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What does it look like to live with YOPD?

We’re happy to report, it’s not what you probably expected.

These are the faces of YOPD. They are young, resilient, active, fit, determined, groundbreakers, and fighters. They are living their best lives and thriving, despite diagnosis and they’re inspiring all of us to do the same.

We encourage you to browse our gallery with images from YOPN events as well as photos received from fellow members. Please know, we only include images of those who have openly shared the news of their diagnosis and are comfortable letting others be part of their story. Maybe that’s you, too. Or maybe you need a little more time. We support you 100% and hope these pictures bring a smile to your face and encouragement to your journey. You can always share your photos on Facebook or Instagram with #yopn

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A program of Parkinson & Movement Disorder Alliance, a national 501(c)(3) nonprofit that educates, empowers, and connects people across the Movement Disorder Care and Support Ecosystem ©.

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