At is core, MStranslate is an online science communication initiative, founded by brothers Brett and Eric Drummond. It leverages Brett's background in multiple sclerosis research to curate and communicate the wealth of information available on MS, removing the complexity of the science to make it easily accessible for every member of the MS community. MStranslate's primary broadcast points are their social media channels (Twitter, Facebook and RU-vid), complemented by their website (www.mstranslate.com.au).
hi. i'm an MS patient here, have been for nearly 30 years, i'm now at near 15 % of my former self, today i decided to listen to those who say it's what you eat is what causes your symptoms, so today i'm not going to have breakfast only 1 table spoon of olive oil and see what happens during the day
Interesting, the CDC in the US looked at early on and porolonged childhood abuse and concluded that the likelihood to develop an autoimmune disease during lifetime is over 50%. New research also shows that the microbiome being unhealthy us a connection. However, stress as in high cortisol levels and adrenaline effect the microbiome. So that is where a possible connection is?! And my question is, how much do hormones play a role in progression of disease. A lack of Estrogen or pregnancy seems to change it.
One three things can cause ms dietary allergies like gluten and heavy metal toxicity in neural tissues and three lack of vitamin D3 massive deficiency and intravenous colloidal silver can reverse brain lesions, remyelinization of the myelin complete remission of ms so you can say a cure but you’ll have to see a naturopathic or integrative medical doctor for that treatment
what about PPMS. I'm done Hsct in Mexico 9 months ago and have worsened. I also worsened on Ocrevus which was all I was offered at Barlo in Toronto. I'll try humbler food portions and staying active. Thanks for your work good Dr. Will Brown.
Been scapegoated, emotionally, sexually and physically abused in different parts of my childhood so I was wondering if my MS had any explanation besides "doctors dont known"
No cure for MS? How about HSCT? Now why dont you try remyelination on those who did HSCT? Then you will eliminate the possibility of myelin damage during repair. Did you look into blocking M1? There are few methods that show huge promiss that no one tends to look at.
I have SPMS and did HSCT in Moscow as in Canada my doctor said it wont help. It helped a lot. Now I need to regrow myelin sheeth. Combination of B12, Clemastin (2mg), and lions mane extract with daily use of UV. Diet change includes reduction of sugar by 80%. Improvment in EDSS within 2 weeks. I can cure it and I am just a biologist. I can even give you set up to findna remyelination that has 70% probability to do the research and trials on. Keep the money, I need cure
I got MS at 49 & now I’m 53 Wheelchair & divorced. Very determined to Change this narrative and Eating greenery fruits smoothies and exercising for good health.
The problem is that it s still not yet "on the market". Years are passing and decades as well. It will be for the patients who aren’t in a critical MS. As my doctor says, often hopes but probably too late for the current patients.
I have MS and there is no way I would introduce an immune thearapy like mRNA into my body. There would need to be extensive and scientifically rigorous studies as to the safety and effectiveness of this kind of treatment before I would ever consider it.
Thank you - that was really interesting and eye-opening (I've just subscribed your channel). I think another significant quetion would be about the amount of casein injected into the mice. They have quite small bodies, so maybe there was realtively a large amount of protein they had to tackle. Tha would lead to another question - do people with MS who have problems with casein have to avoid milk altogether, or reduce it.
How about sunshine for vitamin D or supplements, lysine, monolaurin, methylated B vitamins, flax seed oil, fish oil? You know, nutrients to support your brain?
You definitely don't want people to get better! How many people's lives have been lost so far because of pharmaceutical companies? The year is 2024, there is still no stopping or repairing treatment, this cannot be justice. DO YOU HAVE NO CONSCIENCE OR CHARACTER? EVERYTHING IS MONEY!?😢
I had no idea that myelination stops with age. That’s just another kick up the backside 😢 I have been taking clamastine on and off, and just recently I have managed to get metdormin. What’s interesting, my walking improved by taking 3 pills of clemastin and one of metformin once a day. I usually take them at night. I wish I knew more on how to administer this drugs together. Great update
@@EmekaOkafor-rq2ne I found the clemastine pills in Canada or Turkey … there are not cheap either 😔😥 but try Lions Mane instead; do some research on that. Might work better. I am currently taking lions mane, and if I stop my energy levels, my fatigue is bad. I’m hanging onto anything at the moment. This illness is cruel and hard to bare. Good luck ❤️
I've been pain-free and drug-free for over 2 years with no meds. I know this has worked for others, but I'm not naive enough to say it will work for everyone. My MVD saved my life. I was in such pain that suicide wasn't out of the question. After an MVD I was pain-free and drug-free for 12 years. In those 12 years, I kept an interest in trigeminal neuralgia to learn more about it to help others. When the pain started back I knew what to do. I tried some supplements and settled on taurine, lion's mane, and a B complex, and have been 100% pain-free. I am restoring the myelin sheath (insulation)around the nerve instead of treating the pain with drugs. I learned more in this area from those successfully treating themselves with MS than from any other source. Google taurine and myelination, and lion's mane and myelination. If you doubt demyelination has anything to do with TN, google it. I've been pain-free for over 2 years and have had good feedback from others who have tried it. There are over 30 supplements that claim to help in this area, but when I found what worked for me, I stayed with it.
Living with Multiple Sclerosis (MS) wasn’t the end of life for me, I was cured by a traditional Herbalist called DR ALAHO OLU I met on RU-vid Channel….
Living with Multiple Sclerosis (MS) wasn’t the end of life for me, I was cured by a traditional Herbalist called DR ALAHO OLU I met on RU-vid Channel….
Was NVG-291 or Lucid MS discussed this year? They have shown the most promise at getting close to a cure so far. The reprogramming of our immune cells sounds really good, too.
Watched these one at a time over a week or so. Still terrific to hear your updates - feel I am kept in the know from a distance. Thanks heaps for your work! 😊
