Mast Cell Diseases can be overwhelming. You don’t have to navigate them alone.The Mast Cell Disease Society (TMS) provides trusted resources, community, and research to help you understand, manage, and live fully with mast cell diseases.New Patients – Start HereDonate to TMSTogether, we can make life easier for those facing Mast Cell Disease.Your donation today brings education, advocacy, and hope to people living with mast cell diseases.Donate NowFacing a new diagnosis is hard.We’re here to help.Explore tools, resources, and support to help you understand Mast Cell Disease, prepare for appointments, and feel more confident in your care.Begin Your JourneyA diagnosis can feel confusing and isolating. We’ll help you make sense of what’s happening, connect with others, and take the next step forward.Start HereGet ResourcesOur resource guides help you stay organized and confident, with ready-to-use documents for doctor visits, ER visits, diagnostic tests, and more.Learn MoreSupport the CommunityTogether, we can make life easier for those facing Mast Cell Disease.Your donation helps fund research, community support, and trusted resources for people living with mast cell diseases.Donatelearn with usEducation that makes a difference.Our growing library of expert-led courses brings clarity and confidence to the mast cell disease journey.Learn MoreStay informed, inspired,and supportedFrom research and resources to personal stories — discover what’s new and helpful for navigating life with mast cell disease.TMS goes to American Academy of Asthma, Allergy, and Immunology (AAAAI) 2026 in PhiladelphiaTMS goes to American Academy of Asthma, Allergy, and Immunology (AAAAI) 2026 in Philadelphia By […]Learn MoreA New Opportunity to Encourage Your Doctors to Join Our Free TeleECHO ProgramA New Opportunity to Encourage Your Doctors to Join Our Free TeleECHO Program At The […]Learn MoreColors of SM: Share Your SM StoryColors of SM: Share Your SM Story Blog Post Sponsored by Blueprint Medicines It was […]Learn MoreKicking for a CauseKicking for a Cause: Gary’s Fundraiser for TMS At The Mast Cell Disease Society (TMS), […]Learn MoreShonna’s Summaries: A New Anaphylaxis Definition, Overview, and Tool for CliniciansShonna’s Summaries: A New Anaphylaxis Definition, Overview, and Tool for Clinicians by Shonna Snyder This […]Learn MoreMCDecoded Live and the Importance of CommunityMCDecoded Live and the Importance of Community An inside look at the MCDecoded Live discussion […]Learn MoreGiving Tuesday: A Letter from Our Board Chair, Judi EmmelA Letter from Our Board Chair, Judi Emmel, on Giving Tuesday Today is Giving Tuesday […]Learn MoreReflections from the FAACT Summit: Connecting Communities and Sharing AwarenessReflections from the FAACT Summit: Connecting Communities and Sharing Awareness An inside look at the […]Learn MoreTMS Takes the Next Step: Representing Our Community at the NORD Registry Meeting TMS Takes the Next Step: Representing Our Community at the NORD Registry Meeting By Shonna […]Learn MoreSee how we’re bringing awareness and support to the mast cell disease community with our feature on PBS.Watch NowMore support, straight to your inbox.Join our newsletter for helpful tips, community stories, and the latest updates to keep you informed and connected.
