Cure for Multiple Sclerosis?

Thank you for being straight forward. This is hard to get any dr. To answer questions directly. I love your channel, thank you for what you are doing! <3

The thing that actually helped me the most was IVIG. It got rid of most of my symptoms. I got a divorce and I lost my insurance. So, I am now using supplements to treat the symptoms. Since immunoglobulin is a blood product from thousands of different individuals, I won’t take it because I have no doubt that it is tainted by the Covid vaccine, which I did not take. Next step will be stem cells.

@Dr. Boster - Can you do an updated video on this topic, please? I would like to see how your feelings have changed from then to now?

look into the book "medical medium", I take monolaurin to kill the epstein barr virus that caused it. He sees doctor's won't catch on until the 2030's. re: type 2 diabetes, you can also reverse it by going full carnivore, and stop doctors from just managing your diabetes. The doctors lied and said my immune system is attacking me, when it was actually attacking the toxins the virus was spewing, but couldn't find the virus, because it's hiding deep in our organs.

I’ve had ms since 2008 when I was 19; living very well on fingolimod until this medication was stopped stopped due to COVID I was happy on this medication and felt fear stopping a medication that I knew to be controlling the disease that was in 2020:( im now disabled… and frankly frustrated suffering now ataxia😢 thank you

Sir i am ms patient since 10 yrs i am very fed off this now pls help

Good evening. I suffer from progressive MS with remitting episodes. The last three years the progression stopped. I have lack of recent memory, but worse of all I have vertigo. Most of the time I feel stunned. According to a neuro-oto-rhyno exam it is due to lack of mielin in my cerebelum.
I was diagnosed in September 2018.
Since then I found a very promissing study from Dr. Stu Metcalf from the University of Cambridge.
Basically they use a nanoparticule to deliver the treatment to the brain.
It is called lifnano. LIF stands for Leuchemia Inhibitor Factor.
The lifnano travels through the blood stream and reaches the brain where it starts "knitting" the mielin.
Do you know anything about this?
Thank you so much.

My mom has ms i cant do anything🥺🥺
Im from india

I ask god every day❤

I could share you over and over

❤

i think i have the beginning stages of ms caused by humira

What's the link no with Asperger's ADHD OCD hypomobility inflammation

Beliefs don't really help

I live in Iran and I can't use those medicine . How can I cure it or ....?

Hello can you talk about HSCT please

You have made my night, my tommorow and very probably my week, and my whole new life as a new ms patient. It will be my mantra to hold on to that moment we will have new or more medication so the future won't be that terrifying.

You have made my days ! A big thank you from France ! Merci very much for all your videos

I'm glad to have seen this video thank you for making it.
Can't wait for this sickness is cured and I don't have to deal with it anymore this Multiple Sclerosis is something I can do with out and I also want everyone else to not deal with it also so I definitely am waiting for a cure for this sickness

Will Cannabis help in eye vision and numbness in ms

I really appreciate your videos Dr. B! I have been currently diagnosed with RIS but I'm told that I'm high risk for it to progress. Every little thing like muscle twitches has me on alert and your videos have helped ease some of that stress. While I know that a full blown MS cure is unlikely for a while, I was wondering what your thoughts were on the remyelination research and trials that are going on right now? Do you think that we are looking at repairing myelin as being a realistic part of making MS boring in the next 5-10 years? Thank you!

Does this mean recovering from the damage of MS or, treating it so you can liveva relatively normal life again,

the ‘NO’ made me burst out laughing. i think im having a breakdown

Hey Doctor! I liked this video and your take on the expectation we should have for a cure of ms!Also, would it be possible to make a video on how you view remyelination and eventual drugs for remyelenating the brain(Dr. Beeber made a video on the topic!)

You're right about that dr. Boster most medicines these days treat symptoms we haven't found a cure for too many of the diseases up today but type c hepatitis has been cured recently come on dr. Boster find a cure

Thank u DOCTOR for your honest reply i apreciate it ( ms patient )... Best Wishes to u...

Sir, I hear about a bunch of therapies that are supposed to aid in remyelination. Is it really possible for remyelination alone to regenerate the entire neuron considering axonal loss? Thanks in advance.

What is your opinion of LIFNano?

Do you think the body (if treated correctly)could get rid of M.S? The body can heal itself from many things. Just a thought

I had HSCT last year, it's not a cure it just halts the progression of MS. My latest MRI shows no active inflammation, progression or new scaring. The clinical trials are still available all around the world.

If it gets boring we loose interest and it discourages us on finding a cure for it. I say we keep pushing and not let its severity fade. I'm 26 years old and I've already been in a wheelchair for 4 years. I dont want my future to be a test I want my future to be a solution. I'm willing to help anyone willing to let me help them find the truth to this nonsense called MS.

Yeah u right doc that much expensive drugs we will not expect a cure for ms to be more honest.

How about fibrin or vaccination for ms?Are these promising for cure?What's the latest news?Greetings from Greece .

I was diagnosed with MS almost 2 years after a neck & back injury. It didn't show up when I had a spinal tap 3 months after my accident. But after my MS diagnosis I had bloodwork done again. And my results came back saying I had a vitamin d deficiency. So can the neck, back injury or vitamin D deficiency are both be the culprit behind & reason why I have been diagnosed with multiple sclerosis 🤔🤔🤔 👀👀👀 ...???

What type of treatment would you recommend most of the options out there? I'm currently on Tecfidera for 2 half years now. Thinking of switching, cause sometimes I forget my second doses.

Thank you for this video Dr. B. This is great information. Would you be able to discuss HCST? I have heard many people discuss this and would like to know your opinion on this treatment.

Thanks Aaron!

I'm back Suzanne fr. Sudbury,Ontario,Canada////

My "cure" to date is ability to walk without use of a cane anymore (mostly)...
I wonder what remylineation could do for black holes in my brain and cog fog, though
...takes me forever to compose even a short message
///

Had new dental hygienist* for cleaning this week who told me story of woman she knows with MS who quit taking expensive DMTs and now uses essential oils instead and has been "cured". Didn't ask much more about it b/c a) getting teeth cleaned more imp't to me at time and b) been around that block having an old friend who now makes a lucrative post-retirement living with sales from same company, and with whom I've had several debates about their "research-based findings" (i.e., testimonies) that were not solid enough for me to go the route

*btw hygienist is working thru a temp agency and my guess was that maybe she also sells essential oils--idk/not my business but my choice of therapy is my business
...
and I also like to believe well-wishers are that first

Hi Dr Boster I was watching a video and saw that you are upset with Terri Whals. You mentioned that’s she cured herself but she never said that. She is able to manage her ms through her diet. She took many dmd’s and they helped but she was still disabled. She says it has made her quality of life better. She uses food to treat her ms. I love watching your videos and respect you and so happy o can learn through you. I just wanted to let you know that cause I did read her book. I changed my diet but I am also on a dmd as well.

I never wanted to be boring. BUT, NOW, I embrace it as you define boring. I cannot thank you Dr. Boster and Dr. Nicholas for helping this aspect of me A COMPLETE SNOOZER/boring. You are both my saviors. NO one knows I was ever diagnosed with MS unless I make it known. Thanks to your care!

I did the 5k MS . I was the first woman crossing the line. Was I in pain - yes and would I do it next year- yes. I proved to myself that I could do it. I’m going back to school and the best is yet to be!

Thank you for all the info about MS

Not a cure not still a hopeful thought. I’d love MS to become “boring “

Even with new activity this week on mri I’m still boring so I’m happy with that silver lining. There’s so many people in the online community that think that being boring is wrong, I’ve been bullied today for speaking out positively on my own social media 😑
It’s nice to watch Dr B where it’s a positive and informative environment

Thank you for being upfront.

My neurologist won’t treat my MS with steroids . I’m having a flair but she’s worried about side effects. I asked her pa if it was because I am old and she said yes. I am 75. She the pa said that there aren’t enough studies of older people. Sounds like bs to me. I’m still alive and hurting why can’t I be treated with respect.

Eat nine cups of natural fruit and vegetables daily.

Hello Doc, Thank you for this video. I have been taking Gylenia for the past 4 months and I hate it, i feel worse on this medicine. I am doing my research and realizing that if i keep my diet in check I can come off meds all together. Can I ditch the meds slowly but surely?

Thank you for being honest . There are so many charletons out there touting they've cured MS with diet or chiropractic that makes my head spin some times with frustration and anger because some family will tell me that I can be cured in this manner and don't need to spend hard earned money on my medicines like I do.