The Glass is Half-Full

Okay all of you 'struggling to stand' or 'not wanting to have to use a wheelchair' or others that look upon using a wheelchair as a symbol of failure, you're about to get punched. Punched in the figurative sense. I am about to go on my soap box and my Irish is up which means that I'm fairly peeved (though I've been mulling this over for awhile so I'm not as angry as I once was, which means there will be fewer expletives and a kinder tone). If you've read this blog or know me at all, you know that I did not go easily into using a wheelchair as my primary mode of transport. I too, may have had a little bit of your attitude about the wheelchair being sign of failure or of having given up. My sister, Kerri, helped put it in a different light. She said, and I'm paraphrasing here, "It's actually an energy saver since walking is stressful and you're worried about falling - using a wheelchair will take away a lot of that stress. You will hav

  Years ago as a freelance writer, I submitted an essay entitled "The I'll Nevers of Parenting". It was a list, mostly, of things I had said prior to having children and the crow I was then eating because of the stupidity of the claims. You know little pearls of 'wisdom' that only someone who hasn't experienced the joys of  parenting could utter, like: I will never yell at my child in public or I will never let my child eat dinner in front of the television or my children will never stay up past 9 pm. I yelled at my children (usually when we were both tired and totally irrational!) in public. One time, as we were in the drop off lane at school with a long line of cars behind us, the boys hoped out of the car but Delaney was insisting on something that for the life of me I cannot recall and I was insisting that she get out of the van. We crept along, van door still open, until I got to the end of the line and yelled at the top of my voice, "Delaney get the

I have been living with MS since 1992 - I used the calculator on my phone to determine that it's 29 years (because unlike the man pictured above my math skills are lacking). That's a long time and you don't need to be mathematically inclined to come to that conclusion. And when first diagnosed, my neurologist declared that with all the research he believed a cure was imminent likely 'within five years'. that would mean that we would have had the cure 24 years ago. We don't. So I am grateful I didn't wager any money on Dr. Wiley's prediction.  But what we do have, instead of a cure, is a plethora of pharmaceuticals to help stem this disease's progression and help us live fuller lives, longer. I am happy for that but am also curious and a tad skeptical because these drugs cost a person living with MS a lot of money and pharma has no financial incentive to search for the cure when they can keep us living less gimpy lives for many years reliant on their