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Lou’s Lichen Scleorsus Diagnosis Story

Lou’s Lichen Scleorsus Diagnosis Story

Our sister in Lichen Sclerosus, Lou from Australia, shares her diagnosis story with us. Her trials with everything from doctors to mental health.

Be prepared to smile and laugh because we had fun. And although our stories are individual to ourselves we share a lot of similarities.

If you haven't heard my story yet you can find it at lssupport.net/my-lichen-sclerosus-diagnosis/

So share in the sisterhood of LS. Also, stay tuned to the end for an exciting announcement.

Don't forget to subscribe to be notified of the next episode.

Instagram @lichensclerosuspodcast

Facebook @lichensclerosussupportnetwrok


Video Lou shared with her partner – vimeo.com/168204328

Lou's doctor –

Dr. Kathy Cook 
Mercy Women's Hospital
Heidleberg VIC

The vulva clinic only runs on a Monday, and you'll need a referral from your GP to see her.

By Kathy

I'm 42, a wife and mother of three. I have been suffering from Lichen Sclerosus since 2013. I started this podcast to build community and learn more about this incurable condition.

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