My thoughts on living with lipedema and lymphedema…and other stuff


  • The mandate I wish to give

    Like everyone else in the country, I am overwhelmed by the stupendous success of the Democrats’ efforts to get out the vote and turn the tables on the events of the past two years by taking back the legislature. It is, as all news media are now shouting, a referendum on the heinousness that is… Continue reading

  • The Undermining Effect of AI

    The new controversy of the day is the use of artificial intelligence. I’m not just talking about the drama surrounding the building of giant AI “farms” that are co-opting essential natural resources, or about people’s fears that AI will replace too many jobs for humans. Many people are against it primarily because it’s only as… Continue reading

  • A secret ambition resurfaces

    I’m not exactly sure of the year, but somewhere around 18 years ago, after I had finished library school, I took a class at Otis College of Art and Design (formerly the Otis Art Institute) on how to write a children’s book. I took that class at that specific school because I had met the… Continue reading

  • This day in a lifetime past…

    This morning when I clicked on Facebook, I got one of those updates about what I was doing on this day in various years past, and it shocked me. Since my lipoedema went rampant and provoked the accompanying lymphedema, it has felt like an unending state of being that has surely lasted decades. But 10… Continue reading

  • Navigating sensations

    On a medical drama I have been binge-watching the past few nights, a character made a statement that has been revolving in my thoughts ever since: “Pain is in the body,but suffering is in the mind.” Is it truly that starkly divisible? My answer is, I’m not sure; but I think it’s more complex than… Continue reading

  • The mental state

    I found a quote from someone who was suffering from Parkinson’s. Although that and lipedema are very different fates, I found an affinity with what she had to say… “[Parkinson’s] can affect much more than the body. It can bring anxiety, depression, exhaustion, and apathy. The apathy is particularly strange. You can find yourself lying… Continue reading

  • Healthcare vs. insurance

    And now that I am healing up satisfactorily, there is no time to sit back and enjoy that, because I am being bombarded with messages from my insurance—Medicare and Blue Shield (PPO). I went online this week and tried to decipher them, and also tried to understand the policies and the logic behind them. People… Continue reading

  • Healthcare via social media

    Here is what happens when doctors remain uneducated about your specific condition for more than 85 years after the first mention of it in a medical journal: You start taking advice from people on Facebook. Lipoedema was first mentioned in medical journals, as far as I can discover, in the 1940s. And there is some… Continue reading

  • The long slow road to healing

    I’m still here, still spending most of my time on my reclining sofa with my legs up, still tired, still frustrated and kinda bored. It’s been about three weeks since I left the hospital, but I am far from past this episode. After a week of talking about it and promising to come but not… Continue reading

  • Terrible horrible morphs…

    …into uncomfortable and annoying. I am continuing to blister and peel, the red has further decreased and become more pale, and the heat is mostly gone from my leg; but the nurse from the hospital visited today and opined that there was still infection happening, so she has called in another prescription for antibiotics (a… 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.