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.

New here

Sat, 05/04/2013 - 09:13

Hi,new here.I have a little 5 year old girl with absence seizures.

Comments

Re: New here

Submitted by mereloaded on Tue, 2013-05-07 - 18:37
Hi there. I am new here, my son is 15 and just had a seizure 2 months ago first time ever. I have a question for you, why do you have to wait 2 months for an EEG result? That is unreasonable. I know that you have to wait for the neuro appointment an average of 2 months, but there is no reason that you have to wait 2 months for the results. On most practices, you can call ahead of the appointment and ASK for the results. Neuros know of the waiting times for appointments and usually have a nurse on call that can tell you the results before the appointment and also answer some questions. Call your practice and ask them, there is really no reason to wait 2 months to know. Best wishes!

Re: New here

Submitted by katiesmom2008 on Wed, 2013-05-08 - 16:56
Hi,we had to wait 1 month for EEG and 1 month for the result.And only for our GP and me ringing the hospital a good few times. Thats i guess how things are in ireland. Very slow. My daugther is on medication now and doing better. Did you get a appointment/EGG for your son? Regards

Re: New here

Submitted by mereloaded on Wed, 2013-05-08 - 18:08
I am in the US. Sorry that it has taken forever, I feel your frustration. I had to wait 2 months to see a neuro for my son. The EEG was done within a few days and I had the results within 2 days. They gave me the results ahead of time over the phone. I guess it is because you are going through a general practitioner and not a neurologist. I guess you will need a referral to see a specialist. There is a great website in the UK that gives you a detailed list of neurologist in the UK. here: http://www.epilepsy.org.uk/ My son is been on keppra for almost 3 months and doing great, no relapses. We did lifestyle adjustments: diet, dha pills, vitamins, earlier bed time, no staying up late and very little video games. I think all together it has helped. So far so good. I hope your son feels better too. Please know that you are not alone. best wishes!!!!!!!!!!!!!

Sign Up for Emails

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