My Nonprofit Reviews

My association with CFRI spans nearly 25 years. Our 28-year-old daughter was diagnosed with CF when she was 22 months old, but it wasn't until she was three-years-old that we returned to the Bay Area and began to volunteer our time fundraising for CFRI. We will never be able to match what we have raised to what they have given to us in research/information/education and a shoulder to lean on. They continue to empower and give hope to the parents of children with CF, the children/adults with CF, the family and friends of those with CF through the sharing of knowledge about the disease, resources for care, and continued funding of medical research and education programs. As a former board member, I know the staff and volunteers are totally invested in providing a better future for those living with Cystic Fibrosis, and it shows in their heartfelt relationships with the CF community.

More Feedback