Cure HHT: Summary

Cure HHT

Healthcare, Nonprofit, Genetic Disorders, Rare Diseases

Cure HHT aims to improve the quality of life for individuals with HHT through research, support, and advocacy.

Cure HHT is a nonprofit organization dedicated to raising awareness and providing support for individuals affected by Hereditary Hemorrhagic Telangiectasia (HHT), a genetic blood vessel disorder. The organization focuses on improving diagnosis, treatment options, and funding research to find a cure for HHT.

Remote observational study participation; Access to HHT treatment centers; My HHT Tracker App for personal management; Comprehensive resource library for patients and families

Cure HHT is most valuable for individuals diagnosed with HHT, their families seeking support, and researchers looking for collaboration opportunities.

Strong focus on research and funding for new treatments; Comprehensive support network for patients and families; Established history of advocacy and awareness since 1991

Cure HHT has a robust network of resources, a commitment to research, and a clear mission to improve patient outcomes.

Cure HHT positions itself as a leading nonprofit organization dedicated to addressing the needs of the HHT community through research and support.

The target users include patients with HHT, their families, healthcare providers, and researchers in the field of genetic disorders.

Learn More

• HHT

• genetic disorder

• patient support

• research funding

Be part of uncovering the real impact of HHT

Supportive, informative, compassionate

Cure HHT uniquely combines patient support, research funding, and community engagement to address the challenges faced by those living with HHT.

Cure HHT identifies itself as a cornerstone of the HHT community, focusing on advocacy, education, and research to improve lives.

1991-01-01