PUCK Personal Fundraisers

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Epidermolysis Bullosa (EB) is a devastating disease. Pioneering Unique Cures for Kids (PUCK) was founded and is now run, by parents who sought treatment for their children at the University of Minnesota. The doctors there, led by Dr. Jakub Tolar, are pioneering novel new treatments for EB, which will one day lead to a cure.

The PUCK Personal Fundraisers page was created for families and individuals to celebrate and honor the brave children who fight EB every day. It is also a place to remember those special children who have earned their butterfly wings. It’s a tool to use when friends, family members and coworkers ask, “what can we do to help?”

Pioneering Unique Cures for Kids knows that a family experiencing the diagnosis of a genetic disease, such as EB, needs a lot of support throughout the journey. Funding research for new cures and treatments on a Personal Fundraising page is one way loved ones can show their support. Anybody can support these champions by making a tribute gift to their fund.

Together, we can help find better cures and treatments for our children. To manage a fund you already have set up, visit the PUCK Personal Fundraising Center.

To manage a fund you already have set up, visit the PUCK Personal Fundraising Center.