Each week, a new patient is highlighted. Volunteers are given details about the child's interests, guiding the creation of personalized artwork.
All submissions are reviewed to ensure quality and consistency before being distributed to hospitals or mailed directly to patients and their families.
Completed cards and care packages are hand-delivered to hospitals, connecting volunteers directly with the medical teams who bring them to MCAS patients.
MCAS is estimated to affect up to 17% of the global population, yet it remains one of the most underdiagnosed conditions in medicine today.
Patients spend an average of 7–10 years to receive a correct diagnosis, often cycling through dozens of specialists while symptoms are dismissed or misattributed.
The Mast Cell Disease Society (TMS)Through partnerships with institutions like Mayo Clinic and Cleveland Clinic, as well as the generosity of our donors, we work to create measurable, lasting change for MCAS patients worldwide.
The virtual setting protects patients with vulnerable immune systems, while also encouraging emotional resilience by providing moments of laughter, connection, and companionship during treatment.
