When Natalie Stack wished for her “disease to go away forever” on her 12th birthday, few of us could have imagined the innovation, progress and hope her wish would inspire. 20+ years, 235 research studies and two FDA approvals later, Natalie’s Wish has transformed into something so much more than a wish – but a community, a support system, a research powerhouse and a movement to create a world without cystinosis. But there’s so much more to be done.

Each year, friends, families, and supporters of the CRF community gather to show their commitment to our children and adults living with cystinosis at the Natalie’s Wish fundraiser. Though we will not have an in-person event this year the entire month of April will be dedicated to continuing the momentum Natalie Stack’s wish created, and raising funds for life-saving cystinosis research.

Join us for our month-long fundraiser to celebrate over 20 years of impact and ring in a new era of progress for the cystinosis community.

Because at the end of the day, Natalie’s Wish is our wish. It fuels our dedication and determination to find better treatments and a cure for cystinosis, and we won’t stop until we do.

Thank you!