Is There a Cure For Multiple Sclerosis? | Cure for MS
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- Опубліковано 3 лис 2021
- In this video I discuss where we are at with finding a cure for MS and what are the closest things out there. This was something that I was researching voraciously when I first realised I had MS, because that is the natural thing to do. I then ended up looking into how diet effects multiple sclerosis and that was where I found some really promising signs.
There is obviously lot's of work that is currently going into finding a cure and hopefully there will be some in the not too distant future, as some great work is going on across the globe to find a cure for this horrible disease.
Let me know in the comments your thoughts on the treatment options available and whether you have heard any exciting news on updates in the medical field with regards to a cure.
Stay tuned for more videos and hit subscribe if you would like to follow my journey and hopefully we can learn from one and another and live an incredibly healthy life.
Let me know where you are at in your journey in the comments below and let me know what has helped you come to terms with your diagnosis and what has helped you take control.
- Stem Cell Treatment for MS
- HSCT Mexico
- What is MS?
- Living with MS
- Overcoming MS through diet and wellbeing
- Multiple Sclerosis Best Bet Diet
- A day in the life
- Meal examples
These are a few of the topics I will cover in upcoming videos so be sure to subscribe and let me know any other suggestions!
Music used Lower Loveday - Seeing You Around open.spotify.com/track/6EXChx...
Thank you for sharing your thoughts with us. Since March 2018 I*ve been on Orcrevus. Since then the MRI are unchanged. Despite this encouraging news there is still decline. In June 2021 I started with a gluten free, lactose free, diary free, egg free, sugar free diet. The fatique was much better within weeks. There is still decline in my physical abilities but I can fell that there is almost no inflamtion in my body. And that´s good of course. Greetings from Germany
Thanks for sharing your experience. Sorry to hear you are still in decline. You are definitely doing the right thing by changing up your diet though, this will have massive benefits if you keep at it! Have you also looked into mindfulness and reducing stress levels?
@@tomgarbett77 You are right. I had to reduce my stress level. At some point I was not able to work at all anymore. The motivation and the personal drive is slowly coming back. Gymnastics every day is helping a lot.
@tomgarbett77 How are you doing my friend ?
@@tomgarbett77 But for about 2 months I've noticed that things are getting better.
Thanx again for your positivity...hang in there...there is no cure but there is alot we can do to control flairups...so for now we hold on to that
No problem! But yes we’ve all just got to hang on in there, do all we can and stay positive and happy!
Thank you. Yout right diet plays a big part. Please talk about the role of the HPA Axis, and the role of adaptogens in MS.
Yes it definitely does. And that's a great suggestion actually because I similarly believe that the HPA axis is heavily involved in the process of your body becoming systemically unbalanced leading to MS. Adaptogens is also something I will look into further, have you got any particular that you have found useful?
You are right bro, I think we all should get together and do something to boost the research of ms.. please you have a audiance plan something we have to beat MS!
ALSO think.. there are less research organisation institute of MS compair to other disease , but In the last 20 years we have received many medicines. So if research goes a better way we will solve it.
This is great you are bang on! I think I might need a bit of a larger audience just yet to be able to make an impact but that is definitely one of my goals in the long is to keep looking into research and keep pushing the boundaries so that we can make more steps forward!
@@tomgarbett77 OMG! I'm great full for your response.., I have been research a lot and found really there are not that much resarch are going for MS, pharmaceutical companies are just "thinking" about a 3rd phase of trailer of a medicine, HSCT can be the tool, but no research are going about it, just MS people save there money and go for HSCT ,and hope for living more n healthy life, but..there is also a impressive success rate in HSCT. Think about it bro.. there is a really big hope for us.. we should do something..
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A, In my country I must to pay for all medical needs.... irm are free ....but you need to wait a lot...In this time a lot of things can happen....
I wonder how it's in other'S country.i pay also my vitamins and blood tests
Yes I’m fortunate here in the UK that it all comes with the national health service. Where are you from? But yes you’ve got even more incentive to do what you can on the diet and lifestyle side of things to try and combat the disease!
@@tomgarbett77 I'm from Romania,and we are not 100% sure if it's ms.But in near future I will know.
@@luciancotaie8803 well wishing you luck with the results! But whatever it is you’ve just got to accept it and stay positive and do everything you can to combat it.
But for about 2 months I've noticed that things are getting better.
How are you after 9 months on diet? Just a thought, there are 3 million MS patients in the world. Do you think nobody tried to stop MS with diet? I'm also on diet, but last MRI shows disease activity.
Thank's for asking. You are right, in the meanwhile I'm on diet now for 29 month and there still was decline. Less than before, but noticeably. Especially my heat intollerance and my bladder got worse. 8 month ago I started with 16/8 h intermittent fasting and for about 3 months I've noticed that things are getting better. It's an extremely slow process but right now the decline seems to be stopped. And since 12 month I'm not on Ocrevus.
diet yes... but you're also taking heavy DMT that works quite well no? Differentiating between diet & the DMT will be very tricky! :P
Yes exactly! That's why I am hoping I get an MRI soon so I can see the effects of just the diet before the DMT has had time to take real effect!
@@tomgarbett77 ahh great stuff! Good plan :) I am going to try to do the same and see if it has any impact - eating very clean like you are, taking supplements and have upped my exercise - I hope we both see some good results! :)
I hope it works.....eating healty..
I've been drinking celery juice ....then honey dew melons ...juicing... smoothies
Dry fruit.....stay away from stressful people
Music good music...house .plants help too
Hi Tom they dodnt want us to know to much so true However think if we talk to others besides Neuorogist they wont talk! we have l find some answers Like talking to maybe naturopathic doctors and other MS freinds Diet most important factor in MS I think I'm just eating heathly no specific diet is that same or does have be specific diet for MS?
Yes you're right they definitely don't want us to know because so much money is made off the treatments unfortunately! But yes I think the main step is eating whole foods and cutting out inflammatory foods like gluten and dairy. Then being more specific I think 'The Best Bet' diet is the most balanced and scientifically backed up of all the MS diets. So that's why I chose that diet for me!
@@tomgarbett77 I'm eating healthy but no specific diet vegetables chicken fish lately been making turkey I'm my community theybarbeque often roasted pork all this fatty food American diet is awful Some people do eat right though No gluten dairy in my diet Tom
@@juliettesleeve7452 Yes sounds like you've got a great diet then really! Consistency and doing a diet you can continue with is key!
@@tomgarbett77 Thanks Tom will continue eating like this Its key I also do yoga and like walking on beach near shore I feel we have encourage and support one another to be best person we can possibly be 🌿
@@juliettesleeve7452 Yes Yoga is great too to really help mindfulness! But yes completely agree!
I have PPMS , Had a fetal stem cell treatment in Kyiv Ukraine, the only place In the world this type of stem cell treatment is available . It stopped progressive and reversed many symptoms , So I have a much better Quality of life.They have done This treatment for 30 years with much success . look for the god cells podcast episode EP 14 , for my story .
Its inherited and everyone has different symptoms comes on different way Its comes from Swedish origins Its complex disorder rather than disease Bet has something to do genes and chromosomes my opinion but they dodnt talk about it much Tom
Funny you say that because although I have no Swedish descent people have always told me I look Scandinavian because I'm tall blue eyes etc! But yes I think a lot of people have the genetic susceptibility but only some of us develop it due to many other external factors lining up, like diet, stress, leaky gut, HPA axis etc! I will probably get a video together on my thoughts on all that!
@@tomgarbett77 Yes Tom you definitely do look Scandinavian no doubt about it Even if you dodnt have ancestry Somewhere along line there is might go far back Im Anglo Saxon and and swedish in my heritage I We have gene's from way back personally think almost every thing hereditary MS is bit complex but well figure out!! Look forward to your video Tom
Hello brother how are you now, I'm also think there are so much to do with this disease, but low number of research organisation and MS patient make it more slow, but we are also human we also have right to live a healthy life, we MS warrior's should have to do something for it.. what's your thought.. of it?