GETTING DIAGNOSED WITH LIPEDEMA IS ONLY THE 1ST STEP...
Proud to be a panelist on the monthly Lipedema Patient Roundtables hosted by:
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out the videos!
PRIVATE SUPPORT GROUP
Do you have Lipedema and want to join our private support group, click the link below...
ANNUAL LIPEDEMA TRIATHLON
We created this annual triathlon to help spread awareness of Lipedema and the importance of staying active. This June will be our 6th Annual Event!
FIND US ON INSTAGRAM
Join us for fitness videos, self care tips, product reviews, and all things for living your best life with Lipedema!
PUBLIC FACEBOOK PAGE
If you don't have Lipedema personally, but care about someone who does, click the link below...
In 2007 I was diagnosed with Lipedema (actually primary Lipedema, and because I had gone so long not being diagnosed properly, I also had secondary Lymphedema). I was 35 at the time, had just given birth to our daughter, and had no idea what Lipedema or Lymphedema were. Basically Lipedema is defined as a rare and painful fat disorder, although with 17% of the population believed to be suffering with this, how rare can it be?
Proud to be a Juzo Brand Ambassador. Click the image to learn more.