Sudden inability to sweat

Options
Sudden inability to sweat

Comments

  • soundgirl
    soundgirl Member Posts: 14
    edited June 2010

    Hi,   I am a breast cancer survivor for 2 years now.   I had adriamycin, Taxol and Herceptin.   Now I am taking Tamoxifen for 5 years.   I have been feeling great except for random shocking pains in my body at times and some times aches in my legs.  I have been taking Vitamin B1 & B12 and L-Glutamine to help with the pain.   The past two weeks I have been feeling very little or no pain.  This past Thursday I was in the hot house and busy working so I didn't pay attention to my drinking, eating or the fact that I wasn't sweating at all and I normally sweat a lot.  I felt my tongue go numb and then I was about to pass out.   I was able to force myself to turn on the ac and stand in front of it and get a few glass of cold water.  I felt very dehydrated.   I somewhat recovered from this but I am still not able to sweat and I still feel quite thirsty.  When I get hot I have been cooling off with ice packs.   My Dr said my blood work came back normal.   My ekg was normal.   We can't figure this out.   Anyone ever experience this? 

  • RegulJ
    RegulJ Member Posts: 244
    edited June 2010

    Sounds like your electrolytes are off. Try some Gatorade nex time.

  • pip57
    pip57 Member Posts: 12,401
    edited June 2010

    I spent most of my life unable to sweat.  Now I can.  It really does make a difference with your ability to cope with heat.

  • soundgirl
    soundgirl Member Posts: 14
    edited June 2010

    I've been drinking a lot of gatorade and water.    My oncologist i saying my symptoms can be chemo induced menopause or side effect of the tamoxifen. 

  • chainsawz
    chainsawz Member Posts: 3,473
    edited June 2010

    Wow!  I have a similar experience.  I used to sweat like crazy, and now I don't seem to sweat at all and I live in a very hot desert so I have to be very careful.  I went to a pool party, but since the temp was over 100 I had to sit in the shade and keep ice packs under my shirt!  Another weekend, I was working outside (cooler day) for about 45 minutes and my face became purple!  Everyone was very panicked, but I just drank lots more and put ice packs on my face for an hour or so until it got better.  I thought I was having a heat stroke. 

    I did 6 rounds of TCH at the end of 2008 and have been on herceptin since....tykerb for the last year.  I thought it was related to the tykerb.  I didn't even thing about my chemo induced menopause.  My onc doesn't seem concerned, but it makes it difficult for me to enjoy physical activity and the outdoors.....unless I can carry enough ice packs with me!!   They checked my thyroid and that and all my blood work is fine, too. 

    I guess we are just going to have to find a way to make ice packs fashionable this summer...LOL!!!   BTW - I have family in Tenafly, NJ and we love to visit in the spring and summer - I can see why it is called the garden state....so beautiful!!!  Best to you :>  lisa

  • soundgirl
    soundgirl Member Posts: 14
    edited June 2010

    As I started to feel better today I noticed I had a knot or spasm in my neck and shoulder.. I rubbed it out and put icy hot on it and about 15 min later I started to sweat again?   This is very strange...

  • soundgirl
    soundgirl Member Posts: 14
    edited June 2010

    Still not sweating like I used to.   Still getting the dizzy, stomach bloat and muscle spasms in neck and face.   My doctors can't figure this out at all..  :(

  • carol1949
    carol1949 Member Posts: 562
    edited July 2010

    I also went through a time when I didn't sweat.  Now, I stopped taking the Femara after feeling like a 90 yr, old.  There are so many other ways to negate the bad estrogen in our bodies.  I just wasn't interested in the bad s/e's of the drugs.

    Lugol's iodine negates estrogen in our breast.  Also many other supplements.  Just do your research  and trust that the right information will come to you.

     I don't use antipersperant, though.  I use an organic deoderant w/ no parabens and no alluminum.

  • soundgirl
    soundgirl Member Posts: 14
    edited July 2010

    I also use an organic deoderant with no parabens or alluminum.  I will check out that iodine.   My estrogen is very low right now so I think that's causing a bunch of my issues. 

  • swimangel72
    swimangel72 Member Posts: 1,989
    edited July 2010

    Hi Soundgirl - I hope you get an answer to your question - I haven't been able to sweat as much as before either, but I blame it on the Herceptin. Did you have Herceptin for a year? Also - I'm confused with your signature line - if your tumor was over 6cm, and you had 1 lymph node involved, shouldn't it be Stage 3?

  • bluedahlia
    bluedahlia Member Posts: 6,944
    edited July 2010

    You might want to ask your doc about Peripheral Neuropathy.

    Symptoms of Autonomic Nerve Damage

    Symptoms of autonomic nerve damage are diverse and depend upon which organs or glands are affected.

    Autonomic neuropathy (autonomic nerve dysfunction) can become life threatening and may require emergency medical care in cases when breathing becomes impaired or when the heart begins beating irregularly. Common symptoms of autonomic nerve damage can include:

    # an inability to sweat normally (which may lead to heat intolerance)
    # a loss of bladder control (which may cause infection or incontinence)
    # an inability to control muscles that expand or contract blood vessels to maintain safe blood pressure levels.

    A loss of control over blood pressure can cause dizziness, lightheadedness, or even fainting when a person moves suddenly from a seated to a standing position (a condition known as postural or orthostatic hypotension).

    Toxins

    Toxins can also cause peripheral nerve damage. People who are exposed to heavy metals (arsenic, lead, mercury, thallium), industrial drugs, or environmental toxins frequently develop neuropathy.

    Certain anticancer drugs, anticonvulsants, antiviral agents, and antibiotics have side effects that can cause neuropathy secondary to drugs, thus limiting their long-term use.

  • soundgirl
    soundgirl Member Posts: 14
    edited July 2010

    Hi Swimangel,   At times my sweating does come back.  I didi have Herceptin for a year.   Is that a side effect? 

    Bluedalhia,   I have brought this up to my doctors but they suggest I am either dealing with anxiety or early chemo induced menopause.    So IDK.   Pretty scary.  

  • soundgirl
    soundgirl Member Posts: 14
    edited July 2010

    I think I fixed my diagnosis... :) Thanks for pointing that out.

  • Frankie_
    Frankie_ Member Posts: 422
    edited July 2010

    Interesting topic! I was just having this discussion with my mom when we were away on holidays. I recently read that having a 20 minute sauna/once weekly was good to release toxins from our bodies. I have NOT been able to sweat (release toxins) at ALL since being treated for bc (chemo/herceptin & rads) even in the steam sauna. Others in it were sweating with beads of sweat (their whole body). Me nadda, nothing, zip. Not one bead of sweat! This really concerns me alot. Prior to bc /treatments I was able to sweat. I m planning on having a discussion with my Onc about this.

    Frankie

  • soundgirl
    soundgirl Member Posts: 14
    edited July 2010

    Frankie,   Let me know if your Onc has an answer.   Mine didn't.    I have been out of treatment for a year and a half now and this just happened to me 6 weeks ago.   Prior to all of this I sweat very much! 

  • swimangel72
    swimangel72 Member Posts: 1,989
    edited July 2010

    Yes Frankie - Id be interested in what your Onc says too, especially since you also had Herceptin. Soundgirl - I don't know if the inability to sweat is a SE of Herceptin, I'm just grasping at straws. I'm glad to see your tumor size was less than 1cm though - THAT's good news! BlueDahlia - thanks for that interesting info - I did get neuropathy of my left arm during my chemo tx's (Navelbine and Herceptin) but it went away, or so I thought.I don't ever go in the Sauna at the gym I belong to - and due to the early stage lymphedema, I'm not allowed in hot tubs. My house has central a/c so I really don't suffer at all from heat.........but I wouldn't want to actually TEST my body at all - I'd be afraid of heat stroke!

  • Frankie_
    Frankie_ Member Posts: 422
    edited August 2010

    Hi ladies,

    I have not been able to see my Onc as of yet. When I see him next I will talk to him about this and I will report back here and share his thoughts.

    Frankie

  • Leah_S
    Leah_S Member Posts: 8,458
    edited August 2010

    After chemo (A/C and then taxol) I didn't sweat for over a year. I do now, though much less than before. I didn't have herceptin. What is interesting is that during that time I was peeing more than before, so I wonder if my body was trying to get rid of toxins via a different system.

    I also had peripheral neuropathy in my fingers and the bottom of my feet for almost a year after tx.

    Leah

  • Medigal
    Medigal Member Posts: 1,412
    edited August 2010

    What's the big deal about not sweating?  I don't ever recall sweating for any reason inmy life.  Even when I was having hot flushes with Arimidex I never had a sweat.  I have never had to use deodorants in my life since I don't sweat.  None even when I lived in the real South!  I never equated sweating as being a necessity for our bodies.  Maybe I should mention this to my regular doc next appt. I wonder where the toxins in my body go to.  Like the other poster, I urinate non-stop all day and even at night  so maybe this is "my" form of sweating.  Very interesting!

  • chainsawz
    chainsawz Member Posts: 3,473
    edited August 2010

    I'm not sure sweating is the whole problem for us, just an obvious change to our bodies.  Something has broken my thermostat and now I can't tolerate heat at all.  In this 108 degree desert heat, I get very overheated quickly and it sends me towards a heat stroke.  Sweat on the the skin helps cool it down and I just don't have that and my face turns purple.  I think one of these chemo cocktails broke my thermostat and my body can't regulate itself properly or maybe it's hormone related....who knows?  I just hope it doesn't last forever because staying in the a\c is no fun :>  

Categories