Join Cure Rare Disease as we Strive for Five.
$5 million is the goal, and we will reach it $5 at a time.
In efforts to continue our life-saving work in 2021, we are striving for the ultimate collaboration. In order to continue our work we have set a goal to raise $5 million before the end of this year! And although that seems like a lot, we are confident in the power of collaboration.
How it works: Donate $5 and then ask 5 of your friends to donate and have those friends pass it on to 5 more of their friends until we hit $5 million!
Here's what $5,000,000 could enable:
Develop a new CRISPR system to address 40%+ of the mutations amenable to editing which could correct diseases impacting over 1 million people
Finish development of 5 CRISPR based therapeutics
Build a novel technology to better deliver CRISPR throughout the body for rare disease patients
Meet Our Community
The Klassen Family
The Klassen Family
We are the Klassens, Lee’s and Jeremiahs. We live in MD, CO, and VA. “pop-pop (dad), Greg (me) , Jeff (son), Michelle (daughter) and DeeAnn (sister) have all been diagnosed with Spinocerebellar ataxia #3.
The Bryan Familiy
The Bryan Familiy
Beau & JeanAnn Bryan with sons Sawyer (8) & Wesley (6) reside in Tea, South Dakota just outside of Sioux Falls. Both both have a duplication of Exon 44. Faith, Love & Hope guide our actions to a brighter future.
The Hamilton Family
The Hamilton Family
Rick, Nancy, Kalel (7) and Livvy (2) Hamilton from Ahwahnee, California
The Falger-Jackson Family
The Falger-Jackson Family
Kati, Joe and William (2) living in the Pacific Northwest. Newly diagnosed family in Feb 2020. We enjoy our family time, the outdoors, and house projects.
The Andrews Family
The Andrews Family
Chase Andrews, big brother to Cassidy and Cara, son to Chad and Amy Andrews. Fruit growers in St. Thomas, Pennsylvania.
