Hi, After 4 years watchful waiting on my prolapse, doing my Pelvic Floor exercises, using Estrogen i know I am going to need Surgery in the near future. I was diagnosed with LS last year ( had some fab support on this forum ) Vaginal atrophy and Vulvodynia - all these seem under good control ( at the moment ) my question is - did LS influence the type of surgery you had ? 4 years ago I was offered mesh surgery but I resisted but now with the skin issues vaginal surgery isn't looking like a good alternative so would mesh done laparascopically be a better option ? Both have risks, possible nerve damage , possible adhesions ,horror stories etc etc - will be able to speak to a Urogyn when Covid settles so your advice in the meantime would be welcome. Thank you