watch me run…

ms1

I ran… the wind blew, the sweat started to drip, my breathing accelerated, and still I ran… I became a bullet train of MS glory… muhahahaha

okay… that isn’t me… and my distance my seem trivial to some, but to all you MSers out there, when I say I managed to beat my time on the 25 foot walk, it will mean something… when I first got sick, 25ft felt like miles… a marathon of pain… and then I had to sit down… and that was after I had bounced off the walls as I wobbled down the hall… and my time… HA… a lot embarrassed me back then… now I share everything… bladder issues, jumbled words, or loss of basic abilities… but at the time I wanted to cry… I felt like I needed to push harder, like people (even my dr) would look at me and think “She isn’t even trying… there’s nothing wrong with her!!!”

back then my 7+ seconds time was humiliating… as I grow with my MS, and accept more limits, and strive for goals, I am better equipped to handle the ups and downs… but this one, folks, was definitely an up… 2 seconds… point-5 seconds faster than my last time…  and what fancy foot wear did I don in preparation for my big run???

ms2

HA… no tennis shoes for this girl… I showed up for appointment with my comfy flip flops on my feet… but this 25ft walk (or in my case run) is serious business… lol… so I kicked them off… and my doc, well accustomed to my ways by now, told the little nurse in training to “back out of the way…. she really is gonna run” … lol… in my stance and off I went… it is the small accomplishments that help to balance out the crap… and that 25ft is now my favorite part of the neurologist’s office… that and my doc is funny… that is why I think she will totally appreciate my runners gear…

ms

I soooo need to find something like this… 😛 … day by day, highs and lows, I want everyone to keep shooting for those small moments… it can be anything… a good time on your 25ft walk, a day without headaches, making something that has been giving you trouble for years… each small moment gives hope … and, for me, usually a smile… because I am well aware that I am acting like a silly monger, but for once I am having fun with my MS… tracey

 

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