This morning I am reviewing a video called, “Eating to Starve #Lymphedema & #Lipedema“ by Chuck Ehrlich, MS, MBA via YouTube, as I prepare for the new year. The recommendations that he makes align with the outcomes of a food sensitivity test I did through checkmybodyhealth.com last month as well. Looks like for me, I need toContinue reading “There are Specialists Learning and Teaching about Diets to Help us with Lipedema”
Daily Archives: January 3, 2021
Hypermobility and Lipedema Go Hand in Hand
Hot off the presses! There’s a new book about #EDS called, “Disjointed” out. It’s kind of expensive, and I’m encouraging my library to put it on the shelves for the broadest awareness. I plan to grab it today to see what it’s all about. Grab your own copy by clicking the image below. And if you’reContinue reading “Hypermobility and Lipedema Go Hand in Hand”
Who is LegsLikeMine and Why Are We Here?
Who owns LegsLikeMine? Susan O’Hara, from Yukon, Oklahoma in the USA owns and runs LegsLikeMine. Susan has had lipedema for years, starting with the birth of her first child in 2001 and the condition has progressed through various hormonal changes, stress. Unfortunately, as many women who have this condition also experience, Susan did not knowContinue reading “Who is LegsLikeMine and Why Are We Here?”
