Exercise

This is a tough one for me as I find it hard exercise without a ‘purpose’ – swimming is arguably the best exercise for people with MS – the nervous system can stay cool while the muscles get a work out – but I hate swimming laps.  I enjoy snorkelling or scuba diving because that’s swimming with a ‘purpose’.  Unfortunately the snorkelling and diving in Toowoomba is lousy.  When I’m feeling okay in the leg department I do try to walk more than I do on the ‘bad’ days, simply following the rule, “if you don’t use it, lose it”.  The important thing is not to overdo it.

With any exercise, Nursie Mel says there is a ‘two hour rule’ – if you do exercise and two hours after feel as good as before starting, that exercise was good for you – if you feel worse after two hours, you’ve overdone it.  Here are a few tips I whipped off another website:

  • Always warm up before, and cool down after exercise
  • If you allocate 30 minutes for regular exercise, start with 10 minute sessions and work up from there
  • If balance is an issue, exercise near a rail or bar (I don’t think they mean one in a hotel – that could result in a literal ‘pub crawl’)
  • Avoid slippery floors, areas with poor lighting and rugs or other things that might trip you up
  • Choose an exercise that you enjoy – swimming, water aerobics, tai chi, yoga etc
  • If you begin to feel sick or it starts to hurt, STOP!

Some people with MS are sensitive to heat and, naturally, body heat will rise when exercising.  A few tips on overheating:

  • Exercise early morning or late afternoon to avoid the hot time of the day
  • Drink lots of cool fluids
  • ‘Listen’ to your body – if symptoms pop up that weren’t there before you started exercising, slow down or stop until you cool down
  • Again, swimming and water aerobics are good exercise options but be careful of slippery floors near the pool or in the change rooms 

SUNBAKING

While trolling around the web I found a site that recommended sunbaking for people with MS.  And that lack of exposure to the sun (Vitamin D) could be a cause of MS.  This was based on statistics that more people in Tasmania are diagnosed than in warmer parts of the country.  I grew up in Gundagai, a town that can have hot, dry summers.  We had our annual holidays at the beach in Sydney and I lived in Sydney from age 11 to 45 (before spending three years in Vanuatu).  So the cooler climes have no bearing on my diagnosis. 

And because I grew up in sunny Australia, I had a nasty squamous cell carcinoma removed (in 2009).  Sunbaking may be fine in Scandinavia, but in Australia it can be deadly.  I’d rather have MS as abbreviation for Multiple Sclerosis than a Melanoma Sentence.

Having said that, here’s a link to a calculator that tells you healthy levels of exposure to the sun.  You need to enter the time of day, day, month, latitude & longitude (you can get this from Google Maps), the sky condition (cloudy etc) and your skin type – and voila!  For me to get the required dose in Cairns on a sunny day could be 2 minutes while in Melbourne on an overcast day it would be 39 minutes.  http://nadir.nilu.no/~olaeng/fastrt/VitD-ez_quartMED.html

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About this Blog

‘My MS’ follows my personal journey with Multiple Sclerosis. Everyone with MS has different circumstances, symptoms and stories. Feel free to share yours via comments or email! MS can be a bit mysterious and it can come with a few myths. Hopefully you will find the blog informative and an enjoyable read!