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 TMSTMS Eventsand ProgramsA year-round mix of virtual and in-person opportunities to connect, learn, and engage with the mast cell disease community.VirtualSeptember 2026EMPOWER Workbook WebinarRegister In PersonOctober 2026TMS MastCellCon On Tour- PhoenixRegister In PersonNovember 2026TMS MastCellCon On Tour- RaleighRegister View All EventsSupport the CommunityTogether, we can make life easier for those facing Mast Cell Disease.Every person who supports Team TMS is helping us continue the work that means so much to our community. Your gift, no matter the size, helps us be there for people and families affected by mast cell diseases.Support Team TMSFacing 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 Morelearn 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.Reflections from Our TMS Book Club Discussion of ImmuneReflections from Our TMS Book Club Discussion of Immune By Isabelle Charlot Earlier this week, […]Learn MoreConnecting Across Communities at the EDS ConferenceConnecting Across Communities at the EDS Conference An inside look at the EDS conference through […]Learn MoreClinical Trial FAQsClinical Trial FAQs An Interview with Dr. Jennifer Vaughn The Mast Cell Disease Society recently […]Learn MoreReflections from Our TMS Book Club Discussion of The Body Keeps the ScoreReflections from Our TMS Book Club Discussion of The Body Keeps the Score By Isabelle […]Learn MoreDr. Nathan Boggs, Walter Reed National Military Medical Center, and TMS Have a VisitDr. Nathan Boggs, Walter Reed National Military Medical Center, and TMS Have a Visit By […]Learn MoreShare Your Voice: Help Us Research How Mast Cell Disease Affects Your NutritionShare Your Voice: Help Us Research How Mast Cell Disease Affects Your Nutrition We’re excited […]Learn MoreA Systemic Mastocytosis Journey: From Diagnosis to AdvocacyA Systemic Mastocytosis Journey: From Diagnosis to Advocacy A Q&A with Steve Bashore following his […]Learn MoreTMS 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 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. Notice: JavaScript is required for this content.
