


The Mast Cell Disease Society Email Formats
Research Services • Sterling, Massachusetts, United States • 11-20 Employees
The Mast Cell Disease Society Email Formats
The Mast Cell Disease Society uses 3 email formats. The most common is {first initial}{last name} (e.g., jdoe@tmsforacure.org), used 40% of the time.
| Format | Example | Percentage |
|---|---|---|
{first initial}{last name} | jdoe@tmsforacure.org | 40% |
{first initial}.{last name} | j.doe@tmsforacure.org | 40% |
{first name}{last name} | johndoe@tmsforacure.org | 20% |
Key Contacts at The Mast Cell Disease Society
Jessica Fraser
Executive Director
Celeste Finnerty
Vice-Chair, Research, Board Of Directord
Bonnie Nasar
Member Board Of Directors
Valerie Slee
Chair Emeritus Board Of Directors
Rosemary Schultz
Board Member, Board Of Directors
Company overview
| Headquarters | PO Box 416, Sterling, Massachusetts 01564, US |
| Website | |
| NAICS | 5417 |
| SIC | 839 |
| Keywords | Nonprofit, Fundraising, Medical Research, Genetics, Rare Disease, Medical Literature, Mastocytosis, Hereditary Alpha Tryptasemia, Mast Cell Activation Syndrome, Mast Cell Diseases Support, Medical Symposiums |
| Founded | 1995 |
| Employees | 11-20 |
| Socials |
About 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 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.
Employees by Management Level
Total employees: 11-20
Seniority
Employees
Funding Data
The Mast Cell Disease Society has never raised funding before.
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