@hdsanational

@hdsanational has been a member of Linktree for 1 year and joined in July 2024. The social media accounts linked to from @hdsanational are: Facebook, YouTube, LinkedIn, Email, X. Besides social media accounts, hdsanational has populated their site with Skyhawk Therapeutics Releases Twelve-Month cUHDRS Subcomponent Results from its Phase 1/2 Clinical Trial of SKY-0515 in Huntington’s Disease, Understanding the 2026 Cost of Living Adjustment - Huntington's Disease Society of America, Find Help - Huntington's Disease Society of America, uniQure community letter, Support Tyler Zimmerman, uniQure press release, Petition · Bring Hope to Huntington's Disease Families: Urge the FDA to Uphold Accelerated Approval - United States · Change.org, Emily Richardson, Rare Disease Leaders Convene on Capitol Hill for Congressional Townhall Briefing, Take Action 👉 If you are living with HD:, Support Meaghan Leon, Skyhawk Therapeutics Announces Twelve-Month Interim Results from Phase 1/2 Clinical Trial of SKY-0515 in Huntington’s Disease - Huntington's Disease Society of America, Family Members take Action - Huntington's Disease Society of America, Support Owen Moore, Let's Talk About HD Awareness Month with Tam, Allison & MaryAnn, Support Jennifer Plurad, Planned Giving - Huntington's Disease Society of America, Become a Mentor - NYA & HDYO Mentorship Program, Huntington's disease advocates raise awareness for rare illness, Support Zeke Melman, Virginia Huntingtons Disease Awareness & Education Day - 2026 Virtual Livestream, Take Action 👉 If you are a supporter:, Support Christy Simpson, Woman Diagnosed with Huntington’s Disease at 18 Speaks Out About Living with Fatal Illness (Exclusive), Take Action 👉 If you are a family member:, Support Carol Mendiola, Donate to HDSA Awareness Month 2026, Support Hiren Patel, How it Works - Brain Donor Project, Support Erin Turner, Huntington Disease Awareness Month - On New Jersey, Support Tom Malone, HDSA National Youth Alliance, Twibbonize | The visual campaign platform, Support Kati Janssen, Fighting for a Cure for Huntington's Disease - Heather Thurgood, HDSA Support Groups - Huntington's Disease Society of America, hdsa.org, hdsa.org, www.kcau9.com, Welcome! You are invited to join a webinar: Living with Loss: Navigating Grief in Chronic Illness. After registering, you will receive a confirmation email about joining the webinar., Get Involved - Huntington's Disease Society of America, AMT-130 What does it mean for the HD Community- Q&A - YouTube, Why I volunteer for HDSA…, What the AMT-130 News Means for the HD Community, HDSA Volunteers: Dom Thomas, Disability Tips Resources, HDSA Volunteers: Beth Hoffman, Support HDSA and It's Mission, POWERHD, Donation opportunities - HDSA, HD Human Biology Project - HDSA, HDSA Voice of the Patient Report - Flipsnack, HDSA's National Youth Alliance, Golf for a Cure raising funds and awareness for Huntington’s disease | WWLP, Annual Convention - Huntington's Disease Society of America, Huntington’s Disease Day of Action - Huntington's Disease Society of America, HDSA HD Symptoms and Treatment Impact Survey, Huntington’s Disease Day of Action - Huntington's Disease Society of America, Family Members take Action - Huntington's Disease Society of America, Tune in to our Advocacy webinar 2/26, 2026 HDSA Team Hope Walk in South Dakota Set for May 2 at Sertoma Park - Midwest Medical Edition, 2026 Team Hope Walk Le Mars to raise money for Huntington's Disease, HD Gene Discovery Day, 40th Annual HDSA Convention: Optimizing Sleep in HD, hdsa.org, MSN, app.dvforms.net, HDSA Marker 2025 - Flipsnack, Update from the Huntington’s Disease Society of America (HDSA) - Huntington's Disease Society of AmericaHuntington's Disease Society of America, What We Know So Far: Skyhawk's SKY-0515 Phase 1 Trail Update, Australia Opens The Door for SKY-0515: Skyhawk Seeks Provisional Approval for Its Oral HD Drug – HDBuzz, www.prnewswire.com, Skyhawk Announces Australia's Therapeutic Goods Administration Has Determined SKY-0515 for Huntington's Disease Meets Eligibility Criteria for Registration via the Provisional Approval Pathway, Regulatory Update, Introduction to Disability Services and Financial Planning, Community letter, Will Forte says 'SNL' still makes him nervous when he returns, Vico Therapeutics Announces Patient Dosing in Twice-Annual Regimen of VO659 in Phase 1/2 Trial in Huntington’s Disease, Spinocerebellar Ataxia Type 3 and Type 1 – Vico Therapeutics, HDSA Rare Disease Day - 2026 | AddEvent, Donate to HDSA Rare Disease Day 2026, Disability Tips - Huntington's Disease Society of America, Let’s talk about Huntington’s Disease | Daily Leader, Ask Allison!, Write Your Legal Will Online, Free & Simple | FreeWill, This Month @ HDSA, FInd a Local Event - Huntington's Disease Society of America, Volunteer Opportunities - Huntington's Disease Society of America, 2026 HDSA Annual Convention - Phoenix, AZ, Qualtrics Survey | Qualtrics Experience Management, Sarepta Therapeutics Announces Approval of Clinical Trial Application for SRP-1005, Its Investigational Treatment for Huntington’s Disease | Sarepta Therapeutics, Inc., For More Information-Huntington's Disease Society of America, Will Forte Gets Candid About His Family's Health Journey with Huntington's Disease - YouTube, Honestly HD, Family Members take Action - Huntington's Disease Society of AmericaHuntington's Disease Society of America, Family Members: Urge Congress to Back Fair Review of AMT-130., People Living with HD: Urge Congress to Back Fair Review of AMT-130, Webinar Registration - Zoom, Community Letter, Press Release, hdsa.org, ohiovalley.hdsa.org, UC Health hosts education day on Huntington's disease, Ask The Scientist With HDBuzz, Webinar Registration - Zoom, Petition · Bring Hope to Huntington's Disease Families: Urge the FDA to Uphold Accelerated Approval - United States · Change.org, HDSA Today | January 2026, Team Hope Poll, easternpa.hdsa.org, Sarepta Therapeutics Announces Submission of Clinical Trial Application for SRP-1005, its Investigational Treatment for Huntington’s Disease | Sarepta Therapeutics, Inc., What should we know about HDSA-funded research?, YOUTUBE CHANNEL -Huntington's Disease Society of America, The HDSA Podcast.