I was just diagnosed 6 weeks ago with LS and in fact I am going back to the gynecologists’ today for a check up. Shock is an understatement as I’m trying to grasp straws on what happened for this to occur. I am post menopause and for the past 7 years on Vagifem pessaries to help with the vaginal dryness. I was told to wear panty liners and I did for the last seven years. I started to notice a burn and sting with tingling and I felt a “ring of fire” that I couldn’t get away from. I went to my female GP and she indicated all looked okay down under but she will prescribed a steroid cream. A week later I went back as that made the burning worse. The ring of fire is now visible and it looks like a red and raw line on both sides of the labia minora. Long Story short, I finally got in to see a female gynecologist and at first sight, she instantly said it was LS and said lets try the steroid ointment instead of the cream and also to apply an estrogen cream to the entire vaginal surface while I still use the vagifem pessary every 4 days.
Unfortunately, I am finding no relief and I could be facing a biopsy of the area today. Also to note, I smell like a yeast factory. I look back and I blame myself for the continual usage of those panty liners so they would whisk away moisture from the pessaries. Well, the liners did their job as I have no moisture left. I also have to say that if this was brought on by STRESS, then perhaps I am not the only one during these Covid times who is experiencing such a shock n awe with this LS.