and look forward to chatting again on Friday. Thanks to Teresa, Pam, Helen, Kandy, and Laurie for their attendance today. It was lovely to meet Kandy for her...
and look forward to chatting next week. Thanks to Teresa, Ashlee, Lynn, Steve, and Laurie for their company today. Love and hugs to all, Sue & Kelly...
and look forward to chatting again on Wednesday. Thanks to Teresa, Matt, Pam, Lucy, Jim, Cas, and Misty for their company today. Love and hugs to all, Sue &...
Hello everyone I've been out of the loop since my mother passed but I got an email that has inclined me to come back. Well, I just was curious if anyone heard...
Phase II DIMOND Study [Dimebon] Results Are Very Encouraging HDSA Breaking News by Marsha Miller http://www.hdsa.org/research/news/815.html Not only is it safe...
You might look at www.hdsa.org and search for current research studies going on that are still looking for volunteers. Most Centers of Excellence have studies...
Hey...  I have HD.  I am part of CHORT. I am looking into COQ10 trial too. You ask your Neurologist. Mine helped me and will help me get into COQ10 trials...
As Dave mentioned, the new HDSA website link for Research, under Pipeline, you will be able to find clinical trials in your area...bur right now it shows...
Dear All, Also a quick note that there is an extensive database of Clincal Trials at WeAreHD.org: http://www.wearehd.org/browse.php?s=studies WeAreHD has...
thanks heather, food luck with the trials.............. and thanks to all those who responded, **************Gas prices getting you down? Search AOL Autos...
please forward this to everyone in your address book. All it takes is a quick 10.00 donation. These pups need to get to their new forever homes and the person...
I won't be able to attend today's chat, I'm afraid, as I've got a lot to do and too little time to do it! [:">] I look forward to catching up on Friday...
Reminder from: huntingtonsdiseasesupportclub Yahoo! Group http://groups.yahoo.com/group/huntingtonsdiseasesupportclub/cal HD Support Club Chat Friday July 11,...
huntingtonsdiseasesup...
huntingtonsdiseasesup...
Jul 11, 2008 2:56 pm
9619
I won't be at chat today I'm afraid as I'm still exhausted after spending hours in London yesterday for Twin Research and am in some pain from the biopsy wound...
Hello everyone. My name is Kelly Keller. I am more of a lurker, but definatley relate to all of you. I joined this support group when it finally hit me that I...
Wonderful news Kelly! Enjoy it and look after your family. Â Matt. ... From: Kelly <kwiley3077@...> Subject: [Huntingtons Disease Support Club] I just...
Kelly, I am jumping up and down for you!! I hope your brother has the same results as you. It would be great if it ended with your mother. Too many are...
Congratulations Kelly on your results!!! It's absolutely great that you're negative and I understand what you mean about thinking you had it because I was...
congrats first and for most on your results i know from my own stand point that even though i have h d and i know how ticked i get at times it would be a huge...
That is the best result. I have HD and know what it is like. I wish you the best, free of HD. That's why I got tested. I did not want to sit there and wonder...
Another new update on HDSA's websites from Marsha Miller! As Marsha wrote me: We now have four Phase III clinical trials underway or planned - creatine, ...
and look forward to chatting again on Wednesday, hopefully in our own room if it is working. Thanks to Tripod, Aunty Pam, Pam, Shelby, Angela, and Teresa for...
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