Dating someone who is paralyzed


Fatigue, pain, and spasms are my big problem, but I really try not to let it get in the way of anything I want to do. I have a high sex drive so I like to do it with my boyfriend as often as my body allows!How, if at all, has your disability affected the way you have sex?I've had lengthy conversations with men who are shocked that disabled people have the same sexual desires as them and have sex lives too.I recently spoke with a guy I was at school with and he confessed that he liked me at the time, but couldn't figure out how or if I could have sexual relationships.Like every other woman, I feel desire and arousal; my responses are the same.I guess they depend largely on what my partner and I are doing at the time! Woman A: Dysautonomia, which causes chronic fatigue, dehydration, fainting, and I also have an immune deficiency disease, which means I have a greater susceptibility to infections and a harder time than normal fighting them off. Woman D: I've had Ehlers-Danlos all my life, but it got a lot worse when I was 23.Woman C: Because of my specific disability, I have to be almost hyperaware of my physical body and specifically my heart rate at all times.



I think there is also an assumption that if you date someone with a disability, you will become their carer.My heart rate stays even and lower when I'm lying down, but my symptoms can vary day to day. Woman D: I have difficulty with penetration, which is linked to my pain. I also struggle with non-penetrative acts such as oral or mutual masturbation because my fingers are mostly unusable and my jaw dislocates.Having sex would have to be done very carefully with a considerate partner who fully understands the issues of the Ehlers-Danlos. Woman E: There are certain positions I can't stay in for long (e.g. I can't be restrained by my ankles either as I get random spasms and cramps. Has your disability impacted the way other people respond to you as a sexual person at all? The only visible part of my disability is my port scar on my collarbone and unless you're looking for it, it's hard to spot.As my pain worsened and I have become more limited, this isn't an option anymore. I am unable to do a lot of everyday things because of my pain, which I have a tendency to blame on my body.



Dating someone who is paralyzed comments


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