Every once in awhile you come across something that just makes you want to cry because someone finally actually understands what you're experiencing. It was like that for me and others I know when we stumbled across Dr. Lam's site after reading a blog written by someone very like us.
Suddenly I was seeing myself and my situation as part of a larger community picture where answers are actually given. I highly encourage anyone with lipedema (lipidema) or associated symptom groups to check out Dr. Lam's site https://www.drlam.com on adrenal fatigue syndrome. Brilliant!
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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