u/femragebot

I hope this is okay to post. I reached out to the mods a few weeks ago to ask permission but never heard back.

I have vulvar lichen sclerosus myself, and after years of trying lubricants that either irritated my skin, seemed to trigger infections, or contained ingredients I wasn't comfortable using on already compromised tissue, I became frustrated by how few options there were. I also learned that many conventional lubricants are hyperosmotic, meaning they draw water out of vulvovaginal tissue which causes dryness and irritation. So I decided to create one myself.

Over the last couple of years I've worked with formulators to develop a water-based lubricant specifically for sensitive vulvovaginal tissue. My goal wasn't to make another "luxury" lube - I wanted something that wasn't just less likely to cause irritation, but was intentionally formulated to help support the skin barrier and delicate vulvovaginal tissue.

I'm now at the point where I'd really like feedback from the people I made it for.

I'm looking for women with diagnosed vulvar LS in Canada who would be willing to try a complimentary bottle and give completely honest feedback. I'm not looking for glowing reviews or testimonials - if you don't like it or if something could be better, I genuinely want to know.

There are no strings attached, and I'm not asking anyone to post publicly. I simply want to learn from other women living with this condition so I can continue improving the product.

If you're interested, feel free to comment or send me a DM.

PS - I've been using it for about two years now without issue. It will sting if I have tearing in an area or if I'm in a flare but literally everything stings if I have tearing or I'm in a flare.

PPS - This isn't some random thing I make in my kitchen. It's manufactured in a registered facility and formulated by a formulation chemist and has been third party tested. It's water-based, pH matched, iso-osmotic, made with minimal ingredients and has sodium hyaluronate and aloe for extra soothing and hydration.

Thank you ❤️

I was diagnosed in 2018 and have been mostly fine since then with the occasional irritation. I had a really bad flare in January-February (went through an extreme life stress event). I started noticing that it was harder for me to orgasm/my orgasms felt muted over the past couple months. I noticed last week that my clit has started fusing to my hood on the left side. Has anyone had any success in unfusing? I've made an appointment with a pelvic physio clinic here that does myofascial release and hoping that works.