But let's start from the beginning:
What is Lymphcare anyway?
“The diseases lymphedema and lipedema are visible, chronic diseases. Many patients are overwhelmed, insecure and feel left alone. The good news is, you are not alone! In truth, you are part of a very large community of patients who are enjoying their lives to the full!
LymphCare was developed to make your life with lymphedema or lipedema easier. Here you will find everything you need. Find out more about the clinical pictures, exchange ideas with other patients and your therapist and find out how other sufferers deal with them.
Join the LymphCare platform and become part of the lymph and lipedema community. Here you will find motivation, courage and valuable tips for your everyday life. "
Source: Lymphcare Germany
How can I take part?
It's very easy, go to the page of Lymphcare and log in as a patient on the right side of the page. Of course you can also tell your therapist about it and ask them to register there. The more skilled workers, the better the exchange. You have to answer a few questions when you register, but that's a minor issue.
What to expect
The Lymphcare Forum is currently under construction and is very fresh on the market. It's up to us to fill the page with life. You can ask all your questions about nutrition, compression or illness there. On the site you will also find dates for the latest events throughout Germany. The most important FAQ's on the topic Lipedema and lymphedema are explained again in detail and the forms of therapy are also examined carefully. An all-round package!
So what are you waiting for, register and be there. There is too seldom the opportunity to interact directly with therapists. We from Lipedema fashion say YES! Can I have some more, please!
I just signed up, now it's up to you.