Our AlliancesTMS is grateful to be part of a community of patient education and advocacy organizations that are each doing their part to support the mast cell disease community and the broader rare disease patient community as a whole. Below are the amazing allies that work with TMS to support our community.The American Initiative in Mast Cell Diseases (AIM) works to advance the research, education, and treatment of mastocytosis and related mast cell diseases. One of AIM’s projects is to identify Centers of Excellence and Reference Centers that can treat patients with mast cell diseases. Resources from AIMArticles Resources from the Allergy & Asthma Network The Itch Podcast: Episode 63: Mast Cell Diseases and Systemic Mastocytosis: The Basic ScienceThe Itch Podcast: Episode 65: The Symptoms and Triggers of Mast Cell Disease The Itch Podcast: How to Diagnose Mast Cell DiseaseAnaphylaxis Resources Resources from APSHOThe Advanced Practitioner Society for Hematology and Oncology (APSHO) has developed a comprehensive Toolkit for Systemic Mastocytosis, designed by a multidisciplinary steering committee. Explore 15 reference tables, visual guides, and curated provider and patient resources for diagnosing and managing systemic mastocytosis.Toolkit for Systemic Mastocytosis Resources from FAACTMast Cell Disease InformationPodcasts:Ep. 237: Mast Cell Disease Society – Finding SupportEp. 236: Indolent Systemic Mastocytosis – the Patient PerspectiveEp. 235: Exploring Systemic Mastocytosis (SM)Ep. 194: The Mast Cell Disease Society – Everything You Need to Know Resources from Gryt HealthMastoconnect Resources from Medscape OncologyLiving with Systemic MastocytosisJust an Allergy or Could It Be Systemic Mastocytosis? Resources from NCCNSystemic Mastocytosis Guidelines – English VersionGuia de Mastocitosis sistémica – Versión en español Resources from Patient Power Systemic Mastocytosis Web Resources