HHT Foundation International, Inc, based in Monkton, MD, is a leading organization dedicated to raising awareness, providing education, and driving research efforts for individuals affected by Hereditary Hemorrhagic Telangiectasia (HHT). With a mission to find a cure for HHT and improve the well-being of those impacted by the disorder, the foundation works tirelessly to increase patient access to life-saving care and enhance treatments through scientific research.
Since its establishment in 1991, the foundation has been a pivotal force in the HHT community, advocating for improved understanding and diagnosis of this genetic bleeding disorder, which affects over 1.4 million individuals globally. Through government advocacy, seed grants, and leveraging investments, the organization has successfully turned donations into millions of dollars dedicated to funding new treatments, technologies, and drugs for HHT patients worldwide.
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