Excessive Sweating - face, neck and head
Posted , 14 users are following.
I have the symptoms of Polysysticovaries with the excessive hair, sweating, weight and so on, but the only thing that I can't hide is the sweating. When i dry my hair i have to dry it again and again as my head just drips in sweat. I can walk up a flight of stairs and sit at my desk at work and there I go again - drenched in sweat with frizzy hair! I'm a bigger girl but i'm not unfit. When working out i will look like i've been swimming after only 5 minutes of entering the gym. I've been put on Clonidine in the past which helped for a while, and now i've been put on beta-blockers to try. I've had my thyroid tested and this has come back ok. I'm being treated for PCOS even though all tests say that i haven't got it, but doctors think i must have because i have all of the symptoms. What else could it be and can I do anything to prevent it as it's getting me down!! Thanks
6 likes, 23 replies
betsy422 avic12
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eva96035 avic12
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but over the past two years it's been horrible I take meds for the following, thyroid, blood pressure, gout, IBS, osteoarthritis, cholesterol, and I'm on a hormone patch, I had a hysterectomy back in 2011 but my blood work is pretty much normal. I don't know if it's a combination of the meds I take or if I need to see a doctor for just the sweating alone...
Has anyone got any ideas on what I need to do next?
eva96035 avic12
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Have you got any suggestions what I should do next?
pamela14511 eva96035
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I absolutely can feel your struggle. I can be doing nothing except standing in A-line or sitting at home and sweat will be runningI can be doing nothing except standing in A-line or sitting at home and sweat will be running down my faceIn my hair looks like I just got out of the shower because it is so wet
anne42438 avic12
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eva96035 anne42438
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to the medicine I take combined. I even tried separating the meds somewhat... For the most part this happens to me at work more than at home but where I work I'm not constantly moving or anything, I can be sitting in a chair and just feeding one of my patients and start sweating like I'm starting a workout so I just don't know anymore what to do or where to start... Any suggestions?
sheryl37154 anne42438
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anne42438 eva96035
Posted
pamela14511 anne42438
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I am so thankful for your post I'm going to talk to my doctor about this because I along with you know the embarrassment of sweat dripping Off my face and down my neck always trying to explain it away as hot flashes. Thank you again
eva96035 avic12
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sheryl37154 avic12
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2002 winter, having lunch with senior work colleagues, started 'spurting' from my face and head. Surreptitiously trying to mop up with the dark navy blue paper napkin. Another woman asked loudly across the table, are you ok? I was wondering if the dye had turned my face blue. It had not, but my distress was obvious despite trying to be discrete about it. They all turned and looked at me - ahh, hot flashes!
However, it should not have been as I was happily on hrt (oestrogen pellet implants at the time). For 6 years I suffered this. Coincidently I had been prescribed a strong pain medication for oesto-necrosis caused by haemochromatosis brought on by my full hysterectomy. Must be the medication, they said, so asap I went off the medication. Rather have pain than this severe sweating condition. No change.
You all know it, sweat dripping off the eyelashes, etc, hair constantly wet from sweat or ducking it under the shower, waking up with smelly sweaty hair during the night - back under the shower. Sweat pooling down my front and back. Trying to put on makeup, because I am vain, was impossible.
Finally, after 6 years, decided to investigate botox and went to a gp who did botox to see if she could help me. First, she said, I want to find out what is going wrong. Yippee, me too! Referred to an endocrinologist, hormones tested, excess prolactin, extremely rapid heartbeat, mri confirmed a microadenoma of the pituitary gland.
When I finally started carbergoline, there was almost immediate relief. I searched further and found that women with excess prolactin need extra oestrogen (whether in menopause or not) as it causes the oestrogen to be ineffective thus thrusting us into menopausal symptoms, and bone thinning problems. It can all manifest differently for some, but for me it was severe head sweats - constant and permanent hot flashes.
7.5 years I am still taking carberglone because everytime I try to reduce it, the symptoms come back again. Endocrinologist believes taking carbergoline long term is not going cause any harm, thank goodness.
However last year, I tried a different hormone which failed to work but it took a few months to figure that out, because the temperature was very hot, thus excusing the head sweats, and haemochromatosis symptoms are similar to menopause. Now, it seems to have opened the flood gates again, my prolactin is low, and there appears to be no obvious reason for it. I am sure there is one - just got to make the drs work harder.
I have tried No More Sweat on face and neck, messy on hair of course, to no avail. Currently I use 3B Face Saver which allows me to put on some makeup for a little while.
But my message is, ask for your pituitary gland hormones to be tested, and even try to find if there is a neurological or hypothalamus problem, if possible. That is what I feel could be a cause, just got to find someone who is interested and knowledgable enough to look.
Anne, I don't know how you lasted that long. I am sure I would have gone crazy if a solution had not been found for me. Sounds woosy, but it is very delibitating, soul destroying and stressful on relationships.
I have read there is a microwave/laser? therapy but only available for armpits. I suppose we don't want our head to be microwaved, do we. Miradry, I think. I have not come across Pro-Bantheline, so I will check that out. Also recently heard of Escitalopram but I don't know enough about it yet.
I hope someone gets some relief from my diagnosis.
sheryl37154
Posted
I note that Pro-Bantheline sounds like it is very mucas drying, e.g. eyes, constipation, probably other areas that we need to keep moist. Hopefully the dry mouth effect will make us drink more water to offset it.
Anne, what is your experience in that department?
I also like the idea that it is an anti-spasmodic of the gut - I suffer a lot from that, ever since the hysterectomy. Deemed to be from adhesions.
sharonrf sheryl37154
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sheryl37154 sharonrf
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At the time of my diagnosis, and finding that women with a prolactinoma need extra oestrogen, I found a wikipedia description that says that 5 alpha-reductase enzyme was responsible for the ineffectiveness of my oestrogen (caused by excess prolactin). I had printed it off and took it with me on a visit to my gp (she was not responsible for helping me find a solution - the botox dr did). My gp asked if she could have the copy - sure, I can print off another one.
When I eventually got around to doing so, I could not find it again on Wikipedia. It was referred to as affecting testosterone, but not oestrogen. Strange. My endocrinologist was amazed that I knew about it. He thought I must have medical quals, but no, just desperate research skills.
Good luck for Friday.
pamela14511 sheryl37154
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I am new to this forum but I just wanna thank you because I no longer feel like I'm the only one struggling with this Condition of had and face sweat.
pamela14511 sharonrf
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I could not agree more it is so embarrassing when you have to carry a washcloth with you and hope and pray you can find some kind of air circulating. If I could carry a fan with me everywhere I go I would. I don't even bother with makeup anymore because it is such a waste of time I'm just going to sweat itAway.