The Mast Cell Disease Society, Inc. (TMS) is a 501c3 nonprofit organization 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. We represent all those affected by Cutaneous and Systemic Mastocytosis and their variants, Mast Cell Activation Syndromes, and Hereditary alpha-Tryptasemia. For years, we have been pioneering the path to increase education and research about thus little-known rare disease and bringing compassion and innovation to our mast cell disease community globally. TMS was founded in 1995 and has since grown to a network of over 15,000 patients, family members, caregivers, and physicians; held 23 patients & caregiver conferences, local, regional, and online support groups and forums; granted over $500,000 in research grants and facilitated our patients being able to access support and emerging quality care. Our Medical Advisory Board consists of top experts in mast cell diseases, where we collaboratively aim to serve the mast cell disease community and educate physicians and other health care professionals.