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2,110 Views ā¢ Jul 12, 2024 ā¢ Click to toggle off description
This is a clip from the following video about 10 hot takes about multiple sclerosis: Ā Ā Ā ā¢Ā 10Ā HotĀ TakesĀ AboutĀ MultipleĀ Sclerosis...Ā Ā
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Dr. Brandon Beaber is a board-certified neurologist with subspecialty training in multiple sclerosis and other immunological diseases of the nervous system. He is a partner in the Southern California Permanente Medical Group and practices in Downey, California (South Los Angeles). He has several publications on MS epidemiology and has participated in clinical trials for MS therapeutics. You can follow him on twitter @Brandon_Beaber where he regularly posts about MS news and research.
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he video material by Dr. Brandon Beaber is general educational material on health conditions and is not intended to be used by viewers to diagnose or treat any individual's medical condition. Specifically, this material is not a substitute for individualized diagnostic and treatment advice by a qualified medical/health practitioner, licensed in your jurisdiction, who has access to the relevant information available from diagnostic testing, medical interviews, and a physical examination. To the extent that Dr. Beaber endorses any lifestyle change, behavioral intervention, or supplements, the viewer should consult with a qualified healthcare professional to determine the safety and efficacy of the intervention in light of their individualized information.
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Genre: Science & Technology
Uploaded At Jul 12, 2024 ^^
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RYD date created : 2024-07-15T15:53:16.239424Z
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YouTube Comments - 44 Comments
Top Comments of this video!! :3
Appreciate you providing the statistics. You and Dr. Boster's videos are what I refer to during my neuro appointments.
19 |
It's great to hear a neurologist saying this. I am against drugs due to small benefits and unknown long term side effects. Too many doctors mislead and scare people into taking these powerful drugs. Thank you for your honesty.
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Although itās important to consider risk for me a 24% reduction in disability might be the ability to continue to use my hands - so worth the risk in my opinion.
12 |
I agree with that statement that they are overrated. Im currently on ocrevus. No new lesions but still my mobility worsens.
9 |
Wow, thank you Dr. B.
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These are tasty treats I come for. You are part of who I cite when I bring ideas to my neurologist.
4 |
Great video Dr. B
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Over 20% is possible the chose between being able to use my hands or walk, well I'll take it. Better odds than my brain tumour coming back that I was also diagnosed with the sameday.
And studies also do show that nowadays with the better dmts people with MS are living fuller lives with less disability.
3 |
I would love to see such a study in comparison to dietary interventions like Wahls protocol or OMS instead of placebo. ā¤
1 |
This is a hard truth, and I am here for it. I do not appreciate all the hopium takes. Live strong as u can and take those holidays when u can. Life is no guarantee for anyone.
2 |
Good to know. Age 60 with MS on no DMDs. I have more fun uses for my money!
7 |
So refreshing to see a neurologist consider the facts associated with drugs which provide only modest benefit at great risk.
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Wow! Makes it hard to know what to do.
My B19s are up so I am going back for another O infusion.
I hope I have enough B19s that have gotten to the other side and matured.
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They're gonna keep pushing them when ocrevis is over $60k per iv bag
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Not a good enough reason for me to go on them. We all have to make our own decisions don't we? Thank you for this!
3 |
The side effects were way too much for me. Especially with other health conditions. However, If Ocrevus was used much less often instead of every 6 months, I might've been able to stay. Wondering what other's thoughts are on possibly using an anti cd20 to knock down bcells and then follow up with one of the inflammation blockers such as Frexalimab. Yes, I realize a study like this is a long way off. But that's one thing swinging around in my thinking. I'm hoping the studies being done on Frexalimab are positive for all types of MS.
1 |
After 6 years of anti B-cell drugs, I now came to realisation that I might die of infecton (as demonstrated in 2022 when I had covid). And now I view statistics totally differently, i.e. not in favour for MS drugs š¢
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I have been dealing with this same issue. They have me on Rituxan for PPMS - and supposedly it will give me a few more years of mobility. But always wearing masks, not going out much because of a damaged immune system and just the month it takes to recover from the medicine makes me wonder why Iām doing this. I want to keep walking - but I donāt know if itās worth not really living. And the medicine does nothing for any of the other horrible issues I now have. (Eyesight, hand tremors and weakness, gastroparesis, pain, headaches, flushing and incontinence - all in one year of being diagnosed.
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Also rrms?
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@jb3543
1 month ago
Damn, i wish all neurologists were as honest as you are on that topic !
16 |