Thanks for all your replies. I'll start from the bottom up...
CKLD - I'm amazed not more research has been done. I think I'd happily bet that most crimes committed by women were done during PMS. I know I would go completely *wrong* due to PMS, not to mention suicidally depressed. I was put on Prozac after my PTSD diagnosis, which stopped PMS dead.
With hindsight, my first marriage failed due to my PMS. Not directly, but due to my ex's reaction. He'd mock me and goad me every single month. I swear he had more PMS than me. I'm now extremely happy that I finally divorced him. My current, lovely partner is wonderful. He recognises when I'm not myself (because I'm REALLY NOT), and takes any clumsiness/temper/out-of-sorts behaviour in his stride. No "on the rag" poking from him.
I don't think I'll have a follow-up as I'm no longer in the same place I was when I was referred (suicidal/agitated etc.). I will ask to see him again if my moods start to get bad again, though, as he was excellent. I'll also ask to see him if his advice to my GP and neuro gets ignored and they insist on me going back on Elleste - the reason my mood was so down to start with.
I have no idea why they'd do that as I'm clearly overweight and have high risk family associations with stroke/thrombosis. I repeatedly told the GP that, along with telling her I didn't want to take any more tablets than necessary (I take huge amounts for MS and pain), and asking for a referral to a meno clinic or gynae.
MIS71MUM - I was shocked at how heavy my periods were on Elleste. And I'm used to heavy periods. Thank you for your advice and I hope that others reading might get a bit of comfort knowing that their mood changes have a genuine reason that can be helped. I'm hoping to be prescribed something that will help without causing me mental problems. Kinder is a very appropriate description, and thanks for the good luck wish

Ah, Roseneath. I feel your pain. You're lucky you're getting bloods done. I'm supposed to have regular blood tests for MS and the meds I take, but not been sent for nearly 2 years. I feel that if I complain, I'm being written off as *that hysterical woman* and in some way punished. I also have the problem that a lot of my brain fog and other symptoms are associated with MS. The fact that the flushes are new for me seems to mean nothing to them. Can I ask - your name? Are you in South Wales?