The type of physical activity anyone takes part in depends on personal preference and ability. There are many people with MS who run marathons...there are many who do arm chair yoga. Do what works for you. But do something!! I believe MS is a "use it or lose it" type of chronic illness.
As a fitness instructor I believe everyone should be active. An active lifestyle with someone that has MS is subjective to that person's situation. People with MS should excercise in consiltstion with their treating doctor. This is due to possible mobility issue and the fact heat exacerbates symptoms. The aim of excercise is to get people feeling better not worse. I'd reccomned to see your doctor and ask them on ways you can keep active for your case.
It seems to me that exercise caused me to overstress my body. It depends on how much the body are able to endure with, so i recommend to just follow your own path. Is your body, you know the best.
OF COURSE, IT IS GOOD TO DO SPORT, WITHIN THE POSSIBILITIES OF PHYSICAL OF EACH PERSON, IT IS IDEAL TO SWIM, BUT YOU CAN ALSO DO WALKING OR STATIONARY BIKE.
For me, it is fundamental to any daily physical activity. As stretching and walking, for long enough, and that I find it necessary to not get exhausted.
While the body allows us, the exercises in the patients of E. M. they are very important, as you do not become tired more easily over the muscles of our body
It is advisable to any sport if you try not to force you above your limits,I personally I walk before I ran, but my dizziness and constant tiredness are multiplied.
Outside of my immediate family and a handful of friends, I keep my diagnosis of Multiple Sclerosis hiden. Tucked away in the shadows where I feel it keeps me safe from the pitiful looks, awkward questions or even worse (for me, anyway) the fear that ...
Gosh who'd have believed that a few years ago I was walking around as what I thought was a fully functioning adult with just the odd wince in my left leg and side. Bam!!!!!!menangitus decided it was going to knock me off my feet . Bam!!! Sounding lik...
Life use to be good, then a week or so before christmas I was slurring my speech. mom was like that sounds like a stroke.. I ignored it cause I was going out of town to spend christmas with my dad and sister. while thier i was getting dizzy and even ...
Hace 31 años recibí el primer diagnóstico, paralizada desde el cuello, pero cono no sabia nada de la enfermedad siempre pensé que podría volver a caminar, una de mis hermanas empezó a hacerme intuitivamente moviendo de cada uno de mis músculos...
I would like to know if extreme fatige and muscular weakness can be early symptoms of multiple sclerosis. Should I take more tests to discard ms or these symptoms are not ms symptoms?