Every Family Matters. Double Your Impact This Winter.

We walk beside you with services and programs that ease the burden of HD, providing support, education, connection, information and access to care throughout North Carolina.

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Help, Uplift and Grow with a monthly HUG donation of any size. 

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"HD Reach has provided me with unique opportunities to face challenges associated with Huntington's Disease. I have developed emotional strength, coping skills, confidence, and most importantly a sense of belonging through this community. My life has changed for the better and that change started with HD Reach." H Patton

We all know that Huntington’s disease is a family disease — and that, as of today, there is no cure. Whether you are a person with HD, gene negative, at risk, a care partner, child, sibling, friend, neighbor, physician, or employer, the impact of an HD diagnosis is broad and deeply felt.

Even with the challenges, there is hope, joy, progress, resilience, innovation, adaptation, and companionship along the way.

At HD Reach, we hope you’ll consider us part of your family. We are your boots-on-the-ground resource for support, education, referrals, and community — right here, right now. Wherever you are on the path, HD Reach supports you.

Your gift today will help us maximize a generous $30,000 matching gift by December 31st.

Give in honor of someone special, in memory of a loved one, or just because you can.

Together, we keep HD Reach ready to serve — family.

HD Reach Staff

“Family is not an important thing. It’s everything.” Michael J. Fox

Nathan Wilmoth

byHeather Wilmoth

My husband Nathan was diagnosed on April 16, 2016 with Huntington's Disease. At first, we felt really alone. But after processing Nathan's diagnosis, we made the decision to live our lives as positively as we can. Nathan's disease has progressed, but Nathan is still Nathan. The fun loving, sweet give the shirt off his back, loves his family and friends with all he has. And a smile that has always been and continues to be so infectious you can't help but smile with him. HD has changed the life we thought we were going to have, but it's made us realize how precious life is and how much we truly do love each other. When Nathan was diagnosed, the first thing I said was "Your walk with HD, will not be your Mom's, My walk with HD will not be your Dad's," and it hasn't. Nathan has also participated in clinical trials and wants to continue to do so when allowed. We have two children at risk, we try to fight for them as well as the other families like ours.