Excessive head and face sweating
Posted , 301 users are following.
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.
29 likes, 808 replies
jill94630 gill22568
Posted
cindy102784 gill22568
Posted
I feel like I wrote this myself. I feel your pain. I too have hypothyroidism (controlled) and was just diagnosed with psoriatic arthritis . I've been told by 3 Drs to go on Estrogen which I can't take because I have fibercystic breast and was told by oncologist not to take estrogen. I'm desperate also I understand there is a surgery you can get but not sure I want to go to that extent but if can't find anything else will probably consider it.
Have you gotten any good suggestions?
becky66271 cindy102784
Posted
I feel your pain! I've been suffering with this sweating for years now. I also have thyroid disease (hypo) and PSA as well as Fibro, and Cervical Spinal Stenosis. I'm 47 years old and it sucks to have all this crap to deal with and sweating on top of it! But it's nice to know there are other people that can relate!
carencaren gill22568
Posted
jeanne70329 carencaren
Posted
ihavenonickname gill22568
Posted
This was like reading everything I had to say! ...right down to the thyroid, arthritis, and fibromyalgia ..lost my thyroid to cancer, have had juvenile rheumatoid arthritis for 54 years, and plain ole aggravating fibro.
I hate this dripping business! Feet just fine, underarms just fine, but my head turns on like a garden hose! I keep both my central air conditioning and my furnace at 69F. I run the AC in the car in the middle of winter 7,000 feet up when the Rocky Mountains are at -20F
I need help...once it starts it drips for an hour or more.
kind regards
judith
helene46251 gill22568
Posted
Hi Gill
I really feel your pain. I have suffered all my life from excessive sweating (particularly my hands) but the one saving grace, up until about 20 years ago, was that my head and face were bone dry - even in intense heat. At least other areas are a bit easier to hide! I've been a yoyo dieter all my life but, no matter how high or low my weight, it has made little difference to the heavy perspiration.
What stood out to me in your post is that you mentioned fibromyalgia. I too have been diagnosed with this, and it's since I've had it that the facial sweating has started! None of the several doctors I've seen about this condition has ever mentioned that it causes excessive sweating, so I did my own research and, bingo - it's a commonly-reported side effect of fibromyalgia.
OK, I know it doesn't help either of us with our embarrassing problem, at least it might explain your symptoms.
ihavenonickname helene46251
Posted
but I need the garden hose turned off...do I ask rheumy?
tinaj1962 gill22568
Posted
Hi Gill
I have had exactly the same problem all my life. I am now 53. I also have fibromyalgia. 2 years ago I heard about OXYBUTYNIN, the one I prefer is actually called DITROPAN This has totally transformed my life. PLEASE ask your gp to presctibe it, it is miaculous! I take one 2.5mg tabletevery morning BEFORE I even get out of bed and then 1 -3 more through the day. NO SWEATS AT ALL anymore! I have even holidayed in Turkey in July and all was fine - I did double the dose though. This drug is usually used for bladder control problems, not for sweating, BUT IT WORKS BRILLIANTLY. There are NO known side effects, except a dry mouth, but I always drink plenty of water anyway, even that is less of a problem now my body is used to it!
I CANNOT RECOMMEND THIS HIGHLY ENOUGH
My surgery did try a cheaper generic brand once, but for some reason it didn't work as well, so do ask for the one above - Ditropan.
I am sure it will help you as it did me and many others on here
ihavenonickname tinaj1962
Posted
crystalinabox gill22568
Posted
Hi. I have the same troubles as you. Have you tried DRYSOL ? It is a prescription liquid that is a super strong antiperspirant. I apply to my face all-over and my neck and also it can be used on scalp. I use it around my hairline. So now that I'm using regularly,i use it now just once a week for maintenance. It can be sensitive on the skin, so patch test a spot. It is amazing. I actually have been wearing makeup and it's so nice to be able to smile at someone and not wonder what they are thinkinging of me. I've heard it all.. embarrassing. Please try this. I hope it will help you as much as it did me!!! And oh yes. I still want to try Botox also.
ladybugtwo gill22568
Posted
What a relief finding others that suffer the same conditions. I live in the states - Wisconsin. My sweats began as normal menopausal symptoms at 52. I am now 62. At 55 I was diagnosed with stage 2 uterine and cervical cancer. I underwent a complete hysterectomy, chemo and radiation. Immediately after, all hell broke loose! It's been the most miserable 7 yrs of my life. Anything over 60 degrees sends me into extreme overheating and severe head and neck sweating. Even sitting still. For me, the heat feels as if it's internal. It takes forever to cool down, which acutally I never really do. My feet, ankles and fingers start to swell, and the head sweating is unbearable besided embarrassing. I cannot take HRT due to my cancer. I do take Lexapro (for depression) a diuretic for high blood pressure, adderral for PCCI (post chemo cognitive impairment) and lyrica for severe neuropathy caused by chemo. i have stopped meds to determine if they were the cause and nothing improved. I am desperate for relief! My doctors seem to shrug it off as just an inconvenience. Live a day in my heat! I'm at a loss where to turn next.
diana91800 ladybugtwo
Posted
diana91800
Posted
Let me finish, sorry - SHOWER I cannot take the meds some do because the dry mouth is unbearable. I have done botox to my head and relieves some.
Doctor look at me like - well don't know what to tell you. Read some of the other people's responses relative to meds.
Lyrica is supposed to help believe it or not but did not with me when he increased the dosage. I also take Lexapro. I also developed high blood pressure from this because of palpatations, etc. from these attacks of sweat. We go to very fancy events and I take a blow dryer and brush with me. I live in Miami - so no cold weather here except a few days here and there. In cold weather I do not have to wear warm clothese. Hang in there - we can do this!!! Diana
ihavenonickname diana91800
Posted
ladybugtwo diana91800
Posted
Maybe YOU can do this, Diana....but I'm turning into a puddle! HA! I could never live in FL. I do vacation at least once a year in FL and will be in Pompano Beach 2/28 - 3/15. I'm so miserable but wouldn't give it up for anything. My dilemma with my intense heat, is that it seems to begin internally. Then if the outside temp is anything over 60, or I see any sun, it's over. I could take a cold shower and wash my hair 3 x/day to no avail. Menopause hot flashes were sporadic. This is constant. Living in WI, we have extremely cold winters, and I wear flips every day, maybe a light jacket, and have to sleep with heat OFF! 62 maybe, ceiling fan blasting, and window wide open. I've actually been reduced to tears from misery and just wanting to crawl out of my skin!
Stella567 ladybugtwo
Posted
Hi ladybugtwo! This is my first post and I'm also from the states-Tennessee.I'm so glad I found this page. Your story sounds a lot like mine down to the same meds. No cancer that I know about yet. I'll be 50 and I have been having menopausal symptoms since I was 38. Guillain-Barre' Syndrome in 2012 and I feel like after everything I have been through this is an awful condition! It's right up there with anything else. Everybody wants heat and I have to have air or a fan circulating. My hair stays wet and I now have a rash I guess it's from the scalp staying so wet. I start wiping sweat as soon as I get out of the tub whether it's cool or warm. Can't wear makeup anymore, hair stays up and pinned off my neck. Even my bra had to go so I'm a hot mess pretty much from head to toe. I can't take HRT but I think it's so much more than that. This is turning out to be the biggest and most embarrassing problem and you are right the doctors do shrug it off. I'm going to see what I can find and if I find anything I will be sure and post!