Be Part of the Community and Empower Your Life

LymphConnect is an online platform developed to help you manage your lymphoedema or lipoedema.
Everything you need is right here.

Discover our free resources

or jump right into our starting program

Be Part of the Community and Empower Your Life

Understand Your Condition

Recognise how and why lymphoedema or lipoedema can affect you

Share Your Experience

Be inspired by sharing stories with others in the LymphConnect community

Discover More on LymphConnect

Get tips to manage your life with lymphoedema or lipoedema and find support from others

Improve your Daily Life with Support from the LymphConnect Community

We understand how difficult it can be living with lymphoedema or lipoedema. The journey can be challenging. That's why JOBST developed LymphConnect: to provide you with all the information you need to help you regain control of your life and enjoy it to the fullest. Join the LymphConnect community today, learn more about your condition and share your experience with others. Need some guidance with your first steps? We are here to help you: sign up for our free starting program.

Watch Liv to learn more about LymphConnect

Why Other Patients Love Us

When I first got diagnosed with lipoedema, the LymphConnect community is where I found support when I needed it most

Madita Lipoedema patient

Through the community, I realised that you don’t necessarily have to be limited by lymphoedema

Paul Lymphoedema patient

Getting the diagnosis was scary. Once I saw the full picture, I knew there’s nothing to be afraid of

Claudia Lymphoedema patient


Get Support From Others With Your Condition

It’s important to know you’re not alone. Join our private community and feel empowered by connecting with other lymphoedema or lipoedema patients.

Share stories and tips

with others like you

Find the right expert

for your condition
Discover more helpful tools         
Be Part of the Community and Empower Your Life
Don’t sit around and go through this in silence. Share your story. Doing that was a real eye-opener for me

Claudia Lymphoedema patient