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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.

Image of two people holding hands in a field, amongst a pale purple background.

My Dilator Journey, Part 4

Today, I talk about my dilator journey for weeks 7 & 8. This post will be TMI, so if that’s not your thing, click out. For example, it will include discussions about oral sex, masturbation, lube, etc. In addition to highlighting the physical aspects of my journey, I document how working with dilators affected my mental health. I had a pretty big mental health breakthrough this week, and I can’t wait to share this with you.

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Image of a person walking down a very long beach. This represents my dilator journey. The background is a pale purple.

My Dilator Journey, Part 3

In this post, I continue my dilator journey from weeks 5 and 6. I highlight the physical and mental aspects of the journey. I discuss some setbacks I experienced and how I dealt with those.

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Image of a sunset and a long road stretching in the horizon. The background is pale blue and the title text reads, "My Dilator Journey Part 2" in black font at the bottom.

My Dilator Journey Part 2

Today, I will continue my journey into weeks three and four. I also document how this journey impacted my mental health. Specifically, I highlight mental struggles and some wins throughout the two weeks. It is important to me to be transparent and open about my journey with you.

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Image of a person standing on a sunny, shallow area of an ocean holding a bunch of red balloons over their head.

How Dilators Can Help Your Lichen Sclerosus

yours, there are many other reasons you may want to work with them that do not involve penetrative sex. In this post, you will learn all of the various ways dilators can be helpful to your lichen sclerosus journey in addition to helping with painful sex.

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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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