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Psoriasis and Psoriatic Arthritis Alliance (PAPAA)

Patient association


  • Psoriasis

About this organisation

  • Year of creation: 1993
  • Number of members: 1000+
PAPAA is independently funded and aims to be a definitive source of information and educational material for people with psoriasis and psoriatic arthritis in the UK. To be a support to both patients and professionals by providing material that can be trusted (evidence based), which has been approved and contains no bias or agendas. We will be looking to provide positive advice that enables people to be involved as they move through their healthcare journey in an informed way, which is appropriate for their needs and any changing circumstances. Service provided : Information service, advice and support for people affected by psoriasis and psoriatic arthritis, including carers and healthcare providers. Free information is available and twice yearly magazine called ’Skin ’n’ Bones Connection is available on subscription. Target group : People with psoriasis and/or psoriatic arthritis, carers and healthcare providers.

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SPIN coordination team