LSSN Nonprofit
Were you looking for easy to find information and education when you were first diagnosed? What about a central place for you to ask questions and meet others with LS? Did you crave community to help you cope? That's a natural reaction and that's why I started LSSN. Now I want to make it official so we can scale and provide all the things we were looking for when we were diagnosed.
LS Warriors
Ever wonder if you're doing things right? Do you crave a place where you can get answers and support from people you know and trust? Want to learn about your disease surrounded by people who understand? Looking for 24/7 access to support and information? Then you need to join LS Warriors. A family of warriors learning, fighting, and healing together.
LS Support Virtual Meetup
Does LS have you feeling lonely? How about worried, anxious, unsure? Want the opportunity to talk to others to see how they deal with their LS? Would you like to ask them questions? Now’s your chance to do that! Join us in our next biweekly virtual meetup. Ask your questions, share your concerns and get peace of mind.
Lichen Sclerosus Podcast
Lichen Sclerosus Podcast is our journal of learning about and living with Lichen Sclerosus.
Each week the host, Kathy, speaks to someone about or researches an aspect of LS and brings you the information so you don't have to go searching.
Get your information with a side of hope and positivity.
The Lost Labia Chronicles
Would you believe there's a way to go from crippling pain and vulvar dysmorphia to multiple orgasm lovemaking and self-love? It's true. In less than two years Jaclyn went from painful sex and anatomy changes that made her feel less of a woman to amazing sex and loving her body. Read her blog to find out how.
