Kristen Groseclose's Fundraiser
We can fund a full-time postdoc researcher, supporting ongoing Smith-Kingsmore syndrome research
Join me and help make a difference, please give today.
We are no longer accepting donations on this campaign, but there are other ways for you to support us today!
We need your help. Please support Smith-Kingsmore Syndrome Foundation. SKS research is at a critical point. We have an exciting opportunity to better understand SKS and help people like my 19-year-old son, Jack, who was diagnosed with SKS at age 15.
Since SKS is a mutation on the MTOR gene, the work we are supporting may have broader implications in the areas of aging, sleep, cancer and epilepsy, which are also impacted by the MTOR gene.
In honor of SKS Awareness Day on August 15, 2022, join me in supporting real change. Together we can make a difference.
Just a small donation will go a long way to helping me meet my goal for Smith-Kingsmore Syndrome Foundation