24th TMS National Patient & Caregiver Conference
24th TMS National Patient & Caregiver Conference – VIRTUAL!
October 13-20, 2021
TMS’s 24th National Conference, presenting sponsor Blueprint Medicines, will be virtually held this year and consist of lay-person-focused medical presentations, panel discussions, workshops and support group sessions, with time for questions, and will incorporate breaks to allow for resting periods, and free time to allow for casual socializing through our virtual platform. This conference will provide a uniquely supportive environment in which patients, caregivers and families learn to self-advocate, and will offer exposure to research and clinical trial information to which they normally would not have access. Patients, caregivers, physicians, young or established investigators, and biopharma can interact outside of the medical environment to promote more positive relationships in a casual atmosphere.
Our goals are to:
- Demonstrate the TMS commitment to helping people with mast cell diseases through education, support, and research.
- Highlight TMS-supported research and the development of diagnostics and treatments.
- Initiate a mutually beneficial dialogue among physicians, public and private researchers, patients, patient advocates, and policymakers.
Register by October 1st to receive our new TMS Emergency Alert Card and stickers (US registrants)! US resident registrations after October 1st will receive goodies after the conference. International registrants will receive digital download of freebies.
Join us on Wednesday, October 20th from 8:00-8:30pm ET for our LIVE Closing Ceremony & Purple Tie Evening to celebrate our community on the 4th International Mastocytosis & Mast Cell Disease Awareness Day, featuring special guest speakers and awards.
How to Watch
The virtual conference will take place online and Whova during 9am-4pm Eastern Time (US and Canada). There are no concurrent sessions, to allow for breaks. Recordings will be available for registrants to watch on-demand the day after the event, or catch up utilizing the official event app, Whova. Recordings will be available for registrants until December, 2021.
NORD’s new Rare Disease Educational Support Program provides reimbursement for registration costs for rare disease educational offerings, to include conferences. For more information, please call NORD at this special line (860) 556-2208.
* All scheduled presentations & speakers are subject to change.