Why I Decided to Join the A-Team (Millennials, Look It Up!) — Part 1

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by John Connor |

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heat, quiet, hotel, covid-19

First in a two-part series.

Do I give in or fight?

I’d had all the tests, and in the summer of 2009, my fears were confirmed: I had MS. My first question was, “Would I end up in a wheelchair?” My neurologist, who must have given the answer innumerable times, said it might happen — no one could know. I’m sure the real answer was, “Probably. It doesn’t happen to everyone; hopefully, it won’t for you.”

Several years later, another neurologist who had previously treated me saw me relying on a walking stick and, while breezily walking past, declared, “We’ll have you back walking properly in no time.” Pep talk. False hope. Well, why the hell not?

Then, in February of last year, the probable happened, and I slowly ground to a halt.

It took a while for me to accept it, but the power of the will gets sapped when evacuation of the bowels meets slapstick!

Because of the cocktail of drugs I was then on, I’d have only seconds of warning before an explosion. I’d sensibly taken to wearing adult diapers. I was downstairs and attempting to get into the nearest toilet, which unfortunately required clambering down two steps. I failed on both counts!

Unluckily for my family, they were all in.

I’d fallen in the tight space of a narrow toilet, and also exuded the intense odor of parfum de pigsty.

Working as a team, we managed to get me up and onto the toilet. It took at least an hour. I remember clinging to the rim of the toilet bowl and lifting with all my might, like I was on some kind of survival course.

The laughter was intense. It was either that or cry.

Enter, the wheelchair-accessible van

Walking was no longer an option. If I wasn’t fatigued, I could still stand. Getting in and out of a car was incredibly tiring, so it was time to look for a new vehicle.

We hit upon a trilogy of solutions: an electric wheelchair, adaption of our house so that I could get in and out, and a wheelchair-accessible vehicle.

We started looking at vans with ramps. Then my wife suggested we future-proof the whole enterprise and get something that I could still drive, and even get into on my own.

The closest I’ll ever get to being in the A-Team. (Photo by Jane Davies)

Enter a van with its own liftgate. It wasn’t the A-Team van, but it was as close as I would ever get.

After over a year of dithering, it finally turned up.

Next week: The synchronicity of bureaucracy and the family outing.

Anyone want a lift? (Photo by Jack Connor)


Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to multiple sclerosis.


Hayley Cameron avatar

Hayley Cameron

Hi John
Just want to let you know that I really enjoy reading your column.
Thanks for adding some light and laughter,

Gale Langseth Vester avatar

Gale Langseth Vester


Having MS really brings the question 'Is it easier to start laughing or crying?' to the fore. The answer, as far as I've worked out, is, 'Don't be choosy, as there's no reason that someone can't do both at once.' This is likely a scenario in which not choosing is the only option.

Enjoying your column very much and wishing you all you need.


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