PDSA ITP SUPPORT

🍀Just like a clover, every ITP journey is unique. Every story unfolds differently, yet each one reflects remarkable resilience. Leave a 🍀 in the comments if you’re cheering on others in the ITP community — or giving yourself a little extra encouragement today! #ITP

Expand your ITP expertise with education designed for clinical practice. This no‑cost CME reviews chronic ITP’s impact, current + emerging treatments, and practical tools for real‑world care. HCPs can earn 1.0 CME/CE credit at pdsa.org/itp-cme.

ITP is one of many platelet‑related bleeding disorders. While most cases aren’t life‑threatening, severe untreated cases can lead to very serious complications. Awareness leads to earlier recognition and better support for those living with these often invisible conditions. #ITP

FACT: We can’t see the full picture of ITP without patient data. Your data helps strengthen research and drives progress. Enroll in the PDSA ITP Natural History Study Registry. #ITP #ITPresearch

Today is Rare Disease Day! We stand with the millions of people affected by rare conditions—including those living with Immune Thrombocytopenia (ITP).

Tomorrow is Rare Disease Day. As we prepare to recognize the 300 million people living with rare conditions worldwide, we invite you to hear Michael's empowering journey with ITP and Evan's Syndrome now on Apple, Spotify and pdsa.org/podcast. #ITP #RareDiseaseDay

Rare Disease Day is coming up this Saturday. To get ready, check out our podcast episode with the CEO of NORD, where we talk about the importance of visibility and support for the rare disease community: pdsa.org/s1e12 #ITP #ITPpodcast #RareDiseaseDay

Send a valentine to your #ITPwarrior! These little notes are a simple way to remind someone they’re seen, supported, and never facing ITP alone. #ITP #ITPcommunity

No two ITP stories look the same. Daisy reminds us that the impact of a diagnosis can follow you through different stages of life, and that giving yourself grace is an essential part of your journey. Read Daisy's full story at pdsa.org/patient-warrio…. #ITPWarriorStory #ITP

New year, new ways to support you! Our new website is LIVE! 🎉Redesigned to make it easier to find resources, connect, and get the support you need. Explore what’s new 👉 pdsa.org #ITP #ImmuneThrombocytopenia #Hematology #PatientSupport

A recent episode of THE PITT spotlights a young patient’s unexpected ITP diagnosis — reflecting what many families face in real life. 🔗 Read the full story at pdsa.org/itp-news/2827-…

Save the date: 2026 ITP Conference in Salt Lake City! Whether you’re newly diagnosed, returning for another year, or ready to get more involved, start imagining the conversations, friendships, and empowerment waiting for you there! #ITPConference2026 #SaveTheDate

From childhood bruises to nursing dreams, Caitlin redefines life with ITP. Read Caitlin's #ITPWarriorStory at pdsa.org #ITP #HemOncNurse #ITPwarrior #PatientVoice

Breaking down the science: Not all low platelet counts are the same. Learn how immune thrombocytopenia differs from inherited thrombocytopenias in our latest episode. Listen now on pdsa.org/podcast, Apple or Spotify. #ITP #ITPpodcast

Meet Lilly, our fearless ITP Warrior 💪. Her classmates call her brave, and we couldn’t agree more! Read her story at pdsa.org. #ITP #ITPWarriorStory #LowPlatelets #ITPinChildren #ITPWarrior

Every gift helps PDSA provide hope, resources, and support for patients and families facing immune thrombocytopenia. This Giving Tuesday, we invite you visit pdsa.org/giving-tuesday to help us make a difference in the ITP community. #GivingTuesday #ITP #ITPcommunity

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-….