Why you should tell your gynecologist about lipedema

My gynecologist in Augsburg is great. Not only because she has accompanied me confidently through times of crisis, but also because she is well informed about lipedema. But that's rarely the case with gynecologists, isn't it? Time to change that!

Why then, gynecologists?

Every time we visit, we give ourselves a little update and of course come quickly to talk about lipedema. I learn from her, she learns from me - try it out, it's really fun! But much more important last time was her statement that gynecologists should urgently become lipedema and lymphedema experts.

Why? Because they are the doctors who most often see the bare legs of every single patient.

Awesome, isn't it? Imagine a world full of enlightened gynecologists who could at least ask the visually conspicuous cases whether the most common symptoms sound familiar to them. A whole new movement of prevention would be possible as early as the teenage years.

Put an end to unnecessary hormone fluctuations

If we look a little further into the future and the suspicion that lipedema is promoted by female sex hormones is proven, it is all the more important to have the gynecologist on board. How many contraceptive and, worse still, no contraceptive hormones could be prevented? No unnecessary hormone fluctuations, which in the worst case could affect the course of the lipedema.

Off to the gynecologist - we have a mission

Each and every one of us now has a mission. When everyone who reads this article tells their gynecologist about their disease, a very special movement will be started! Take flyers, information material or magazines with you into the treatment room and show the possibilities of how to draw attention to lipedema and lymphedema even in the waiting area. Of course, my doctor has z. B. the Lipedema Awareness Cards already out.

Share the message and the idea and together we can really get something going. Höhö, ... legs.

Here we go!



lipedema gynecologist gynecology hormones estrogens education
Caroline Sprott Lipedema Health Influencer Avatar

Author: Caroline Sprott

Caroline Sprott is a remarkable personality involved in the world of lipedema. Born in Bochum in 1989, she now lives in Augsburg. Her professional career began as a trained media designer and she works full-time in marketing. But that's not all - Caroline is also a lipedema speaker, author and model. She is committed to the fight against lipedema and is passionate about supporting the community of those affected. Caroline founded the Lipedema Fashion Blog to share her experiences and knowledge with other sufferers. She wants to create a place where women with lipedema can find information without having to go through private Facebook groups. She combines her passion for fashion with her commitment to the lipedema community. Some interesting facts about Caroline Sprott: Style and fashion: Caroline loves fashion and sees it as a passion and therapy at the same time. She doesn't let compression stockings limit her and opts for creative outfits. Style Icon: Your style icon is Grace Kelly, a woman of natural elegance and inspiration. Favorite colors: moss green, yellow, pastels and navy blue. Weakness for animals: Caroline greets every cow - a loving gesture that shows her love for animals. Important life philosophy: Stay inquisitive, curious and optimistic - life is too short to waste even one day. In addition to being a model and entrepreneur, Caroline Sprott is a health influencer who advocates for the lipedema and lymphedema community. Her commitment and positive attitude are inspiring.

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  • Dear Caroline,

    your reasoning does not convince me. Why this reduction to gynecologists - as if our legs and we patients had not been seen by many doctors of various specialties since childhood. General practitioners, orthopedic surgeons, etc. Who have to be just as familiar with hormones. I expect all of my doctors to know about lipedema and if you don't they should learn. Quite simply - we patients should actively demand this and not allow ourselves to be instrumentalized for providing information to the doctor. Your appeal has a taste for self-interest ... or to put it another way: a doctor has repeatedly said this to the gynecologist in his interviews - perhaps because his sister also operates on lipedema - and we patients are supposed to parrot it. I appeal to all doctors to be more self-confident about lipedema and lymphedema!

    • Hello Katja,

      Do I understand you correctly, that you would rather wait for the doctors to find their interest in the disease on their own than for them to be actively sensitized to it?

      Unfortunately, I also do not understand your argument regarding self-interest. Which one should I pursue? Incidentally, I have nothing to do with the doctor you are talking to, if you could have thought so.

      You can start somewhere and get some attention. When you are dissatisfied, you don't wait in silence for the world or politics to change, but take to the streets and make you visible. In any case, it is never wrong to ask your doctor about it and just because all doctors should be informed there is no reason not to start with the gynecologist.

  • Hello dear Caroline; my gynecologist said if I had liplymphedema I would look very different. That wouldn't be true! When I asked several times, I asked for a blood test to determine the estrogen level, which I have to pay for myself anyway. And oh wonder, the mirror was way too high !! But I didn't get any further help!

  • Hello dear Caroline,

    you mentioned in your post that you found a great gynecologist in Augsburg who knows about lipoedema and is informed about it.
    Could you perhaps give me a tip on how I can find this gynecologist, as I also come from the Augsburg area and am desperately looking for a gynecologist who is familiar with this area and has an open ear for my problems.

    Best regards,
    Kristina