My Nonprofit Reviews

Stephanie, the President and Founder of CWL is so committed to helping and educating families. I found this group as I was sitting in the waiting room of the OR anxiously hearing the word Laryngomalacia for the first time. My 3mo old baby girl had just had a triple scope and I sat there trying to pass the time until she was finished with her procedures. That was just shy of 3 years ago. In those 3 years, I have seen Stephanie's advocacy and unwavering support for newly diagnosed families and families who have been on this path for a while. It is an honor to be a part of this great charity.