Stefon J. — I first developed lymphedema when I was about 13 or 14 years old but I was not fully diagnosed with lymphedema until I was 18 or 19. So, for about four or five years as I was trying to figure out what was going on. I was not able to try any treatments for my leg due to lack of resources and knowledge on the condition and not even receiving a proper diagnosis until years after my symptoms developed. I learned about AIROS when I went to Camp WatchMe 2022 this past June, where I was a volunteer and patient advocate. I was prescribed the use of this device from a plastic and reconstructive surgeon in Orlando, FL.