Showing posts with label sensation. Show all posts
Showing posts with label sensation. Show all posts

May 13, 2010

MS and lust, lethargy and lipgloss

Okay, I'll admit it.  I'm a fifty-one year old who has rediscovered the joys of lust after a long marriage where sex was the only medium used to indicate displeasure (unfortunately, ex didn't get that message). Let's just say it was a bit sparse near the end, say the last five years or so. (or 10)

One of the best best things about leaving my marriage was meeting a lovely man that taught me that it wasn't ME that couldn't respond, didn't like touch, etc.  It was the situation that cooled me off. I was overwhelmed with joy and sensation and still love the guy, years later, though he is no longer part of my life.

So I find it terribly unfair that MS has sucked away my sensations in certain, ahem, key areas. Not that it has slowed me down. I argue to my friends that I am so fatigued from the MS that there comes a point on a date where it is just easier to lie down and do something that doesn't require much chat. It passes the time, remains fun, provides physical activity, I don't have to be witty, and the men seem to like it.

It's a bit dangerous, though, as it becomes my fallback position (as it were) when I am tired at the end of the evening. When I was dating more, I'd go out for dinner, say, go for a walk, wander about, then feel, really, I HAD to lie down right away.  Y'all with MS know this feeling.

The men - well, they were only too happy to keep me company. Add to that my main sensations left are located in my lips, and after a few kisses, well, life became rather scandalous pretty quickly.

But, I reasoned, if I don't use it, I might lose it. And, like eating chocolate when I knew diabetes was pending, I felt I should pack in as much as I could before the boom fell and I wouldn't be able to enjoy it any more. Well, they do say MS impairs some cognitive functions, too...

Alas, even using it hasn't helped me not lose it. MS marches on, and now I am a seriously lascivious woman trapped in a body with seriously impaired sensation. I tried to tell my neuro about it and had to revisit it a lot before he (always he, always he) would listen.  I'll just bet if I'd been a man and told him I couldn't get it up, he'd have been all over it with ideas.  But it remains that women lacking sensation is still deemed rather unimportant, despite so many studies talking about how sexuality is essential for intimate relationships, self-esteem, bonding, etc.

I'm still interested, and thank heavens I am in a relationship now with a kind, loving man who seems willing to explore options, but the fact remains there are times when I can't feel him touch me. And no matter how aroused my mind may be, if I can't sense his touch, my body doesn't respond. It's frustrating. I miss that thrill of neurons firing up and down my spine and tickling my lust centre. I miss the feeling of an aroused body. I miss the increasing heartbeat, the warmth speeding to the skin, the hairs raising. It often doesn't happen, and it's definitely not his fault.

It's tempting to give up, but I've never been a quitter...and I'm not quite ready to retreat to memories of my explorations.
But I've had to give up chocolate.
Unfair.

April 26, 2010

Pain and sensation and all that jazz

They're finding out all sorts of new things about how we actually sense pain and temperature and all of that - the link above talks about researching the cold and heat pathways (which apparently are separate and involve key proteins of some sort).  I'm having a foggy foggy day today after trying to help out at the MS Walk yesterday so took three times through the article and still don't get it quite, but feel free to explore on your own. The key thing is that the cold/hot sensors which prevent us from burning ourselves are regulated from the spinal column..
What I still puzzle about is why the patchy sensation I feel - the places where I can feel touch but the places next to them where I cannot - why I can feel coolness, but pin pricks and injuries are unnoticed. While this is helpful when I chop off different parts of my fingers whenever I make salad (added protein?), I do wonder about the variability in sensation that is part of MS. Any ideas out there?

June 23, 2009

But what about sex?

Woke this morning thinking about love and lust and all those things that make the world go 'round and the birds sing their throats out in my backyard. And got to chuckling about what the MS clinic had to say about it all. I told them that I was lacking sensation, and that as a young 50 gal, this was leading me to some frustration...
So, here was their suggestion. "Some people find that if they put a bag of frozen peas on the area for a few minutes beforehand (as it were), the sensation gets better..."
OMG. So, so here you are, in amongst the awkwardness of dating sex, where you are trying to undress without revealing too many stretch marks or that unwise tattoo or the fungal toenail or whatever body imperfection is playing with your head that day (I remember obsessing for a week about my short toes, for example), AND you are trying to get socks off without bending into an unattractive pretzel, all the while trying to keep the sexual tension high because let's face it, over 50 guys need that....
And now you are supposed to excuse yourself for a minute, race to the freezer, and put frozen food on your groin, all while "maintaining the moment"?
The mind boggles.

Hmm. Maybe Cool Whip.....