There are some photos at _http://www.myelitis.org/gallery/index.php?cat=2_ (http://www.myelitis.org/gallery/index.php?cat=2) I urge you all to put your photos up if you haven't yet. :) And put your name with them -- not everyone has done that. It is nice to put faces to names. Barbara H. _http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) In a message dated 5/14/2007 1:10:05 PM Eastern Daylight Time, [EMAIL PROTECTED] writes:
I was diagnosed with TM in 2002 and in Dec. diagnosed with MS. I did try an MS website and it just wasn’t the same. I’ve been with this group so long… I know I should learn more about MS and I will but right now this TM group takes good care of my questions, problems, etc… I do take copaxone every day. One problem with e-mail is that you don’t see a face or hear the “inflection ” in someone’s voice and many times people can be misunderstood. I would love to see pictures of everyone and see if they match up with what I think they will look like! Bobberino you’re so popular you could do a “bobberino” land!! J I’d come.. I would love to meet the “Missus” Trudy In Virginia where the weather is awesome!! And thanks for the Mother’s Day Wishes and birthday wishes! It was a great weekend. I hope all Mothers had a great day on Sunday! ************************************** See what's free at http://www.aol.com.
