I received a nice letter from a member of MSW board, that I was considered MIA. hmmm, I guess I have been found.

I am still on copaxone. I really struggled about staying on it after some wild side effects. The side effects finally got better, and i started to feel better.

Got a call from the MS clinic to tell me my last MRI showed 2 new lesions, and that my Glioma had not changed. MY WHAT? I guess the local guy spotted a glioma last year, and forgot to tell me. The good news is that it hasnt changed in a year. I am told most of the time they are not cancerous, and left alone it should be fine. To go get a peice of it may trigger siezures or headaches, and since I am siezure free now, I dont want to tempt the hand of fate.

have had several flairs, and struggled along. I have thus far refused all steroids.

Just wanted to wave, and say hello and thanks for the well wishes. My PM box was full. you guys are awesome.

Welcome back!

Greetings, Dejibo !

Might be a blessing you weren't told about the glioma -- one less thing to worry about. Glad it's not getting worse.

Good to see you back, m'dear!!!

Waving back, HIIIII!!!!