HDSA also leads in providing care for HD patients and their families at our 21 Centers of Excellence. HDSA's 12 regions and 37 chapters and affiliates and 150+ support groups help educate the general public and healthcare professionals. This dedicated circle of people provides networking and information and creates fundraising opportunities through a wide range of exciting and worthwhile events nationwide.
Dear Family & Friends, It's once again time to walk for HDSA's Team Hope Walk at Crissy Field in San Francisco, CA. As many of you know, my Grandma, Aunt and Mom all died of Huntington's Disease. Now my sister, Karon, is struggling with the effects of this devastating disease, which means her son, Jesse, has a 50-50 chance of contracting this horrible killer. Because of HD's "orphan status", the big corporations aren't willing to step-in and fund the research. We must do everything in our power to find a cure.That's why I'm walking again this year, to try and help all the HD families!! Thank you for visiting my fundraising page! Donating through this website is simple, fast and totally secure. It is also the most efficient way to support my fundraising efforts. Many thanks for your support -- and don't forget to forward this to anyone who you think might want to donate too! With Sincerest Appreciation, Lynn Zinkl