#TeamPSOR Launches!

On the eve of Psoriatic Disease UK presenting at the EADV Congress in Paris, we are excited to officially launch #TeamPSOR—our new community project that brings together our wonderful and rapidly growing group of supporters, volunteers, and fundraisers.

Whether you’re organising a fundraiser for us, courageously sharing your story on our website, joining us at conferences to amplify the patient voice, helping to moderate our peer support spaces, distributing our flyers, or cheering on our runners from the sidelines, we want you to be part of an exciting community and be recognised for your hard work and commitment.

Think of it as a club of volunteers all working toward the common goal of achieving better outcomes for everyone affected by psoriatic disease—and the best part is that anyone can join!

Stay tuned for social media campaigns, calls for involvement in awareness projects exclusive to #TeamPSOR members, a new private WhatsApp community, new volunteer roles, community meet-ups, and much more!

Psoriatic Disease UK is run entirely by patients and volunteers, and we simply couldn't carry out any of our peer support and awareness work without you. We also underestimated the number of people who would want to help in our first year, and we know many of you want to do more while patiently waiting as we work through the backlog. We hope that #TeamPSOR provides an exciting opportunity to get involved with our organisation and connect with a social and supportive community of like-minded individuals.

If you’d like to be among the first to hear about #TeamPSOR news, please join our mailing list below or fill out the form on our dedicated, and regularly updated, #TeamPSOR page.