My Nonprofit Reviews

My son was born with Primary Hyperoxaluria type 1. Finding out he had this and being a young 22 year old mother back in 1990 was a very scary thing. First time he went into kidney failure he was six months old. I didn't know what any of this meant and what was going to happen to my first born. I heard about OHF and contacted them. I was cryin and scared. OHF was there for me. They gave me information and helped support me. I was absolutely amazed and greatfull! I cannot thank them enough!!! My son is now a Doctor and wants to help others. I believe OHF, all of their support toward finding a cure and for their patients has contributed toward my son's healthy and happy life. OHF is number one!!! THANK YOU!!!