Skip to content
Huntington's Disease News logo
Newsletter
  • About Huntington's
    What is Huntington’s disease?
    • Juvenile Huntington’s disease
    Diagnosis
    Living with Huntington’s disease
    Symptoms
    Causes
    Stages
    Treatments
    • Approved treatments
    • Experimental treatments
    • Non-drug treatments
  • Community
    Columns
    • A Family Tradition — Carlos Briceño
    • HD in Color – Tanita Allen
    Archived columns
    • Negative to Positives — B.J. Viau
    • A Genetic Lottery – Rebecca Field
    • Always Looking Forward — Alexus Jones
    • Gene Positive — Steven Beatty
    • From Where I Stand — Erin Paterson
  • News
  • Resources
    Advocacy partners
    Navigating Huntington’s disease
    • Videos: Bracing for the long haul
    • Anticipatory grief
    • Talking to children about Huntington’s
    • Huntington’s support groups
    • Huntington’s early diagnosis
    • Huntington’s progression
    • Adaptive devices for Huntington’s
    • Huntington’s genetic testing
    • Chorea and Huntington’s
    • Huntington’s and diet
    • View all

Throughout May, Huntington’s Disease News is recognizing Huntington’s Disease Awareness Month with a variety of stories that represent different perspectives on life with Huntington’s that we hope help to inspire and empower our readers. These stories highlight some of the unique challenges of living with Huntington’s, as well as stories of hope, inspiration, and other topics that help to generate awareness among the Huntington’s disease community. Follow along with the series here or visit us on Facebook or Instagram using the hashtag #HDSpotlight

Huntington’s disease took so much from my family

Porcia White and her husband, Jamie, found out together the results of her genetic testing for Huntington’s disease. (Photos courtesy of Porcia White) This is Porcia White’s story: Huntington’s disease was a part of my life from an early age. My earliest memory was sitting against the wall…

The trauma of Huntington’s disease is shared by the family

Jennifer Ushe’s grandparents, Jean and Edward Moshier. (Photo courtesy of Jennifer Ushe) This is Jennifer Ushe’s family story: Both of my grandparents died 10 years before I was born: Grandpa, unexpectedly and tragically, of a heart attack, and Grandma, expectedly but no less tragically, of Huntington’s disease. My…

News

This awareness month, spotlight is on the patient experience

May is Huntington’s Disease Awareness Month, and this year the focus is on the patient experience. Huntington’s disease (HD) is a neurodegenerative disorder thought to affect 4.9 per 100,000 people worldwide, including about 41,000 U.S. residents, and can impact many aspects of everyday life. While each patient’s journey…

  • Prev
  • 1
  • 2
  • Prev

Recent Posts

  • Understanding how Huntington’s disease affects my cognition
  • Guest Voice: We hold onto hope while fighting for new treatments
  • Top 5 Huntington’s disease news stories of 2025
  • Another year means treasuring more moments of shared joy
  • Faulty cellular waste disposal system may drive Huntington’s: Study
  • What the holidays mean when living with Huntington’s disease
  • $12M grant will back first trial of stem cell therapy for Huntington’s
  • A tribute to the kindness of strangers in life with Huntington’s
  • How to support someone who is planning for future care
  • Antipsychotics improve functional capacity, independence in HD


  Subscribe to our newsletter

Get regular updates to your inbox.

This field is for validation purposes and should be left unchanged.

Bionews Logo Bionews, Inc.

3 W Garden St
Suite 700
Pensacola, FL 32502
Website: bionews.com
Email: [email protected]
Phone: 1-800-936-1363

  • Huntington's Disease News on Facebook
  • Huntington's Disease News on X
  • Huntington's Disease News on Instagram
  • About Us
    • Our Culture
    • Leadership
    • Careers
    • Contact Us
  • Explore More
    • Advertising Policy
    • Corrections Policy
    • Editorial Policy
    • Privacy Policy
    • Terms of Service
Disclaimer

This site is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.

Copyright © 2013-2026 All rights reserved.

Log in/Register

[wppb-login register_url="/register" lostpassword_url="/recover-password" ajax=true]

Don't have an account?

Log in

[wppb-login register_url="/register" lostpassword_url="/recover-password" ajax=true]

|

Register

[wppb-register redirect_url="/welcome" ajax=true]

Already have an account?

Register

Create your account by filling in the information below:

[wppb-register redirect_url="/welcome" ajax=true]

By creating an account, you are agreeing to the Privacy Policy and Terms of Service.

Reset Password

[wppb-recover-password ajax=true]