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Al's avatar
Al
Member
14 years ago

Night sweats and hot flushes!

Hi all,

I have just had my 3rd cycle of AC chemo and am finding that the sweats and hot flushes seem to be a new side effect this time time particularly at night. I am still on antibiotics, a result of my neutrapenic episode so I have put it down to this as a possible cause. They are keeping me awake at night and I'm having to wash sheets each day. AAGGH! Not sure whether this is also the beginning of early menopause either!

Any thoughts would be appreciated,

Thinking of you all,

Al xxx

 

4 Replies

  • Thanks Kathy for you message and your honest and revealing comments. Must have been very hard for you and I'm glad things are improving and you're learning to live with it. I'm only 47 (27th of this month!) and feel too young to be going through this but I guess this my fate at the moment. Emotionally I dealing with it quite well but the nausea and associated side affects with the chemo are what are getting me down a bit. i have a great support network but at times it doesn't seem enough. It is as you've said life changing and I am only beginning to see this. I know I still have a long journey ahead of me and it does gets me down as I'm such an active, in control type of person who is fiercely independent and isn't very good at asking for help!  I learning slowly though!  Yes it is a scary process but many have been their and "m glad that I have this site to get advice and vent when I need to.

    In regards to the sweats and hot flushes I do wear cotton and I'm learning to drink more water and cutting down on hot drinks! I used to enjoy a wine as well but haven't the taste for it anymore which is probably a good thing.  There will a big party at the end of all this, I'm sure!!

    Anyway thanks for the great advice - great to hear how others have fared!

    Look after yourself and keep in touch,

    Al  xxx

  • Thanks Sarah for you message. Some great advice. I'm nearly 47 ( 27th!!) and feel at times that I am too young to be going through this but realise that it is part and parcle of the whole chemo treatment. It isn't really getting me down too much but not sleeping well is frustrating. I wear cotton to bed which does help and I am not drinking alcohol at all - no taste for it anyway! I've had to increase my water intake as I am not a good water drinking and with the 'furry" mouth it tastes aweful!

    Thanks Sarah and good luck to you too,

    Al xxx

  • hi al, i was 42 and had early menopause after first chemo. it did hit me and it would have been good to have this forum then to get some feedback from others.

    i am now 55. i had some " rough " years for a while and i " pushed" myself; too much i now think.( i think i was in a denial phase and not wanting to face certain things, plus not knowing where to turn to get help ). but you cannot go back, so my advice is to take it easy, and not do too much or heavy work, while having all these vasodilations and night sweats. they do settle eventually.

    i also take a low dose antidepressant ( zoloft ). i pace myself, and have learnt to try and go with the flow. what you do not get today, you can do tomorrow perhaps, is one of my mottos these days.

    some days i have more " energy " than others.

    i also have slight lymphoedema, which i can stirr up depending on the weather and certain things i do. i get some discomfort in arms, hands and right leg at times. i think the antidepressant helps to " switch off " some pain/ discomfort feelings also. 

     anyway i took it for two weeks and felt better, so i am staying on it for now.

    i did get some suicidal thoughts and i sought help ( but not initially, and i think it is best to seek help early rather than later. ) it was after the first chemo.. i remember thinking to myself " i can always gas myself if it gets too much"..sounds odd i know.. and i was never one to think like this before. i think it was physical effects on my  body( reduced hormones ) and dealing with the emotional effects too.

    please take time to adjust to all the changes and  just try and go with it. so many emotions and things to cope with all at once. treatments that go for many months, and often years, physical changes to our bodies, and mental changes too from chemotherapy drugs.

    my advice is to take a year or two to adapt and ask for help if you need to.

    life is good now, but different; better in some ways, not always easy to adapt to. i have met some great new friends and had experiences i would not have had if it were not for the BC journey. take the time to reflect and adjust, while you go through this unique experience.

    you realise you are stronger than you think.

    re meonpause: well i do not have night sweats now, nor flushes so severe as i had before. i wear layers so i can take one off if needed, and wear natural fibres like cotton, etc.

    i am interested in diet/ foods to help with menopuase, like beans and lentils perhaps?

    it IS a scary experience and you do face your own mortality, but so will everyone else at some stage. you realise the best thing is to just keep living today, and try not to worry too much about the future. you cannot always control the future, but you can control how you deal with it.

    when having hot flushes and night sweats your body does feel out of your control. i think that was hard for me to cope with at the time. i fought it, but i now realise it is best to go with it and try and find ways around it.

    best wishes, kathy.

     

     

  • Hi Al

    From what you are describing it will be the chemo putting you into early menopause, I went through the same thing and as I am 52 and on tamoxifen am still going through it ! I can't remember after how many chemos it started but I was certainly having them by the end of 6 cycles.

    I am now taking a very low dose anti-depressant to help and have only taken it for 2 weeks but it seems to have helped a bit. I have adjusted my life to not drink hot drinks in the morning when I get up cut down on alcohol and always have a fan with me. I drink lots of cold water and have it by the bed too. I also try and wear cotton or "breathable clothes to try and keep as cool as possible.

    Good luck

    Sarah x