May 11

I miss my body

Posted by: Michelle

I miss my 20-year old, pre Multiple Sclerosis body. This was my thought while walking the second half of my morning run today. I’m not prone to whining. But heck, if I can’t vent in a blog, where else can I do it. I’m not talking about the way my body looks. I’m okay with the exterior (and posterior) of my 41-year old self. Nope. It’s the inside stuff that needs a facelift. It’s downright saggy. And because I have MS, it’s hard for me to determine if my digestive, breathing, and muscle weakness problems are caused by the disease or just the natural aging process. The fact is it doesn’t really matter. There’s not much I can do about MS or being over 40, except exactly what I’m doing. Eat right (my big downfall), exercise, and keep my stress levels low.

But the reason I run has always been less for my health and more for the way it makes me feel…which used to be good. Now it’s a little like gambling. I still bet each time I go out that I’ll catch a little glimpse of that athlete and connect with that effortless motion akin to my childhood dreams of being able to fly. Today, I couldn’t get off the ground. And maybe tomorrow will be the same. But, if I keep trying, I believe I’ll get there again. I always say that my health is where it needs to be when I can run 5 miles. Right now, I’m running downhill 1.5 and walking the remaining 1.5 back home.

That said, there’s always something good about being out. Everything’s in bloom right now in Boulder. You have to love purple and fuchsia blossomed trees. It’s like something out of a Dr. Seuss book. The Boulder Creek is also running fast. Makes a nice soundtrack with the beat of my feet. Complements the new Counting Crows playing through my iPod Shuffle. And hard as the run was, it still beats sitting in this office typing. I feel cleansed and awake. Because with running, there is an afterglow. So for now, I’ll stop my whining and bask in it for a while. Thanks for listening.
–Michelle

Published in: Michelle's Blog
  1. jillmlong Said,

    Hey Michelle–the fact that you are going out there and doing it–is HUGE. Keep it up and the glimmer of your former self will catch up from time to time. After reading your blog, I wonder what my excuse is not to go play! Now whenever I waiver on even the opportunity to go–I’ll remember your words for my green light.

  2. dlovejoy Said,

    Michelle, you have my empathies, and I so commend you for getting out there and enjoying the beautiful aspects. I’m a competitive triathlete with a history of chronic fatigue and a challenging case of psoriasis (which compromises the immune system further). My sporting life is full of highs and lows; sometimes I can’t get my body to move or have strength. But, I keep doing it.
    I do believe there’s an “up” cycle in your future. If you keep listening to your body, and keep the movement going, it can only strengthen you!

  3. becca Said,

    Can you bike? I am torn up in lots of joints but I can bike, which I have come to love. You are so lucky to live in Boulder. I would love to live anywhere in the Rockies. It is my dream for myself when I grow up. I am 46.

  4. kathyp Said,

    keep doing all you can, I have ms as well but find the more active i am the better i feel, both mentally and physically

  5. Michelle Said,

    Wow. Ya’ll are so great with all your encouragement. Good news is that I’m running the 3 miles on good days now. Still searching for the magic 5! To answer Becca, I’m not a biker or a skier…those are about the only two things I don’t do. I’m keeping sports like swimming in my back pocket for when my knees give out :-)

  6. sarahengle Said,

    MIchelle,

    I was diagnosed with MS nine years ago after having a seizure in the middle of the night that freaked my husband out so bad he had trouble sleeping for the next year and a half. I was not a very active person at the time, and with the diagnosis I just became depressed. I was on Avonex and anti-seizure medication for a year and a half after the seizure. I went off of all of the drugs to have my son, who is five now. I felt so good being off of the medication and since I did not relasp after my pregnancy the doctors didn’t insist that I go back on them. I am very active now, but everytime I had the least little thing I panicked that it was the MS. Sometimes good things come from bad. Last year I had some trouble with my eyesight. My vision got so blurry I couldn’t see for about a half hour. I rushed to the emergency room panicking that this was a symptom of the MS. After many tests and a visit to my neurologist he looked at my MRI results and told me that he no longer thinks I have MS and the problems with my eyesight were due to a retinal migraine (which is fairly common). I still have leisions on my brain but they don’t really know what caused them and they are not multipling. The news had a unique effect on me, I hadn’t realized the motivation I drew from having the MS diagnosis in the back of my mind all those years. It is supernatural. But I also don’t need to panick anymore when I am unusually fatigued, either. Take the good you can draw from your experience and don’t dwell on the negative part it serves no purpose. You never know, one day they may tell you your healthy and fine, just tired!

    Sarah

  7. curlyag Said,

    Hi, Michelle–
    I totally identified with your posting; I will be 50 on June 3, which is WEIRD; I still want the energy of my 22 year old body that backpacked or ran. I have Hashimoto’s, an autoimmune disorder, and they are hopefully going to rule out rheumatoid arthritis; my rheumatoid factors are high, but I don’t have any swelling or pain in my hands. However, fatigue has been the thorn in my flesh for many years. I love being active, and as I transition into this next phase of life (my youngest will be a Senior in high school) I SO want to be active. Sometimes when I run, or do anything a little too much, I may pay for it for days. But I REFUSE to quit! My desire is to climb a 14er in Colorado this summer! Keep moving!!

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