I'm hard at work on a book about MS and intimate relationships. It's been an interesting process.
I've been to our excellent local sex shop, Venus Envy Halifax, and interviewed the funny, smart and wonderful Kayleigh Trace, who provides sex education through the shop and advocacy everywhere.
I've wandered the aisles of hardware stores, looking for things shy men could pick up to spice up their sex lives. I've done the same at Dollar stores and pet stores, I've cruised so many websites, looking at furniture and various equipment and ideas and such.
I have to say I have NOT gone to porn sites. I personally find porn boring and degrading, so I asked someone else to do that research for me. He's got a background in that stuff, so can judge better. I always find myself wincing or giggling.
I've read every sex and intimacy related book in the Halifax Library system. There are a lot. My favourite is A Tired Woman's Guide to Passionate Sex, by Laurie Mintz, because even the title sounds right.
I've done the same with MS related books. Fewer of them, and more focused on things like taking meds to control pee, or helpful advice like "Talk to your partner". Oh, and full of grim info on what can happen with MS and such as it progresses. Not cheery reading for me.
I even started a survey on Survey monkey about what people wanted to know, about challenges they had, etc. Belatedly, I added a second survey for partners, because I want to know what they want, too. Being as how good relationships often require partners....
But I need more responses. I've had over 100 responses to the MS-ers survey, and I would love to have more to the partner's half. Could I ask you to circulate this to your contacts and partners?
Partner survey
Oh, and another question - regarding illustrations. I don't have the budget to hire actors to pose in sexual positions for me, and trust me you don't want me in the book, so I was going to either use:
a. Wooden dolls
b. Needle felted dolls
to show positioning. What do you think? All comments welcome.
Here's one of my needle felted dolls (dressed) for perspective:
A blog about living with MS. Why Mad Sow? In homage to Denny Crane, on the TV program Boston Legal. Every time he forgot something, he'd point to his head and say "Mad Cow." I refer to my MS, primarily a cognitive thing at present, as my Mad Sow.
Showing posts with label relationships. Show all posts
Showing posts with label relationships. Show all posts
January 22, 2013
Impaired social cognition in multiple sclerosis
http://www.ncbi.nlm.nih.gov/pubmed/23315621
Oh goodie.
Oh goodie.
As if it weren't enough that our bodies turn on us and make us dependent, and our minds lose things and start storing socks in the freezer and ice cream in the hall cupboard, it appears that we lose the ability to interact appropriately with the people around us, often the very people we need to keep us from falling apart.
This study looked at how people with MS responded to a film of four people sitting around a dinner table having a discussion. At various points in the movie, it is stopped and the patient is asked to identify the emotion being expressed by the person at the table.
Apparently we don't do so well at that.
Like autistic people...we seem to lose the ability to read people's faces appropriately, which might account for a few mixed experiences I've had lately.
Of course, this study also gives us an excuse for misunderstanding people. We can just trot out the statement, "Remember - we MSers fail the MASC! You have to tell me what you are thinking!"
Finally, a reason to have real discussions, instead of being expected to read minds.
Huzzah!
July 15, 2012
A Helpful Book
As a youngish and dating woman with MS, one of the things that has filled me with the most despair over the past several years is my loss of sensation in the...ahem...sexual areas. I consulted with my docs, whose recommendation was to place a bag of frozen peas over the...ahem...area in question and that that would help me feel increased sensation.
Well, I dunno about you guys, but frozen anything DOWN there doesn't sound too enchanting for me or the fellah involved. As one friend said, it's like going swimming in the Atlantic Ocean - cold at first, but okay once you're in...
Yikes.
Now, other than developing a jaundiced eye whenever I see a bag of frozen peas in the market, I haven't had much success with that advice. A friend of mine (who works with people with disabilities and their sexual health) and I got to talking. What if we combined the power of her knowledge of everything sexual and battery operated, and my nursing knowledge and the experience of someone living with MS, and we put together a helpful book?
Not a deadly boring one, but a light, useful one, with advice and drawings and some laughter and fun. That. we figured, could be a help to other people like me.
After all, MS is being diagnosed earlier and earlier, and it sounds gruesome to be sentenced to years and years without any idea of how to have a rewarding sex life. We deserve one, no?
But maybe that isn't what's needed. So we thought we'd ask you. In a short little survey, with no chance we can identify you, compiled on machines somewhere in the deep dungeons of the internet, impossible to trace. Well, maybe not completely impossible to trace, but I've got better things to do than find you. There are all those other frozen veggies to experiment with...
Here's the Blurb:
Dorothyanne Brown, a person with MS, nurse, and epidemiologist, and her
writing partner Karen Kalinowski, a Natural Health Consultant and Sex and Kink Awareness Educator, are collaborating to create a resource for people with MS and their partners about sexual intimacy.
We've created a short survey, ten questions, to get a feeling for what your
needs are as a person with MS or a partner of a person with MS.
The survey is completely anonymous. We have no way to figure out who answers
it, we plan no cross linkage to any database or physician services.
It will help us create a resource that will be most useful to you.
Just click on this link and you will be taken to the survey:
http://www.surveymonkey.com/s/LSLN9XN
Please share widely with others with MS or their partners. Help us create a resource that will work for you.
Questions? respond here or email msandintimacy@gmail.com
And thanks!
Well, I dunno about you guys, but frozen anything DOWN there doesn't sound too enchanting for me or the fellah involved. As one friend said, it's like going swimming in the Atlantic Ocean - cold at first, but okay once you're in...
Yikes.
Now, other than developing a jaundiced eye whenever I see a bag of frozen peas in the market, I haven't had much success with that advice. A friend of mine (who works with people with disabilities and their sexual health) and I got to talking. What if we combined the power of her knowledge of everything sexual and battery operated, and my nursing knowledge and the experience of someone living with MS, and we put together a helpful book?
Not a deadly boring one, but a light, useful one, with advice and drawings and some laughter and fun. That. we figured, could be a help to other people like me.
After all, MS is being diagnosed earlier and earlier, and it sounds gruesome to be sentenced to years and years without any idea of how to have a rewarding sex life. We deserve one, no?
But maybe that isn't what's needed. So we thought we'd ask you. In a short little survey, with no chance we can identify you, compiled on machines somewhere in the deep dungeons of the internet, impossible to trace. Well, maybe not completely impossible to trace, but I've got better things to do than find you. There are all those other frozen veggies to experiment with...
Here's the Blurb:
Dorothyanne Brown, a person with MS, nurse, and epidemiologist, and her
writing partner Karen Kalinowski, a Natural Health Consultant and Sex and Kink Awareness Educator, are collaborating to create a resource for people with MS and their partners about sexual intimacy.
We've created a short survey, ten questions, to get a feeling for what your
needs are as a person with MS or a partner of a person with MS.
The survey is completely anonymous. We have no way to figure out who answers
it, we plan no cross linkage to any database or physician services.
It will help us create a resource that will be most useful to you.
Just click on this link and you will be taken to the survey:
http://www.surveymonkey.com/s/LSLN9XN
Please share widely with others with MS or their partners. Help us create a resource that will work for you.
Questions? respond here or email msandintimacy@gmail.com
And thanks!
December 31, 2009
Love, romance, and the eternal doubt of life with MS
It's all very twee, isn't it? The whole vision of love and romance and walking through a landscape filled with hearts and flowers, babbling brooks, sunlight, and sweetly chirping birdies to add music....Well, I've always had a hard time believing all that - typical first love broke my heart thing. And, as an overweight, very short gal, I've spent quite a bit of my life feeling unloveable. Having MS for years and not knowing it made me feel even more unworthy - tired all the time, cranky when I was too tired to think, numbing and filled with pain in alternates.
Add to that the full MS cover. Now it becomes almost impossible to think that anyone would ever want to be around me for more than a short time, for more than a quick roll in the hay, for more than the good times. Who in this big world would be willing to take on a moody with MS, falling apart lass, who has difficulty with everyday tasks and regularly forgets things on the stove? Who will probably get worse and worse and worse?
I mean, I can be brazen and tough it out, tell myself I am good on my own, be more fiercely independent than ever. I can wear my push up bras and mock men for their attention to silly things such as breasts, I can educate myself and fool myself that I am perhaps alone because I am too smart, I can push away everyone who tries to get through the armour.
I do all of this, deny my need for support, contact, affection, touch, love.
Because I know there are storm clouds beyond the sunny meadow, and I don't want to inflict those on anyone. Not even a dog.
It makes me unwilling to trust in love, to let myself fall into it, to accept it when given. Like the rest of my life, which has become undependable, I figure it's a wobbly thing, given to short-circuiting like my fraying nerves. And who knows? Perhaps I have a lesion on my "accepting love" gyrus or something.
It would take a very patient, persistent, and kind man to lead me down the meadow past the hearts. I'm balky.
I may, may have found just such a man. Fearfully, I take a step into the warmth...
Subscribe to:
Posts (Atom)


