It is hard to believe that six years ago those newly diagnosed with Lipedema were being advised to NOT exercise, as doctors thought it would make our symptoms worse.
Six years later and new members of the Lipedema Fitness Facebook support group are telling us their doctors recommended they join our group!
That is huge progress! We are changing how Lipedema is treated!
Keep fighting for your mobility, keep spreading awareness, and keep being awesome! We are stronger together and we are changing how Lipedema is treated and hopefully we learn even more next year and get to some real answers and one day maybe even a cure!