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nic

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I just wanted to say Thank You for this site.

Developing epilepsy at the age of 41 has been very hard for me to get my head around. I feel very confused and out of my depth. I don't have any friends with epilepsy and up until now it's something I've given little thought to.
I get very confused when my consultant throws information at me..I always come out with lots of unanswered questions.

Over the past few weeks this site has given me a sense of belonging. It's also full of good advice and there is a sense of hope. This will not ruin my life..it's changed my life for sure..but I'll deal with it one day at a time.

:hugs:
 
Hi Nic,

I'd suggest you ask him/her to write the info down for you.
You can also use your search engine to look it Yahoo,google or whatever it is.

live with your epilepsy one day at a time now that is the best way to go there.
It has been a lifetime for me but at any age it's just as hard for the person, I just happened to grown up with it. I was two when I was diagnosed with E.
 
nic

You are very welcome as Belinda5000 said take it one day at a time and remember people here will support you and try to help you just as you will help us.
 
I feel very confused and out of my depth. I don't have any friends with epilepsy and up until now it's something I've given little thought to.
This was what brought me to CWE when I developed epilepsy at age 35. I discovered an ongoing party with incredibly warm and wise guests. I've never left. CWE is badass. :)
 
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