Lipedema Awareness Interview with Lilith Nix

Jun 04

Lipedema Awareness Interview with Lilith Nix

June is Lipedema Awareness Month and I’ve got some great things planned for this year.

If you’re not familiar with lipedema, you can start out by reading the posts I made last year for the 2014 blog hop – I Have Lipedema Part 1, Fat Legs Aren’t Our Fault, Lilith’s Road to Recovery, Taking Action – the Lymphedema Treatment Act and More. If you’re not familiar with lipdema, you can find out more at, (I’m a contributing lifestyle blogger) and Lipedema Simplified and the Life with Lipedema Facebook page.

Remember to visit the Fight Lipedema T Shirt Campaign to support me and fellow lipedema sisters with health care needs. 

This year I have three four! special guests I’ll be introducing to you. These ladies are only a few of my lipedema sisters that I’ve met online. We interact through several Facebook groups nationally and internationally as well as state by state in the US. We pray together, we’ve helped support one another, and we continue to fight for our disorder to be recognized and understood by the medical community and society.

Lilth NixMy first special guest is Lilith Nix. I wrote an article about Lilith last year during Lipedema Awareness Month but this year I’m happy to have her share her story in her own words. There will also be a transcript available to download below the recording.




Show notes:

Lilith’s Road to Recovery Facebook page

Fight Lipdema T Shirt Campaign

Interview Transcript PDF

Do you have Lipedema or know someone who does? Let me know in the comments or get in touch on Facebook or Twitter.


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