There is danger in giving a name to a condition. To carry the burden of "having a disease" can be discouraging--especially when that "disease" has no cure, no treatment, no hope of reversal, as with the current status of lipidema in medical research.
In fact, I reject the "disease" and prefer to consider my condition only as a symptom of a dis-EASE, or im-BALANCE somewhere in my body. Lipidema is not a dead end. It is rather a great clue to a complex mystery.
It involves
metabolism, immune systems, hormones, capillaries, digestion, mineral balances and other intriguing signs. I do not suffer from lipidema. Rather, I am challenged and intrigued by it. And I do have hope--lots of it--that with God's help and inspiration, we will solve this mystery together..
Betty B. Ready
"In God We Trust"
see also www.lipedema.com, learntobereadyblog.com, bereadyinc.com
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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