Hi everyone, Tylenol w/ Codeine could be making her stomach upset, it did me & others I have talked to. (I don't takany meds they scare the hell out of me!) Ny...
Hi Sabrina, Can you call your doctors in Hawaii and ask them if they know anyone they can refer you to in your new area? Where are you now? Jeanne...
AMOUR49@...
Jul 1, 2002 1:23 pm
10307
Sabrina -- I know it isn't easy --- I watch my son struggle with some of the same issues you have --- he makes it through each day and I'm sure you will too...
AMOUR49@...
Jul 1, 2002 1:33 pm
10308
In a message dated 6/30/02 4:52:23 PM Pacific Daylight Time, ... You must have the magic touch! Its taking us months to have my son's records transferred!...
AMOUR49@...
Jul 1, 2002 1:36 pm
10309
In a message dated 6/30/02 9:16:12 PM Pacific Daylight Time, ... I lived in the San Fran/Bay Area for 18 years - it always surprised us to see the tourists in...
AMOUR49@...
Jul 1, 2002 1:42 pm
10310
Has anyone had good experience with a neurologist in the Baltimore/Washington area? I am having increasing problems breathing. A complete cardiac workup was...
Marshal Levine
mslevine@...
Jul 1, 2002 2:29 pm
10311
For those of you who use wheel chairs I thought the following URL might roof interesting. JohnE ...
Great Idea, try it Kay ... From: <AMOUR49@...> To: <CMT-Support@yahoogroups.com> Sent: Monday, July 01, 2002 9:22 AM Subject: Re: [CMT-Support] Sabrina ......
Hi all: My husband, son and I just returned from a 5 day road trip (after flying to Las Vegas from Portland OR) thru Zion Nat. Park, Bryce Canyon, and the...
Hey - I am still lurking...working on my web stie, getting lots of counciling... A friend of mine has been taking Flexeril and I was hoping to get some...
Hey Yall! Just thought I'd let ya know that Kaitlins hearing test was normal. She can hear perfectly fine. LOL, Kara P.S. TO all the new members of the...
Rita here and wanted to say HI to everyone, my first time posting here, I know Sue, she found me on my page it is below and plain on coming back soon :-) and...
Lamar, The MDA wants CMT people to go to their MDA support group. It is combined of all Neuropathic diseases, Muscular Dystrophy, Als, etc. They didn't want...
Sounds like you had a great trip. Isnt the Golden Access Card a wonderful thing. I have had it for a year now and just to let you know it will get you half off...
Hi, I am new to the group and the puter, so please be patient with me. I am really glad I found you and can't wait to start making friends with the people who...
Patsy, I have had much the same result, but MDA does have CMT specific support groups in some areas. I heard every line possible from them about forming one....
I was diagnosed with Friedrichs Ataxia 22 yrs ago. Went to MDA and dx with cmt along with two other problems that they could not in their words- pinpoint. My...
Vicki, First, Welcome to the group! You will find many answers, but aside from that you will find a friend when you most need one, we are all walking if-it-be...
Kara, That's wonderful news!! It's always great hearing 'Good News" we don't get a lot of that, our kids mean so much to us all we hurt when they do. Thank you...
HI Vicki, Welcome to the group. I am sure you will make LOTS of new friends..We are all here for each other. I am so glad I have all of you to help me get...
Well here it goes and I hate to put it this way, since you have been so nice about your situation, stop being nice and take a stand, you know your body and how...
My redneck email goes for Sabrina too Kay ... From: BRI420_69 <bri420_69@...> To: <CMT-Support@yahoogroups.com> Sent: Saturday, June 29, 2002 1:59 AM ...
Welcome Vicky, Candice Ralston here, you will not only receive information, you will have fun just knowing the people. I have CMT1A. Good luck to you. Candice...
James & Candice Ralston
notslar@...
Jul 2, 2002 3:25 pm
10333
I have also been interested in learning some yoga in order to breathe better, relax and increase my own body awareness. The current issue of MDA's Quest...
Lamar wrote..<<I do feel that group that includes all MDA covers is far from ideal. Yes, CMT is a neuromuscular disease, but all such neuromuscular diseases...
