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katie8288
Jun 20, 20240 min read
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Epilepsy in Pediatric-onset Huntington's Disease Survey.
In less than 15 minutes, you can participate in an anonymous survey as an adult (over the age of 21) caregiver of someone diagnosed with...
katrina4384
Jun 18, 20241 min read
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katrina4384
Jun 12, 20240 min read
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Sage Therapeutics Announces Topline Results from the Phase 2 SURVEYOR Study.
"The study met its primary endpoint, demonstrating a statistically significant difference as measured by the HD-Cognitive Assessment...
katrina4384
Jun 11, 20241 min read
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Are you taking the right medications based on your unique DNA?
Are you aware that genetics are more than just lineage? Within your family, you may have very different experiences with medications or...
katrina4384
Jun 10, 20241 min read
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Jamie Holloway ~ Help 4 HD's newest team member!
When you first meet Jamie, you will notice her warmth, smile, and genuine interest in those around her. We are excited about what this...
katrina4384
May 20, 20242 min read
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Forbes Features Tanita Allen in Why Self-Advocacy Can Help You Become an Invaluable Collaborator.
As Tanita Allen, author of the book We Exist, explained in a recent conversation, “We all need to be self-advocates, because our society...
katrina4384
May 7, 20241 min read
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Teva’s New Real-World Evidence Confirms Effectiveness and Patient Satisfaction for HD Chorea with the 4-week Titration Kit for AUSTEDO® (deutetrabenazine) Tablets
https://www.tevausa.com/news-and-media/press-releases/tevas-new-real-world-evidence-presented-at-the-2024-aan-annual-meeting-confirms-eff...
katrina4384
Apr 19, 20247 min read
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Help 4 HD is Coming to HOUSTON!
On April 27th, Help 4 HD International will host our first in-person HIPE education event for 2024. We have a great line-up with...
katrina4384
Apr 15, 20241 min read
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"WE EXIST" - by Tanita Allen: Together we exist; together, we rise.
Welcome to the heart of “We Exist,” a compelling autobiography and memoir penned by Tanita Allen. Experience a journey that goes beyond...
katrina4384
Mar 26, 20241 min read
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21 with Juvenile Huntington's disease: An adult, not a Child; feeling stuck in a unique and difficult place.
Hi, I’m Ashley Harmon. I am 21 and have Juvenile Onset Huntington’s Disease. I am an adult, not a child, but yet, in many ways, I feel...
katrina4384
Mar 18, 20243 min read
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katie8288
Mar 12, 20240 min read
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CEO/President of Help 4 HD International, Katie Jackson, Speaks to Sage Rx About Huntington's Disease.
This link will take you to a video of Katie and her daughter, Madison, who are talking about the impacts of HD and what they hope to see...
katrina4384
Mar 5, 20241 min read
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Announcing a New Support Group Style with Help 4 HD - Stay Connected
People in our community have reached out to Help 4 HD requesting a different type of support, and we are excited to announce that we have...
katrina4384
Feb 19, 20242 min read
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HDYO Brings Back the North American CAMP for Young People Impacted by HD!
HDYO is hosting its 6th North American HD Young Person Camp on August 11-15 from Camp St Charles in Maryland. The camp offers young...
katrina4384
Feb 7, 20241 min read
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HD Community Letter from Prilenia
January 26, 2024 Dear Huntington’s Disease Community, We hope 2024 is off to a great start for you and your loved ones. To build on...
katie8288
Jan 26, 20243 min read
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European Medicines Agency (EMA) Greenlights Mitochon Pharmaceuticals to Initiate Phase I/IIa Biomarker Study in Neurodegenerative Diseases
BLUE BELL, Pa.--(BUSINESS WIRE)--Mitochon Pharmaceuticals today announced that it was awarded approval from EMA to begin enrollment for a...
katie8288
Jan 11, 20241 min read
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HD Deserves a Voice; Fill Out the FDA Accelerating Access to Critical Therapies Public Docket
Accelerating Access to Critical Therapies for ALS Act – ACT for ALS - Action Plan for Rare Neurodegenerative Diseases including...
katie8288
Dec 19, 20233 min read
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