Hey y’all!

Tune in as Randie sits down with Kathy, host of the Lichen Sclerosus Podcast.

Kathy was diagnosed with LS 5 years ago at 40 and the life-changing diagnosis paved the way for her podcast and organization on a mission to educate women about the auto immune disease that commonly affects the genitals.

In this episode, Kathy details the symptoms she experienced before diagnosis, the sub-par medical care she initially received, and how living with this diagnosis affects her body, marriage, and children.

It’s a wonderful, informative conversation that highlights how powerful women are (In Randie’s humble opinion).

You’ll not only enjoy the interview, but you’ll get insight into how to maintain a healthy vulva and what to do if you are experiencing LS symptoms.

Items Mentioned:

**As Amazon Associates we earn from qualifying purchases at no additional cost to you. It’s a great way to support the show and there’s also no pressure or hard feelings if you’d prefer to skip the links.**

• Listen to the Lichen Sclerosus Podcast: https://followthepodcast.com/lspodcast
• Follow Kathy on IG: https://www.instagram.com/lichensclerosuspodcast/ and every where else at
• Lichen Sclerosus FAQ: https://lssupportnetwork.org/lichen-sclerosus-overview/
• DONATE to the Lichen Sclerosus Support Network: https://givebutter.com/lssn

• To hang out with us and support our work as independent creators, join us on Patreon at http://bit.ly/JOINBMM there you’ll get access to our Discord channel, unedited, edited and ad-free episodes, zoom meetings with us, and more.

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