MS (Multiple Sclerosis)

Most Recent Posts

MS and Low Dose Naltrexone

Shell17 (Victoria, Australia) on 12/27/2022
5 out of 5 stars

My experience with LDN... after being diagnosed with MS in 2018 (symptoms of neuropathy, fatigue, bladder problems, lack of balance, gait problems). I was put on Tysabri and had no improvement in symptoms. I developed a brain tumor in 2020 and had that removed - whether it was that drug, nobody knows.

I subsequently went on LDN in 2021 and this year (2022) the tests from my neurologist showed that I have improvements in all of my nerve tests and no new symptoms. Of course he tries to sell me new pharmaceuticals at every visit but I say no and continue with the LDN.

It must be filled at a compounding pharmacy and it costs $105 for 100 capsules in Victoria, Australia - I take 1 x 5mg tablet daily.

I found this website helpful - https://ldnresearchtrust.org/what-is-low-dose-naltrexone-ldn

It may not be a cure, but I have experienced zero side effects and the regular MS drugs have a massive list of side issues.

REPLY   3      

Wahl's Protocol for MS

Mary (NY, NY) on 06/08/2021
5 out of 5 stars

Dr. Terry Wahls wrote the book The Wahls Protocol: A Radical New Way to Treat All Chronic Autoimmune Conditions Using Paleo Principles. She offers some very interesting information on how cells work in her book. Dr. Wahls had MS so severe she was confined to a wheel chair. She was a vegetarian. She switched to a paleo based diet and slowly reclaimed her health. She advocates eating food for vitamins and minerals. She recommends foods like chicken liver, bone broth for collagen, coconut oil and vegetables broken into 3 groups – greens, sulfur like onions and broccoli and rainbow vegetables like red bell peppers and anti-oxidant fruits like strawberries and blueberries. She also limits her sugar intake to 1 teaspoon per day. I found her book very interesting. She has videos on youtube you can view explaining her principles and amazing recovery:

Minding Your Mitochondria with Dr. Terry Wahls

http://terrywahls.com/minding-your-mitochondria-dr-terry-wahls-at-tedxiowacity/

Dr. Terry Wahls presentation

https://www.youtube.com/watch?v=oW6njb4ZVpA

Bone broth recipe: Cover a whole chicken in water in a pot with 1 Tbl iodized salt. Bring to a boil on the stove, then simmer covered one hour. Pull off meat. Return bones to the broth. Add 1 Tbl vinegar. Simmer 6 hours.

REPLY   5      

Budwig Protocol for MS

Mary (NY, NY) on 06/08/2021
5 out of 5 stars

Here is an excerpt about Dr. Budwig, a doctor that helped cure people of many different diseases including MS from the website http://www.cancertutor.com/Cancer/Budwig.html

Dr Budwig was born in Germany in 1908. She passed away in 2003 at the age of 95. She has been referred to as a top European Cancer Research Scientist, Biochemist, Blood Specialist, German Pharmacologist, and Physicist. Dr Budwig was a seven-time Nobel Prize nominee. In Germany in 1952 she was the Central Government’s Senior Expert for fats and pharmaceutical drugs. She’s considered one of the worlds leading authorities on fats and oils. Her research has shown the tremendous effects that commercially processed fats and oils have in destroying cell membranes and lowering the voltage in the cells of our bodies, which then result in chronic and terminal disease. What we have forgotten is that we are body electric.

The cells of our body fire electrically. They have a nucleus in the center of the cell which is positively charged, and the cell membrane, which is the outer lining of the cell, is negatively charged. We are all aware of how fats clog up our veins and arteries, and are the leading cause of heart attacks, but we never looked beyond the end of our noses to see how these very dangerous fats and oils are affecting the overall health of our minds and bodies at the cellular level.

Dr Budwig discovered that when unsaturated fats have been chemically treated that their unsaturated qualities are destroyed and the field of electrons removed. This Commercial Processing of fats destroys the field of electrons that the cell membranes (60-75 trillion cells) in our bodies must have to fire properly (i.e. function properly).

The fats ability to associate with protein and thereby to achieve water solubility in the fluids of the living body---all this is destroyed. As Dr Budwig put it, “the battery is dead because the electrons in these fats and oils recharge it." When the electrons are destroyed the fats are no longer active and cannot flow into the capillaries and through the fine capillary networks. This is when circulation problems arise.

Without the proper metabolism of fats in our bodies every vital function and every organ is affected. This includes the generation of new life and new cells. Our bodies produce over 500 million new cells daily. Dr Budwig points out that in growing new cells, there is a dipolarity between the electrically positive nucleus and the electrically negative cell membrane with it’s high unsaturated fatty acids. During cell division the cell and new daughter cell must contain enough electron rich fatty acids in the cells surface area to divide off completely from the old cell. When this process is interrupted the body begins to die. In essence, these commercially processed fats and oils are shutting down the electrical field of the cells allowing chronic and terminal diseases to take hold of our bodies.

She pointed out that this can be reversed by providing the simple foods, cottage cheese and flax seed oil, which revises the stagnated growth processes. Dr Budwig discovered that when she combined Flaxseed oil, with its’ powerful healing nature of essential electron rich unsaturated fats, and cottage cheese, which is rich in sulfur protein, the chemical reaction produced makes the oil water soluble and easily absorbed into the cell membrane.

I found testimonials of people from around the world that had been diagnosed with terminal cancer (all types of cancer), sent home to die and were now actually cured and living healthy, normal lives. Not only had Dr Budwig been using her protocol for treating cancer in Europe, but she also treated other chronic diseases such as Arthritis, Heart Infarction, Irregular Heart Beat, Psoriasis, Eczema (other skin diseases), Immune Deficiency Syndromes (Multiple Sclerosis and other Auto Immune Diseases), Diabetes, Lungs (respiratory conditions), Stomach Ulcers, Liver, Prostate, Strokes, Brain Tumors, Brain (strengthens activity), Arteriosclerosis and other chronic diseases. Dr Budwig’s protocol proved successful where orthodox traditional medicine was failing. Dr Budwig pointed out in her book that she often took very sick cancer patients from the hospital with only hours or a few days left to live and had very good results with her protocol, most of the time. She pointed out that in some of these patients she would start their therapy with an enema of 500CCs of an oil mixture and “that their subjective awareness of well being increased immediately.”

REPLY   14      



Ann (Timbucktoo) on 08/18/2019
5 out of 5 stars

In reply to Birdie from Timbucktoo on the Asperger's page:

Birdie from Calgary, Alberta Canada February 4, 2012 at 3:10 pm

Finally after 55 yrs, I realized I had asperger syndrome after seeing a program on TV about it. I suspected mercury poisoning (identical symptoms) so I had all my "silver" mercury dental fillings removed. MUCH relief was obtained doing this. I could not believe the difference! Then I used Olive Leaf Extract capsules to remove the candida yeast and zeolite powder to detox my system of any remaining heavy metals. WHAT a difference! I punted major fear and depression with this stuff!

When I was in my twenties, I had 17 mercury fillings removed because I had symptoms of multiple sclerosis. Within 3 months all symptoms improved and that was 30 years ago!!

REPLY   3      

AHSCT for MS

Kelli (Franklin, TN ) on 12/13/2020
5 out of 5 stars

AHSCT Autologous haematopoietic stem cell transplant (also known as bone marrow transplant) for MS

I had AHSCT in Moscow, Russia in May, 2018. It uses your own stem cells which you then harvest and put in liquid nitrogen. Then you have 4 days of chemo which erases your immune system and the memory of MS. Then they give you back your stem cells to rebuild your immune system. You spend about a week to 10 days in isolation until you reach a safe level to re-emerge. Then you can go home.

The whole process takes 30 days. You can find out more at www.msclerosis.com. First developed by Dr Burt at Northwestern University in 1995. Stuck in FDA testing because of drug company pressure. Been doing it in Moscow for past 10+ years and at least 8 years for foreigners.

I am 2 1/2 years post treatment and have zero MS after 22 years and every treatment both medical and alternative with little success. I had an EDSS of 4.0 and had relapsing remitting but starting to go secondary progressive. There have been over 1000 patients from outside Russia and an effective rate of about 98%. I consider it a cure. They say it may be available in US in 2024, but the sooner you get it the less chance of permanent damage as if the nerves are damaged (demylienated) they cannot be fixed.

REPLY   13      

DMSO for MS Pain (Translated From German)

Gerti (Gallspach) on 07/22/2017
5 out of 5 stars

DMSO gehőrt in jede Hausapotheke

Meine Krankheit MS musste viele Jahre mit der Schulmedizin mehr schlecht als recht zurecht kommen. Bis ich letzten Jahres von natűrlichen Mittel erfuhr. Mein Weg fűhrte mich zu DMSO. Seither ist dies mein tgl. Begleiter ( nehme 2-3 TL oral ein ).Ich fűhle mich seither schmerzfreier, vitaler...., außerdem wird es ebenso erfolgreich bei Insektenstichen, Verbrennungen usw.eingesetzt. Kann diese Erfahrung nur weitergeben.

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Google Translation from German:

DMSO belongs to every home pharmacy

My illness MS had to cope with the school medicine for many years more badly than right. Until last year I learned of natural resources. My way led me to DMSO. Since then this is my daily companion (take 2-3 Teaspoons orally). I feel since then painless, vital ...., besides, it is equally successful with insect bites, burns, etc. used. Can only pass this experience on.

REPLY   7      

Dietary Changes, Supplements Helping MS

Karen (Raleigh, Nc) on 02/12/2017
5 out of 5 stars

I have been following the Swank diet and Terry Wahls diet for about 6 months, and I feel that has helped diminish multiple sclerosis symptoms. Current research has pointed to problems with gut bacteria in ms patients, and lack of nutrients due to this digestive issue. I added a very tiny amount of iodine through kelp supplement, about 50 mcg daily, and felt blood flow to my feet and warm hands and feet, helping blood circulation. (have to be careful taking iodine due to thyroid) I started taking biotin 8 mg daily and that has improved my energy and strength. Also take multi vitamin, vitamin d3, b complex vitamin, magnesium malate and turmeric.

The 9 cups of leafy greens and colorful vegetables and fruits, along with no processed foods, gluten free, low saturated fats and low sugar, per the above diets has helped. I lost 13 lbs on the diet. I was diagnosed with secondary progressive multiple sclerosis previously. I can now drive, as the vertigo and nausea is gone, and my leg strength is better. I have not been to the hospital with breathing problems from "ms hug" since starting the diets. The pain is better. I am currently excited about the biotin, as my energy has improved since taking it. There was a recent study done on biotin which had good results, so neurologists are recommending it and vitamin d3 now. If you take vitamin d3, make sure you take a calcium citrate supplement and magnesium to balance electrolytes.

I drink low sodium V8 juice to get the potassium so it all balances out. I do low salt diet, sea salt only to get the other minerals. Salt was found to aggravate ms, and I found it to be true. I drink a lot of water too, since I believe dehydration was worsening ms. You need about 9 cups water a day for a woman, about 11 cups for a man. I set timer on my phone to remind me to drink glass of water.

Pinching skin on back of hand and raising 1 cm and releasing it, skin should snap back quickly. If skin sinks back slowly, you are dehydrated. I thought I was drinking enough water, but I wasn't! Also take a good probiotic supplement. I still have good and bad days, but the improvement is definitely there!

REPLY   6      

Dave's Protocol for MS - Now on YouTube

Earth Clinic (Atlanta, Ga) on 08/08/2014

Hi everyone!

We just posted a video on YouTube of Dave talking about how he cured his wife of MS 18 years ago. Check it out here: http://youtu.be/CJTRiSFcVLY

REPLY   1      

Re: Friend with MS

Serena (Clover Sc) on 02/17/2014
5 out of 5 stars

This is to Ga_bass from Atlanta, Ga 05/01/2013 concerning friend that was diagnosed with MS. Please tell her to research low dose Naltrexone. It has stopped MS symptoms for many. Good luck and stay away from artificial sweeteners.
REPLY   2      

Inclined Bed Therapy for Multiple Sclerosis

Stephanie (San Francisco, Ca) on 11/03/2013

MS (Multiple Sclerosis) Remedies Needed

Inclined Bed Therapy (IBT)

I would like to suggest people with MS look into Inclined Bed Therapy, which by definition, is the process of sleeping on a bed that is inclined by 4 to 6" at the head of the bed so that the entire body is sleeping on an angle(not just the head, or top half of the body, like with a pillow). The easiest way to do this is to put risers(square, plastic or wood blocks) under the two posts at the head of the bed.

Inclined Bed Therapy takes the pressure off the spine, allowing circulation into the brain stem, allowing new stem cells to develop. People with MS that have practiced IBT nightly for several months report MS symptoms going into remission. There are several websites dedicated to Inclined Bed Therapy and several testimonials, even one man that claims he can walk again due to IBT after only 6 months.

Some of the other reported benefits of IBT include sleeping better through the night, reduced back pain, reduced snoring, reduced sleep apnea and reduced acid reflux, reduced need to urinate in the middle of the night(due to gravity separating the heavy particles from the water particles forcing more water elimination through the lungs as oppose to the bladder). For testimonials regarding many other benefits to sleeping this way, refer to IBT listed here on earthclinic and other websites online, or refer to Andrew K. Fletcher, he is the original person trying to help get the word out. He claims that even the Egyptians, who were brilliant, knew to sleep this way!

If you do have MS, and decide to give IBT a try, please talk to your doctor first and report back your experience here to help others.

REPLY   1      

MS Natural Treatments

Stenya (Los Angeles) on 08/02/2013

What options are available regarding cure/improving MS? Thank you.
REPLY         

Low Dose Naltrexone (LDN) Helping Wife with MS

Fred (South Africa) on 05/17/2013
4 out of 5 stars

My wife was diagnosed with MS seven years ago. The Neurologist started treatment with Rebiff and ocasionally she had to go to hospital to receive a cortisone drip. She had constant headaces, fever and spasms after the injection. She was only allowed to use Panado as a pain killer. (Sometimes up to 8 every day) As time progressed and relapses ocurred the spasms headaces and body pains worsened to such an extent that she could barely walk. Speech and bladder controll was also severely affected. She was introduced to LDN little more than a year ago. We started with a daily dose of 2mg after 9 pm, and she is now on 4. 5mg per day. She has no more headaches, never had a spasm again and can walk short distances without any aid. Her speech and bladder controll also improved. Although the MS caused a lot of damage the LDN improved her quality of life to a great extent. Pity we did not know about LDN sooner
REPLY   2      

Eliminating Artificial Sweeteners and Taking Ldn Helping Ms Diagnosis

Chip (Playa Hermosa, Guanecaste, Costa Rica) on 03/18/2013
4 out of 5 stars

Hello, I have Primary Progressive MS, and unlike most people I know what started it. I used to drink Aspartame sweetened diet soda. In 2004 I started to have significant neurological symptoms, numbness, severe word sluring, loss of muscle control and hot flashes in my left arm. I saw at least a dozen doctors and spent 4 days in the hospital, no one could figure it out. Then in May I went to a Chiropractor and he convinced me to give up Diet Coke, which I was drinking about a 6 pack a day. Immedieatly the symptoms started disappearing and within 2 weeks they were completly gone, except my right thumb and 2 adjacent fingers had some numbness, they felt like anything I touched was through cloth. A follwup MRI showed that I had lots of damage to my brain, and much of my cerebellum was gone (the nerves that control the fingers are in there). I continued to push for a real cause and in December I was diagnosed with MS by a doctor of neurology who was also a professor of Neurology at the University of Miami.

She said I had R&R MS, and I disagreed because I said that I never had a relapse or remission. In any case I did not take anything and seemed to be fine except for the numbness in my fingers. Then 5 years later I started to experience weakness in my right leg, which I attributed to Planta Fascitus which I had in my right foot. I went to a podiatrist and he fixed the foot, and I then went to a physical theripist to strengthen it, she said that the problem was neurological. I than went back to a neurogist and he proclaimed I had MS. Over the next 3 years I steadily declined, never having a relapse or a remission. I saw 3 more neurologists and they all said I had MS.

I tried the Wahles Diet, lots of supplements, the Swank Diet, and acupuncture, all to no avail. Then last week I got a prescription for Low Dose Naltrexon (LDN). I initially got my Doctor to write it for 4.5 mg, but the pharmacist at Skip's Pharmacy in Boca Raton told me to start with 1.5 mg, then after 30days up it to 3 then after 30 more days go to 4.5mg.

Although it has only been a few days already I do not get fatigued by midmorning and my right leg does not cramp up or shake a lot in the morning, like it was. My disease progresses slowly, but I am hopeful that it will now stablize.

I have now retired to Costa Rica, where I got a Doctor to write the prescription for LDN. Since I go back to Florida to visit frequently I hope to be able to keep up the LDN.

REPLY         

Cheryl (Brisbane, Qld, Australia) on 11/02/2012
5 out of 5 stars

I have MS, and have been following Swanks MS Diet for the past 2 years - I have no symptoms of MS (other than brain fog - but that could just be me! ). His diet is all about reducing saturated fat intake. Dr Roy Swank did over 50 years of research on MS. There was a 20 year study completed on this with MS patients which shows remarkable results. And all it takes is changing the food you eat. Please have a look at the following 2 websites - http://www.swankmsdiet.org/ and Dr George Jelinek's site - http://www.overcomingmultiplesclerosis.org/ . These 2 websites have great forums which show that the diet can slow/reverse symptoms of this disease. Both these doctors also have books that are my bibles. Take care and please look into Swanks MS Diet.
REPLY   1      

Protocol for Ms Improved Quality of Life Dramatically

Arkanestudio (Tucson, Arizona, Usa) on 05/22/2012
4 out of 5 stars

My name is Jessica and I was diagnosed with relapsing/remitting MS roughly 4 years ago. I was told that it was most likely the culprit of some issues I had been experiencing for over 15 years. I am going to be 35 this year in October and truly outside of childhood have never felt better. I have had on and off again numbness along nerve paths throughout my body and on my face. I have had phantom "tingles" and "bugs crawling", chronic fatigue, weak bladder control, nystagmis, optic neuritis (I do a really great impression of Marty Feldman every once in a while), restless leg syndrome, a horrible case of shingles in my 20s, and run at a usual temperature of at least 99 which in Arizona leads to heat exhaustion quickly.

I had tried both Rebif and Copaxone and was miserable with not only dealing with the sore site injections and immediate discomfort throughout my body but crappy side effects... I was not me anymore. I also developed a bad case of depression as a side effect and had to be put on more medication. Got to love the drug companies.

I started looking in to things on my own and found that taking a few more supplemental vitamins and adding in other extracts and such while subtracting things like meat, bad sugars, and dairy I could be me again and live virtually symptom free. Stress is not always something easily avoided but it really is my only set off anymore for the disease. I can tell when an exacerbation will most likely rear its ugly head and usually stave it off with relaxation and meditation. Here are a list of my daily vitamins and supplements in case anyone out there is interested in researching and trying a few or all of the suggestions for themselves.

Once a Day:
Alpha Lipoic Acid 100mg
Acidophilus 10mg
Chelated Manganese 5mg
Black Currant Oil 535mg
Chelated Zinc 50mg
Vitamin D3 2000mg

Twice a Day:
Pycnogenol 60mg
Ginko Biloba 60mg
Transfer Factor 600mg
St. John's Wart 300mg

Three Times a Day:
Co Q-10 30mg
Vinpocetine 10mg
Soy Lecithin 520mg
Omega-3 Fish Oil 1000mg
Spirulina 1000mg
Pure Vitamin C Crystals 5000mg per teaspoon (1/2 tsp. ) dissolved in water to take vitamins each time.

I have a smoothie that I make most mornings with frozen fruit, fresh blueberries, protein, and coconut water that I add a tablespoon of extra virgin raw coconut oil to along with a teaspoon of turmeric. I also do a small concoction of 4.5g or 2 rounded teaspoons of magnesium citrate (raspberry-lemon flavored CALM) mixed with 2oz of apple cider vinegar and water.

This may seem a to be a lot to do... But man I tell you what... I am active, awake, and in a good mood about 90 percent of the time. This disease does not run my life and the regimen is small stuff in the grand scheme. A little bit of exercise goes a long way. I walk, hike, swim and dance my booty off because I want to these days and I feel great not to mention dropped weight.

REPLY   10      

Need Feedback on Hydrogen Peroxide for Ms

Orshi (Exeter, Devon, England) on 01/21/2012

Hi all! I was diagnosed with MS 14 months ago, I had a rubbish year, needed steroid every 3-4 month, havent been able to work as I constatly have problem with fatigue, pins and needles and pretty bad numbness in my feet, bladder dysfunction, constipation, weakness and balance trouble, difficulty with walking, blurry sight with one eye and lots of other symptoms.

Steroid works but every time I get some, by the time I start to get back to normal, the problems slowly come back and I'm going down within two month again. It's very depressing. Now, I'm trying to be positive but right now I can't even walk again for ten minutes without sitting down for a rest. When I was diagnosed I was also told that I have EBV and they couldn't really tell 100% that my symptoms are caused by ms or EBV but most likely ms I guess.

I have been reading about Hydrogen Peroxide therapy for about two weeks and it gave me so much hope that I decided to try it. I am on 14 drops today now, climbing up to 25 and then do the whole protocol as it's in the books... I was wondering if anyone with the same problems has tried HP therapy? Please would you share your experiences with me, and maybe give me a little hope that I will get better one day. I am only 30 but I feel like my life stopped a year ago:-( I know I can't expect anything in a couple of weeks but I believe in this now so much that I tell myself every single day that this stuff will help me and I'm willing to do, even be patient for six months for results as long as I can walk, and after if I get better I am going to drink or inhale hp for the rest of my life.

Please give some good news here dear everyone or Ted! This site is great by the way!

I wish you all good health, and I'm looking forward to some answers. Also here's my email if anyone would share their experience with hp therapy in private orsika(at)hotmail.co.uk

Thank you!

REPLY   1      

Diet and Supplements for Ms

Debbie (Melbourne, Australia ) on 12/23/2011

I read this article yesterday from Dr Mercola on a Doctor who cured MS with a paleo diet and some supplements so thought I would pass it along.

http://articles.mercola.com/sites/articles/archive/2011/12/23/overcoming-multiple-sclerosis-through-diet.aspx?e_cid=20111223_DNL_art_1

REPLY   1      

Alkaline Diet for Ms

Dwan (Atlanta, Ga) on 11/21/2011

Hi! Dwan here, in Atlanta, GA who has MS and is now eating mostly alkaline rather than acidic foods - and drinking water with baking soda mixed in.

For those times I decide to eat out eat a restaurant in Atlanta, I want to eat at a restaurant that serves alkaline food.

Is there a directory online that lists restaurants that serve alkaline meals - especially in Atlanta?

Thanks,

Dwan

dwanpete3(at)yahoo.com

REPLY         

Dave (Fountain Inn, Sc) on 10/06/2011
5 out of 5 stars

Both my maternal grandfather and my mother had full blow MS. So I have an intense interest in the subject. After much study I offer these four helps to rebuild the myelin sheath.

First: It is likely that a virus has made inroads allowing lesions after attacking the myelin sheath. This is an open wound on the nerve. The sheath has been made suceptible to attack because the wrong oils have been consumed over the years making the sheath "wall" weak. To build the wall back the patient needs good oils especially evening primrose oil in large quantities; 2-3 thousand IUs daily. The good oils must be used for consumption like Olive Oil. Hydrogenated oils must be avoided at all costs. Most restaurants use hydrogenated.

Second: To kill the virus, the patient must ingest colloidal silver daily for at least 6 months, one eighth cup a day, twice a day. One will not turn blue if you are taking true colloidal silver properly diluted. If one does not want to take the silver then there are other virucydes such as echinacea. Hydrogen peroxide can also work. One will need some professional help to administer that.

Third: The patient must take Calcium AEP, up to eight tablets spread throughout the day. Dr. Adkins in his book Vita Nutrients used Calcium AEP as the most important part of his protocol for treathing MS patients. He would give the patients Calcium AEP by IV drip. But one can get the effect orally also. Google Calcium AEP and you will find the many many great helps AEP can give. (Not just MS. ) The key is not the Calcium. The active worker is the AEP. AEP works on the cellular level to do remarkable things. When ever my mother would have a painful leg/ MS "flare up" I made sure she took an extra four or six AEP tablets. That never failed to give her relief. Please read more on AEP. I do not have MS but I take two daily.

Finally, get on line to find a good source for "sphengelin" and I probably have that spelled wrong. This will actually rebuild the myelin sheath.

Also, get Dr Robert Adkins book "Vita Nutrients" and his treatments for all kinds of problems are at the back of the book including MS. He will recommend much more than I have suggested. He does not go after the virus that many believe is an important element in onset MS. That is my only addition to his excellent treatment program.

REPLY   4      

Nutrition and Chronic Disease

Iowama (Pella, Ia) on 08/29/2011
5 out of 5 stars

Let me start by saying that I do not have MS. In fact, it has been through my own search for a nutritional prevention for Macular Degeneration that I have become familiar with the work of Dr. Terry Wahls, a member of the faculty of University of Iowa Medical School. It was through her newsletter that I began to learn thorough explainations on how nutrition can protect us from chronic disease. Her newsletter led me to look into Oil-Pulling, which led me to this website. Dr. Wahls is a practicing physician who spent four years in a tilt/recline wheelchair before reversing her own MS through a protocol of nutrition and electrotherapy. She is currently conducting a clinical trial of her method. Like I said, I don't have MS, but I don't want anyone else to have it either.
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