Hereditary Neurological Disease Centre

Hereditary Neurological Disease Centre HNDC is a non-profit specializing in Huntington's disease. The Hereditary Neurological Disease Centre is a free-standing. non-profit organization.

They provide genetic testing, counseling, monthly support groups, medical clinics and research study activities. We often use the short version- HNDC- and this has apparently brought some confusion with the national HD organization, Huntington's Disease Society of America (HDSA). We are not, and never have been an affiliate of the national organization. While we share a common goal to assist those

with Huntington's disease, our direction, purpose, mission, and funding sources are dramatically different. All HNDC funds provide direct research and patient care programs for our regional area. ALL MONEY is used for these important program services, none is used for overhead, salaries, or sent out of state. If you want to know where your dollars are used, please contact us and arrange an opportunity to learn more about WHERE your donations go, and to WHOM they help directly in this area. PLEASE...Be an informed supporter and know where your time, talent and donations are going. Our MISSION:
At the Hereditary Neurological Disease Centre, we are dedicated to walking alongside individuals and families on their Huntington’s Disease (HD) journey. We provide compassionate guidance, comprehensive support, education, and advocacy—at little to no cost—empowering those affected to navigate the challenges with dignity and hope.

06/17/2026

Read more about ANX005 and the science behind it: https://bit.ly/4anmyoo

New research is exploring ANX005 as a potential treatment for Huntington's disease, with the goal of slowing disease progression by targeting inflammation in the brain.

While more research is needed, studies continue to advance our understanding of potential therapies for the HD community. 💙

06/15/2026

Click here: https://bit.ly/4e5dNSl to read the full story.

For people living with Huntington's disease, nutrition is about more than food—it's about supporting your body through the challenges of everyday life.

In this column, the author shares how shifting their mindset from perfection to nourishment has helped them manage HD symptoms and prioritize their well-being.

💙 "I don't have to eat perfectly to care for myself well."

06/12/2026

New trial data suggest SKY-0515 may help slow Huntington’s disease progression, offering hope for a potential disease-modifying treatment.

While research is still ongoing, these early results are encouraging for the HD community. 💙

Click here: https://bit.ly/4xd7y6c to learn more.

06/10/2026

Click here: https://bit.ly/4dQe9vX to learn more.

While there’s no cure for Huntington’s disease yet, therapies like physical therapy, occupational therapy, and speech therapy can help people maintain independence and improve quality of life.

Every step toward better care matters. 💙

06/08/2026

The Allen Institute in Seattle says scientists have now learned enough about how the brain works to start fixing it when it breaks.

06/08/2026

Address

9300 E 29th Street N, Suite 350
Wichita, KS
67226

Opening Hours

Monday 9am - 4pm
Tuesday 9am - 4pm
Wednesday 9am - 4pm
Thursday 9am - 4pm
Friday 9am - 4pm

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