Wyatt Warrior FundA fighter from the start, he was born with a rare disease, Diffuse Cutaneous Mastocytosis. Wyatt’s tiny body produces too many mast cells. His skin blisters easily and he is at risk for severe anaphylaxis. There is little known about Wyatt’s disease and there is a need for research, education, advocacy and resources for patients, their families, doctors, and caregivers. Please join us and become a WYATT WARRIOR! Annually, Wyatt raises awareness through a fall Wyatt’s Walk and you may support the advancement of pediatric research by donating below. Donate NowSarah Gittleman FundOn February 21, 2004 our life changed forever. Our daughter, Sarah Gittleman, had an anaphylactic reaction to medication and almost died. During her recovery, we found out that she had Systemic Mastocytosis. We did not know what that meant but found out quickly. Within the next four months her symptoms were rapidly increasing and by July, Sarah was diagnosed with Mass Cell Leukemia. Sarah passed away on December 21, 2004.Sarah was a typical 23-year-old. who was a Michigan State graduate in accounting and wanted to be a CPA. As a Family, we wanted there to be a way to honor and remember Sarah. Since finding a cure is the most important thing to us we decided to create a research fund in Sarah’s name. We hope that someday we will find a cure for this horrific disease and thank you for donating to this campaign.Donate NowThe Adam Thrasher HCP Education FundThis fund is established in loving memory of Adam Thrasher by his family to support the healthcare provider education programming of TMS. Adam’s smile, sweetness, and steadfast desire to share life with everyone around him will never be forgotten by those who were lucky enough to know Adam.Now more than ever, there is a need for more physicians and healthcare providers to treat our growing patient needs. Investing in healthcare provider education of mast cell diseases is imperative for us to continue the delivery of world-class care to our community.Please help us honor Adam’s memory with a donation to the Mast Cell Disease Society.Donate NowThe Julie Smith YollesMast Cell Activation SyndromeWellness Research FundThe JSY Fund supports scientific studies aimed at improving the quality of life for individuals diagnosed with Mast Cell Activation Syndrome (MCAS). It prioritizes research that helps patients more effectively manage the complex symptoms and triggers associated with MCAS including severe food and skin reactions as well as sensitivity to sunlight and environmental exposures. The Fund is committed to making a meaningful impact on how those living with MCAS can better navigate this chronic condition.Donate NowTMS General FundDonate NowResearch FundThe Mast Cell Disease Society is a 501(c)3 nonprofit organization. Your donations allow us to provide support to patients, families and medical professionals through outreach, education and advocacy. Thank you for supporting us in our mission to support others. This fund supports research efforts related to mast cell diseases.Donate NowMany families also create their own fundraisers to support the work of TMS. You can find all of the fundraisers that have been set up to support our work by clicking HERE.
