My Nonprofit Reviews

The OHF has given our family a sense of community and strength in challenging times. In 2010, when Kate was diagnosed, my husband and I attended the patient day in NYC. That day provided information, support, and more importantly, a feeling that although we may stumble along the way but that we are not alone in this journey. About a year later, Addie was diagnosed too. I never forgot that day in NYC. I walked up to the check-in at the conference and when I said my name, others at the desk knew my children by name and it was a little surreal. By providing opportunities for education, networking and support, my family has grown in knowledge. We are very grateful to the Oxalosis and Hyperoxaluria Foundation for its assistance and may we all be more resilient as a result.