Lilith’s Road to Recovery

Jun 19

Lilith’s Road to Recovery

June is Lipedema Awareness Month. I’ll be talking about my journey with this mostly unknown disorder. Follow the links below the post to read more great blogs by some awesome people who are part of the Lipedema Awareness Blog Hop.


 

Lilith is an awesome lady I met on one of the Lipdema support groups on Facebook. She doesn’t have a blog, but she does have a public Facebook page where she’s sharing her journey with late stage Lipo-lymphadema. Lilith traveled to Germany with a caregiver at the end of 2013. She had three surgeries with German doctor Josef Stutz. She knows these surgeries saved life.

Visit Lilith’s page, read her articles and see her pictures at her Facebook page – Lilith Nix Lifesaving Road to Recovery.

Do you know someone with lipdema or lymphadema? Or do you have it? Let me know in the comments or get in touch on Facebook or Twitter.

 

One comment

  1. Lilith Nix /

    Thanks for sharing my story Christina. There are so many out there suffering alone with lipedema and/or lymphedema. Raising awareness for early diagnosis and effective treatment is the key. Thanks for all you do. You really are making a difference in the World!

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