Help raise the flag about how important copays are for people living with rare disease. (Senate Bill 203)

Join WI Rare and fellow advocates at the Wisconsin State Capitol on January 8 for a short, but powerful, press conference highlighting the real impact of copays on our community.

Time: 11:00 AM

Let’s pack the room in solidarity. Copays can affect anyone — so bring your friends, bring your family, and show the press just how much this issue matters to us.

After the press conference:
You’re invited to continue the conversation at a Rare Disease Meetup at Michelangelo’s Coffee Shop, just across from the Capitol on State Street.

RSVP today!

We can’t wait to advocate alongside you. Together, let’s make sure copays count.

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