Latest Mastocytosis Society Events


INSPIRE WEBINAR:

There will be an Inspire webinar offered for all TMS FB members on Wednesday October 3 at 2pm ET. The Inspire Team will be answering the questions and concerns that you submitted to us and some we copied from the FB page posts. This webinar WILL be saved to be viewed after the live showing – You can view a recording of the webinar here. https://www.youtube.com/watch?v=9QQd0gAiVfQ&feature=youtu.be

Please don’t hesitate to reach out to us with any comments or questions.

Thanks,

Judy and the rest of us here at Team Inspire


2017 TMS Member Meeting: 

Please Join The Mastocytosis Society’s Board of Directors for our 2017 TMS Member Meeting:

Each Chair will give a brief report about their year’s activities and the initiatives planned for 2018.

Monday, December 4, 2017, 8:00 pm- 9:30 pm (ET)

To reach as many people as possible TMS is trying an online meeting this year.
Information is being emailed to all registered TMS members.
This emailed invitation contains the link needed to access the meeting.
Members may sign in on their computer at no cost, or call in by phone and local rates may apply.
We look forward to updating you on all that is to come in 2018!

 


Misbehaving Mast Cells in POTS and Other Forms of Dysautonomia

Join The Mastocytosis Society and Dysautonomia International for a review of the relationship between autonomic dysfunction and misbehaving mast cells. Guest speakers, Dr. Andrew White, an immunologist at the Scripps Clinic in La Jolla, California and Dr. Jonathan Bernstein, an immunologist at University of Cincinnati, reviews the current approaches to diagnosing and treating mast cells disorders, how MCAS is distinguished from other mast cell disorders, and theories on what may be causing mast cell symptoms in some people with POTS and other forms of dysautonomia. The doctors answer your questions during the Q&A at the end of the webinar.

Support Group Meetings

*Click Here* to see a list of upcoming Support Group meeting dates.  See you there!

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TMS 2018 Walk-a-Thon

Each year, thousands of people participate in our annual walk-a-thon to raise money and awareness for Mast Cell Disorders. This year we invite you to create your own “Fundraiser Page” and share it with friends and family who will contribute to your effort of raising money for TMS.

Learn More

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2018-2019 Conferences

The Mastocytosis Society, Inc. will hold its next large scientific and support conference for patients, families and health care professionals in 2019, in Northern California.
In 2018, we will be hosting six regional one-day conferences with a presentation by a mast cell specialist and a support group session. Stay tuned for updates!