Hello all, I am hoping for some help.
I have been now advised of my endocrine treatment and what that looks like for the next 10 years.
can anyone who has had a similar experience please share with me.
I am due to start ovarian suppression injection next week following letrozole daily which will start 3 weeks after my first injection.
The one that I am worried about is abemaciclib which is targeted treatment and will have to take it for 2 years.
I have read up on the side effects and they are very similar to when I was having chemo.
can anyone explain to me what there experiences were?
Many thanks
terri
I am on zoladex and exemestane. I had my first zoladex implant at the same time as my 2nd chemo cycle, which I think made everything particularly intense. I had read that you have the same oestrogen levels as a post menopausal woman 3 weeks after the implant. I have to admit, I thought I'd got away with mild symptoms but then they hit me at 3 weeks.
It was an intense menopause, which my oncologist has warned me about, but I do suspect having chemo at the same time made it worse.
The good news is that things have significantly improved since then. Everyone is different, but at the 2 year mark, I was still getting mood swings that were out of character. I started on a low dose antidepressant and have felt like me again in my mood ever since.
I still have hot flushes and other menopausal symptoms, but I figured I was going to be going through the menopause anyway so at least this way, I know what it is!
Good luck with it all.
Thank you for replying. I have the added drama of my treatment being via the private sector then having to dip back to the nhs as private does not cover it. I am worried I will find it hard to navigate my menopause via the gp. I think I find this part of my journey more unnerving that the chemo and surgery put together.
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