Rare Disease Day 2026
PAPAA is marking Rare Disease Day today, 28 February, by shining a light on the lesser-known but serious forms of psoriatic disease that affect people and families worldwide.
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Autoimmune Awareness Month
March is Autoimmune Awareness Month. This year, PAPAA is joining our Connect Immune Research partners to highlight the impact of autoimmune conditions and the importance of working together to…
NSAIDs and psoriasis
Non-steroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen and naproxen, are often recommended as first-line treatments to ease pain, stiffness, and joint inflammation in mild psoriatic…
Hit or myth?
Psoriasis and psoriatic arthritis (PsA) are well known to many of us, but common myths can add to the emotional burden, shape how others respond, and delay recognition and treatment. Read some of the …
PAPAA is a trusted UK charity for psoriatic disease support. We empower individuals through evidence-based education, comprehensive support, and effective advocacy. Our trusted, holistic approach provides deep insights into psoriatic disease management, benefiting both patients and healthcare professionals. PAPAA's commitment to scientific research and positive, patient-centred care drives our mission to improve lives affected by psoriasis and psoriatic arthritis. With more than 30 years of experience, we offer free access to expert information, treatment guides, and real-life stories, ensuring trusted support for all aspects of psoriatic disease.