Our website uses cookies to improve and personalize your experience. We do not sell your information. Our website may also include cookies from third parties like Microsoft Clarity, Google Analytics, Google Adsense. By using the website, you consent to the use of cookies. We have updated our Privacy Policy. Please click on the button to check our Privacy Policy.

I have Lichen Sclerosus. Hello.

I have Lichen Sclerosus. Hello.

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.

Kathy Ruiz-Carter Lichen Sclerosus Support Network Vice President

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.

Leave a Reply

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Related Posts