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Joint Statement on Diversity and InclusionThere is a serious diagnosis gap in skin diseases. For too long, training materials have centered European images, shaping physician's understanding of psoriasis and related illnesses. People with non-white skin have more difficulty receiving a correct diagnosis. As a consequence, their treatment is delayed, often causing further health complications.
It's time to break these obstacles. As the global organization representing all people with psoriatic disease, no matter where they come from or what kind of psoriatic disease they have, inclusivity is at the heart of IFPA's work. All the Colors We Are is an initiative to call attention to psoriatic disease and the way it presents on diverse bodies.
This image gallery features images of psoriatic disease from around the world in real-life contexts. Join us to promote inclusion in your educational brochures and training materials. All images are available for free download.
IFPA recognizes the bold individuals who have contributed their powerful images to this library. Thanks to you, we are raising awareness of the true diversity of psoriatic disease.
You are invited to credit IFPA when you use these images.
News Care and Treatment, News
Joint Statement on Diversity and Inclusion
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All the Colors We Are Launch Kit
BIPOC Patient Voices
Every day, IFPA and our member associations are in contact with people living with psoriatic disease. Worldwide, our organizations have witnessed the real consequences of information gaps when it comes to the diversity of psoriatic disease. All the Colours We Are is a project to fill those gaps. It's time to represent all persons living with psoriatic disease irrespective of their gender and geographical location.
Together with IFPA members, partners and supporters, IFPA will give the public a more balanced and accurate understanding of what psoriasis can look like among different skin colours.
Sofia Lovi
Exco Secretary - Psoriasis Association Malaysia
Sofia was diagnosed with psoriasis and psoriatic arthritis at age 12. More recently, she was further diagnosed with fibromyalgia syndrome. Her journey to advocacy in 2015 when her first newspaper article was published on World Psoriasis Day. Since then, she has appeared on radio, television and in magazines and was even crowned Miss Amazing Malaysia in 2019.
Paul Mendoza
President of PsorAsia+Pacific
Paul Mendoza is the President of Psoriasis Philippines and the President of Psoriasis Asia-Pacific. He is the Chairperson of PsorCoach University where he empowers patients to lead other patients. He is part of the Technical Working Group in drafting the National Psoriasis Policy under the Department of Health. He is also part of the Philippine Alliance for Patients with Chronic Illness, Healthy Philippines Alliance, and Alternative Budget Initiative for Health where he engages the Philippine government for patients' rights, access to medicine, social protection, and universal health agendas.
Tamsin October
Psoriasis Advocate - South Africa
Tamsin is a community development practitioner from Athlone, Cape Town, South Africa. She was diagnosed with psoriasis at age 13. Tamsin works with youth from socio-economically challenged areas, and is devoted to promoting diversity and equality in the global fight against psoriatic disease.
Sicily Mburu, M.D.
Scientific Officer
Sicily injects the patient perspective into every stage of the research cycle. Sicily is a health professional with a clinical background and over 10 years experience in the field of global health. Sicily holds a dual MSc in Epidemiology, and Health Economics & Policy.