The June 2025 edition of the Platelet Journal is now available. This edition includes reports from our recent Patient Convention in Manchester, some great news from some of our fundraising heroes, upcoming meeting dates and much more. Platelet June 2025 - bit.ly/plateletjune25

Congratulations to consultant haematologist Prof. Nichola Cooper on ‘ITP & Me’—a new book for teens exploring Immune Thrombocytopenia, a rare blood clotting disorder. 👏 Here's Prof. Cooper and colleagues at the House of Commons during the ITP Support Assoc's 30th anniversary!

This is a recording of Dr Andrew Morgan’s Virtual Patient Meeting covering ITP and Stress, this is Session One in what will be a series of three virtual meetings. youtu.be/M4Uo2bw_KNQ?si…

ITP and Me – An ITP Book for Young Adults and Teenagers Are you a young person who has been diagnosed with ITP? Then this book is for YOU! ITP and Me – An ITP Book for Young Adults and Teenagers Filled with the real-life experiences of teenagers with ITP, you’ll find everything

The ITP Support Association are pleased to share some exciting news, Iris Web Media will now be supporting and managing the social media accounts for the ITP Support Association. Iris Web Media specialises in values-led digital communication - from smart websites to impactful

Teenagers and ITP Prof Nichola Cooper This is a presentation from our 2024 UK and Ireland ITP Support Association Annual Patient Convention which was held at the Cavendish Conference Centre in London. As we have just published our new ITP guide to teenagers and young adults we

This is a recording of Dr Andrew Morgan’s Virtual Patient Meeting covering ITP and Stress, this is Session One in what will be a series of three virtual meetings. The interest in this meeting was outstanding with scores of people joining online. You can download a copy of Dr

ITP Support Association Online Support Group The second of Dr Andrew Morgan's support group meetings via Zoom is taking place on 26th August at 6pm GMT. Dr Andrew Morgan will be talking to us about living with ITP and Stress. Anyone with any interest in ITP may join us but

We are pleased to be able to share the video recording of the first session of our ITP Support Association Annual Patient Convention which took place at the Bridgewater Hall in Manchester on Saturday May 10th. youtu.be/JYVCqPdJwrs This is a recording of the first session

In 2024, hundreds of locations around the world turned PURPLE during September to help raise awareness for those living with Immune Thrombocytopenia. This is the 10th year of our community celebrating Global ITP Awareness Week (22–28 September 2025) and as part of the

Join us online on Tuesday 16th September 2025 at 7pm for the Scotland ITP Support Association Virtual Patient Meeting, an opportunity to connect with fellow patients, caregivers, and the advice of ITPSA Medical Advisor Dr Catherine Bagot , to learn more about living with ITP.

Are you a young person who has been diagnosed with ITP? Then this book is for YOU! ITP and Me - An ITP Book for Young Adults and Teenagers Filled with the real-life experiences of teenagers with ITP, you’ll find everything you need to know about the condition, along with lots

📘 ITP & Me is here - a heartfelt guide for teenagers and young adults living with Immune Thrombocytopenia. Packed with real-life experiences, practical advice, and honest reflections, this 48-page book helps young people navigate diagnosis, treatment, and everyday life with

💜 Become a Member – Support the ITP Community Whether you’re newly diagnosed, supporting a loved one, or simply want to help raise awareness - joining the ITP Support Association is a meaningful way to stay informed and connected. Annual Membership UK Members: £15 per year

#LightUp4ITP – Let's Raise Awareness Together Each September, monuments, buildings, and landmarks across the UK and beyond light up purple to mark Global ITP Awareness Week — showing support with those affected by Immune Thrombocytopenia. 💡 We’re inviting local landmarks,

Emma Roger-Lund’s story is a powerful example of living with ITP from childhood through adulthood. 🎓 As the 2024 ITP Support Association Scholarship Winner, Emma shares how her experience shaped her perspective and commitment to raising awareness. 📍 Read her full journey on

👋 Meet Mervyn Morgan - Chief Executive Officer (UK & Ireland) Mervyn has been with the ITP Support Association since 2016 and became the CEO in 2018 on the retirement of the Charities founder Shirley Watson MBE. He works closely with specialists, patients, and volunteers to

Whether you're a teen with ITP, a parent, or a teacher — this free book helps start the conversation that changes lives. ITP & Me is filled with real personal stories and advice from teenagers who know what it’s like to live with Immune Thrombocytopenia. It’s a fantastic

What’s a normal platelet count, and why does it matter? For most people, it’s between 150–450. For those living with ITP, it can drop dramatically… sometimes without warning. 💬 Understanding your numbers helps you manage the condition and speak up for your needs. Learn more

💡Help Light Up Your Town for ITP Awareness! 💜 Every September, landmarks across the UK turn purple for Global ITP Awareness Week and you can help make it happen in your area. Know a local town hall, library, NHS building, or heritage site with exterior lighting? Reach out and