Platelet Disorder Support Association

10/07/2026

Thank you to the City of Dublin, Ohio - Government for participating in as part of ITP Awareness Month! 💜

10/06/2026

Asking questions isn’t being difficult, it’s being informed. It’s advocating for yourself and partnering in your care.

The ITP Patient Bill of Rights reminds every patient that they deserve clear explanations, open conversations, and a care plan that reflects their goals, values, and lifestyle. You have the right to understand your diagnosis, explore all treatment options, and participate in shared decision‑making with a healthcare team that listens to you.

If you ever feel unsure, overwhelmed, or need help preparing for appointments, PDSA offers tools and resources to support you. Explore the ITP Patient Bill of Rights at pdsa.org/treatments/bill-of-rights.

10/01/2026

Tune into to hear PDSA President and CEO, Caroline Kruse, talk about ITP and ITP Awareness Month!

09/29/2026

Jumbo the Elephant Lights Up for ITP! Thank you to the City of St. Thomas for supporting ITP Awareness! 💜

💜 Jumbo Shines Purple for ITP Awareness 💜

Jumbo is shining purple in recognition of Immune Thrombocytopenia (ITP) Awareness!

ITP is a rare autoimmune blood disorder that causes a low platelet count and can lead to increased bruising and bleeding. Lighting Jumbo purple helps raise awareness, show support for those living with ITP and their families, and encourage greater understanding of this often-unseen condition.

Tonight, we join communities in helping shine a light on ITP. 💜

09/28/2026

More than a platelet count. More than a diagnosis. More than the challenges ITP can bring.

A platelet count is just one part of the story. Behind every number is a person with goals, dreams, relationships, and a life that extends far beyond a lab result.

This ITP Awareness Month, we celebrate the resilience of everyone in the ITP community who continues to move forward, advocate for themselves, and live life on their own terms.

09/27/2026

💜 What an incredible first Pump It Up for Platelets event in St. Thomas, Ontario!

More than 80 people came together to raise awareness, connect with the ITP community, and show their support for those living with ITP — including 6 ITP warriors who helped make the day so special. 💜

We were also honored to welcome Andrew Lawton Andrew Lawton, Member of Parliament for the local area, as a special guest. Having a local elected representative join us is a meaningful way to bring greater visibility to ITP and the experiences of patients and families in the community. Andrew, thank you for taking the time to be there, learn more about ITP, and stand alongside the ITP community. We truly appreciate your support!

A huge thank you to everyone who helped make this first St. Thomas event such a success — the organizers, volunteers, ITP warriors, families, friends, and everyone who showed up to Pump It Up for Platelets! 🩸💜

Here’s to the first of many!

09/26/2026

💜 We loved seeing our PDSA team sporting purple for platelets. Now we'd love to see how YOU participated in Sport Purple for Platelets! Day!

We're collecting photos for PDSA's 2026 Sport Purple for Platelets! Day Photo Album, which will debut on our website and be featured in next week's September e-News.

📸 Post your photo in the comments
📩 Send us a DM
📧 Email your photos to [email protected]

Thank you for helping make ITP Awareness Month visible, meaningful, and community-driven. Together, we're raising awareness and showing the strength of the global ITP community, one purple photo at a time. 💜

09/26/2026

Living with ITP isn't always about reaching a perfect platelet count. Sometimes, it's about finding stability, confidence, and a treatment approach that allows you to live your life.

Meet 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 and discover the perspective that helped her navigate life with ITP.

🔗 Read Julia's story at pdsa.org

09/25/2026

💜 is a global movement founded by the International ITP Alliance. By illuminating landmarks across the United States and Canada, we're joining hundreds of buildings, bridges, monuments, and iconic landmarks around the world in raising awareness of and showing support for the global ITP community!

📸 Visiting one of these locations? We want to see it! Share your photos, tag PDSA, or send us a DM, and help us showcase the incredible support for the ITP community from coast to coast.

09/25/2026

💜 Today is I Sport Purple for Platelets! Day 💜

The global ITP community is coming together to raise awareness for Immune Thrombocytopenia (ITP), a rare autoimmune blood disorder in which the immune system mistakenly attacks platelets, resulting in increased platelet destruction and, for some people, reduced platelet production.

Whether you're wearing a purple shirt, rocking purple accessories or hair, lighting up a landmark, or going all out in purple, every photo helps spread awareness and make ITP more visible.

📸 Don't forget to: ✅ Wear purple
✅ Take a photo
✅ Tag PDSA or send us a DM
✅ Encourage friends and family to join in

Let's show the world the strength of the ITP community and turn social media purple today!

💜 We can't wait to see your photos! 💜