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Indian dating with more relationships and no rocks around you looking for relationships. After describing my dating escapades to a friend one day, she asked me: Have you ever considered dating a man with MS? And I felt a bit irritated by the question because she seemed to offer it up as some kind of solution to my man problem, which it is definitely not. To my mind, meeting a man with MS seemed similar to meeting someone who shares the same interests one might have such as golf or wine-tasting.

That said, the notion of sharing a common disease seemed very freeing in a way, too. I was getting tired of making the MS speech to every man that thought he was interested in me, having to explain the disease and how it affects me, then waiting to be judged worthy dating material. Nice, but I would still face the same chemistry challenges that exist with any prospective boyfriend. I cannot, in all fairness, begrudge any able-bodied man his preferences, including not wanting to get involved with a chronically ill woman.

I feel intimidated and awkward around them.

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He was so big and powerful that his hugs squeezed the breath out of me and knocked me off balance. And I had to crane my neck to look up at him, which aggravated my herniated cervical disc. So I will not abandon my preference for shorter men. Recently I challenged myself even further.

After a protracted and difficult online communication with an able-bodied man on Match came to an end, I met a guy on the disabled site who has Cerebral Palsy.

He was genuine, appreciative, discreet, upbeat, smart and funny. He wrote that he wanted to meet me soon. We met for lunch at my favorite Lebanese restaurant.

Jake was just as genuine, smart, pleasant, and charming as he was in writing. We talked for a long time and found so much common ground, sharing similar online dating experiences with the able-bodied, sharing a developed sense of humor and upbeat attitude about being in the world.

At one point, Jake told me he had dated a woman with MS for two years. He expressed one gripe about the experience: It bothered him that she grieved over what she had lost, always talked about being free of disability one day, yearning for it, rather than accepting her limitations and doing her best with what she had. I told him that we all pretty much feel that way. It might have to do with the difference between CP and MS. Cerebral Palsy is diagnosed in infancy and is not progressive.

Multiple Sclerosis is acquired in adulthood, so the patient has memories of being able-bodied and recalls those traumatic events of disease onset, testing and diagnosis. We harbor anxiety about our future and what kind of decline we might be facing. These things do not encourage us to accept our lot. They give us hope that some day we will be free of it. It was the biggest challenge of all and the thing that did me in that day. His physical affectations made it very difficult for me to understand his speech.