In my 50 blogs to go post, I put out a call for any subjects I hadn’t written about and a reader suggested tackling the topic of sweating and myasthenia.
Here’s what I’ve found out: it’s a common discussion topic for people with myasthenia. Forum after forum comes up about this so you are not alone.
The neatest explanation I can find is that profuse sweating is one of the side effects of the medication you may take, mestinon.
This is far too much information, but why change the habit of a lifetime: I’ve always been a bit sweaty so it’s hard for me to tell the impact that mestinon has had. Both at work and in my spare time, I tend to run on high adrenalin and that’s normally enough to give me a rosy glow (and sweat patches).
I’ve always thought it was due to having a high metabolism – my core is usually ‘nuclear’ according to Elaine. But when reading about this, I do think it has become worse since starting medication. I say this as sometimes I can be doing absolutely nothing, free from any kind of stress, and be in a sweat. Others have commented that they get sweaty when they are pushing themselves too hard – the body trying to keep you cool in amongst all the effort.
I also recently read this Women’s Health article about why people sweat in different ways and it explains a bit of the biology behind why we’re all different.
One thing I have changed recently is the times I take mestinon. Like caffeine, I don’t take mestinon after 5pm as otherwise I have difficulty sleeping and, more relevant to this post, I am in a sweat for most of the night.
Another thing I try to do is carry a spare top and deodorant with me. When I’m feeling uncomfortably sticky, having a change with me is a great relief.
Does anyone else have any tips or insight to share?