Letrezole

FormerMember
FormerMember
  • 30 replies
  • 279 subscribers
  • 8244 views

Hi , I've been taking letrezole for 8 months now and the side affects are awful, flushes and sweating being the worst,  some women I  know have stopped taking itfor better quality of life,  do I or don't I continue to take them???

  • Hi Moomy! 

    I'd love to read that article if you can remember where you saw it! 

  • Ask if you can be put on Zoledronic infusions instead Moomy!

  • Heres the article

    Hugs xxx

    Moomy

  • FormerMember
    FormerMember in reply to moomy

    Hi 

    I typed it all out and got the website as a link - Just click / tap here

    Must admit it is a bit of an unnerving read :-/

    Hugs, G n' J

  • FormerMember
    FormerMember in reply to FormerMember

    Hi all .

    I've dripped and hobbled all day today. We have had a busy week so I'm hoping I'm just a bit tired. Not a lot planned for the weekend so I can keep my feet up.

    I'm going to read the article now, I hope it's not too depressing.

  • FormerMember
    FormerMember

    I am about to start taking Letrozole. Frankly I am terrified!

    Do any of you take any supplements to counter some of the SE's? I have read about magnesium being useful and omega 3.

    Also, is there a preferred time of day to take them?

    Any thoughts?

  • FormerMember
    FormerMember in reply to FormerMember

    I found taking it at night was better. If you do have problems try a different brand or different AI until you find one that suits. I started with letrazole generic, then switched to Femara, then changed to Arimadex which I’ve been on for a few months now. Everyone reacts differently so don’t worry. I know people who don’t have problems with it at all. I get the flushes and bones/muscles hurting but it is better than it was at first. If you’re not happy speak to your oncologist. 

    I do take Omega 3/6 and multivit as well as B6 but again good to check with onco.

    Best of luck.

  • FormerMember
    FormerMember in reply to FormerMember

    Hi

    Please don't be terrified. Not everyone gets everything or even any. I did read today that some of it isn't actually a side effect of the drug. The symptoms are more due to the hormone being reduced.

    I was very late going through menopause about 57. The doc did say that was good at the time because you don't age. I wasn't sure what he ment then but I do now. Another doc said things dry out without the hormones , including the joints. The trouble is oestrogen also caused the cancer. 

    I did start taking mine in the evening and I thought the sweats got less, but the weather changed at the same time so hard to say.

    I've only been on it for a couple of months so I'm hoping things improve.

    You've got this far, it's just another step.

    Hugs

  • FormerMember
    FormerMember in reply to FormerMember

    I have been on Femara since January. I do get sore joints, especially knees, but had been quietly satisfied that it was bearable.  Until last week!  I woke up with trigger thumb one day. My wrist couldn’t be trusted to hold up a mug of tea. I couldn’t get up the stairs.  I felt awful.

    When I started letrazole I also started cod liver oil and glucosamine with condroiton, (on recommendation of someone on this sight.) About a week ago I ran out of glucosamine/ condroiton.  When I realised the coincidence yesterday I rushed out to get some more. 24 hrs later, on the maximum dose for 2days now, I am back as before. I really cannot believe the difference it made. 

    So I would recommend trying glucosamine with condroiton. I just bought mine in Superdrug. I won’t be running out of it again.

    good luck xx

  • Yes , I take glucosamine/chondoitin, and so does , find it helps xx

    Onwards and flatwards (don't do hills) and keep walking if you can!