Our first-ever Vulva Salonwas a smashing success. Together, the SSL community raised money to donate to the Lichen Sclerosus Support Network, and raised awareness of this under-represented and often misdiagnosed intimate skin condition. We are so grateful to have a community filled with like-minded vulva owners actively searching for answers!
No worries! We recorded the event for you to enjoy when you have time. Click here to watch the video.
For continued lichen sclerosus support, here are a few of our favorite resources.
Dr. Jill Krapf
Our fantastic guest speaker is the go-to expert for all things vulvar pain. Click here to follow her on Instagram!
Lichen Sclerosus Support Network
LSSN is a nonprofit near and dear to our hearts. Check out their provider database to find a specialist near you or join their biweekly meetups! Click here for more information.
The Lost Labia Chronicles
Dedicated to all things LS, The Lost Labia Chronicles offers a whole host of great resources, including a free ebook, a rich blog and an awesome podcast! Click here to check it out.
Wellbeing by Penny
Follow @wellbeing.by.penny on Instagram for yoga specifically intended for pelvic pain plus a healthy dose of laughter!
If you’re looking for soothing support for LS symptoms like dryness and itching, give Rescue Balm a try. We’ve heard from so many SSL lovers living with lichen sclerosus who have found sweet relief inside that little pink tube.
Lastly, be sure to sign up for our emails for information about future events like this one!