In a message dated 5/13/2007 8:47:38 AM Eastern Daylight Time, [EMAIL PROTECTED] writes:
First off, I am glad Bob feels like part of the family and that he feels comfortable sharing here. And I hope to one day stop in Elvis land and say hello & hug him and the missus. I'm not sure but I don't think there is the support and friendship in the MS support groups I'v checked out. I could be wrong. I am sure there are those in their groups that have found the connection that we share, but folks....you gotta amit, we've got a special group here and welcome anyone to be part of the discussion. I too give kudos to Bob for always being there for any one of us in the group and for sharing his wealth of knowledge and love, which is great. I wasn't putting him down, I just wondered if the MS information applied to us, with TM. Like, they take different types of medication than is appropriate for us and I am sure that there are other differences in the manner of treatment between the two illnesses. I am thankful for any information, from anybody, from any reliable source, regarding TM. I appreciate the caregivers and the people who donate their time and money to our daily burdens. And, I love you Bob, Kevin, Lynn, Barbara, Ken, Trudy, and all of the others in our TM club. Peace and Prayers, Jude ************************************** See what's free at http://www.aol.com.
