Dietary Approaches to Treating Multiple Sclerosis-Related Fatigue with Terry Wahls, MD 

Agreed

Pam Bartha in Canada is doing more for reversing MS. "Multiple Sclerosis is a Parasitosis" by Dr Alan MacDonald, look it up.

So sorry what you've been through😔❤

Sorry to hear about your family :/ I was diagnosed 3 days ago - I am a 26 years old and honestly scared about these stories. What green veg do you eat & what vitamins do you recommend from your experience? Any help is much appreciated. Currently blind in one eye - my first optic neuritis bout never healed :(

@@__Wanderer I was diagnosed this year March. I take Vitamin D3 with K2 (MK7), Vitamin C, Probiotics, and Omega 3. I was on Keto but because of Dr. Wahls I switched to Paleo. I eat a lot of foods rich in sulfur like Onions and Garlic. Green leafy veggies (Dark ones the better), Cruciferous, Fruits as well. Also Celery is good too. I also introduced Animal Organs like Beef Heart, Liver, and Kidney (Grassfed). Exercise, PT, OT, and Meditation highly recommended

@@BlasianGoddessTM77 Hey Blasian, thank you for the amazing comment :) The help is much appreciated! Will definitely try to incorporate some of your suggestions :)

I'm so sorry. My family treats me the same. No one really understands this until your going through it. ♥️🙏 And the vitamins mentioned are a must. And keep moving as much as possible. Hurts, but helps. If that makes any sense.

How's your MS now?

Do a RU-vid search: Dr. Howard Liebowitz/ozone/MS.

Terry didn’t mention clumsy behavior dropping things losing grip. Falling. Is there is a reason for weakness in left leg in particular. How do I get your book, protocol, and diet plan? Also the feeling of spiders crawling on face an legs. How or who do I see for this. I also have vision problems. When I ask dr’s what this means they don’t know an have no suggestions. Who can I turn to for help?

@@cathlynpollom2545 she has an Instagram account. May be write to her there and she could recommend a specialist to you. Best of luck!

Ditto!!

Yes she does! What a remarkable human being 🤍

Agree

V I mo mi ni

You might also find the Clint paddison program helpful.

She found a solution for her illness, she is a doctor, and she is trying to capitalise on it with her “walls” protocols … She didn’t lead a rebellion against allopathic medicine that cheats patients but also doctors!!! Yes she is very “caring” lol

Yes. Works for my ME too

Hey ! I am dealing with MS and I am struggling . What did you eat to treat it ?

The cure for ms is in vitamin D. The cure exists and it is this vitamin d. Look for a treatment called "Coimbra protocol". This treatment was developed by the Brazilian doctor Cícero Galli Coimbra, it consists of mega doses of vitamin d. I have witnessed countless cases of healing, people go back to walking, seeing and living life normally.

@@franciellenunes8552 What about B vitamins? Thank you for the info though - the info on Coimbra looks very helpful. Have you read the works of Grant Genereux? Have you heard of the hypothesis of vitamin A poisoning as the cause of MS and other auto-immune diseases?

@@franciellenunes8552 I was just diagnosed with ms the doctor put me on a high once a week vitamin d med

@@facemango4780 If you keep taking it, it will help you a lot. Be sure to take vitamin D, take it with magnesium bisglycinate.

@@franciellenunes8552 sure will do thanks 👍

She absolutely does not deserve a Nobel Prize for her work. She seems to have no idea what facet or facets of her diet change cured her multiple sclerosis. The underlying cause or causes of MS remain a mystery. And she has made no efforts, as far as I know, to fund or help fund clinical studies on nutritional cures for MS. Read the works of Grant Genereux for better information on MS and other so-called auto-immune diseases.

If you have MS do a RU-vid search for: Dr. Howard Liebowitz/ozone/MS.

It’s called Ehler-Danlos Syndrome

Wow this is great news, Curious how you are doing now three months later? I have fibromyalgia and myofascial pain syndrome which is also connected Tissue disorder. Thanks will look forward to hearing from you.

Diet is an incredibly powerful too. By any chance, you do not have Ehlers-Danlos Syndrome? I do.

@@nataliab5879 I dont yet have a diagnosis but I'm beginning to think you are right. I am much better on the diet.

Congratulations!

Good for you! It is the best thing you can do. Diet and lifestyle currently the only treatment I'm receiving for my RRMS. A word of caution, Terry Wahl as a fraud using peoples desperation to make money. She nuked her entire immune system with chemo (Novantron) and went into remission, before publicly claiming her diet cured her. Not trying to devalue the importance of diet and exercise, but she is a despicable human being.

Get tested for connective tissue disorders . :-)

What was the book? Do you recommend reading that as well?

What kind of algae I wonder

@@ketogenicvegan4970 probably chlorella or spirulina

She cares about money. She is a fraud and a despicable human being. Do a little research.

How are you now?

How are you now?

Bastaría bajar el archivo de subtítulos, traducirlo al español y pedirle al canal que lo añada. Se puede hacer.

You could use an auto-translater I think.

Appreciate video content! Apologies for chiming in, I would love your thoughts. Have you heard about - Seyrooklyn Salient Supremacy (Have a quick look on google can't remember the place now)? It is a great one off product for overcoming the symptoms of multiple sclerosis without the headache. Ive heard some pretty good things about it and my old buddy Taylor got astronomical results with it.

Wow! I hope your mum sees some results and cures herself! This lady is amazing, all the best!

The cure for ms is in vitamin D. The cure exists and it is this vitamin d. Look for a treatment called "Coimbra protocol". This treatment was developed by the Brazilian doctor Cícero Galli Coimbra, it consists of mega doses of vitamin d. I have witnessed countless cases of healing, people go back to walking, seeing and living life normally.

@@franciellenunes8552 - And doesn't he also say you should take K2 along with the extreme high dose vitamin D? I bought a book about the protocol last year though I've still to read it. Vitamin D is a really a magical thing though with MS there is at least potential for the K2 to be the star of the show due to its effects on the brain. Having said that it is probably more likely they work together in synergy. Do you know if Portugese speaking countries have lower rates of MS and/or higher rates of recovery?

@@colinthomson5358 In relation to taking vitamin K together, yes at first it is part of the protocol. Fuction of it has to do with helping calcium to go straight to the bones and not stay in the kidneys and let the excess calcium generated by high consumption of vitamin D occasionally cause kidney failure. However, over the course of many years of study by Dr. Coibra, the creator of the Protocol with the treatment of high doses ended up realizing that although vitamin K is very good it is not entirely effective for this, however he found that instead of vitamin k2 which would prevent patients from having serious renal failure on a calcium and magnesium restricted diet. It is not that vitamin K2 is not good, it is still included in the protocol (especially for patients who can afford it), but the reality is that many financial conditions exist to buy everything. So the basis of the protocol today is a high dose of vitamin d (it will depend on each case), magnesium, omega 3, and the other vitamins dependent on the financial situation of the patient (k2, coenzyme q10, riboflavin, zinc, complex b. ..). In view of my research, I believe that yes, vitamin K2 is very good, but the great cure star for ALL autoimmune diseases and that includes multiple sclerosis is vitamin D. Now these days I have had the joy of knowing that a scientific work international study on the Coimbra protocol was accepted in the international health journal. This work was entitled: "Resistance to vitamin D as a possible cause of autoimmune diseases: a hypothesis proven by a therapeutic protocol of vitamin D in high doses". I believe that the title of scientific research itself was self-explanatory and demonstrated why vitamin D is the big star. Regarding epidemiological data, I have nothing concrete, but I can tell you what I have seen the doctors citing, I have seen somewhere a data that says that only 5% are not fully cured (however, these would be alcoholic patients or smokers, in advanced states of the disease and who almost certainly have emotional problems such as stress and worry). Honestly speaking to you, I have never seen a single case that has not healed. I have been looking for information over the years to help my husband to heal (which in fact came about with this protocol). Here in Brazil, I follow social networks and several people who have done / do the treatment. All are healed or are healing. It is even exciting to talk about it, because I saw and witnessed many cases of people who were no longer walking and running again, people who did not see seeing again, in short the cure for everything. I think the treatment is a little better known here (in Brazil), although even many doctors are unaware of the treatment or do not specialize in order to treat patients with vitamins, the vast majority of people / patients / doctors kill themselves until today hostages of the pharmaceutical industry that always brings more problems as side effects than any cure. I do not know where you are from, but I know that there are doctors qualified in several countries to prescribe this protocol, although they are few, I am not afraid to do it without the help of a doctor, it is necessary to have frequent tests to evaluate the kidneys and so on. Even here in Brazil, I believe that we have around 30 doctors in the entire country alone. For those who came to know the cure this is very sad to know. Sorry for the long text and my bad English, I am not a native speaker. I hope I have clarified some of your doubts.

Congrats!!! And thank you for the comment. 38 years here, undiagnosed but all my symptoms indicate MS... It's too early to see effects (1 week) but I'll keep this diet for a while

eat more fatty meat. The brain , nerves and muscles as well as; intracellular mechanism need tons of fat and cholesterol to function properly. #MetabolicMind #ROBLOX #MetabolicHealthSummit #BestFoodReviewShowEver #DrDaleBrenesen #CharlieFoundation #paleoMedecina

Apply what you read in her book to your daily routine. Mainly foods. Trust me, I was diagnosed this year and got her book and such drastic changes. Sending you good vibes

Did it work? 3 months relatively early but every answer is appreciated

what are some of the ingredients that are available in US/taste good for 'average american' (for me - no nightshades, which means no hot peppers/peppers - thnx)

None. This woman is a fraud and a despicable human being. I have MS. Diet and exercise are the only treatment I can afford. Terry Wahl nuked her entire immune system with chemo ( $25000 Novantrone) and went into remission. Now is using sick people's desperation to make money.

All the best..hope u don't have it

How are you doing? Hoping you’re ok? 🤍

is their any specific test for MS? in my case doctor rules out the possiblity of the rest of other autoimmune diseases like NMO ROG SLE etc and then came to conclusion that ok you have MS.

@@mayankyadav2720 dont rush to conclusion.....its a deficient syndrome rather than disease...they will put in panic state and then you know every thing.....write down here...jmayaank@gmail.com...all what your symptoms are.write as much as possible so that i can reach to conclusion.then i reply...

Did you find out ?

why not go a step further and look at foods that resemble the same supplements your taking :)

Absolutely!

Carnivore diet.

Because its simply the fact they need the greens

Just make sure it's organic because I just read that potatoes are sprayed with glyphosate/herbicides.

Nightshades should be consumed periodically or not at all.. the glycoalkoids, solanine and nicotine outweigh the benefits if your gut bacteria is not diverse and plentiful enough to handle the extra toxins. Gotta make sure your lymphatic system can filter those said toxins as well.. meaning do NOT cover your armpits with aluminum based deodorants... or any at that. If you have bo.. u need to detox.

I cannot eat potato or I immediately get random shooting pains for hours. Maybe yams and sweet potatoes work similarly?

@@HammyGirl999 Sweet potatoes are not part of the nightshade family, so they should be okay. You may have a potato allergy.

High dose d3 20,000 a day. Also k2 to push calcium into the bones.

@@katherine9798 it's medicine cost or Wat. Pls tell me

@@yogeshkumar-up4bj D3 and K2 are vitamins. You can find them at amazon.com

Keto carnivore actually helps. It improve my ms in so many ways. I look like normal person. I got diagnose in 2006.

@@revealedbynaty Are you on ttearment?

How are you managing on a vegan version of this diet? I am vegan too and want to try :)

No better way but to try and see if it works. 🤷🏽‍♀️

"Goji berries could interact with some drugs. If you take warfarin (a blood thinner), you may want to avoid them. Goji berries may also interact with diabetes drugs and blood pressure drugs, so talk with your doctor first. Otherwise, it's probably safe to eat goji berries in moderation."

@@treegreen941 heard goji canbe problematic lately . Take for a week then forget em. That should be enough to end fatigue that's worse than pain. Forever. Safety profile goes threw the roof. Goji is nightshade family