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But what is it like to live with Parkinson’s at a young age? Weinschreider, who is now 43, says she worked for 10 more years after her diagnosis.

At that point, the side effects of the medications she was taking became too much.

“A lot of my good friends still don’t know, but I’ve gotten more open with it,” she says. I just want to be as normal as can be.”That extended to her romantic relationships as well.

Weinschreider kept her diagnosis under wraps for a few months when she first began dating her now-husband, David.

She started taking medication right away, which she says made a “big difference” in her quality of life.

But she didn’t come to grips with her diagnosis until later.

Weinschreider and Miller also both ended up joining forces with the Parkinson’s Disease Foundation—Weinschreider is an advocate for the PDF Women & PD Initiative, while Miller is a member of the PDF People with Parkinson’s Advisory Council—and both say it’s been incredibly helpful to know other people with their condition.

But they also stress that their Parkinson’s doesn’t define them.

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“Then I got upset and was really nervous.” The specialist reached the same conclusion—it was likely Parkinson’s, a chronic and progressive movement disorder.

“It was really hard to tell him because I was afraid it would be a bad turning point in our relationship,” she recalls.

She was surprised by his reaction: He asked what her diagnosis meant and how it would affect their life together.

“I shared the news with friends and family right away,” she says.

“I also made the decision at work to be open about it, particularly because people see me slightly limping and ask about it.” Miller admits that sometimes it can be “awkward and uncomfortable” to share her diagnosis, but overall people have been “so loving” and regularly ask how she’s doing. Both women are on medication for their Parkinson’s symptoms and regularly see specialists about their condition to make sure it’s under control as much as possible.