The Mast Cell Disease Society

The Mast Cell Disease Society

Research, Po Box 416, Sterling, Massachusetts, 01564, United States, 1-10 Employees

tmsforacure.org

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phone no Phone Number: +17*********

Who is THE MAST CELL DISEASE SOCIETY

The Mast Cell Disease Society, Inc. (TMS) is a 501c3 nonprofit organization dedicated to providing multi-faceted support to patients, families, and medical professionals in our community ...

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  • Po Box 416, Sterling, Massachusetts, 01564, United States Headquarters: Po Box 416, Sterling, Massachusetts, 01564, United States
  • 1995 Date Founded: 1995
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: $5 Million to $10 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Research

SIC SIC Code: 2834 | NAICS Code: 541511 | Show More

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Frequently Asked Questions Regarding The Mast Cell Disease Society

Answer: The Mast Cell Disease Society's headquarters are located at Po Box 416, Sterling, Massachusetts, 01564, United States

Answer: The Mast Cell Disease Society's phone number is +17*********

Answer: The Mast Cell Disease Society's official website is https://tmsforacure.org

Answer: The Mast Cell Disease Society's revenue is $5 Million to $10 Million

Answer: The Mast Cell Disease Society's SIC: 2834

Answer: The Mast Cell Disease Society's NAICS: 541511

Answer: The Mast Cell Disease Society has 1-10 employees

Answer: The Mast Cell Disease Society is in Research

Answer: The Mast Cell Disease Society contact info: Phone number: +17********* Website: https://tmsforacure.org

Answer: The Mast Cell Disease Society, Inc. (TMS) is a 501c3 nonprofit organization dedicated to providing multi-faceted support to patients, families, and medical professionals in our community and to leading the advancement of knowledge and research in mast cell diseases through education, advocacy and collaboration. We represent all those affected by Cutaneous and Systemic Mastocytosis and their variants, Mast Cell Activation Syndromes, and Hereditary alpha-Tryptasemia. For years, we have been pioneering the path to increase education and research about thus little-known rare disease and bringing compassion and innovation to our mast cell disease community globally. TMS was founded in 1995 and has since grown to a network of over 15,000 patients, family members, caregivers, and physicians; held 23 patients & caregiver conferences, local, regional, and online support groups and forums; granted over $500,000 in research grants and facilitated our patients being able to access support and emerging quality care. Our Medical Advisory Board consists of top experts in mast cell diseases, where we collaboratively aim to serve the mast cell disease community and educate physicians and other health care professionals.

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