The Mast Cell Disease Society

The Mast Cell Disease Society, Inc. (TMS) is a national rare disease nonprofit founded in 1995. As the United States’ largest mast cell disease nonprofit, we believe in patients first. We represent patients affected by cutaneous and systemic mastocytosis and their variants, mast cell activation syndromes, and hereditary alpha-tryptasemia.

Our Mission

We are dedicated to providing multi-faceted support to patients, families and medical professionals in our community and to leading the advancement of knowledge and research in mast cell diseases through education, advocacy and collaboration.

Join us in finding a cure.

Learn more and join our network of over 15,000 at tmsforacure.org.