LS community Archives

TLLC Blog Posts

TLLC's blog is moving!

In January, 2023, TLLC partnered with Lichen Sclerosus Support Network (LSSN). This means my new 2023 blog posts will be published on LSSN’s page. For full details on what the partnership entails, watch this video.

Image of a single candle, burning brightly, amongst a background of tiny irridescent lights representing Ellen and the LS community.

Honoring the Life of Ellen Swanborn-de Lange

Click to learn more about and honor Ellen Swanborn-de Lange the work she did for the lichen sclerosus community.

Jaclyn May 22, 2023

I am often surprised that she captures what has been on my mind.”

Jaclyn manages to put into words many of the thoughts, feelings, fears (oh, so many fears), and questions, that come with a diagnosis of LS. She captures both the physical and often more importantly the mental health aspects of learning to live with LS. Her generosity in sharing her personal journey and speaking truthfully about LS provides much needed hope and perspective

Joanne

Reading her blogs has helped me deal with LS in every way – physically, emotionally, and mentally. -Maria

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