It really is a lottery isn't it and it shouldn't be. My heart breaks for all the ladies who like me, can't get prescribed what they need or even diagnosed. I first had signs of VA about 15 years ago and had no idea what it could be - I was 40 then and hadn't even thought about menopause. Then about 10 - 12 years ago it flared up to level its back at now. No diagnosis from GP, to GP to gynea all diagnosed other things I did not have. Finally I self diagnosed from information on this forum. The first GP I saw gave me pessaries and Ovestin straight away and the pain went from 10 - 2 in weeks. But when I saw her again once I was using twice a week because my symptoms were again getting worse, she then decided I needed further investigation into what I might have. She didn't tell me it could be VA in fact I'd never heard of that until I eventually came here. Then more misdiagnosis from other GP's and I saw a gynae who, when I mentioned the fact the pessaries helped at the loading dose, rejected the idea my problems could be hormonal. I asked if there were any menopausal symptoms I may have and she said "no". When I finally asked for local anesthetic cream to ease my pain, she reluctantly gave me it saying it wouldn't work as my pain was nerve pain. Next visit, I told her it worked, all be it temporarily, and she looked me in the eye and said " There is nothing more I can do to help you so I will close your file down. You'll have to see your GP ".
Sorry if I'm repeating myself but I know you won't all have read my history in the past.
Why do we have to go through this? I cannot understand it.