March for Epilepsy
Things are a bit better these days, my daughter's seizures are coming less frequently, but still aren't out of the picture. I'm always in a state of stress, hoping for no news and dreading news when it comes.
On March 27th I'm going to Washington D.C. for the Walk for Epilepsy. It's quite a long ride (10 hours) but worth it. It feels good to feel the love and support from all the other people who suffer in the same way we do. Also feels good to be a part of something that hopefully raises awareness of the problem and money towards research. Research, .... slow, but our only hope.
Maybe I'll see some of you there?
On March 27th I'm going to Washington D.C. for the Walk for Epilepsy. It's quite a long ride (10 hours) but worth it. It feels good to feel the love and support from all the other people who suffer in the same way we do. Also feels good to be a part of something that hopefully raises awareness of the problem and money towards research. Research, .... slow, but our only hope.
Maybe I'll see some of you there?
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