I set myself up on my floor peddler and did an hour in 5 minutes forward and 5 minutes backwards repeated. I ought to do this every day to keep the circulation in my legs. I’m getting twitching in them on and off now so my days of transferring from my RR chair to wheelchair using my walker and going to the loo independently are numbered but I’m fighting it all of the way. Xx
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Lynne K An hour of non-stop exercise sounds a lot Lynne, especially pedaling if your legs are weakening 🤔
Certainly if your legs feel tired or shaking afterwards, it might be advisable to do maybe 3 x 20min sessions throughout the day, but you know your body best. xxDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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Originally posted by Ellie View PostLynne K An hour of non-stop exercise sounds a lot Lynne, especially pedaling if your legs are weakening 🤔
Certainly if your legs feel tired or shaking afterwards, it might be advisable to do maybe 3 x 20min sessions throughout the day, but you know your body best. xxALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my balance.
I'm staying positive and taking each day as it comes.
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Originally posted by Deb View PostHi Lynne K. Its fantastic that you're exercising and fighting. Go girl !
I really really don't want to be the voice of doom and I know I'm probably stating the obvious but please take special care not to have a bad fall during this really hard stage, Hugs to you x😘🤗ALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my balance.
I'm staying positive and taking each day as it comes.
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It's great you're keeping as independent as possible Lynne K . I was advised gentle exercise was ok but never to the point of increased fatigue....it's a balancing act....for us literally😃😘Initial diagnosis 7-4-2021 'suspected MND' confirmed by 2nd opinion 4th June 2021 ALS. Began with R foot limp and lots of falls. NIV overnight. Generally weak. Mostly terrified.
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Still transferring with my walker to wheelchair. Steve rearranged my chair and side table so now my RR chair is next to my wheelchair. That’s making transfers easier as only a couple of steps but my table is now on my weakest side with my weakest hand but he’s doing his best for me. Catheter tomorrow morning so less transfers needed xxALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my balance.
I'm staying positive and taking each day as it comes.
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