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June is HHT Awareness Month

For individuals and families affected by hereditary hemorrhagic telangiectasia (HHT), awareness and support are vital. June is our opportunity to come together, share our experiences, and educate others about this often-underdiagnosed condition. Explore resources, connect with the community, and find out how you can help amplify the voices of those living with HHT.

What Can You Do To Get Involved?

Every year on June 23 — and throughout the month of June — local, state, federal, and national organizations come together to shed light on the impact of HHT and to show support for those at living with and caring for those with HHT.

After a successful campaign in 2025, this year we'll be taking the theme "Beyond the Visible" one step further by shifting the theme to "Visible Together". We are honoring 35 years of dedication to the HHT community and looking towards the next 35 years of progress.

Children - Back to School

Raise Awareness

Jessica Hammer - Finish Line

Host a Fundraiser

FUNDRAISER BALL FOR GRACE NOLAN ARTICLE

Donate

Upcoming Events

Diagonal Therapeutics Open House & HHT Patient Forum

Open House and HHT Patient Forum at Diagonal Therapeutics Friday, June 26  |  9:30am-1:00pm ET   Join patients, caregivers, clinicians, and researchers for a day of connection, learning, and community focused on hereditary hemorrhagic telangiectasia (HHT) in celebration of HHT Awareness Month at Diagonal Therapeutics (200 Arsenal Yards Boulevard #220, Watertown, Massachusetts, 02472). Register to…

State of HHT: An Update from Cure HHT’s CEO

Upcoming Event: State of HHT: An Update from Cure HHT’s CEO Tuesday, June 23  |  6:00-7:00pm ET   Join Cure HHT’s CEO for a comprehensive update on the state of the organization and the organization’s work on behalf of the community. This webinar will highlight key milestones from the past year, including progress in research,…


Kate is a teacher, an avid swimmer, and addicted to green tea lattes. She loves traveling, dogs, and dreams of having a family.

Kate lives with HHT.

Stand with Us on Global HHT Awareness Day

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