It was a great pleasure to take part in this concert ❤️

Great

Is there a night time bed one

Touching

Thank you to each and every one of you for the work you're doing for those living with MS whether you are yourself or you're dedicating your career and time to helping people like me.

Mrs Janis Winehouse and comments made from watching her do her alone shopping in London Retail Shoppers store #

Loved the explanations from Dr. Smith. ☺️ great format!

Great video. It would be good to see more of this type of video!

please get moving

𝖨 𝖫𝗈𝗏𝖾 𝗒𝗈𝗎 𝖬𝗈𝗆

I broke both my legs and this was very helpful. Thank you.

Amazing! 👏

Mary my outside teacher

I scoffed at the whole thing when it was announced, a drug that I take for type 2 diabetes and a cancer drug mixed to restore the myelin sheath? Two drugs that individually have horrible side effects, both produce stomach problems and diarrhea? What would that produce? I'm sure the results were explosive!😄 A product called Myelin Sheath Support worked for me years ago, but the demand was high, and they couldn't keep it in stock. A product called Megarelief is made for migraine sufferers but heals the myelin sheath. Here's the most controversial one out there, but I can't argue with success, and it does make sense to me because the myelin sheath is a fatty acid, the Carnivore diet! All of these have worked for people with trigeminal neuralgia. Those with other autoimmune issues might find this information helpful as well. There are over 30 supplements that help in the restoration of the myelin sheath, and that's where it's at. Keeping the myelin sheath healthy. What I take is taurine, alpha lipoic acid, multivitamin, turmeric curcumin, and lion's mane. I take sublinguals whenever possible.

Look into lion's mane mushroom as well.

I got hit with Transverse Myelitis; immune reaction after a fly shot; Jan. 2020. Recovered from total paralysis in lower body. Presently abt. 20/30 normal leg strength ; no pain 90% no feeling at all. On good days can stand using walker and walk app,20 ft. I am determined to strengthen my legs. Lower back very week this program lets me really focus on lower back, core strength. The 40 min. is tough but I do as well as I can. Tough program, I like.

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Damn had no clue. Big inspiration. I was on Avonex back in the day!!!

Damn had no clue. Big inspiration. I was on Avonex back in the day!!!

What tests? How do you diagnose MS? What tests?

Is there something a patient can do to keep his nerves alive?

Clemastine fumarate trials have been halted.

Thank you for trying & for all the hard work & dedication. I was diagnosed in 2006 RRMS although I think I had it a few years by then so I estimate I have had it 30+ years. Spent years being told there was nothing wrong with me & it was all in my head. I asked for a second opinion as I knew I was ill. I saw a wonderful Neurologist who actually did some work for the MS Society Mr Mike Boggild (genius man) who within a fortnight diagnosed me not only with MS but a DNA test confirmed I had been born with a rare muscle wasting condition which other family members were subsequently diagnosed with too. ALWAYS ask for a second opinion if you are not happy. I’m not sure how that works these days but it’s worth asking. I don’t advocate this for every one of course but for me it was a complete change in diet. I eat low carb 50-80g a day but not Keto & most of my carbs are completely organic vegetables & plenty of them every day. I eat plenty of fish, red meat once a fortnight & I eat lots of nuts & seeds. I avoid most supermarket food & additives especially artificial sweeteners. I can’t remember the last time I had a significant relapse. I genuinely cannot remember. My greatest struggle is fatigue, weakness & tremors but changing my diet definitely had a significant positive effect. I do not & never have taken MS drugs. As I say I absolutely do not advise anybody to do this. Always follow your Neurologists advice & trust your own instinct. Nobody knows your body like you do. I have no idea if MS drugs would have made my life better or worse. It is an individual choice as every body is unique. I have no idea if it is connected or not but my MS appeared to slow down in terms of relapses once I started taking a series of drugs for my heart. It’s only looking back years later that I could see the pattern & how it changed. Life is hard with this disease for sure but trying to have a positive mindset helps greatly.

What a great video, so so true 🙂

Ty 4 postn awareness! I was diagnosed with RRMS in 1998... prayers up for all with this illness and their caregivers 🙏🏽🙌🏽

Ahh. He's SOOOOO dope. The MOST underrated rapper out there. This was a nice interview, thank you!!

It is 3 years ago, is there any news in 2024?

Will this work for leukodystrophy?

I wish these videos have more promotion I'm recently disabled with cauda equina syndrome and this means alot with your help

Excellent information. I am a pilates instructor who has a new young client with MS. Very informative.

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

This is quite moving man. Shout out all people active and not giving up.

Too much music

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. ❤🎉❤

YES !

Greetings from Alaska. I strongly resemble the fellow in blue. I have ms.

Greetings from Alaska. I strongly resemble the fellow in blue. I have MS.

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

Excellent, but why disabled the download?

❤🎉❤🎉❤🎉thank U sooo very much!! 🙌🏽🙏🏽

It's been 3 years, any success in this trial?

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.

Micro manage the energy to not end up in bed for months or yr. or permanently, on end, not able to move at all.

thank you its very helpful

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!