Cyndi Lauper has joined the community to help people understand that the reality of PsOriasis is PsO much more — and to encourage everyone to take the next step in their psoriasis journey.

You know living with moderate-to-severe plaque psoriasis (PsO) doesn't just affect your skin——it can affect your life. Help spread the reality by sharing your personal psoriasis experience. And don’t miss That’s PsO My Reality—a special docu-series that follows real people like you as they take on the challenges of managing psoriasis each day.

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SPREAD THE REALITY

SHARE YOUR EXPERIENCE

I HAVE HAD PSORIASIS SINCE I WAS SEVEN, I AM NOW 28. I HAVE IT ON MY HEAD ALL THE TIME. I'M SICK OF IT. I'VE GOT IT ON MY LEGS, MY CHEST, MY SIDES.

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THAT'S PsO MY REALITY

Take a closer look at life with psoriasis, as we follow real members of the PsO Me Community and see the challenges they face each day.

I FEEL DISGUSTING AND I HATE IT WHEN MY GRANDSON PULLS AWAY FROM ME. HE DOES STOP ME FROM SCRATCHING. BUT I DO NOT GO ANYWHERE WITH IT BEING EXPOSED.

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I'VE BEEN STRUGGLING WITH PSORIASIS FOR 3 YEARS NOW. IT STARTED ON MY SCALP AND IS NOW AFFECTING OTHER PARTS OF MY BODY.

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I'VE HAD PSORIASIS FOR OVER HALF OF MY LIFE- 27 YEARS. IT'S PAINFUL AND QUITE FRUSTRATING AT TIMES ESP. WHEN IT BLEEDS.

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I HAVE LESIONS. MY MEDICINE DOESN'T WORK LIKE IT USED TO. I AM TIRED ALL OF THE TIME.

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MY DOCTOR DOESN'T UNDERSTAND WHAT I'M GOING THROUGH.

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I ONCE GOT TIRED OF THE DISCRIMINATION.

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LIKE A LEPER. I AM BEING TREATED, BUT MY PSORIASIS KEEPS SPREADING.

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PsO HERE WE ARE

where to find others with psoriasis

members in the West

members in the Southwest

members in the Midwest

members in the Southeast

members in the Northeast