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.
Read the latest contribution to The Grief Project by a fellow LS warrior, Louise. Louise is an incredibly gifted writer and takes us through her journey of grief, sadness, and growth.
This week on The Grief Project we have Jen, a fellow LS warrior, who will be discussing her journey with grief from Lichen Sclerosus, a traumatic birthing experience, and episiotomy scar endometriosis. Jen is one hell of a woman, she has faced some serious hardships and beat them all.
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.
In this post, I dive into the details of my diagnosis and what it entailed. I highlight some of my red flags (i.e., painful sex). I discuss when and how painful sex started for me, how I dealt with it mentally and physically, and how I finally got diagnosed.
Introduction Welcome to my blog page where I will be writing about my experiences with Lichen Sclerosus! So, here is the deal: my labia
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