My 2 1/2 year-old grandson has just been diagnosed with Absence Seizures. He was seen by his pediatrician last week after we had observed a few weeks of staring off into space. His parents and I questioned what we were seeing and when we all discussed it, we realized there was a problem. He was seen today by a neurologist, scheduled for the first-available outpatient EEG (2 months away) and started on medication. He is bright and outspoken - already knows his numbers, colors and alphabet.

I guess I'd like to hear from other families who have experienced this. Right now, prior to starting his medication, he is experiencing upward of 20 witnessed episodes daily. The goal of the medication is to control this number.

Any advice out there?

Welcome to NT -
You've found a wonderful forum for care and support.
I'm very sorry for what you and your grandson are going thru.
This must be a very difficult time.

There are several forums here that you might benefit from.
Please feel at home here and holler if you need help in finding your way around.

Wishing you the best
Rae

Hello and welcome to NeuroTalk. Happy to see you have come to be with us. Just let us know if we can be of any help.

There are great number and caring fellow members here, just let us know how we can assist, you see we are are supportive and relaxing place to be. Our shoulders are here for support in many ways.

Check out the following forum. there are a great number of members there to help you out. I myself have epilepsy. I developed it when I was ten years of age, but I am now controlled.

http://neurotalk.psychcentral.com/forum11.html

Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Darlene

Welcome to NT

I hope you're finding your way around.

THere's lots of good info here.

Just take your time and ask if you need something.

Hello and Welcome, I am new too.