Smouldering MS?

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Is there hope for the future of MS Care? In this video, I share 3 things that give me hope for the future of MS care and research in July of 2023. If you want to hear more, then start watching right now!

The Boster Center for Multiple Sclerosis accepts new consults and is actively enrolling MS clinical trials! Contact us today: www.BosterMS.com or call 614-304-3444 to schedule!

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COMMENT with your thoughts and questions below! Hope for the future of MS care. I look forward to reading and responding!

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NOTE: Make sure to talk to your provider before ANY treatment decision. We hope to educate, empower and energize those impacted by Multiple Sclerosis. This channel consists of a collection of formal lectures and informal video clips about MS to help educate others. These videos do not provide medical advice and are for informational/educational purposes only. The videos are not intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of a qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or seen in any of our videos. They are just to help educate you about the condition guys!
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That exactly how it’s going for me sadly. Diagnosed during the (ongoing) pandemic, which psychologically hasn’t helped at all. An MS diagnosis is obviously a life changing diagnosis and I have found the psychological support to be non existent; every conversation that I have about it seems to be a battle. Quite the opposite of what a newly diagnosed individual requires. I’ve been truly left to my own devices to sort this out. Truth is the fatigue makes this borderline impossible and makes me want to throw the towel in at times…Thank you for just being here Dr Boster.

markthorne
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Man I wish you were my neurologist! Thank you for the time and effort you put into these videos for those of us impacted by this disease.

mahkell
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Dxed at age 15. Was in and out of hospital for six months. Made my mind up that i was not going down like that and started running track and cross country in high school. Became the CO of my NJROTC my senior year. Became a five season lifeguard. Got my EMT and certified as a volunteer firefighter in MS. Became a mom. Now 25 years later I’m in a power chair and on disability since 2013, just in the last five years have gotten to where I can not do much for myself.

daphnesalang
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This is me. Very few lesions. Diagnosed RRMS in 2003. SPMS by 2012. All of the DMT monitor relapses and brain imaging during clinical studies. My primary care physician has been saying, “A woman your age shouldn’t have this much trouble walking” for the past ten years. This is MS.

daisyjo
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You're such a unique blessing to us, Dr. Boster! Thank-you!

GODEED
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I notice this with my left arm and hand they’re getting more spastic especially if I get upset
My hand is getting less useful like tying my shoes or butting my pants are becoming a real problem 😞
I’m going to see a ms therapist team at Mayo next month so hopefully they can help me 🤞
I have RRMS

tinytattoomike
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I don't need a neurologist or diagnostic testing, to know what I could do before the Corona pandemic and what I can do now. 😔

Jerusalem_Warrior
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I thought we can't see smoldering disease... ?

donnabolt
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I was diagnosed with primary progressive. Multiple sclerosis. To start with, and it's only gotten worse

henp
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És mi lenne, ha más oldalról tekintenének a betegségre? Pl más autoimmun betegségek jelenlétére. Pl gluténérzékenység. Enzimatikus rendszer hiànyos működése!

lorantvarga
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I haven’t walked in over a year and I reverse it and get better and walk again?

abelsamora
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What do you think about doctor Terry Wahls who reversed her MS with a diet.. literally from wheelchair to no symptoms ?

christinabee
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Dr, is it true that a root canal can be the cause of Ms and other diseases .
Like they say in the documentary (Root cause) on tubi?

stephaniesantiago
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Science is mistaken forwards to the truth. Hope you all get it right. Translation from german to englisch could be wrong. 😅

But anyway, also in medicine we always and still progress in our understanding and knowledge.

I guess you have an entire video about this topic. I need to watch. How can we see if one is suffering this smouldering MS. Different type of MRT (MRI?) needed?

Best regards 🙋‍♂️👍

in-kognito
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I read an article today about Why I’m drinking more water because of my MS ..on " multiple sclerosis news today " website and I noticed that they mentioned your name, well done, sir👍🏻👍🏻👍🏻

AC-Milan