This week four Lichen Sclerosus Warriors share their diagnosis stories with us. Although each of their stories is individualized they all have similarities to our own.

LS can be such a lonely disease but by sharing our stories we realize there are thousands of women feeling and going through what we are going through.

I hope you feel a little less alone today after listening to this episode.

Don't forget to signup for the Lichen Sclerosus Podcast Virtual Meetup - https://lichensclerosuspodcast.com/connect/

Other episodes mentioned:

The Mental Side of Lichen Sclerosus - https://lichensclerosuspodcast.com/the-mental-health-side-of-lichen-sclerosus/

Why I hesitated to check my vulva but you shouldn't delay. - https://lichensclerosuspodcast.com/time-to-check-your-vulva/   Do you need a support group? - https://lichensclerosuspodcast.com/do-you-need-a-support-group/   How to still have a great relationship despite Lichen Sclerosus - https://lichensclerosuspodcast.com/how-to-still-have-a-great-relationship-despite-lichen-sclerosus/   Get in touch with me: Instagram @lichensclerosuspodcast FB @lichensclerosussupportnetwork Website https://lichensclerosuspodcast.com/ Email [email protected]