Join Our New Lymphie Strong Pop-Up Community!

This new program is aligned to the Lymphie Strong online virtual community. The average member takes about 3-6 months to onboard lymphedema self care. We aim to shorten that timeframe. Our focus will be on the individual and assisting them in building their Move That Lymph virtual toolbox in a small, personalized setting. Click here to get started.

We Care Because We Live With Swelling Too

Launched in 2015 by a father and daughter from Texas initially hoping to spread awareness about multigenerational hereditary lymphedema with a blog and a small Facebook group, Lymphie Strong has grown into a global patient support and advocacy community with thousands of members who live with lymphedema and lymphatic disorders of all types.

Lymphie Strong is an online resource for people with lymphedema by people with lymphedema who know from firsthand experience how challenging living with chronic swelling can be and how it impacts your life in both big and small ways.

Find Treatment Information & Support

Support Communities

people forming round by shoes

Whether you want to learn about lymphedema self-management treatment options, get anecdotal advice from real people on coping with flare ups and symptoms, learn more about topics like surgery, or have questions on diet and exercise, our members are here to help get you started.

Move That Lymph Challenge Fitness Series

Want to workout with others who know what it is like to deal with your symptoms?

Take your lymphedema fitness training to the next level and join an upcoming virtual Move That Lymph challenge.

Empowerment Series Events Calendar

composition of notepads and calendar of new month

The 2021 Empowerment Series Events Calendar will highlight all events for our support groups with the aim to fulfill our mission of helping to close the gap in finding information and to help end isolation. This includes group speakers and conferences available to the patient community.

Lymphedema Resources

Here you will find a starter list of lymphedema resources that may help you on your lymphatic journey.

This includes the websites of our compression garment sponsors, product ambassadorships, patient organizations and resources, financial assistance programs, public lymphedema provider directories, and some lipedema resources.

Member Testimonials


Lymphie Strong is a global patient support and advocacy group for people living with lymphedema founded and owned by Veronica P. Seneriz.

Social Channels

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We Are Stronger Together

Lymphie Strong would like to thank our industry partners and sponsors who help bring our patient initiatives and programs to fruition.

You Are Not Alone

Lymphie Strong partners with products and programs designed for people who live with chronic edema and swelling. We understand because we live with it too and have for over 3 generations.

Find out more information on the new event from Ninjas Fighting Lymphedema Foundation. Help us Win Our Fight against lymphedema.

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