Patients Helping Patients®
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| The Ladies' Room For the specific issues faced by Women with MS. |
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#1
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Intimacy issues
Sex or walking.
Choose one. This seems to be my problem with being intimate with my partner. This is kind of embarrassing to talk about but as I am here "with the girls" I am just gonna say it: If my partner and I are, ahem, intimate, even if I am not very active at all (lucky me ) I may get spasms in my legs or loose feeling during AND I get completely fatigued (weak, wobbly, shaky, vibrating) legs after. Since I was thinking lately I might be going into a flare or whatever for the past weeks (as I have had a marked increase of most of my usual stuff/symptoms/crap including lots of spasticity. Like if I do anything I feel like I was run over by a truck while my muscles get stiffer and I get slower and slower )So my partner being extra special nice to me basically means that for the rest of the day I would actually need to rest to "recover" (which of course is not possible and so I drag my limp footed, spastic legged, tired, snail paced person to work, the store etc.) ![]() It just all seems wildly out of proportion with this kind of activity. Since I can't walk any distance without my cane and I am struggling anyway, but c'mon I was just laying there doing virtually nothing!!! ![]() Plus it seems kinda mean. Puts me off of sex because the consequences are just too high... Anybody else know what I'm talking about? ![]() Lynne
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*undiagnosed and just hangin' in there somehow* |
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#2
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Sorry, you are having trouble! I wonder if taking a Baclofen before sex might help? My husband has ED problems, so we haven't had sex in a while...
Sara |
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#3
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Thanks Sara for your help!
I am definitely going to the dr. this week anyway for baclofen (although I can't decide which is worse: the spasticity or the weakness. I am afraid baclofen will make me even more tired and weaker and might take away the support I am getting through the spasticity. Hmmmm...) I guess some things you just have to accept and move on. This whatever-illness-I-have (I am undiagnosed) has taken so much already, guess my sex life is just the next new thing. But I will just hope it will come and go... Best, Lynne
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*undiagnosed and just hangin' in there somehow* |
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#4
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Lynne - thanks for sharing your experience. So often people are not willing to discuss how symptoms affect their sex life.
There are times when I experience L'Hermittes, numbness, pain, and/or fatigue during sex - it can really take away from the moment (or, like you said, the entire day). My husband and I have tried new positions that are more comfortable or require less energy from me and that helps some. Good luck at the doctor - I hope you find out information that will help you feel inspired and strong. Warmly, Lisa |
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#5
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Thank you Lisa!
It helps me a lot that you relate and answered ![]() yes, I bet your right: a lot of folks may not feel comfortable talking about their symptoms and sex life. I think in general I am just sad and feeling so limited because having physical problems is hard enough on a relationship and sexuality is such an important part of of maintaining intimacy. I am hoping when this phase of fatigue and spasticity moves on things will get better too. (and until then I will be at least trying to get relief with baclofen) Quote:
Lynne
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*undiagnosed and just hangin' in there somehow* |
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#6
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Hi Lynne. I hope the Baclofen helps - please do keep us posted.
Warmly, Lisa
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Warm Regards, Lisa ______________________________ RRMS Dx 5/2006 | DOB 1977 | Copaxone |
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