Question about hot flashes

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nosurrender
nosurrender Member Posts: 2,019
edited June 2014 in Life After Breast Cancer
For all of you who are post treatment and in meno, whether chemically or surgically induced, or naturally in meno-

If you went into chemo pause and got hot flashes are the chemo induced ones STRONGER than the ones you get after? Like after you got an ooph?

I cannot imagine these chemoflashes getting any worse but I am worried they will when they do the ooph on me after tx.

Thanks in advance.
g

Comments

  • Fitztwins
    Fitztwins Member Posts: 7,969
    edited July 2007
    I just posted something about hot flashes. LMAO. Actually, chemo flashes were more intense. Right now mine are bad, but When the weather is cool, I take my meds and don't drink...they are very tollerable.

    hang in there.

    Janis
  • nowheregirl
    nowheregirl Member Posts: 894
    edited July 2007
    To me, chemoflsahes and hormone therapy induced hot flashes which I have been getting since February of 2006 are equally annoying as hell. I was so hoping them to be gone when I finished with chemo but they are still here. It took a whole year to finally finish with chemo as I did three chemo (12 Taxol before surgery, 4 EC and another 12 Taxol after surgery) Can you imagine how hard it was to be tortured by chemoflashes for a whole year? Now I have another three years ahead of me before I finish with Tamoxifen.

    How long before you complete your chemo? Hope you get to feel better soon.

    Hugs,
  • rumoret
    rumoret Member Posts: 685
    edited July 2007
    Chemo Flashes were the worst! I have been on Tomoxifen since January 2007 and the hotflashes are very mild during the evening. I have my ovaries and uterus.....but blood test showed my Estrodial below 7.......and my vaginal scan showed my ovaries shrinking from 1 year ago.

    Love,
    Terry
  • BMD
    BMD Member Posts: 1,492
    edited July 2007

    Gina--I think chemo flashes were just terrible and much more frequent. Femara flashes are no picnic either. I had my ooph about a month ago. The week I had it I thought I would be flashing all the time. I did not have one hot flash for 3 days. They are back now though. Not quite as intense maybe but now my skin gets very itchy all over right before I get one. It is extremely hot and humid this week so I am sweating like crazy. I also switched my anti-depressant from Lexapro to Effexor over the last 3 weeks. Shirlann said that might help. To hot to tell right now. Alcohol definetly makes them worse and more frequent.

  • DragonladyTina
    DragonladyTina Member Posts: 371
    edited July 2007
    Hi Gina,

    I had a few hot flashes with chemo but NOTHING like the ones I had after ooph and arimidex. The flashes are tapering off some now but the sweats are horrendous. I was one of the lucky folks who never lost a drop of sweat even in 90 degree weather, now forget it. I am drenched especially at work.
    I have to say the meno/ooph/hormonal therapy flashes/sweats are worse for me.
    Best wishes to you!

    love Tina
  • JustOne
    JustOne Member Posts: 226
    edited July 2007
    For me, the chemo flashes were more frequent but the ooph flashes were unbearable. Nighttimes were the worst, waking several times not knowing if I should get up and change t-shirts or just climb in the fridge.

    Now 7 years out and at age 52, I’m on the other ‘side’ and the flashes have stopped. Now I’m chilly most of the time. Can’t win.

    ~Pam
  • nosurrender
    nosurrender Member Posts: 2,019
    edited July 2007
    Oh boy,
    It looks like it can only get worse when I am done and they give me the ooph and start me on AIs.
    What meds do you take Janis?
    Fumi, my chemo started in April and it will most likely end the end of October if all goes according to plan. I thought 7 months was bad- you did a WHOLE YEAR??

    I have been putting Sea Breeze on my head the minute I get home and take off the wig. I think they are worse under a wig.

    Thank you for your responses!

    g
  • nowheregirl
    nowheregirl Member Posts: 894
    edited July 2007
    So are you wearing a wig? Poor girl, I know exactly how miserable it feels. I started my first Taxol in July of 2005. Needless to say it was summer. Our summer isn't that easy to deal with, too much humidity and it gets 100F in the afternoon and hardly goes down any lower than 82 in the night. Although I had my last Taxol (another 12 rounds after surgry) in July of 2006, I had to keep wearing my silly wig until April of this year as my hair didn't grow back that fast. I don't know what you are doing for living but hats, bandanas etc weren't my option for some business reason. When my hot flashes got really bad, an ice pillow helped me fall asleep. Other than that, I haven't found anything that really works, unfortunately. I put an ice pack on my forehead but it only caused me headache.

    Wearing a wig certainly makes you feel worse with those annoying hot flashes. I just hope your hair grows back quickly.

    Hugs,
  • gsg
    gsg Member Posts: 3,386
    edited July 2007

    my chemoflashes were much more intense than my post-ooph hot flashes. post-ooph flashes i don't even break into much of a sweat...it's just more a feeling of suddenly being very warm.

  • notme
    notme Member Posts: 161
    edited July 2007
    I was menopausal before chemo. I had pretty much completed the hot flash and night sweat period and just run warm all over all of the time.

    Then I went on Arimidex and get hot flashes in my head. I just seem to sweat through my head now insteqad of the rest of my body. Any heat producing activity, house cleaning, heat outdoors, coffee drinking results in a wet head. Since growing my hair back, it is curly and then the wet head enhances the curl and destroys any styling I had done.

    But hey! I have hair and there is nothing like feeling the wind though your hair after not having any hair. And when you hair is wet, that wind feels even better. I make my own wind now with Asian fans left at various locations in the house.

    notme
  • Fitztwins
    Fitztwins Member Posts: 7,969
    edited July 2007

    I am on Zoloft. It helps. some. So does a fan...directly on me!!

  • nosurrender
    nosurrender Member Posts: 2,019
    edited July 2007
    Fumi, I am like you- I am wearing my wig. I can't go out in public without it. I am not brave like some girls here are. I WISH I WAS! It would be a lot cooler. I remember that picture you posted a few months back and your hair looked so pretty- how long did it take you to get it to that length?

    gsg, I get that all over warm feeling and then, like Notme, break out into a sweat from my head only. I think my wig will slide off some times!

    Zoloft helps, Janis? Maybe after chemo I can ask for some. My onc doesn't let me take anything while on chemo. Not even the Glutamine for the nueropathy.

    Thanks for helping me out girls.

    Love,g
  • nowheregirl
    nowheregirl Member Posts: 894
    edited July 2007
    I finished with my last Taxol in July of 2006 and got my first hair cut in April of this year. So it took 9 months to get my hair to that length. My hair has never been good at growing back fast. And like I said in my previous post, I don't find any difference between chemoflashes and hormone therapy induced hot flashes. I'm a lot like you, it's a sudden onset of a sensation of intense heat which in my case always starts in my head. It's like my head is burning. Although I'm wig-free now, it still starts in my head so I guess it doesn't matter whether or not you wear a wig. To be 100% honest, I felt better when I was bald in this aspect. At least I was able to have my head "naked" when I was home. To get those annying hot flashes in this heat with thick hair on my head makes me nuts. But it's just my case. Like so many others, hopefully yours will get better once you complete your treatment.

    Hugs,

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