Compression Facial Care: My Second Face

I have seen many restorations since my diagnosis and am always keen to learn as much about lymphology and other sufferers as possible. This is how I met the feedback from a reader who feels very alone with her situation. There is a suitable compression supply for practically every part of the body, because even if lipedema theoretically only affects the extremities, lymphedema can develop almost anywhere. And so there is the compression facial care, which I am able to bring you closer to today.

One of our readers has bravely agreed to report anonymously about her facial care. If there is someone out there who shares their fate and wants to exchange ideas, they are very welcome to contact them via email ( or via the Contact form turn to us and we will arrange everything else. I would be very happy if this would help me make contacts.

My second face

I have secondary lymphedema on the left side of my face. It was created through an ear operation. It took the doctors two years to make this diagnosis. Unfortunately, the edema presses on the trigeminal nerve causing pain. Tension, pressure and pain are my daily companions. In addition, my face is disfigured, swollen, etc. every day.

I have to wear a compression face mask, which is not always possible in everyday life. In addition, I tape my face and neck, which puts a lot of strain on and disfigured my skin - I am desperate. I get lymphatic drainage at home twice a week and look for someone who has experience in what can still be done. Unfortunately, I don't know anyone who has it on their face.

Professionally, I can't wear the mask, which doesn't make it easy, and I also take medication to endure the pain. I received a recommendation from rehab to submit an application Reduced earning capacity to ask, which burdens me a lot.

Alone with my compression face supply

I'm also currently looking for talk therapy to somehow deal with it, but unfortunately I'm on the waiting list. I feel so alone and would be happy to meet like-minded people, I haven't found anyone in self-help groups or in rehab.

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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