Have you seen "The Lipidema Project" websites for Massachusetts, Hawaii, SoCal, etc? They're starting to spread. That's good. Except............
Have you noticed that the only solutions offered still are either compression garments, liposuction or air compression?
I don't for one moment accept that those are my only options.
For that reason, I haven't joined up with any of them, nor will I until more serious attention is paid to other avenues for holistic change. The answers are out there, and I'm looking hard every day for them. I don't choose to be stuck with only those limited options.
This blog is NOT ABOUT fad diets, liposuction, compression or surgery. I am not a doctor. The average doctors don't even know what lipidema is. So I will share what I've learned from experience and from decades of research to give hope to those who feel hopeless and see if we can cure the supposedly "incurable".
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