Hi! My name is Kathy. I have been diagnosed with Lichen Sclerosus for two years but have suffered much longer. I had minimal knowledge of the condition and was okay with that. That was until about two weeks ago when I had the worst outbreak since I started my medication. I had no one to talk to or ask questions. I decided to find my community and learn as much as possible about this illness. Lichen Sclerosus Support Network, a nonprofit organization dedicated to sharing evidence-based education to help people living with LS improve their symptoms and quality of life. We have a private, off-social network community through our Membership to help people living with LS.
This is a journal of my learning about and living with Lichen Sclerosus.
Please join the community, and let's give each other hope and support!
Edited in 2022 to add: Fast forward two years, and I founded the Lichen Sclerosus Support Network, a nonprofit organization dedicated to sharing evidence-based education to help people living with LS improve their symptoms and quality of life. We have a private, off-social network community through our Membership to help people living with LS.
