In a message dated 9/13/2007 4:56:14 PM Eastern Daylight Time, [EMAIL PROTECTED] writes:
Thanks Jude... and the other folks who have welcomed me into this community. I have been lurking and learning about how to cope with TM since July and I have to say you are an amazing group of people. I don't have much wisdom to offer (okay, I did email Frank about Hen3ry and Tom Lehrer as my husbands a fan and has the complete collection) but that's about it. and I haven't tipped over backwards in a wheelchair yet but if my sense of balance takes one more hit I'm gonna need a cane to avoid embarrassing encounters with lampposts and local officers (this college town has a real reputation for being a party school) I see my neuro Oct 1 and am trying to think of all the questions I could possibly write down to ask him about meds, treatments, recovery etc. Anybody have suggestions for my list? Mindy the artisan Mindy, We are all so happy that you decided to make yourself knowns to us. It is a gift to meet one more unfortunate TM'er, willing to share a bit of herself, her disease experience, and her ability to feel free enough to discuss upcoming events and the willingness to ask for help and ideas regarding her first trip to the neurologist. I did my forte'...that of welcoming you and helping you feel safe enough to open up and ask the questions you need help with. Now it is up to some of the others to help with your questions because I know next to nothing about who runs what, who is going to give you an idea of what to ask the neurologist when your time for your appointment nears, and all of that kind of stuff. Best of everything, my dear. Make a list and stick to it.! Jude, from Michigan "Our present troubles are quite small and won't last very long. Yet they produce for us an immeasurably great Glory that will last forever" 2 Corinthians 4:17 NLT ************************************** See what's new at http://www.aol.com
