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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.

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Title text reads: "The Grief Project: Paulina's Journey" in black cursive font. Underneath is a graphic of pink, purple, and yellow flowers with green leaves.

The Grief Project: Paulina’s Journey

Without further ado, let me introduce you to Paulina, a beautiful soul living in Germany. Paulina has been a part of the Lichen Sclerosus Support Virtual Meetups for quite a while now, and also speaks with such strength, asks wonderful questions, and gives great support to others. Thus, I will now turn the metaphorical floor over to her.

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Jaclyn September 22, 2021
Image of a a person with their hand on their face, with a grief struck look on their face. They have pale skin, white hair, and wear a blue top. The background is a pale purple.

Grief: The Forgotten Feeling of Living with Lichen Sclerosus

Today, I want to touch on another aspect of mental health that often accompanies living with Lichen Sclerosus: that is, grief. Grief is a multifaceted feeling and can present itself in several different ways. In this post, I will discuss how grief can manifest and why grief is normal when you have Lichen Sclerosus.

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Jaclyn September 14, 2021

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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