Robin was diagnosed with OCNDS shortly before he turned 2 years old. We were grateful to have an answer but scared of the path ahead. The CSNK2A1 Foundation became, and continues to be, our guiding light. The research that has been done so far and what is planned for the future will make a significant difference in the lives of families like ours. Please consider donating to help fund further research and tackle the priorities identified at the recent family conference.
