My Nonprofit Reviews

My daughter was born with laryngomalacia, but we didnt get a diagnosis until she was a few months old. My husband and I did a ton of research, but felt so lost and overwhelmed. Until we found Coping with Laryngomalacia. this group gave us a community, a wonderful network of parents who have been there before and those who were on the same path. CWL gave me purpose. I help to fundraise to give back to other malacia families, those who need the love and support, those who will be there for the next wave of malacia moms and dads. Coping offers families with upcoming procedures care packages, to remind them they are never alone on this journey. I would be so lost without CWL