me again from downunder.
Just asking if anybody has the same symptoms, I get weak and I sweat, drip down my back my hair gets wet i feel like everybody is looking at me its terrible. any suggestions.?
me again from downunder.
Just asking if anybody has the same symptoms, I get weak and I sweat, drip down my back my hair gets wet i feel like everybody is looking at me its terrible. any suggestions.?
I sweat from the back of my head and neck from over exertion and excessive heat. Crushing fatigue and night sweats are symptoms of a flare for me.
Pete
dx 1/11
"Every day is a good day. Some are better than others." - unknown
"Take your meds as directed and live your life as fully as you can." - Michael Chacey, MD
You could be flaring. I report all symptoms to my doc.
Phil Berggren, dx 2003
I have those symptoms a lot but for me it means a hypglycemic episode since I have diabetes and that makes my blood glucose levels jump around. I think pred might cause some similar symptoms but there can be other causes and should be checked out so they can figure out most likely cause and recommend some appropriate treatment or plan to prevent those episodes.
Last edited by drz; 09-14-2012 at 11:58 PM.
I sweat really badly from my hair/back of head when I'm out n about, like when shopping etc. Not really from over exertion but just moving around. It's horrible and I feel like everyone is just looking at me. The moonface doesn't help make me feel any better either :/
For me, I think the sweating is down to preds. I am on 40 mg at the moment and I remember last time I was on preds I had similar problems, it's a bit like hot flushes you might experience when going thru menopause or something.
I remember some of those when I was in Nursing Home and on higher dosage of prednisone. A couple times the staff had to change my bedding and night clothes since they were drenched like I had spilled water on myself. The feeling of being way too hot and way too cold also happened at times back then and I could go from having no bed covers to asking for heated blankets to warm me up. Ah, the joys of Wegener's and side effects from the treatment. Good times?--nope, but it is great to now be able to look back at them and be thankful some things have changed for the better.
yep thats it the same isnt it terrible
Check the side effects for your meds. I'm guessing some of them will have sweating as a side effect. I think about 7 of my drugs have sweating as a side effect. Yeah, I sweat a lot.... There are times when I'm in a social environment where I don't want to sweat, so I will actually put anti-persperiant on my head and face (really stings when it gets in your eyes). I have also switched out all of my shirts for dri-fit nylon polos.....
Wegener's (GPA )- Apr10, Granulomatous Hypophysitis - Apr10, Diaphragmatic Paralysis - Feb16, Bradycardia - Dec16, Fibromyalgia - 2017, Hypoparathyroidism - 2017. (my story)
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I sweat constantly unless I am doing nothing - it's so disgusting.
I don't sweat at night though, but if I am out or working I am sweating...
Lots of hairspray and a good backcombing.
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