Disease won't keep J.T. Scott quiet

| Melissa Leavitt

J.T. Scott of Lake Stevens, Wash. has had psoriasis since age 4 and psoriatic arthritis since age 11, but it hasn't stopped him from enjoying life.

Scott, 14 now, gets good grades, holds the role of the social butterfly between (and yes, even during) class and enjoys playing defensive lineman on the football team. 

Scott's position as a National Psoriasis Foundation Youth Ambassador fits him perfectly. When asked about the lesions on his arms, he says he has psoriasis, an autoimmune disease appearing on the skin, and it's not contagious. Twin sister Mikayla admires how well her brother has handled his medical challenges. 

"He's had a few bad comments toward him and it does make me feel bad," she said. "He just laughs it off and doesn't let it get to him." 

Even though Mikayla doesn't have psoriasis, she's spreading the word, too. She recently helped a friend who was having skin problems connect with a doctor who diagnosed the friend's psoriasis and helped treat it. 

"We joke I got hit with the medical stick," J.T. said. 

Like many, J.T. was misdiagnosed with eczema initially. It never improved, but he didn't get teased for it much when he was young. As he got older, though, the teasing started. That's when his persistent rashes were diagnosed as psoriasis and he started accessing more effective treatment. 

"It's not on my face anymore, it's not on my legs anymore," J.T. said. "It's just on my arms and that's great." The Scotts will move from Washington state to Virginia this summer. J.T. said he's nervous about the move and the changes, but knows he'll make friends and continue to make others more aware of psoriatic diseases. 

"I'm pretty social. I'll talk to you even if you don't want to talk to me," Scott said.

Learn more about the Youth Ambassador program »

Driving Discovery, Creating Community

This year, we’re celebrating 50 years of driving efforts to cure psoriatic disease and improve the lives of those affected. See how far we’ve come with this timeline of NPF’s history. But there’s still plenty to do, and we can’t do it without you! Learn how you can help our advocacy team shape the laws and policies that affect people with psoriasis and psoriatic arthritis – in your state and across the country. Help us raise funding to promote research into better treatments and a cure by joining Team NPF, where you can walk, run, cycle, play bingo or even create your own DIY event. Contact our Patient Navigation Center for free, personalized support for living a healthier life with psoriatic disease. And keep the National Psoriasis Foundation going strong by making a donation today! Together, we will find a cure.

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