and look forward to chatting again on Wednesday as long as my hospital appointment doesn't interfere with my plans. Andy.... sorry I got booted at the end and...
Dear Friends and Family, Most of you know that Huntington's Disease, a neuro-degenerative, genetic disease of the brain haunts both Dave's family and my...
Dear Susie - I want to help and I want to be committed to doing something for HD. I don't doubt your truthfulness and good intentions. But may I ask you to...
Frank, TEAM HOPE-Walk For A Cure is an HDSA annual fund raising effort, and the money goes to HDSA, usually as unrestricted funds. You can go to HDSA.org and...
Remember the gala celebration will be at the HDSA National Convention scheduled in Oklahoma City June 15-17th 2007! Never too early to start making your plans...
Nice to hear from you again, and to read that you are doing ok. Hope this year 2007 will bring something good for you and all of us in here. Love from ...
and look forward to chatting again on Friday. I hope the room won't be so keen to boot people out next time as it gets very frustrating and confusing when that...
I know this conversation probably wasn't intended for me to read but I do check every now and again. I would like to say my name is Madison, I am 29, and have...
... Maddy, check with your local Indiana State Chapter and see if they're holding a Walk-A-Thon. If not you as well as any others in the Greater Chicagoland...
Hi it is me Maddy. I havent talked to you in awhile but I just wanted to say hello and that I do think of you. You are one of the few pwople I speak with, with...
Maddy, the world is full of great ideas like your son's...he's an HD Hero! Here's another story of one young girl's idea for fund raising that's become a...
Hi Maddy! Thank you for writing! I am so sorry I did not respond earlier, but things have been pretty crazy around here. My mom is moving in with us so I can...
Hello everyone- I'm new to the group and thought I would take a moment to introduce myself. My name is Kelly, I am 36 yrs. old and my family and I just moved...
Hello Kelly and welcome to the Huntington's Disease Support Club (HDSC). I am so sorry to hear that your mother has HD and that your baby sister is gene...
Sourve: technologyreview.com <http://www.technologyreview.com/BioTech/18002/> Thursday, January 04, 2007 The number of genetic tests that can be performed...
Source: NIH News <http://www.nih.gov/news/pr/jan2007/ninds-03.htm> The National Institute of Neurological Disorders and Stroke (NINDS), part of the National...
Source: sacbee.com <http://www.sacbee.com/107/story/102445.html> Published 12:00 am PST Thursday, January 4, 2007 Story appeared in SCENE section, Page E2 ...
I need help........... my doctor just left for the military, and I am lost. I have developed an eating disorder, (which has been underlying for years) that I...
Hello Kelly, I am responding to this because I have no where to turn too. I am 29. I am HD Positive. I was diagnosed last year of May. May 5th to be exact....
Thank you for your response. I generally do not check my Huntington's email. simply because, it is depressing, and I wish to ignore it. However, time is going...
Sue, Thank you for the warm welcome and let offer my condolences in the loss of your husband. Thank you, also, for reminding me about the speech eval. I spoke...
Hi Kelley, Welcome to the group. I don't post very much but read everything. My family is plagued by HD. My father had it (d. 1994) and now my brother has ...
Source: pitchforkmedia.com <http://www.pitchforkmedia.com/article/record_review/39761/Ramblin_Jack_\ Elliott_I_Stand_Alone> Record Review Ramblin' Jack Elliott...
Source: falkirktoday.co.uk <http://www.falkirktoday.co.uk/ViewArticle2.aspx?SectionID=927&ArticleID\ =1956577> YOUNG people with brain disabilities in Forth...
howdy there kelly welcome to our group i am tonia and i am 31 i have hd now and so does my little sister emily we got it from our dads side of the family but...
