Hello everyone and thanks for accepting my request.
I was diagnosed with stage 3C metastasized ovarian cancer in December 2018.
I started chemo in Feb 2019 (delayed due to having severe sepsis) I was too weak for monthly chemo and had it weekly instead. My oncologist noticed that after id taked the oral dexamethasone 6 hours hours after chemo i was very hyper, so i was told not to take it in future.
Fast forward to my second cycle which started in May this year, i immediately went down hill mentally follwing my first chemo session. My oncologist said that id been given a massive dose of dexamethasone pre-chemo via IV.
The problem is that its been 6 weeks now and it doesn't seem to wearing off.
I literally went from being normal and happy considering the circumstances to severly depressed, extremely anxious and irritable, no interest in life, suicidal thoughts, terrible nerves and crying.
I was wondering if anyone else had had this kind of reaction and how long it had lasted. Ive shut myself of from my family and life for 6 weeks now, ive just been in bed hiding.
I was prescribed antidepressants before the cancer, and my Dr switched them to Mirtazapine when I phoned her and told her how dreadful i felt, but it hasn't help one bit.
Hi
Welcome to the community although I am sorry you qualify to join our exclusive group of incurables. I am sorry to hear about the problem that brings you here.
I can only talk about my own experience, point out I’m not a doctor and stress the importance of you talking to your own doctors. So having said all that...
I had chemo first in 2014 after being diagnosed with grade 3c2 serous womb cancer. The steroids turned me into a hell hound. My husband brought back pink roses and I would cry because he knew I only liked yellow. Or vice versa. I was very depressed and likely to snap at the kids or indeed anyone who had the misfortune to come within striking distance.
I realised I couldn’t go on when I was hiding under the duvet one day and my husband said to me that I should just look forward to our family holiday. I couldn’t. All I could think was let the family go and I’ll just stay under the duvet.
That was when I went to my GP who diagnosed anxiety and depression and gave me, yes you’ve guessed it, mirtazapine. I didn’t find it particularly helpful at the time although in retrospect it may have been more useful than I thought. I took it for about a year than decided I didn’t want a crutch anymore.
I don’t remember how long the steroid madness lasted, just that I came out of it at some point.
I have to say that what you’re going through sounds very distressing. I think worse than I went through although maybe you have more insight than I did.
I am now on chemo for the fourth time and with it the steroids. I don’t seem to have quite the same reaction these days. They give me energy for a day or so but not the madness.
I hope this helps. It can be a lonely place to be feeling the way you describe. I hope you’ll find that things change with time and that you feel less alone for sharing your story.
With love and hugs xxx
Hi
Lovely to meet you but I really wish we had met elsewhere.
Sorry to hear that you are going through a rough time. I have a rare blood cancer which was diagnosed in March 2015 and like Annette, I haven't had chemo or the meds you are taking.
I have had antidepressants, though not Mirtazapine. I was given them when just 4 months after diagnosis, I was diagnosed with a spinal condition that means I can't stand or walk, only for very small periods of time so outside of the house I need a wheelchair.
I started to have hallucinations about 3 months ago, mostly when waking from a sleep or a short nap. Not nice at all, quite frightening. I hope you can find your way out of your present circumstances.
Take care and stay safe Rubyjane.
Tvman x
Hi RubyJane,
Wishing you a warm welcome to this very friendly group.
I had dexamethasone,4 years ago each time via the canula before the chemo,but must admit I had no problems with apart from the fact that it stopped me sleeping for the first few days. i suppose like all drugs we are all effected differently & maybe the doses are different for each person.
Hopefully these side effects will pass eventually, although maybe you should try and contact your Oncologist again & let them know how you are feeling.
Take care,
Georgette x
, Hi and welcome!
I was on Dexa for a while after my brain surgery, and i can tell you it did change me alot, i did become very aggressive and angry ( poor hubby) i could not sleep but eat all the time weird things. But the worse has been coming of it, very very slowly, that's important, but it was like falling in a big hole!!!
Pet
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