In this post, I reflect on my over a 10-year journey to get a diagnosis. I then share why I…
In this guest post, Jen shares her story about living with lichen sclerosus and trauma. It is a reflective piece…
The Grief Project is a collection of voices from people around the world with Lichen Sclerosus, sharing their experiences and…
Gina is a fellow LS Warrior whom I had the pleasure of meeting (virtually) over a year ago at one…
In the latest installment of The Grief Project, Denise bears their soul and opens up about their diagnosis story and…
Since you were diagnosed with Lichen Sclerosus, have you ever given yourself a timeline to get better? Perhaps you gave…
Introduction A few weeks ago, I had the pleasure of sitting down and interviewing an amazingly brave soul. We had…
A few weeks ago I had the pleasure of (virtually) sitting down with a friend and fellow LS warrior, Megan…
In this post, I continue on the topic of mental health and Lichen Sclerosus, but instead of focusing on a…
Do you feel alone and isolated because of your Lichen Sclerosus? Do you want to share with others that you…