I have lichens sclerosis on my mons pubis. I wanted to share my experience with it, in hope it could help someone else. I am 32 , my lichens first appeared 3 years ago as a tiny itchy bump. The more I itched the bigger it got and as it didn't disappear over time I decided to see my GP. I was sent for a punch biopsy and the results came back positive for LS. At the time my symptoms improved, I didn't follow up on getting any medication and in all honesty I didn't realise the seriousness of the condition. A few months ago I had a flare up in the same area, it was itchy and got slightly bigger. I decided to do some research into why and what treatment options were out there. I learnt that the condition never goes away and certain foods can make it worse. I then looked into medication and the go to is dermovate cream/ointment which is a steroid. A lot of researched showed the steroid cream thinned the skin and caused more problems. I then found some studies where Tacrolimus 0.1 ointment was used which contains no steriod. The study showed LS lesions went into remission or completely disappeared. I asked my GP for the Tacrolimus ointment, as wanted to try something steroid free first. I have used it for two weeks, I apply a thin layer before bed. I was really sceptical about it working, but it has! the lesions and scarring I had have shrunk, and I have no itching what so ever. Honestly a miracle ointment! I would recommend any one with LS to try it!