Your worth isn’t defined by your platelet count. It’s shaped by how you feel, what you’re managing, and what matters to you. Shared decision‑making and patient rights support your ITP journey every step of the way. Learn more at pdsa.org/treatment-opti… #ITP #SharedDecisionMaking
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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Asking questions is being informed, advocating for yourself and partnering in your care. The ITP Patient Bill of Rights reminds patients they deserve clear explanations, open conversations, and a care plan that reflects their lifestyle. Learn more at pdsa.org/treatments/bil….
A platelet count is just one part of the story. Behind every number is a person with goals, dreams, and a life that extends far beyond a lab result.
We celebrate the resilience of everyone who continues to move forward, advocate for themselves, and live life on their own terms.
We celebrate the resilience of everyone who continues to move forward, advocate for themselves, and live life on their own terms.
Meet #ITPWarrior Julia from Germany, a medical assistant living with ITP. Through her journey, she learned that stability matters more than perfect numbers and that quality of life is about much more than a platelet count. 💜
🔗 Read Julia's story at pdsa.org
🔗 Read Julia's story at pdsa.org
💜 Today is I Sport Purple for Platelets! Day 💜
The global ITP community is coming together to raise awareness for ITP. Be sure to wear purple, snap a photo, and share it to help make ITP more visible. #ITPAwarenessMonth #Purple4Platelets #LightUp4ITP #Global4ITP
The global ITP community is coming together to raise awareness for ITP. Be sure to wear purple, snap a photo, and share it to help make ITP more visible. #ITPAwarenessMonth #Purple4Platelets #LightUp4ITP #Global4ITP