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Encouraged on several fronts
Things are happening—some by chance, some purposefully, all fairly positive, some even hopeful. First of all, I “met” Carol on Facebook in one of the lipoedema/lymphedema groups I follow, after she reported a seemingly miraculous transformation illustrated by pictures that were hard to believe. She, like me, has both lipoedema and lymphedema, and she, like Continue reading
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ACCESS granted…
I finally received my ACCESS identity card that will enable me to schedule rides in easily accessible vehicles to get to my doctor’s appointments, art seminars, or whatever. As the office had indicated, it took until late February to arrive, but now that I have it in hand, I can start thinking about leaving the Continue reading
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Brain fog…
The biggest enemy of self-care when it comes to lipoe-lymphedema isn’t physical tolerance so much as mental disposition. Yesterday was a good day, and I was able to think clearly enough to come to the realization that I have fallen down on the job and my recent poor physical response is a result of that. Continue reading
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Experiments, long overdue
I lately, finally, made the decision to put my health first (and get over being angry about it). I went back to see what seems to be the sole doctor on the West Coast who knows what lipedema is and also specializes in the treatment of lymphedema, and when she discovered I had, yet again, Continue reading
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Unmeeting Wishes
Lipedema is a loose connective tissue (fat) disorder that occurs almost exclusively in women (about 11 percent of them) and is triggered by hormonal changes. It is a chronic medical condition characterized by a systemic buildup of pockets of adipose tissue (fat) in the legs and arms. It may be accompanied by an unusual texture within Continue reading
About Me
I started this blog to talk about a genetic, fibrotic fat-storing (some say autoimmune) condition called Lipoedema, which is something I began to experience in my 60s, although some see early onset at puberty, or post-pregnancy, or at menopause. The other “L” condition from which I suffer is Lymphedema, as a common secondary effect of the fibrosis that blocks lymphatic drainage. Despite the fact that one in 11 women suffer from lipoedema, most doctors have never heard of it, so on top of the pain and embarrassment of this extremely obvious malady, millions of us are out there being fat-shamed for a condition that isn’t contingent on diet or exercise for its growth. This blog was intended to share my reactions.
I have, however, reserved the right to discuss “other stuff” here and, increasingly, since January 20th, 2025, that is politics, because what else, after all, are we legitimately obsessed with in this age of fascism in these United States of America? So while the “theme” of this blog may be confusing, it is my blog, where I can talk about whatever I wish. You are not constrained to read the parts you don’t like. But I feel compelled to write about them.
MEdoubleLL 