CURE FOR MS??

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  • Опубліковано 8 сер 2022
  • Link to my bands' new song: open.spotify.com/track/21yzEW...
    In this video, I wanted to discuss a contentious opinion that some people have that there could be a cure already out there for multiple sclerosis, something that is literally staring at us in the face every day!
    Let me know your thoughts below, and also if you have any suggestions at all for future videos!

КОМЕНТАРІ • 49

  • @idraculaa
    @idraculaa Рік тому

    Ha, makes sense why I had a hard time finding your intro song. Thumbs up on the intro song

  • @faduji3935
    @faduji3935 Рік тому +2

    Hi all,
    about the questions
    "How can it be that sunlight on the stomach influences the intestinal gut flora positively?",
    "How much is Vit-D supplementation able to replace (healthy) sunlight exposition?",
    "How does infrared light (of the sun) affect the body?"
    you need to know, that infrared light is penetrating quite deep in the body even through bone structures. It so reaches easily internal cells (of your own body and also "third party flora" cells). I learned that recently in more detail watching the for this relevant YT-videos of the channel MedCram (for ex.: "Near Infrared Light Reduces Inflammation...", /"Sunlight: Optimize Health and Immunity..."/"The Case for Sunlight in COVID 19 Patients....") which I highly recommend.
    So far it seems a regular sunlight exposition (likely also artifical sunlight with no/reduced UVA/UVB) therapy should help mitigate or even avoiding many diseases/ physical ailment. You could call it a sun-diet.
    I Wish the best 2 you all.

  • @kerryrosker3881
    @kerryrosker3881 2 роки тому +1

    Keep doing videos, it helps all of us with MS find ideas and different treatments than we may know and helps a sense of community! Also maybe more people can talk about their experience on ocrevus and how they live amongst current viruses like covid when the immune system is gone

    • @tomgarbett77
      @tomgarbett77  2 роки тому +1

      Hey Kerry, thank you for the kind comment, but that’s exactly what I do it for so that hopefully it can help others with MS! But with Ocrevus I know from my experience I have been fine and have not been ill once since starting treatment. I think this is because it only depletes B cells and not all immune cells so the immune system is compromised but still functioning. Hope this helps, would be great to hear from others on this topic!

    • @kerryrosker3881
      @kerryrosker3881 2 роки тому

      @@tomgarbett77 thanks Tom! Appreciate you!

    • @tomgarbett77
      @tomgarbett77  2 роки тому

      @@kerryrosker3881 No problem!

    • @rayshoesmith
      @rayshoesmith 5 місяців тому

      ​@@tomgarbett77research neuroquant brain anylitics, this software measures brain atrophy of every section of the brain and is a fr superior method than what uk uses of simple lesion measuring!
      Also blood markers:
      Tgfb1
      Mmp9
      Msh
      Vegf
      C3a
      C4a
      There have been cases when the above markers are restored with vasactive intestinal peptide brain atrophy reverses. Due to msh stability increases innate immune function and reduces cytokines.

  • @petro3441
    @petro3441 2 роки тому +1

    Congrats with the release of single🥰 nice to see again. You look good.tganx for the info

    • @tomgarbett77
      @tomgarbett77  2 роки тому

      Thanks Petro! Have you heard the song? Would be great to know what you think!

    • @petro3441
      @petro3441 2 роки тому

      @@tomgarbett77 I love it. If you just know how many times I would just link on your Chanel to hear the entry song

  • @juliette1884
    @juliette1884 Рік тому +1

    Hi Tom this video was so interesting I really believe that low vitamin D play role in MS symptoms But also believe that any vitamin where missing or low can cause other problems Low b12 can cause neurological issues low magnesium can cause muscle spasms But if body doesn't digest it it can also cause low vitamin levels Then you have to add probiatic Hereditary and environmental are definitely case low vitamin sets it off So true Tom make more video like this 🌸

  • @pelletey
    @pelletey Рік тому +1

    Hi mate, well spoken - you are a good advocate for us with MS. You should be getting your serum D levels checked, you want to be above the normal range, in the low 200's. I take 10kIU a day unless I need to increase my level in which i'd take a one off 100kIU(as directed by my doctor) - this is also suggested by the OMS plan(Overcoming MS book/group). When I clicked on your video I thought you would be refering to EBV-it is the real culprit and researchers are scrambling to understand how it is triggering MS. I have shit genetics when it comes to converting D2->D3 plus another SNP. Vitamin D must have massive effects on keeping EBV/MS under control. I live in sunny brisbane and try to spend time in sun/ouside.

    • @tomgarbett77
      @tomgarbett77  Рік тому +1

      Yes it sounds like you are well on top of your vitamin D levels which is great. Being in sunny Brisbane must really help too. I've never actually had my serum levels checked as this has never been suggested by my doctor so I think I am going to request it be done, because otherwise I am just shooting in the dark. But yes I agree the evidence behind EBV does well seem to be one of the main triggers. Vitamin D is likely to the control the response to EBV in non-MS individuals. I very much see MS as a chain of events that need to line up in order to activate disease and I am a firm believer that EBV, Vitamin D and also diet are key factors that all lead to the autoimmune response that leads to MS. But yes hopefully they find more out about EBV because that could be the one clear route to cure MS.

  • @kitty.bradly
    @kitty.bradly 2 роки тому +1

    I am currently low in everything that my diet is high in, it makes no sense to me. People will automatically think I have a poorly planned veg diet but literally everything I eat is iron fortified or helps asorb iron so it's weird I'm so low I should need an iron transfusion.. ugh. Explains why I feel like garbage though. Being low in vit d makes sense though, even if I felt ok it's freezing and there is no sun in Australia right now. Anyway, I love your song!

    • @tomgarbett77
      @tomgarbett77  2 роки тому +1

      Yes I think this is probably a common problem in most of us MS'ers in that we are struggling to absorb nutrients, which causes the deficiencies that leads to the autoimmunity. I would suggest maybe finding a functional medicine doctor if you can that can help look at your diet and what might be causing you not to absorb these nutrients. I know for me, before I made changes to my diet and lifestyle I was passing urine like nothing else! Needing to go every hour. So I think that is definitely something you can look at! But thanks for checking out the song, really appreciate it!

  • @demoskunk
    @demoskunk Рік тому

    We've known about this for awhile. I've raised my vitamin D level above 80 and my PPMS has still been getting worse. It's relentless.
    Vitamin D won't reverse damage caused by MS, but it might make it less common. For repair, we need advances in MSCT and the completion of the NVG-291 trial.

  • @CodeyWi
    @CodeyWi 2 роки тому +1

    Hey, Tom. Noticed you said “thrive and survive,” which reminded me of CarnivoreMD as that’s something he says. I wanted to let you know that since starting his diet, I’ve never felt better. There are similarities between it and the Walz protocol, but I just wanted to share it. Every but helps.
    Also - you should check out the nano bots studies at a few universities in the US. Nothing is out yet, but they’re researching.

    • @tomgarbett77
      @tomgarbett77  2 роки тому +1

      Yes I realised when I was editing the video that I must have picked that up from Paul Saladino because I have been watching some of his videos recently! That’s really interesting the diet has worked for you. Are you strict carnivore or do you have some plant based foods too?
      I will definitely look into the nano bots study you’ve mentioned as well!

    • @CodeyWi
      @CodeyWi 2 роки тому +1

      No, not strict but I stick to it about 5-6 days of the week.

    • @tomgarbett77
      @tomgarbett77  2 роки тому

      @@CodeyWi ahh nice. I’m already on the best bet diet which removes a lot of similar things but I have thought one day I might try the carnivore because it seems like people have great results with it.

  • @kathytaylor1102
    @kathytaylor1102 Рік тому

    Could you do another video on your diet please.

  • @matutexpro
    @matutexpro Рік тому +1

    Tom, is ghee allowed or considered as dairy in the diet protocol you are following ?

    • @tomgarbett77
      @tomgarbett77  Рік тому +1

      Hi Matias, Ghee is a bit of a grey area, some people don't take the risk whilst others will because it should have had all the dairy molecules removed. So it is very much a personal choice. I personally will have ghee very occasionally when going to a restaurant but wouldn't choose to cook in it. However there are many benefits of Ghee to overall health so I can see why people would decide to use it. Hope that helps!

  • @donnamoore8479
    @donnamoore8479 2 роки тому +1

    Hi Tom, I have 2 sisters that had low vitamin D and they don't have MS. Me and 1 sister have it. I don't recall having my vitamin D checked until my diagnosis

    • @tomgarbett77
      @tomgarbett77  2 роки тому +1

      That’s interesting! I think there also might be something in the theory that people with autoimmune conditions don’t absorb vitamin D as easily as others and this could be what causes the deficiency initially which creates the autoimmune issue! Because you’re right I don’t think any doctors check vitamin D levels until a diagnosis

    • @donnamoore8479
      @donnamoore8479 2 роки тому +1

      @@tomgarbett77 testing Vitamin D seems to have started about 20 years or so ago in my experience. Not sure it doesn't decrease in many other conditions. Until we find out the cause of MS there will be no cure, only treatments, some work some don't. The treatments results seem to vary in different people just like MS severity varies in people. Guess we may just have to remember to enjoy each day as much as we can and take care of ourselves as best we can until a true cause/cure is found. Take care.

    • @tomgarbett77
      @tomgarbett77  2 роки тому

      @@donnamoore8479 Yes I definitely agree with you there. I am however a strong believer in the fact that lifestyle (including sun exposure) and diet play a massive role and we can use this to our advantage in slowing the progression of the disease.

  • @goddess.110
    @goddess.110 2 роки тому +1

    The HPA axis and MS as a next topic please.

    • @tomgarbett77
      @tomgarbett77  2 роки тому +1

      Thanks! I’ve been meaning to do that so I will definitely look to do it!

  • @TK.000
    @TK.000 Місяць тому +1

    My mom got MS at 24 and she was a sun worshipper. Always laying out in the sun.

    • @tomgarbett77
      @tomgarbett77  Місяць тому

      That's interesting to hear. With some people the absorption of Vitamin D is the issue.

    • @TK.000
      @TK.000 Місяць тому

      @@tomgarbett77 I was wondering the same thing. Maybe she is not able to absorb it very well.

  • @CharlesMichaelSidwell
    @CharlesMichaelSidwell Рік тому

    Where is the link for your band?

  • @beastywild
    @beastywild 2 роки тому +2

    Have you read about the Lymphoma drug called Rituximab? They've recently done clinical trials and it appears to be 5 times more effective at preventing relapses in MS patients than current RRMS drugs

    • @tomgarbett77
      @tomgarbett77  2 роки тому +1

      Yes I have heard of Rituximab and that it is promising, but didn't realise it was that effective! This is a positive, hopefully it will continue through trials and be available to treat people with MS in the next couple of years or so!

    • @jeffkameny9492
      @jeffkameny9492 Рік тому +1

      @@tomgarbett77 Greetings all . I am in the Untied States and have had 4 treatments with Rituximab. I was diagnosed 2 years ago this coming November. Along with a drastic change in my diet and increasing my exercise level 2 to 3 times what it was prior I feel that The treatment has been extremely successful.As you were mentioning in this video I also take 4000 vitamin D daily…..Just want to thank you Tom for sharing your journey with us….Stay Blessed and be well

  • @drakulie
    @drakulie 2 роки тому

    I had my vitamin d level checked after diagnosis. It was a 20 level. Started taking vitamin d nutrients 10,000 iu and getting sun. A month later I was at a 120 level. Had to back off the nutrients.

    • @tomgarbett77
      @tomgarbett77  2 роки тому

      That’s interesting and shows your levels were obviously low pre diagnosis. Maybe us MS’ers naturally absorb less vitamin D and so need to spend more time outside and with supplementation!

    • @drakulie
      @drakulie 2 роки тому

      @@tomgarbett77 I got checked after my diagnosis (rrms). I live in south Florida. Very odd to me. I might have them checked again.

  • @kristaplacide36
    @kristaplacide36 2 роки тому +1

    I am going to buy some more vitamin d today. Do you have pins and needles?

    • @tomgarbett77
      @tomgarbett77  2 роки тому

      Yea I would definitely recommend getting some vitamin D tablets! Great for overall health too. But I used to get pins and needles as an early symptom however I am symptom free at the minute which I put down to my diets changes

  • @angelbabycards3595
    @angelbabycards3595 Рік тому

    Yes.., a very interesting hypothesis on the causes of MS. Here, I was diagnosed in Spring, 2016. I never 'Accepted that Diagnosis, so I began looking for, either [Effective Research], [Effective Treatments], and or.., a Potential Cure. Here, what I found several years ago, was [Liquid Stevia was purported to be a Cure for Lyme Disease, which is known to some, as a Cause for what We call...umm.. 'MS'
    And So: I began looking into it, as my legs were weak, and I wasn't getting any stronger fer sure, lol. Well.. One Day.., Well.. One Evening.., Once I watched the videos, I did my own research, and came to certain conclusions.., it kinda made sense to me; that Spirochetes, could certainly.., Be inside my body at the microscopic level, chewing on that Fatty Tissue, located in and around the Connected Spine and Brain, and could have a 'Taste for that particular Fat in the Body.. And so.., I said to myself: These microscopic worms, living in my body, and burrowing, and eating fatty tissue, look very much like tiny [Earthworms]. Then I said: So: if they behave in the same way earthworms behave, then how do I exterminate earthworms, outside, in my garden.. Answer: I use a particular pesticide, and when I spray the ground, the earthworms simply come to the surface, and die.. Then I said to myself; So: Since I might need a Pesticide, that I myself can ingest, what then could I ingest, that's safe, and won't harm Me...... The Host...? Answer: Well, as I watched many many of those videos several years ago, alot of folks were talking about cures, that involved Ordinary Tree Bark; Sarsaparilla.. Yup, seems they used that wood long ago for infections, and for critters that for some reason, were making them sick long ago.
    Then: As I continued looking, I came across another video, that said: Stevia in Liquid - Not Crystal Form, was responsible for killing Spirochetes that cause MS..! - Excelsior..! So guess what I did...:
    - I got up, went to the store, purchased some Liquid Stevia.., I took it by mouth, under the tongue, swished it around for about 2-3 minutes, and then I waited... Well guess what happened...
    About 20 minutes later, somehow..I sensed, that my legs were slowly coming back online.. I felt, that I just might be able to stand up properly.. And so.. after that 20 minutes passed, I decided, and I held onto the portion of the fence next to me.., and I stood up.. I walked slowly back into the house.. I couldn't believe it.. It made absolutely 'No Sense Whatsoever, that something as simple as Liquid Stevia could help Me.., but it actually did. And So: I bought two more bottles, I use them every now and then when I feel I am getting weaker again.., and the same thing happens... And so: It's Just the way that lady said, about Liquid Stevia. It's been many months now, if not a few years since, and though they did diagnose me.., I really haven't had any symptoms anymore. So.., I think I might have been onto something, because I really have had [No Signs or Symptoms of MS ever since], - so I do believe, at least for Me.., That the Stuff Actually Works. I do hope this helps. You Take Care. MDM, JD Candidate, Central California. - Peace. \\//

  • @plaziesmith9348
    @plaziesmith9348 Рік тому

    4000iu but want more now lol think diet is involved to feel real bad if eat the wrong food had kefir yoghurt few days ago never again it was mango and something else thought it would be ok i was very bad off it

  • @steviestevens1247
    @steviestevens1247 2 роки тому +2

    Nice tan 💋💋💋💋