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Please help us educate and support both people with mast cell diseases (MCD) including mastocytosis, MCAS and HaT, as well as health and medical practitioners. Many people with MCD are provided with limited correct information especially when trying to adjust to their diagnosis. We seek your help with fundraising and developing these resources to make a real difference to these people’s quality of life.
BECOME A MEMBER
TAMS is a volunteer-run, membership association. TAMS members receive discounts for TAMS conferences and events, member e-newsletters, online and face-to-face support groups and more.
The TAMS committee advocates on behalf of TAMS Members to the medical community and government.
TAMS receives a lot of emails, calls and messages from people seeking diagnosis and treatment for their mast cell dieases. A lot of these ask the same questions, so we have put together some information to help you on your diagnosis and treatment journey.
LATEST NEWS AND ALERTS
20 October 2021 marks the fourth annual International Mastocytosis and Mast Cell Diseases Awareness Day.
When mast cells, usually from bone marrow, skin, and GI biopsies, are exposed to a special dye in pathology labs the granules of the mast cell or their cartilage matrix shows up in a distinctive purple colour. Once mast cells are highlighted in purple, pathologists...
Our second Explaining Mast Cell Disease info sheet and post focus on Adult Onset Cutaneous Mastocytosis.