Hi ladies, my consultant is offering me to be put into a chemical induced menopause, via injections to shut down my ovaries for 6 months to see how I feel, then perhaps the possibility of a total hysterectomy including removal of the ovaries. Has anyone else experienced this? I'm very anxious to have my ovaries removed because of the increased risk of all the other diseases and rapid ageing, although I would be offered hrt. Just wondering if it would actually be worth going through all that and putting myself at risk of heart disease and osteoporosis or shall I just stay as I am and out up with all this..?
Induced chemical menopause : Hi ladies, my... - Endometriosis UK
Induced chemical menopause
Hi. Only you can decide what to do ultimately, it's not an easy decision.I had the chemical injection 2 weeks ago and things have changed for me. I'm choosing a hysterectomy.
But I feel like I really couldn't stay the way things were.
The injection for me will stop my period, monthly kidney pain ect.. I've been given hrt which has helped me sleep, stopped joint pain, but the combination gives me spots and I had pain for most of the 2 weeks, but I'm hoping it'll settle soon and things will even out. I realised I was stuck between a rock and a hard place. It wasn't easy either way.
I took some time to think about what the implications of each decision were and decided to leap into the unknown because I couldn't take any more of what had been happening to me.
I'm not sure if this will help you, but I hope so.
I’d say it’s worth a try. I had one ovary and tube out in December(I’d had a large cyst burst in September which they think must have been leaking for some time) and I’ve really struggled with recovering from the operation. I actually think it might be adhesion problems rather than Endo because it’s different pain to what I’d had before and I’m on zoladex. I’m having another scan next month to see how things have progressed. I’m on tibilone. I hadn’t head aches in the first month and my emotions are a bit up and down. I think that might be linked to the difficulties I’m having with recovery, looking after my children and working though…
Good luck! It’s such a difficult journey. 💛
HiyaI have had 2 Zoladex injections now, got one more left then gynaecologist again in July. I’ve not had a diagnosis of anything yet, nor do I know what I will happen when I go back 🤷🏼♀️
Anyway I gave them a go to see if made a difference with the pain, it has! I’ve still had some pain, been keeping a diary and scoring each day out of 10. I’ve had some pain free days, the rest about a 3, the most a 6 but before I started the Zoladex it would be round 8/9 so is doing something, still early days as well as believe can take a little time to settle
Hope this helps even if in a small way, it’s so hard trying to work out what’s for the best
Hi there. Have you had an MRI to determine whether it is deep infiltrating endo and/or adenomyosis? I was on injections for three months and really messed up moods, had nausea, headaches and still relied on painkillers.
But I had a severe case and hysterectomy is only way forward. My advice would be to get it thoroughly checked out before starting such a harsh treatment- go privately if you can.
Best of luck
Vic_Sponge x
We endo girls are prone to depression (any wonder) and I suppose they don’t tell you about side effects or you’d not try Zoladex! It may work for you but definitely write all your questions down and ask about Plan A, B,…X