffects which we should look for? Would fatigue/exhaustion be one? What about effects on memory? What about increased likelihood of headaches? I recently fell and badly injured my knee -- and have absolutely no recollection of the actual fall. Unfortunately, noone was around to see what happened. Thanks for any insights.

Comments

Re: Juvenile Myoclonic Epilepsy

Submitted by pongosmommy on Mon, 2006-03-20 - 13:14
Hi Michael I am sorry that I really don't have any insites into JME myself. I don't have that type of Epilepsy. But there is some really great info on the main page about JME. www.epilepsy.com/epilepsy/epilepsy_juvenilemyoclonic.html here are a couple more I found on the web for you to look at http://www.emedicine.com/NEURO/topic416.htm http://www.epilepsy.org.uk/info/juvenile.html I hope it helps, Dayna

Re: Juvenile Myoclonic Epilepsy

Submitted by Ssuuzzyy on Tue, 2006-03-21 - 09:13
Mom of 16 yr old boy diagnosed with JME in Nov 2005. Michael, I understand your situation. How old is your son? Mine is 16 and fell 3 times in the shower one morning before school before having a tonic clonic (grand mal) seizure after my husband pulled him out. The falls were the result of the myoclonic jerks which were so strong they knocked his legs out from under him. After the first fall he said that he was very tired while in the shower and he thought that was why he fell. We had no family history. We got him into a pediatric neurologist who did an eeg and confirmed JME. He has been on Depakote ER since Thanksgiving. Fatigue/exhaustion has been on ongoing issue but has gotten better overall. Part of that problem was that the Dr. ramped him up on the meds within 4 days instead of 3 months so he had a difficult adjustment period. He has not had any jerks or seizures since being on the medication. He is also very active -- a distance runner -- which is exhausting by itself, often running 9 miles/day. He has mentioned having some memory/concentration problems which seem to be getting a bit better. His school work suffered but his slowly improving. He did miss a lot of school initially because of being exhausted. I have read that oftentimes people have the "twitches" for some time before actually having a seizure. Onset of JME is typically between 12 and 20 years old. If it is JME the eeg should be definitive as to the seizure activity. Good luck to you both.

Re: Re: Juvenile Myoclonic Epilepsy

Submitted by Ashley on Wed, 2006-06-07 - 21:31
hey, im 15, and i have JME, i got diagnosed in febuary i was having the small twitches like you and your son are having, and then when i would get really upset, or if i would get stressed out, it would lead to passing out, i wouldnt be out completely, i could hear ppl it was like i really light sleep and it would only last for a few min. and i wouldnt shake or anything. and then after i woke up i would start twitching again, and i would usually twitch for about 10 min, before i "passed out". When i got my EEG done, it just showed slight abnormalitys and nothing major, but my symptoms matched perfect to JME, so they went ahead and put me on medicine for it, i have been through 3 different medicines since febuary, we are still trying to find one that works for me :S...i got put on a new one today and i dont really like it. But im feeling better seizure wise, but Good luck xx --ashley

Sign Up for Emails

Stay up to date with the latest epilepsy news, stories from the community, and more.