We take you by the (flat knit) hand
Mein Name ist Caroline Sprott and I've had lipedema in my arms and legs for over ten years. After three liposuctions I decided to use the blog Lipedema fashion to found. Unfortunately, I did not remain symptom-free after the operations and had to look for something that would give me new courage, strength and, above all, self-confidence.
Since then I have been combining a new outfit every day and transforming this "flat knit armor" into shining armor. My own fashionable therapy was born. But the work does not stop there; it forms the foundation for successful self-management.
Together with a great team and a wide variety of guest authors, I will show you that the diagnosis does not have to be the end, but rather offers the chance to grow with unusual challenges.
# lipedema fashion
Life with lipedema is about a lot more than just fashion. Lipedema Mode is your advisor who accompanies you through everyday life - with full energy, concentrated knowledge and many years of experience.
Many women suffer from the second flat knit skin and are easily unsettled by their appearance. We hope we can show you that the supply of both arms and legs does not have to be limits for you. It is a tool that reduces our pain and lets us struggle a little better through everyday life. So let's tackle it together and make this life with lipedema as worth living as possible.