My Nonprofit Reviews

We have had a long journey with our son who was diagnosed with Laryngomalacia at 4 months old after we struggled for answers for so long. Very few drs in our area know much about LM so we travel out of state for our son's care. When we were told he needed to have surgery at 6 months old I was a mess. Then I found CWL! The support we have received from them has kept me going when I didn't think I could anymore. We are headed back into the OR for the fourth time (2nd due to the LM) and CWL is there again. Even for the surgeries that weren't related to the LM, they were there!