PDSA ITP SUPPORT
@PDSA_ITP
Platelet Disorder Support Association ~ the premier source for information, treatments, and support for people with ITP (immune thrombocytopenia).
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This episode demystifies clinical trials, explains how they differ from standard treatments, when they might be the right choice, and how they’ve already shaped major advancements in ITP care. 🔗 Listen now: pdsa.org/podcast or on Apple and Spotify #ITP #ITPpodcast
Meet #ITPWarrior Tierney! From childhood bruises to Broadway costumes—discover how she stitched strength into every step for the past 17 years! Read her full story at pdsa.org. #ITPWarriorStory #ITP #Global4ITP #LowPlatelets #PaintThePlanetPurple #LightUp4ITP
Meet #ITPWarrior Kayla! From monthly hospital visits to eight years symptom-free—Her ITP breakthrough will inspire you. Visit pdsa.org to read Kayla's story. #ITPWarriorStory #ITP #WhatImpactsPlatelets #LowPlatelets #ITPAwarenessMonth
Next week is Global ITP Awareness Week! Let’s show the world that every voice matters. Join the global movement to raise awareness and support those living with ITP by downloading your template today at pdsa.org/itp-awareness-….
ITP Awareness Month is here—Patients are sharing what they wish others understood about living with ITP. Hear directly from patients about what it’s like to live with ITP by visiting pdsa.org/personal-stori… and reading #ITPwarrior stories.
Diagnosed with ITP at 12, Dr. Kristin Hunt turned her journey into a lifelong mission to help others. Hear how she went from patient to pediatric immunologist in our latest episode! Listen now at pdsa.org/podcast or on Spotify. #ITP #ITPawareness #Hematology #Immunology
Meet #ITPwarrior Hadley! Living outside the bubble, read how Hadley and her family found community and clarity through her ITP diagnosis at pdsa.org. #ITPWarriorStory #ITP #LowPlatelets #ITPandSports #ITPandSoftball #ITPinTeens
ITP is an invisible illness—but the impact is very real. From unexplained bruises to relentless fatigue, life with immune thrombocytopenia often goes unseen and misunderstood. #ITPawareness #InvisibleIllness #Global4ITP #PDSA #RareButReal #LowPlatelets
You’re invited to the Canadian Regional Meeting on ITP! Whether you’re newly diagnosed or have been navigating ITP for years, this meeting is a space for education, empowerment, and community. 💜 Visit pdsa.org/canada to register today! #ITP #CanadianHealth #ITPcanada
Enjoy 20% off for ITP Awareness Month throughout September! Shop now at pdsa.org and wear your support proudly! No code needed—prices shown already include the 20% discount! #ITPawareness #LightUp4ITP #PDSA #ITP #LowPlatelets #ITPstrong #ITPwarrior
Big news for the ITP community! Rilzabrutinib has just been approved—a groundbreaking new treatment option for immune thrombocytopenia! Read the full press release at pdsa.org/itp-news 💜 #ITP #Rilzabrutinib #PDSA #HopeForITP #ITPtreatment #ITPresources
💜Purple with Purpose 💜 Mark your calendars for Sport Purple for Platelets! Day on Friday, September 26th and let's turn awareness into impact! Every photo, every post, every person helps raise awareness for ITP! #ITP #ITPAwarenessMonth #SportPurpleForPlatelets #LightUp4ITP
September is ITP Awareness Month 💜 Listen to our latest episode of Bruised but Not Broken to learn how you can get involved on pdsa.org/podcast or Spotify. #ITPawareness #ITPresources #ITPpodcast #BruisedButNotBroken #LivingWithITP #LightUp4ITP
As we age, managing ITP becomes more complex—and more critical. Tune in to hear expert insights from Dr. Craig Kessler on this often-overlooked intersection of aging and autoimmune disease. Head to pdsa.org/podcast or Spotify to tune in today! #ITPandAging
September is ITP Awareness Month and we need YOUR help! Let's shine a light on ITP by lighting up monuments purple across the U.S. and Canada. Tag friends and encourage them to join the movement. #LightUp4ITP #ITPAwarenessMonth
The Annual ITP Conference was unforgettable—and now you can relive it. Recorded sessions will be available to PDSA members starting September 1st. Not a member yet? Join us: pdsa.org/membership It’s more than access—it’s belonging to a community that truly understands!
Save the Date, Canada! Join us in Ontario for a powerful weekend of purpose and connection! Mark your calendars and register now at pdsa.org/canada Let’s walk, learn, and lift each other up! #ITPAwareness #ITPStrong #PDSACanada #WalkForITP
What’s the best approach to getting vaccinated when you have ITP? Get a platelet count before and after? Wait? Avoid it altogether? Dr. Bussel weighs in with clear, evidence-based answers in our latest episode to clear the confusion between vaccines and ITP. #ITP #ITPresources
Aging with ITP brings new challenges—but also new wisdom. In this episode, three longtime patients open up about what it really means to live well with a bleeding disorder later in life. Listen now at pdsa.org/podcast or on Sportify. #ITP #ITPpodcast #AgingWithITP
Philly, here we come! ONE MONTH till #ITPConference2025 and we have over 250 people registered! ✔️ Review the “Know Before You Go” ✔️ Pre-register for the Saturday night fun event bus tour ✔️ Bring your ITP questions Learn more at pdsa.org/conferences!
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