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Lou’s Lichen Sclerosus Diagnosis Story

Lou’s Lichen Sclerosus Diagnosis Story

Our sister in Lichen Sclerosus, Lou, from Australia, shares her diagnosis story with us. Her trials span 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 many similarities.

If you haven't heard my story yet, you can find it here lssupport.net/my-lichen-sclerosus-diagnosis/. If you need help dealing with appointment anxiety, check out the podcast episode “How to Overcome Appointment Anxiety so You Can be Your Best Advocate”.

Share in the sisterhood of LS and stay tuned to the end for an exciting announcement. If you need help preparing for a visit with a practitioner, check out LSSN's guide for advocating for yourself.

Don't forget to subscribe to be notified of the next episode, or find all the podcast episodes here for more education and diagnosis stories.

Instagram @lichensclerosuspodcast

Facebook @lichensclerosussupportnetwrok


  • Video Lou shared with her partner – vimeo.com/168204328
  • Lou's doctor is Dr. Kathy Cook at Mercy Women's Hospital in Heidleberg VIC. The vulva clinic only runs on a Monday, and you'll need a referral from your GP to see her.

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