Hey Tammy,
I have read your posts too, and I love hearing all the things your Megan is doing.
My Megan had a roguh night last night but most nights are better. It is not as bad as the summer she turned 8. That was awful. She was so depressed and tired and thin. It ripped my heart out. I am hopful still that she will outgrow it, thats what the dr. at UCLA thought. Our neuro is kind and understanding but baffled. We are lucky that most days (nights) we don't have to deal with it. She has sure proved to me she is strong, she continues to get straight A's but has had understanding teachers too. Now she has a 504 that allows her to take her time on tests due the fact that she has night time episodes as well as severa sleep obstructive apnea.
As we opened up and shared with family and friends what she was experiencing we found a lot of people who has experienced seizures too. But this site and reading about "your Megan" and others has been the so helpful :)
Thanks for asking and is your Megan off school for the summer?
Jamie
--- In epilepsy@yahoogroups.com, Tammara Wolfgram <tammy@...> wrote:
>
> Jamie, how is your Megan doing now? I always think of you because our Megans' names are spelled the same, and my Megan was dxed at the age of 10.
>
> Tammy
> Megan's Mom
>
Wednesday, June 29, 2011
[epilepsy] Re: Complex Partials/First Post
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Just a friendly reminder: Please remember to sign your post and remember to clean up messages when you reply to them. This is especially important if you are on digest. This not only helps out the list owner but, it makes messages much easier to read when they arrive in our inboxes.
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