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They also have the added challenge of determining when would be the best time to reveal (and then consequently explain…thoroughly) their condition to their date.

After all, no one truly understands what it’s like to live with psoriatic disease unless they have it too.

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Help us raise funds to support research by joining Team NPF, where you can walk, run, cycle, play bingo or create your own fundraising event.

“I just wanted those anxieties taken away because it can be extremely liberating to be yourself and know that you are not alone.



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