Welcome to our website, created BY people with LS, FOR people with LS. We wanted to have an avenue to share information about the condition, Lichen Sclerosus, (also spelled with 'sis' ending) to make the public more aware of this not so rare condition as some assume it is. As well as being able to share tips and suggestions that those of us with LS have found helps us to manage our disease.
We want to let those just diagnosed know that there IS HOPE. This condition can be managed, and it can improve to the point that you can lead a pretty normal, pain-free life.
Also, we highly recommend you join us in the yahoo group: LichenSclerosis. You will be encouraged and enlightened by the support of thousands of women with this condition, many who have been able to turn their lives around.