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Helping Families with Huntington's Disease

HD Reach is working to improve the care and quality of life for those affected by Huntington’s disease. Founded as a nonprofit in 2009, we provide connections to medical providers, referrals to local services, care management, family support, education, and anonymous genetic testing.


 

We’re here for you. Call or Email: 919.803.8128 or info@hdreach.org

If you’d like us to know how to help you better, let's be friends. HD Reach is a private nonprofit organization. All information collected is held in strict confidence. All HD Reach services are provided through community based funding, donations, or private pay. 

  • Olivia * Living with JHD
    Olivia * Living with JHD

    My name is Olivia and I’m 17 years old with Juvenile Huntington’s Disease. I was diagnosed right before my 13th birthday a few years after my father. Living with this terrible disease has changed so much of my life. However, I still attend school and am a senior this year. I also participate in Girl Scouts. My favorite thing is PT where I get to ride Fritz a horse at hippotherapy. I also have a service dog Larry who helps me with walking, retrieving items and can go get my mom if I need help. Everyday I fight this disease.

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  • People served through our family system model of care.

    15,000

  • People affected by HD in the US including 1,000 in NC.

    41,000

  • Americans at-risk for HD, including 5,500 in NC.

    200,000

Game, Stories, and Huntington’s: Students Learn From Real Experiences in Game Over HD

Recently, we were reached out to by genetic counseling students wanting to participate in a Game Over HD session. We worked with 5 incredibly brave individuals from Game Over HD who immediately volunteered to tell their testing experiences and help the students understand the complexity around testing for Huntington’s disease. While playing a lighthearted game, these individuals shared very personal and vulnerable stories. They talked about the different ways they found out about their results, what they wish they knew then, why some choose to live at risk, survivor’s guilt, caregiving, their hopes for the future, and how they cope while being impacted by HD. They each shared unique perspectives that brought to the forefront why testing for Huntington’s disease is an individual experience that deserves to be guided with empathy, understanding, and care.

Just because someone receives a negative result does not mean it is always a celebration. That someone at risk would immediately want to know their results or should know their results. That HD is not always known within family lineage. Receiving any result may be the start of a journey for identity. Because of these members, there are faces put to stories that will be remembered forever. Students who bonded over gaming with this group left feeling even more interested in HD while also declaring their desire to remember these stories as they move forward with their academic and professional careers. Stories are powerful and it doesn’t hurt to add a little gaming in too!

 

 

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