Lipedema Friendly Outfits – The Halloween Edition, Part 1
Hi friends! Who loves Halloween but hates the store-bought costumes that start with the word, SEXY. Like Sexy witch, Sexy cheerleader, so on and so
Hi friends! Who loves Halloween but hates the store-bought costumes that start with the word, SEXY. Like Sexy witch, Sexy cheerleader, so on and so
Hi friends, I’m sharing a news story that I stumbled across from YouTube, originally published a few years back from Fox News. The more we
Hi friends! Let’s just start with this. This isn’t medical advice, but information I’ve actually experienced, plus a ton of research on doctor websites and
Hi friends! Take a look at this awesome pamphlet we’ve created for you all about conservative measures just one patient takes daily to manage her
Hi friends! As I head over to Atlanta this weekend for the Lighthouse Lymphedema Network 25th annual meeting, I’m doing a little prep work. The
Hi friends! I’m continuing my series of downloading good things from the Lipedema World Congress that was in Potsdam Germany a couple of weeks ago.
Hi friends, this one’s a long article. But ultimately, I want to know, if you had to pick ONLY ONE supplement that you’ve experienced using
Warning to the READER: A problem with a lot of fibrosis treatments out there right now, is that there can be some serious side effects.
Hi friends! One of the most specific reasons I travelled to Potsdam, Germany was to hear a presentation called, The Role of GLP-1 Receptor Agonists
Hi friends, When the world doesn’t fit you and then you find out that you’re part of 11% of people not being served, you either
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