Top Tweets for #TMSforacure
At TMS, we believe every story matters! The 2026 RARE Artist Awards celebrate creativity in the rare disease community.
Explore the artwork and cast your vote until the 23rd: https://t.co/ct3dPCATFX
#TMSForACure #RAREArtist
Need support in your medical journey? TMS nurses are standing by to answer questions and help navigate you to the best resources! You can reach us at: [email protected]
#tmsforacure #tmslistens #patientsupport #MCAS #mastocytosis #HaT
October 20th is just around the corner! Do you have ideas about how to commemorate International Mastocytosis and Mast Cell Diseases Awareness Day? We want to hear all about it! Please let us know by replying below!
#mastocytosis
#MCAS
#HaT
#tmsforacure
#mastcelldisease
Earlier this week, TMS joined NORD (@RareDiseases) and more than 75 other rare disease patient advocacy organizations to call on Congress to pass the #RareAct. Read the letter here: https://t.co/IJVxLiW9hJ #mastcell
#tmsforacure
#mastcelldisease
#careaboutrare
#raredisease
Planning an event to benefit the lives of those affected by mast cell disease and research towards better treatment outcomes? We can help!
Learn more at: https://t.co/7ybHuT5TUQ
Contact us at: [email protected]
#tmsforacure #tmslistens #careaboutrare #fundraising
TMS is actively recruiting nurses & support group leaders! If you're interested in #volunteering in our community, please submit this form: https://t.co/ZyFGWW3fFB
#tmsforacure
We have exciting news! This weekend TMS will be taking part in the AAAAi conference in San Antonio, Texas! Stay tuned for drop in's from us on Facebook Live as we say 'hi' from our booth. 🦄
#tmsforacure #aaaai
#GlobalGenes is still accepting applications for the 2023 RARE Compassion Program. Apply before Feb. 24th!
#TMSforacure
#TMSforacure is growing! Please welcome Rachel Hellman. In addition to the Nurse Line, she will be leading a #POTS support group and contribute in the development of patient resources.
This month's theme at The Mast Cell Disease Society is Medications and Treatments! Please watch this webinar by Dr. Castells as she shares updates on effective treatment for Mastocytosis and MCAS.
#tmsforacure
https://t.co/ilN01S6o4W
Don��t forget to register for our support groups this week!
Advanced Disease 11/16, 6:30pm EST
Comorbidities 11/16. 7:30pm EST
Mast Cell Trivia 11/19, 1pm EST
Men's Group 11/20, 1pm EST
Register here: https://t.co/pr310oczC1
#TMSforacure
Happy Friday! Kick-start your weekend by joining our Inspire page, which is moderated by TMS Nurses. It's a safe space to anonymously ask questions and receive support.
https://t.co/7xLZjJTKMy
#tmsforacure #tmslistens
“YOU CAN SUPPORT THE ADVANCEMENT OF MAST CELL RESEARCH IN OTHER UNIQUE WAYS, SOME AT NO EXTRA COST YOU.”
Shop for Official TMS Merchandise here: https://t.co/GeRXem754Q
#tmsforacure
📣TMS has released UPDATED Adult and Pediatric ER Protocols!
These are completely FREE to the community, please download here: https://t.co/Hp14oMCELX
#tmsforacure #tmslistens #mastcelldisease #mcas #hereditaryalphatryptasemia #raredisease #mastocytosis
The average time to diagnosis for Mast Cell Disease patients is ten years. We are working tirelessly to close this gap and to advocate to physicians to help lower this number. Read one patient's diagnosis journey: https://t.co/sBB8Ild7x4
#tmsforacure #mastocytosis
In honor of 5th International #mastocytosis & #mastcelldisease awareness day, please consider making a donation. Your support ensures continued patient support, education & advancement in research until we find a cure! Give today at: https://t.co/P6kxKJTMYC #tmsforacure #MCAS
I am speaking at Mast Cell Disease Patient & Provider Symposium. Please check out my talk if you're attending the event! #TMS2022Symposium #tmsforacure #mastcelldisease - via #Whova event app
Hi! I'm attending Mast Cell Disease Patient & Provider Symposium. Let's start connecting with each other now. https://t.co/NRERsQeOhp #TMS2022Symposium #tmsforacure,#mastcelldisease
Join TMS and organizations across the world in raising awareness and funds to advance research and our understanding of #mastcelldisease. Download this year's social media campaign: https://t.co/s8ZuJSApX5 #mastocytosis #MCAS #tmsforacure ##rarediseaseawareness #raredisease
Join TMS and organizations across the world in raising awareness and funds to advance research and our understanding of #mastcelldisease. Download this year's social media campaign: https://t.co/s8ZuJSRsZ5 #mastocytosis #MCAS #hereditaryalphatryptasemia #tmsforacure
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