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Partner Opportunities

Bridging the Gap Between Industry and Treatment

Hereditary Hemorrhagic Telangiectasia (HHT), also known as Osler-Weber-Rendu Syndrome, is a genetic blood vessel disorder that affects approximately 1.4 million worldwide and yet remains largely undiagnosed. The familial and societal impact of HHT on a national and global scale is immeasurable.

The success of the Cure HHT scientific and medical education programs, along with our awareness activities, would not be possible without the financial support of the HHT community and our sponsors.


We invite you to join our list of supporters by reviewing the Cure HHT Partnership Opportunities including HHT Academy Patient & Physician Conferences, International Scientific Conferences, awareness activities, and the Cure HHT website.
Questions may be directed to Courtney Kasturiarachi at 410-357-9932 or[email protected].

HHT Academy: Patient & Physician Conferences

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Cure HHT hosts 1-3 conferences in North America each year to educate patients and physicians in geographic areas that are underserved by the medical community, but also have HHT Centers of Excellence in neighboring states. In the event that in-person conferences are not feasible, virtual options may be offered as an alternative. Our next regional conference will be held March 28th-29th, 2025 in Denver (Aurora), Colorado.

HHT Academy Patient & Physician conferences are a perfect opportunity to share information with patients and physicians.

Sponsorship Benefits:

  • Increase your base with a proud partnership with our Cure HHT Community
  • Showcase your products and services by distributing samples or promotional materials
  • Promote presentations and activities specific to your niche of the HHT medical community

International Scientific Conference

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Connect with researchers unraveling the mysteries of HHT mechanisms of disease and discovering potential therapies for patients around the world. We just had our 15th HHT International Scientific Conference in Mandelieu-la-Napoule, France from October 15-19, 2024. We will announce 2026 soon!

Get more exposure to the HHT community by becoming a sponsor, exhibitor or advertiser.

  • Directly reach global opinion leaders.
  • Increase your visibility and build brand awareness through exposure to over 370 healthcare professionals, researchers, and patients worldwide.
  • Integrated meeting and exhibit space to facilitate greater networking and relationship building with the HHT clinical, scientific, and patient community.
  • Partner with the only not-for-profit organization in the world committed to serving those with HHT and bringing together international thought leaders working collaboratively to find a cure for HHT.
Alizée Palomba
Alizée Palomba

Cure HHT Webinars

Cure HHT recently celebrated 30 years of building awareness of HHT, educating, the public and medical professionals, leveraging funding for research, and advocating for patients and families affected by the disease.

Our webinars showcases our tireless work to make an impact on the medical, scientific and patient communities.

For more information please email Courtney Kasturiarachi at [email protected]

Questions may be directed to Courtney Kasturiarachi at 410-357-9932 or [email protected]

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