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I went from crutches to walker to power chair. People do look but try to hide it. I don't have time to look at them, figure I'll never see them again. Going into chair was sort of tramatic, but get more done and save energy now - for me, no one else. As a good friend said "you're still you, aren't you."
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I have a rollator and I only use it when I really need to. My husband basically won't be seen with me if I have it. He walked at the MS walk with me, but he didn't walk with me. He pretty much stayed away from me, and any time I tried to talk to him, he tried walking away like he didn't know me. My mom cried when I got it. My grandmother in law laughed and didn't believe I needed one.
The good news is that I don't need it often at this point. I do if I'm walking for any length of time or distance... even down to the end of my street and back. I wonder if I went to the gym and got on the treadmill with a walk pace, and just walked and built up my muscles some more (I'm not very out of shape, but there is something playing into this), I wonder if that would help me be able to walk longer distances without the walker... or maybe even run. I still have a dream of competing in a triathlon... I guess we'll see how that goes. Quote:
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Giovanna, I'm so very sorry about how your husband is acting. I can't begin to imagine how much harder this MS crap would be with an unsupportive spouse. Shame on him.
I believe exercise helped me in the long-run. It can't hurt, right? Keep active as long as possible with whatever type of exercise you can manage. |
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