The Grief Project: Louise’s Story
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.
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.
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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