Excessive head and face sweating

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I am 63 and for the last 22 years have suffered with excessive sweating on my head and face, which seems to be getting worse.  This is uncomfortable and embarrassing.  If I do anything even slightly energetic (hoovering, ironing etc.) it is worse, and it takes a long time for me to cool down.  I was referred to a dermatologist who prescribed pills, which just dried up my eyes (red, sore and bloodshot within 30 mins) and mouth (making it impossible to eat or even speak).  She point blank refused to consider any other treatment, even telling me botox does not work for the face, which i know is untrue.  This condition, to other people, seems trivial but it is not.  In the summer I cannot go outside, so I can't even play with my grandchildren.  I certainly couldn't go out shopping or to a social event, the sweat drips off me and my hair is drenched within minutes.  I obviously cannot use make-up, or even have a decent hairstyle, which zaps the confidence.  I do have a thyroid problem but that is well controlled.  I am a little overweight but not much.  I have other non-related medical conditions (arthritis, fibromyalgia).  Has anyone any experience of the new gadget around which includes a mask for the face, plugged into a machine - sorry I can't remember the name of it.  I know they are very expensive but I am desperate.  Any helpful tips would be great.  Thank you. 

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  • Posted

    I started Oxybutynin 5mga week ago and I am so happy.  My sweating is now strictly in the normal range.  I did yard work today and had beads of sweat on my forehead, but I didn’t look like someone poured a bucket of water on me!  Normally My eyes would be burning from all the sweat .  I am dry when I’m working inside and I wake up with dry pjs and dry hair.  It feels so good!  The only side effect is a somewhat dry mouth, but it’s an easy fix, drink more water or chew gum!  Any of you who haven’t tried this, please do! You may have to tell your doctor that this is an off label use for this medication. Otherwise they’ll tell you the only treatment is a prescription antiperspirant or surgery. I had to tell mine, but he checked it out and then prescribed it!  I have a new life!
    • Posted

      Hi Jan,I have the same problem,I am going to ask my doctor about this medication.Thank you.
    • Posted

      Gonna ask my doc about the med you suggest an I wonder if anyone else feels warm when just sitting as well? I'm 48 an beginning to have to run to the bathroom to urinate.. My doc says premenopause, but after reading about others, it can't be just that.. I'm so glad I'm not alone in this..

    • Posted

      This is such a horrible problem. I tried the oxybutynin but had unbearable dry mouth and while it helped with scalp & facial sweating my face was so hot to touch and flushed. Maybe i should try taking half a pill and see how that works. I do take oxycodone for chronic arthritis pain but I can't do without it for my pain. It seems so futile. Thanks for your post.

    • Posted

      I have a 5 mg. tablet and 90% of the time I only take 1/2 tablet.  I have noticed that even when I don’t take any my sweating is reduced by 2/3.  I just pray it never stops working.  I’m able to work in the yard, take my grandsons to the park, go to festivals.  These are all things I couldn’t do before without being humiliated by my drenched face and hair.  I just keep a bottle of water and a pack of gum handy.  Good luck.
    • Posted

      AXLeenie, I don't have the urinary problem really but I am hot all the time even just sitting down. It's so bad that when it's cold out and I'm driving the window and windshield on the drivers side fog up from the heat radiating off of me. Has that ever happened to u? I can't believe how identical my symptoms are to yours and other here. I am glad that I'm not alone!!

  • Posted

    Hi, I get Probantheline or Probanthine(some Docs have it as), I take one or two tabs in the mornig, they work better on an empty tummy, so take before breakfast and give them 10 mins to start working before eating, thats what i have found, i sometimes have to take 3 tabs all depending how hot the weather is and how bad my sweats are, but when you first start taking them i advise 1-2 tabs to start with, they last for about 6 hours with me, sometimes only a couple of hours, all depends how many i take and how hot the weather is, but i cant live withought them now, they dry everything up tho, i can hardly open my mouth to speak if i take them and dont suck a sweet or something, i get gums off the Doc which are part sweet part salty and they do the trick nicely, the pills also leave a not very nice taste in your mouth so mints come in handy too, its a small price to pay for no more embarrassing situations outside, i will never really know why this happened but i do know it started when i had been sterilised in Hospital, the day after was when it started, for years the Doc's said they didnt know what started it and they wouldnt be able to fine out withought an operation to look at my ovaries etc, i wasnt going throu that, the Doc i was with for years and complained constatntly about the sweats, didnt even mention about Probantheline to me, it was my sons girlfriend that told me about them, she had the same problem and got them from her Doc,  i had to go and ask my Doc for them, i asked him why he didnt tell me about them and he just shrugged his shoulders, didnt get a proper answer, however i am so greatful to my sons girlfriend for telling me about them or i would still be sweating like a mad women, Hiperhydrosis is the name of what we have and the Doc didnt even tell me that, i had to look it all up for myself,  ihave been taking them for about 4 years now, and some days i have to take 2 twice, in the morning then again in the afternoon if its a hot day, which doesnt happen often at all tho, being in a country thats mostly cold is a benefit and i usually just take 1 or 2 tabs per day and i try not to take any at all if im not going out anywhere, and no vistors are coming round, these wee tiny tabs are a god-send and i would recommend them to anyone with this condition, because they work, they keep you dry and thats the important thing, im so glad im not on my own with this horrible problem, tho i do feel sorry for anyone that has it, its the most embarrassing horrible affliction to have, i ruined jewellery and jackets because of the sweats i had, the collars of jackets were ruined and although the jewellery was only costume jewellery i ruined lots of chains and necklaces, my hair was always dripping wet as was my face and neck,I had to take a face flannel with me everywhere and some days i need two it was so bad, the stares i used to get off people will haunt me forever, it was sooo embarrassing!, so i hope this works for you, give it a try anyway because you never know until you try it, i just wish they could do something a bit better so i didnt have the horrible taste in my mouth, it would be nice if they could cure it or put an implant in that lasted a year or two and didnt give you all the bad symptoms, ie horrible taste in mouth, dryness of mouth, etc, that would be ideal but i guess will never happen in my lifetime, at least i have something that works and the side effects are worth putting up with for being dry, so good-luck all you sweaty peeps, hope it helps.xAnne.

    • Posted

      Thank you so much. Mine started after I had one lobe of my thyroid removed and coming out of the anesthesia I was burning up. I went to a hyperhydrosis doctor years ago and he gave me a pill but it didn’t help. Not sure what it was. I will for sure ask my family doctor for this. Thank you sooooo much!
    • Posted

      Thanks so much Anne. I'm in the UK, but I'm sure we must have those tablets, or something similar. I do sympathise about the uncaring doctor. Mine told me, "Well, you'll just have to learn to live with it!"

    • Posted

      Hello, Like others, I am glad I am not the only one. Besides sweating like crazy just putting dishes in the dishwasher, I feel hot through the day just doing nothing. I am 48 an have to run to the bathroom to urinate so etimes an wondered if anyone else had these problems to..? I am going to ask my doc about the meds you mentioned. At this point, will try anything.
    • Posted

      Hi Anne,

      I was just wondering whether you have urinary symptoms from the probanthine. I had to stop taking them as they caused urinary retention (as well as the terrible dry mouth). For the first few days I was so happy as I thought I had found a cure but the discomfort in my bladder was too much to deal with. My condition (cranio-facial hyperhidrosis) started when i was 37 and having chemotherapy for breast cancer as well as my ovaries being removed the year after. It used to be limited to the summer months but the past couple of years.... since I turned 50 it affects me all year round. My social life is non existant and I am truly miserable.

    • Posted

      Anne, I don’t know if it is available in your country, but maybe you should try oxybutynin instead, it doesn’t taste bad and it works great!
  • Posted

    Hi Gill I have just found this website I am 63 and have the same condition as you,I've no idea what it is,its been going on for more than 20 yrs my hair is cut very short,I have Rheumatoid Arthritis which was confirmed 15yrs ago,I don't know anyone else who has this condition,can you advise me please.Thank you

  • Posted

    I am 53 and have suffered with excessive sweating on my head and face for most of my adult life, although it has been worse the last 20 years. I agree it is very uncomfortable and embarrassing. I can get ready in the morning and do my hair and make up and it can come on that fast in the matter of minutes. Its not Menopause. My hair is simply drenched within minutes of it coming on. and I feel cold and clammy. If I can get to a hair dryer and dry my hair, I can almost outsmart it and it stops,.. weird huh? besides carrying around a hair dryer...... any suggestions? Besides this, I have RA, FIBRO, Chrons, gastroparesis, diabetes and osteo arthritis.....
    • Posted

      oh and I have a thyroid condition also....

       

    • Posted

      Hi Dawn I'm the same,I have RA,and Sjorgrens syndrome just saw this site today I didn't know it was a condition just thought I was unlucky my hair is soaking wet several times a day yet the rest of me is cold and clammy its been going on for 20 yrs + I'm 63 its a relief to know it's not just me.

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