The Mast Cell Disease Society, Inc. OFFICIAL

Transforming lives of patients and families while finding a cure for #mastcelldisease since 1995. #Mastocytosis #MCAS #HereditaryAlphaTryptasemia #raredisease

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

MastCellCon is going on tour in 2026.

We’re bringing our in-person conference to two locations this fall to make it more accessible, with the same programming at each.

Phoenix, AZ • Oct 9–10
Raleigh, NC • Nov 13–14

More details coming soon. Save the dates.

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

New Awareness Day merch is coming soon! In the meantime, select current Awareness Day clothing is 10% off through October 1, 2026.

Use code MCDAWARE at checkout and shop through our Bonfire
store: https://t.co/PvVxLpwZV2

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

Join our Board Chair, Judith Emmel, on October 15 in Bethesda for Together in Strength: Community Conversations on Living With Systemic Mastocytosis. Connect with patients and caregivers and hear directly from members of the SM community.

Register: https://t.co/BTdeCbkR9p

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

MastCellCon ON TOUR is getting closer!

Phoenix: October 9–10
Raleigh: November 13–14

What are you most looking forward to? Let us know below, and make your plans to join us!

Register: https://t.co/IyyVO6j8fq

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

TMS is proud to be part of a Patient & Family Seminar on indolent systemic mastocytosis on October 3 in Baltimore! TMS’s Vlai Ly will be among the speakers sharing information with patients and caregivers.

Register: https://t.co/ICInlMrBxF

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

Awareness Day is coming up! As you prepare to raise awareness in your community, explore our Awareness Day resources for information and materials you can use and share.

Explore Awareness Day Resources here: https://t.co/NWhYhUXocQ

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

TMS support groups provide a welcoming space for patients and caregivers to connect, share experiences, and feel supported.

Explore the full schedule and learn more: https://t.co/8sy5uuQ5rR

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

New Awareness Day merch is coming soon! In the meantime, select current Awareness Day clothing is 10% off through October 1, 2026.

Use code MCDAWARE at checkout and shop through our Bonfire
store: https://t.co/PvVxLpwZV2

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

Last month, we asked our community how long it took for them to receive a mast cell disease diagnosis. Thank you to everyone who shared. Your responses truly help us guide future conversations in our community.

Stay connected through our newsletter: https://t.co/SDoKgg4Pa7

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

Tomorrow is the last day for early bird registration for MastCellCon ON TOUR Phoenix.

Join us October 9–10 for expert-led mast cell disease education and the opportunity to connect with the TMS community in person.

https://t.co/kW1QdJvuKl

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

TMS support groups provide a welcoming space for patients and caregivers to connect, share experiences, and feel supported.

Explore the full schedule and learn more: https://t.co/8sy5uuQ5rR

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

FLASCO, in partnership with Blueprint Medicines, is hosting a free Living With Systemic Mastocytosis patient education webinar on September 9 from 5:30–7:00 PM EST.

Learn more and register: https://t.co/DpZVoyEUmN

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

TMS Book Club is tomorrow! We’re discussing Immune by Philipp Dettmer.

Join us for the conversation: https://t.co/FWYNmZk6tW

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

TMS support groups provide a welcoming space for patients and caregivers to connect, share experiences, and feel supported.

Explore the full schedule and learn more: https://t.co/8sy5uuQ5rR

Please note: time zone is EST

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

Early bird pricing for MastCellCon ON TOUR ends soon! Phoenix early bird pricing ends September 9, and Raleigh ends October 13.

Secure your spot while early bird pricing is still available: https://t.co/kyUiKZkEx5

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

A message from TMS Executive Director Jessica Fraser as we enter the final day of the Rocket Community Challenge. We’re so close to first place and an additional $22,000 for TMS. Help us finish strong.

Donate now! https://t.co/pgj9fFKPeF

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

Tomorrow is the final day of the Rocket Community Challenge! There’s still time to help Team TMS finish strong.

Donate today: https://t.co/b0M2jTvoef

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

TMS Book Club is back!

Join us September 2 from 12–1 PM ET to discuss Immune by Philipp Dettmer and connect through conversation.

Register: https://t.co/Qpcn9MKuWD

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

Phoenix is getting closer, and we’d love to see you there.

Join TMS for MastCellCon ON TOUR on October 9–10, 2026. If you’re planning to attend, register soon.

Register for Phoenix here: https://t.co/kW1QdJvuKl

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

TMS support groups provide a welcoming space for patients and caregivers to connect, share experiences, and feel supported.

Explore the full schedule and learn more: https://t.co/8sy5uuQ5rR

[The Mast Cell Disease Society, Inc. OFFICIAL @MCDiseasesUnite]

TMS staff member Isabelle Charlot recently represented TMS at The Ehlers-Danlos Society’s Global Learning Conference.

Read her reflection on connecting with patients and sharing TMS resources across communities: https://t.co/V2LjD8irVW