The Mastocytosis Society
is a non-profit organization dedicated to supporting patients affected by Mastocytosis and Mast Cell Activation Diseases as well as their families, caregivers and physicians through research, education and advocacy.
ConferenceJoin us May 1-3, 2019 in Northern California for the 2019 Patient Conference.
THE MASTOCYTOSIS SOCIETY CONFERENCE
InfographicsPrintable Infographics and brochures! Use these for handouts and display.
DonateTMS works tirelessly for those people affected by Mast Cell Disorders. Your support allows us to assist and support patients, fund research and raise awareness. Join us as we look for a cure and provide hope to so many.
Emergency room guide
2019 RESEARCH AWARD: TMS Partners with the AAAAI to Fund MCAS Research
In 2018, The Mastocytosis Society, Inc. (TMS) conducted a survey on Mast Cell Activation Syndrome (MCAS) with over 1700 respondents,…
Mast Cell Activation Syndrome Patient Survey: UPDATE
Mast Cell Activation Syndrome (MCAS) Patient Survey This survey was open from August 17 – 25, 2018. (THIS SURVEY IS…