huntingtonsatrisk at Yahoo! Groups

Fw: Faith and Hope First NEWSLETTER!!! please take a moment and see

Dave Hodgson — Mon, 08 Feb 2010 20:35:02 GMT

I tapped into Kim Gibson's Faith and Hope HD organization through Jean Miller. I'm passing this on to my HD Family in hopes that some of you will be able to

FW: Promising results of a new therapy to treat motor symptoms of HD

Terry Hagopian — Sat, 06 Feb 2010 18:45:32 GMT

To my very supportive Family and friends , this is the Latest therapy and treatments available to HD patients and the clinical trials that have been made

For those who live in LA., MS, AR, KS and TN

Jean E. Miller — Wed, 03 Feb 2010 21:53:17 GMT

There are a lot of HD families living in Arkansas, Louisiana, Kansas, Mississippi and Tennessee. However, right now, there are no HDSA Chapters in those

Re: Good News re ACR16 [Huntexil] European Study 2-3-2010

Terry Hagopian — Wed, 03 Feb 2010 20:26:04 GMT

I signed up for this study two yrs ago. Terry To: ; From: jemiller@... Date: Wed, 3 Feb 2010 11:43:30 -0500 Subject: [huntington's at risk] Good

Re: Love child and mother don't know about HD

Scott — Wed, 03 Feb 2010 20:22:34 GMT

Thank you ALL for the advice so far. It sucks to be in this position but someone needs to be informed. Should my brother be Gene+ then this effects not

Good News re ACR16 [Huntexil] European Study 2-3-2010

Jean E. Miller — Wed, 03 Feb 2010 16:46:16 GMT

HDSA's website has an important research update on the ACR16 studies in Europe Neurosearch Reports Good Results from the European Trial of ACR16

Re: Life changes

Scott — Mon, 01 Feb 2010 19:25:53 GMT

Amanda, don't let this get to you. (easier said, I know)... But you musn't let the stress of HD stop you from raising and loving that baby. He may never

Life changes

emtchic7 — Mon, 01 Feb 2010 15:46:45 GMT

It's been a while since I've posted anything to tell the truth I try to forget about HD but I can't deny it anymore. I tested positive in 2005 I had

Re: Another HD Angel

Scott — Mon, 01 Feb 2010 14:17:32 GMT

crying for you and your family, rejoicing for the new Angel ________________________________ From: Kelly McGrath To:

Re: Another HD Angel

Kelly McGrath — Sun, 31 Jan 2010 19:28:16 GMT

I'm sorry to here about your loss. You are all in my thoughts and prayers. "If you stare at someone who is different, you are what is wrong in the world." Cure

Another HD Angel

Toni S — Sun, 31 Jan 2010 18:43:23 GMT

My DIL's siter passed away during the night from complications of HD..she was in her mid 40's with teenage daughters..she suffered alot and I know she is in a

Walk For A Cure

Dave Hodgson — Sat, 30 Jan 2010 20:37:52 GMT

For those of you in the Greater Chicagoland Area from Milwaukee to Rockford to Peoria (and South) to Chicago to Indiana to nearby Michigan, the Illinois

Stem cell research

Toni S — Thu, 28 Jan 2010 16:50:34 GMT

My son [whose wife has HD] just informed me there is a doctor in CA ..Dr. Nola who is doing stem cell research..has anyone heard of her and her work?..peace to

HDSA's On-Line Center of Excellence Survey

Jean E. Miller — Tue, 26 Jan 2010 01:17:21 GMT

For those that didn't know, HDSA launched an on-line survey [in the last few weeks] on their website for families seen by an HDSA Center of Excellence [CoE] to

Re: Love child and mother don't know about HD

Laura Quinn — Thu, 21 Jan 2010 20:25:59 GMT

Scott- First of all I think “love child” is an adorable way to refer to it. I have relatives who use far worse. Love child reminds me of…Forrest Gump