This is the official RU-vid channel for the MS Society.
We’re the MS Society - a community of people living with MS, scientists, campaigners, volunteers and fundraisers. We understand what life’s like with MS, and we support each other through the highs, lows and everything in between. And we’re driving research into more - and better - treatments. For everyone. Together, we are strong enough to stop MS.
I wish the person in white could have used this as an opportunity to model adaptive strategies for exercise, their form is quite poor due to fatigue. Instead of pushing through and having terrible form, demonstrating how to modify the exercises would have been empowering and helpful
My M.S. is the most challenging thing in my life that I have had to deal with, but like my dear father would tell me, GOD, gives the hardest battles to his strongest followers. May the dear loard give strength and resilience to us all . I know that we may not have our previous full lifes, but remember we still have LIFE and we need to learn to put ourselves first. My son is my voice of reason and understands my daily challenges, and those others who have to live with this challenging condition, and he would say to us M.S. should stand for My Self. Basically put myself or yourself first. Never give up, just do and focus on what you can do rather than what you can't. Love and blessings to everyone, stay strong, a fellow M.S. warrior. ❤🎉❤
Okay, WHYY did you purposely omit to mention what "MS" stand for? I had to go in the comments to learn that means "Multiple Sclerosis" Thanks @vaso4261
definitely be careful with the bar bells, i once put a hair brush into my eye ball, from trying to style a hair cut, that required me to keep my arms up, and my arms fell, and i put the hair brush bristles into my eye ball. It is one of other injuries to my eye, but it was not pleasant. so be careful with the barbells over your head. the longer with the exercise, the less stability, with some things. the problem with physical therapists, is they usually want to see improvements, and there is not always improvements, and can lead to a great deal of down time. The issue with sedintary life, is weight gain even if watching the calories, with the amount of exercise, and trying to maintain to not lead to diabeties, or any other conditions. etc. it is not a matter of mind control, like when i was in the military it was by mind over matter, that is not how it is with ms. it is not whether you want to, or if you are trying or not, etc. that is not it at all. etc. Most times the damage is done. I have also had bad injuries, lyme disease also. etc. so it is several things, it maybe a little different..
exercise at this point for me, is that I get some exercise, aside from just being down, or not moving at all. Exercise and being in shape, was always important for me. that is not so much the focus any longer as much as continueing to move. Physicians do not seem to be up to date and society absolutely has no clue, at all and and the information, maybe helpful for patients and their environment as too the childrens, social environment in cruel environments. i loved being in Army in shape. but we have to adapt, I had to learn that not pushing it, to end up in bed for months not able to move at all, etc. which includes alot of things we take for granted. This is important for others to realize also as much as stubborn or independent selves. etc. of course quality of life medications, are extremely beneficial that the physicians no longer believe in quality of life so my thoughts and prayers for those struggling with the conditions. patients may get a day, once in ten or more years, that is not quality of life, or beneficial for anyone. when you cannot keep the body moving, or down for too much physical energy spent, trying to keep the mind active is important too. when you do not feel like engaging in anything at all, its ok to take a break, but trying to find interests, or atleast something, to try to engage in, while down, and not giving up completely that can be very easy to do. Never give up, even society or no one else, understands any of it. be sure to take rests, as necessary, for any potential risk factors. the brain is a muscle too, as everything the entire body can be involved. so take rests as necessary, regardless of society or others. listen to your body, not everyone else.
I noticed when pushing the individual without the chair, a little bit much. The beginning of shaking, etc. of course, it is up to anyone individual, what is too much or the intensity of inability or pain or both.
It is one of the most important points, in ms. in my opinion. listening to the body and knowing too much or too far is too much to not end up, completely down. It is not just lesions, etc. which is a part of it.
I think the instructor should watch the people to see if they’re having trouble or needing help. We know he can do the exercises. Good job everyone, except he didn’t see how anyone was doing!
This has been a terrific find!! After three months recovering from hip and leg surgery this past fall, Finding this video is bringing me some cadence back that I can fully recover (and perhaps even improve ) my strength,, balance and proprioation back. I will be joining you from a chair with a textured tethered half balance ball and a bench until i get back onto a floor. This is great and thoughtful assistive example. Thank you,
Intravenous colloidal silver can repair brain lesions and has been shown to remyelinization of the myelin also copper and vitamin b12 can regrow the myelin
This is the time of information, medicine is changing every moment for better, scientists study the brain more than any other organ, so this brings hope. I do not believe the current generation will live with MS for life❤ because there are lots of researches going on.
