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katrina4384
Nov 5, 20233 min read
This Quarter, Help 4 HD Asked a Few Questions, and the Community Responded!
I wish I knew that it would be possible to find happiness again when I found out about Huntington's disease. I wish I knew that most of...
306 views1 comment

katrina4384
Nov 1, 20231 min read
A Research Study about Anonymous Genetic Testing for HD
Survey Overview We are conducting a research study at the University of Texas Health Science Center at Houston about anonymous genetic...
304 views0 comments

katrina4384
Oct 25, 20233 min read
Let's Talk About GEN HD1 and GEN HD2
Can you explain what happened in Gen HD1 and why you have a Gen HD2 study? What we realized after we looked at generation HD1 was the...
333 views1 comment

katie8288
Oct 18, 20231 min read
FDA Grants Orphan Drug Designation for the Treatment of Huntington’s Disease
Dear Huntington’s Disease Advocacy Community, We are proud to share that today Sage Therapeutics announced the U.S. Food and Drug ...
230 views0 comments

katrina4384
Sep 26, 20231 min read
INGREZZA - For the treatment of chorea associated with Huntington's Disease (HD) TOOLKIT & RESOURCES
Find out more here: INGREZZA HDC Launch Toolkit_FINAL.pdf
221 views0 comments

katrina4384
Sep 21, 20231 min read
Help 4 HD Announces Symposium Schedules & Night Events!
Welcome Party: Luau Style! 4 Rooms Packed Full of Education, Resources, Support, and Community! Award Gala and Farewell Party! Thank you...
88 views0 comments

katrina4384
Sep 14, 20231 min read
Neurocrine Biosciences
Neurocrine Biosciences Announces U.S. FDA Accepts New Drug Application for INGREZZA (valbenazine) Oral Granules Sprinkle Formation
251 views0 comments

katie8288
Aug 20, 20235 min read
Understanding the Clinical Trial Process for Huntington's Disease Families
The clinical trial process is an essential part of the research journey, a critical step in bringing new treatments and therapies to our...
340 views0 comments

katie8288
Jul 28, 20239 min read
Help 4 HD International Exhibits and Presents at the Crisis Intervention Team International (CIT)
Help 4 HD International's LEEP program began in 2014 when Help 4 HD International exhibited at its first International Association of...
394 views1 comment

katrina4384
Jul 16, 20232 min read
Please stop saying that about HD...
1. So, this isn't quite on topic, but the one thing I'm tired of seeing..... I'm THRILLED Hollywood is recognizing HD, but my issue is...
279 views0 comments

katrina4384
Jul 6, 20234 min read
Testing, what to do first; words from the community.
We asked our social media followers, 'What is one thing you should do before getting tested?' the discussions were great! One of the very...
293 views0 comments

katrina4384
Jun 28, 20233 min read
We Asked, and the Community Answered.
We Asked, and the community Answered. When friends or the community ask how they can help, are you always at a loss for ideas? Let's...
341 views1 comment


katie8288
Jun 21, 20235 min read
PTC Therapeutics Shares Positive Interim Data from PIVOT-HD Clinical Trial
PTC Therapeutics Shares Positive Interim Data from PIVOT-HD Clinical Trial in Huntington's Disease Patients June 21, 2023 PDF Version -...
267 views0 comments

katie8288
Jun 21, 20232 min read
uniQure Announces Update on U.S. Phase I/II Clinical Trial of AMT-130 Gene Therapy
Dear Huntington’s Disease Patient Organization Leaders, We are writing to let you know that this morning uniQure issued a press release...
256 views0 comments


katie8288
Jun 8, 20232 min read
Eyes, Ears, Nose, and Paws help Olivia, who lives with JoHD, find her forever partner
Olivia Eiger is a social teen, who recently celebrated her 17th birthday and is planning to commemorate both her birthday and going into...
386 views0 comments

katie8288
May 26, 20238 min read
HD Awareness Month 2023, Some Patient/Family Response.
What do you wish healthcare workers were more mindful of with HD patients? Community Response: · I wish they were educated about...
326 views1 comment

katie8288
May 23, 20231 min read
Help 4 HD is featured on Movement Disorder Policy Coalition
https://www.movementdisorderspolicy.org/news/2023/5/11/help-4-hd
241 views0 comments


katie8288
May 16, 20230 min read
421 views0 comments


katie8288
May 8, 20231 min read
An HD Awareness Message from Charles Fisher
Hello, my name is Charles Fisher. This is my story about Huntington's disease. I got made fun of when I was younger, and I still get...
290 views0 comments


katie8288
May 1, 20236 min read
What has your family endured due to a lack of awareness about HD? The community responds.
• We planned a friend trip to Vegas after my husband’s diagnosis. We all sat down at a poker table to play. The whole table was just our...
309 views7 comments
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