Natural Remedies for MS

The comments below reflect the personal experiences and opinions of readers and do not represent medical advice or the views of this website. The information shared has not been evaluated by the FDA and is not intended to diagnose, treat, or prevent any disease or health condition. Always consult a qualified healthcare professional for medical concerns.

Low Dose Naltrexone (LDN)

5 star (13) 
  87%
4 star (1) 
  7%
(1) 
  7%

Posted by Paul (NY, NY) on 09/15/2006
★★★★★

Editor's Choice

You have nothing written about LDN. I was on the floor drooling this new years day from a bad ms attack, i could not swallow, speak,stand,walk etc. I started LDN www.ldninfo.org and within a months time it reversed all my symtoms and after 8 months im now on my way to walking normal again. LDN works and has been the most effective drug I have ever taken for my MS, my MRI from 2002 had 11 lesions and my MRI from last month after being on LDN for 8 months had zero (0) lesions on the brain. email me for an article I wrote on LDN. email:[email protected] and paulnicholasonline.com

Replied by Pat
(London, England)
10/26/2008

I have a friend. he is 42 been ill for 2 years now. just released from 4 month stay in london hospital. he has been disagnosed with progressive ms. I have never heard of ldn. what is it. and where can he buy it. many thanks pat .x

Replied by Dudley
(Virginia Beach, Va)
12/15/2009
★★★★★

Naltrexone is a cheap generic pharmaceutical approved by the U.S. Food and Drug Administration for treating drug and alcohol addiction. In very low doses, it is proving to be remarkably effective in treating multiple sclerosis--with minimal side effects and at a price anyone can afford.

For more information about Low Dose Naltrexone (LDN), visit

http://tinyurl.com/intro-to-ldn

The above site features links to LDN-related research, case histories, discussion groups, books, articles, and video clips.

Replied by Hristinad
(New York)
03/23/2016

Where can I buy LDN, or a doctor must prescribe it?

Replied by Rsw
(Oh)
03/24/2016
★★★★★

Hi Hristanad,

LDN is an inexpensive prescription drug in the US. It is gaining recognition among doctors and many will prescribe it. If, however, you can't get a prescription, you can buy it overseas, online. There are also several doctors in the US who will prescribe after a phone consultation. You can buy 50mg pills that can be diluted with 50ml of distilled water to make your own solution, where 1ml of solution equals 1mg of LDN. Measure the dose with a $1,5ml dropper, available at any drug store. Very easy to do. It will keep in your refrigerator for up to 90 days. The new updated, comprehensive book, "The LDN Book" by Linda Elsegood is available on Amazon. If you join the LDN Yahoo Group and ask how to get some, the members will give you details about where you can buy it. I'm not sure that I can post it here. If you look on the www.ldninfo.org site, it will give you a list of reliable compounders in the US to use if you get a prescription and the Yahoo LDN Group address. My doctor told me LDN would be very helpful for my autoimmune problems, and to try to get some because she wouldn't prescribe it off-label. I buy mine overseas for the past six years and have never had any problems, and about half of the 12,000 members also buy their own. I think you can google "buy LDN" and you will see some sights, but most buy from the one run by Ian, who also takes it himself and donates to the LDN community. It does not come from China. If you have any further questions, please join the Yahoo Group that is listed on the LDN site listed in this post, and you will be welcomed and your questions will be thoughtfully answered. By the way, for the Crohn's people here, there are several posts right now from experiences of member users, about the current research and Dudley(the moderator) has posted links to first-hand accounts from other Crohn's users, and many links to research and helpful information. LDN is completely non-toxic, taken by mouth, with no side effects except possible short lived sleep problems, and that can be remedied by taking it in the morning. It is helpful with many autoimmune diseases, including Crohn's, IBS, Hashimotos, RA, (many others listed on the LDN site)by modulating the immune system, not killing it, is extremely helpful for MS, and mitigates the damage to healthy cells in cancer treatment. Some have successfully used it with other supplements and/or allopathic or holistic treatments for cancer. Best wishes! You have nothing to lose and much to gain.

Replied by Deb
(Florida)
03/24/2016

LDN must be prescribed by a MD & comes from a compounding pharmacy. Around $20 a month. I think you should start low to see how you react 1 to 1.5 mg, then 3 mg, then 4.5 mg if it doesn't bother you. It makes me VERY dizzy, then nauseous. Good luck!

Replied by Tom
(Los Angeles, California)
03/24/2016

Hi,

I am also looking at LDN to treat my daughter diagnosed with Crohn's disease.

I have heard good things about LDN to treat gut issues.

Please share all the details about LDN if anyone has used it to cure their gut issues.

Thank you. Tom

Replied by Deb
(Florida)
03/24/2016

LDN must be prescribed by a MD & comes from a compounding pharmacy. Around $20 a month. I think you should start low to see how you react 1 to 1.5 mg, then 3 mg, then 4.5 mg if it doesn't bother you. It makes me VERY dizzy, then nauseous. Good luck!

Google Burt Brekson MD PHD.. Dr. Brekson sen uses LDN & IV Alpha Lipoic Acid for everything, cancer, MS. Start low 1 to 1.5 mg, then 3 mg, then 4.5 mg. call a compounding pharmacy ask if anyone in your area prescribes it, they'll know. It makes me very dizzy.

Replied by Rsw
(Oh)
03/24/2016

Hi Tom,

The moderator of the Yahoo LDN site has given me permission to post his page on Crohn's here. He is very generous with his knowledge and time. I think you will find it helpful. Best wishes.

https://sites.google.com/site/dudleyslowdosenaltrexonesites/treating-crohn-s-with-ldn

Replied by Rsw
(Oh)
03/25/2016

Dudley's page can be found about half way down this page that displays. There are also other LDN sites listed.

The one caveat I didn't mention on my current post that is important, is that LDN can be taken with ANY other drug, including steroids during flares, if necessary, but CANNOT BE TAKEN with OPIATE based drugs. They both compete for the same receptors and LDN will always win, which could throw an opiate user into an unexpected and potentially dangerous withdrawal. LDN will block the effect of an opiate. If surgery is anticipated where opiates will be used afterwards for pain, LDN should be discontinued a few days before the surgery or another kind of pain reliever needs to be used for a few days.

Replied by wuan
(singapore)
07/03/2026
3 posts

LDN- request to Rsw(OH) posted did 2016 about buying LDN oversea

Dear Rsw

i saw your posted mail did 2016 stating of buying LDN oversea ( as nonprescription)

would appreciate that you can advise where you are buying from oversea ( whether Alldaychemist can be trusted)

thanks

hendor


Low-Dose Melatonin


Posted by Art (California) on 11/17/2025 2892 posts
★★★★★

Low Dose Melatonin Helps People With Multiple Sclerosis In A Human Study

In the following randomized placebo controlled trial (RCT) it was found that just 3mg per day of melatonin offered beneficial effects to people with Multiple Sclerosis (MS).

Here is a link to an abstract of the RCT :

https://pubmed.ncbi.nlm.nih.gov/39849681/

Here is a relevant quote from the RCT :

' Based on this study, the 12-week melatonin supplementation was effective in improving knee muscle strength, manual dexterity, static postural balance, mood, and cognition in multiple sclerosis patients. '

Art


Mercury Fillings Removed


Posted by Ann (Timbucktoo) on 08/18/2019
★★★★★

Editor's Choice

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!!


MS Natural Treatments


Posted by Stenya (Los Angeles) on 08/02/2013

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

Replied by Rsw
(Uniontown, Oh)
08/02/2013
★★★★★

Low dose naltrexone is 89% effective in stopping MS progression. It is inexpensive, an FDA approved drug, has no side effects except possibly vivid dreams for a week or two, and is taken by pill or liquid. See www.ldninfo.org.

Another all natural product that has been excellent in several MS people I have talked with or heard of, is a Lion's Mane mushroom product made by Mat--x Mushroom. The person I talked with had been taking Avonex for 13 years, had loss of feeling in the legs, began taking the mushroom product and can now ride her horse since she now can once again feel her legs. Her other symptoms are also gone. A man in CA was in a wheelchair, took the mushroom product and now can swim, walk, and works 14 hour days for the mushroom company. He was so happy with the product that he asked for a job and got it. They are now making a product especially for MS people, that contains Lion's Mane, Reishi and Cordyceps. (I have no financial or other interest in this company) Best wishes!

Fritzi
(San Francisco)
06/29/2025

Can't find Mat-x Mushroom company. Has anyone here been able to locate them?

Replied by Just A Thinking Guy
(Kansas)
08/02/2013

I was impressed with Dr. Terry Wahls cure for herself. You can see it on youtube: http://www.youtube.com/watch?v=KLjgBLwH3Wc


Nutrition, Electrotherapy


Posted by Iowama (Pella, Ia) on 08/29/2011
★★★★★

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.

Replied by Wongoblly
(San Diego, Ca, Us)
02/02/2012

I just came across Dr Terry Wahls too. It really is amazing. Please if you now anyone who has MS let them know about her. They can decide for themselves. She has Secondary-progressive multiple sclerosis (SPMS). again she is a Physician who went from four years in a total recline wheel chair only able to walk a few steps with two canes to riding a bike. Have a peek at her website & youtube videos. I don't have MS but it's nice to see what God's food can do to heal us.

Replied by Debbie
(Melbourne, Australia)
02/02/2012

Here is a video by Dr. Terry Wahls which tells you what she ate to cure her MS and get out of her wheelchair. It offers excellent information for everyone needing advice for better health and I really recommend everyone watch the 17 min video. These are the foods we all need to get back to eating. She also mentions foods for liver and kidney cleansing, really helpful stuff.

Replied by Debbie
(Melbourne, Australia)
02/02/2012

Here is Terry Wahl's website. She cured her own ms by eating a paleo diet and adding certain things to her diet. She also has a YouTube site. We should all be eating this food.

Http://www.terrywahls.com/

Replied by Iowama
(Pella, Ia)
02/03/2012

I was looking around on Amazon regarding the latest edition of Minding My Mitochondria and found a review/ response in which the author went through the diet point by point and created a very thorough overview of it (and it has undergone a few updates since I purchased my copy. ) If this is posted under MS, I hope that it will also be posted on the "Healthful Diets" page under "Paleolithic Diet". Thank you and best wishes to all. The link is as follows:

http://www.amazon.com/review/R2LW87M7BQOUQE/ref=cm_cr_pr_cmt?ie=UTF&ASIN=098217508

Replied by Wongoblly
(San Diego, Ca, Us)
02/03/2012

Oh yes I agree with setting another category "Healthful Diets" page under "Paleolithic Diet". Pella, EC suggests you put in a request form to them to add another category page.
Does anyone know how to request a new page at EC? I did notice a drop down menu at top of page submit feedback

I didn't know I could post links here. Everybody should see her history video above link. I saw it last month on youtube plus others.

Also watched "Food Matters the Movie" another excellent video.

Duration 1:18

http://www.youtube.com/watch?v=KmJme9yjLqU

This EC site is awesome. wongoblly

EC: Yes, it was cross posted to Diets section under "Paleolithic Diet".

Liza

Replied by Wongoblly
(San Diego, Ca, US)
02/04/2012

Thank you for the update from Liza at EC. I had no idea it was there too.

Replied by Timh
(Louisville, Ky Usa)
02/04/2012
2041 posts

Living near a Mennonite community, one can't help but see how easily the healthy diet comes to these people. Yes, we all have choices, BUT most of us have limited ones in the context of our modern lifestyle/environment. Solitary, disabled, limited budget folks like me don't have many choices. My best option is eat as healthy as possible AND supplement. I will pose this option/combination ---diet and supplementation as superior to the (either) (or) "choice".

Several yrs gone my dad had finally reached the age of retirement but his health was in steady decline. Fatigue, short term memory loss (forgetfulness), overweight, malice, irritability, depression, etc. Then comes debilitating arthritis. Dad agreed to my recommendation to a good wholefood multivitamin/mineral ---2 daily. 2 mo later and after being out-of-town for 2 wks Dad returns and walks into the hospital room where I was bedridden and I didn't even recognize him until probably 10 sec. later. The results was astounding ---lost 20 lbs, color returned to eyes & skin, mentally sharp w/ no more depression; this was from only 2 multi's day.

If one can eat a very healthy organic (paleo) diet there are yet limitations as far as quantity of nutrients goes, so I would suggest supplementing w/ advanced nutrition (for the topic of mitochondria) like CoQ10, NADH, Alpha Lipoic Acid, d-Ribose, Quercetin.

Of course clean air & water is a must as is exercise to keep the "fire" of the mitochondria burning (cellular respiration yielding high energy Adenine Triphosphate ATP).


Selenium


Posted by Wendy (Plover, WI U.S.A) on 10/29/2007
★★★★★

Hi, Se helps the thyroid which slows down due to celiac. Faster working thyroid helps increase oxygen to the brain cells. Brain cells need more oxygen than other cells. Heavy metals block the thyroid medicine from being used and may block how the hemoglobin works. I was full of heavy metals. Colloidal siver poisoned me. It was the worst hell. I don't recommend anyone take colloidal silver. They may build it up like I did.

Replied by Bessie
(Vancouver, Canada)
10/30/2007

Regarding Earth Clinic's query about "Se" in someone's post. It stands for Selenium which is extremely helpful for those who have problems with their thyroid. By the way, I love this site and check it regularly. I've learned so much. Thank you!

Replied by Dr. J
(Bombay, Maharastra)
03/16/2009

Silver is not a "heavy metal" wendy!!! Its up there with calcium and copper and "correctly made colloidal silver" does not and can not build up in the tissues, argyria which is caused from adding salt etc to silver making process and which causes this silver skin is reversible anyway and harmless. Your high level of sheavy metels were caused by other things such as diet, lifestyle, bad water and amalgum fillings etc. EDTA, cilantro and antioxidants can remove your heavy metals.

For those who are fearfull from this "confused" comment please read now:
http://www.argyria.info/
http://www.silvermedicine.org/argyria.html

Replied by David
(Fountain Inn, Sc)
12/30/2012

One theory concerning MS is that it is virus based. But it is more complicated than most viruses because complicating the onset and progression is an underlying heavy metal in the system. Typically this is mercury.

I have had a lot of family history with MS. When my wife was stricken I used what I'd learned over the years. An MRI demonstrated two lesion in her dorsal vertabra. Hence, she suddenly could barely walk.

Well I knew the road ahead using the conventional treatment so quickly moved to get the mercury out of her system. She did have highly elevated mercury. Only four months earlier she had dental work using mercury amalgams. We killed the virus using colloidal silver drinking three tablespoons daily. She had the fillings removed and chelation to get the mercury removed. Ala Dr Robert Adkins book "Vita Nutrients" who used Calcium AEP in IV form for his MS patients, we added three capsules of that to her vitamin routine. Finally, we got on line "sphengoline" which is a myelin substance and can repair the lesions.

In only two months there were no more symptoms. She keeps her Cal AEP close by in case she can feel a coming "flare up. " That was fifteen years ago.

I have seen this formula work with at least ten MS patients with amazing results.


Supplements


Posted by Arkanestudio (Tucson, Arizona, Usa) on 05/22/2012
★★★★☆

Editor's Choice

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.


Ted's Remedies


Posted by Rich (Boca Raton, Fl) on 01/30/2009
★★★★★

For the "Partial Leg Paralysis" or "Arm Paralysis" claim, I have to admit that I found myself somewhat skeptical about the "Edgar Cayce Electricity claim". However, it appears that one electrical device has now been clinically verified to "repair this symptom". This device was recently showcased on the Doctors TV show.

Bioness Announces NESS H200 and L300 Systems to Be Available at 88 HealthSouth Hospitals Nationwide
http://www.healthjockey.com/2007/05/26/nes-l300-electrical-stimulation-device-for-partial-leg-paralysis-unveiled/

There is a fungalbionics book which seems to implicate the Aspergillus fungus as a possible cause of MS (Ergot poisoning). It seems to say MS is responsive to Nystatin, a non-absorbed antifungal medication. Note: Many nystatin medications are mixed with sucrose(sugar), and so this may reduce effectiveness. I suspect that the SSKI remedy would be beneficial to many ms patients, but I have no experience dealing with the matter, so defer to Ted on the matter.


The Liberation Procedure


Posted by Laura (Denver, Co, Usa) on 03/03/2012
★★★★☆

WORKED TEMPORARILY

I had the Liberation procedure 3x. The 1st time (June 2010 India) good results but very temporary, the veins weren't opened up wide enough. The 2nd time (Aug 2010 Los Cabos Mexico) great results that lasted 6 months, then symptoms came back. The third time (Mar 2011 California) veins were still open, even though symptoms had returned. So I had to look for other options.

Replied by Jowl
(Maine)
07/06/2023
21 posts

Nobody gets this procedure anymore.

The inventor of the Liberation Procedure had to admit after RCTs that the procedure did not do anything beneficial. Sounds like you had placebo effects.


The Liberation Procedure
Posted by Travel Girl (Salt Lake City, Utah) on 07/20/2011
★★★★★

I have had venoplasty or what is called the liberation procedure two times now. The veins that drain the brain and spine are stenosed causing blood to back up in the brain and spine which in turn causes the placques or sclerosis. It is and continues to be the best thing I have ever done for my MS. (I still take LDN. ) The interventional radiologist performs angioplasty/venoplasty and baloons the veins that are stenosed. After the first venoplasty my fatigue went away, I had less brain fog and could feel my fingertips for the first time in years. I also started to dream again. My veins stayed open for about 5 months. Around month 6 the fatigue started in again and I knew my veins must have collapsed. I went back in for another MRI and my brain scan actually showed improvement. I did have 5 lesions on my brain and then after venoplasty I had 3. This procedure works. Nine months from the original venoplasty, I had another one. This time they put me on blood thinners and I am hoping I get more time with this procedure. I recommend looking at the web site www.ccsvi.org or ccsvi facebook for education into this new procedure to help with MS.


The Liberation Procedure
Posted by Sofie (Tyler, Texas, Usa) on 04/09/2011

is anyone familiar with this procedure by Dr. Zamboni in Italy and is there anyone in the usa that performs the procedure?

Replied by Annapt
(Medina, Oh)
04/10/2011
★★★★★

I had this procedure done in February in Albany, NY. Absolutely amazing results - no more spasms, great balance/gait, no more brain fog. Only thing that truly helped me and made me feel normal again.


The Liberation Procedure
Posted by Joyce (Joelton, Tn) on 05/20/2010 489 posts
★★★★★

I seem to recall a number of people on earthclinic.com seeking help with MS. You might want to put a link to this site on EC.

http://www.healthiertalk.com/new-discovery-liberation-treatment-multiple-sclerosis-1789

Seems that Dr. Zamboni (Italy) seeking help for his own wife determined that it is a vascular problem rather than an autoimmune disease. Thank God for the Zamboni's of this planet earth.

Of course they will probably have a little trouble finding someone in USA doing the liberation procedure. I would suggest contacting some place like Mayo Clinic for information.

Replied by Julie
(Buffalo, Ny)
03/16/2011

Hello, I just wanted to say that I've been doing research on the liberation treatment for some time and have come to the conclusion that I want to be tested for CCSVI. Yes, Dr. Zamboni is running trials here in Buffalo, NY but with such high numbers with people having MS here it is a difficult study to get into. I decided I would go to Poland or another country performing the procedure because I am only 29 and was diagnosed in'08 and I have two young children. Upon researching I found a Dr. Here in New York State that does do the procedure and I finally got my referral to see this doctor for evaluation. The staff there is very polite, via talking to them, and I look forward to going. I was also told by staff at the office that some insurance companies are on board now with paying for this procedure to be done. I will post an update after I go for my initial visit.

Replied by Phyl
(Ocklawaha, Fl)
07/17/2011
★★★★★

I had the procedure done in Feb, 2011 with good results and if my veins close up, I will go back and do again. Most of the people on our facebook page who have had it done, some 4 times with great results along with doctors who have ms. I have went off the shots and now only do LDN. There are alot of places in the US now that do the procedure. I had mine done in FL at SHands, also the Moffit Center in Tampa is doing it. Also try this web site, http://ccsvi-ms.ning.com/ and join that, there is alot of info on there and it show you places in the US close to you for the procedure. It is an easy procedure, in and out the same day with no problems. Don't tell your dr you are having it done, just make the arrangements on your own and they know how to word it so the insureance co's will pay. (most of them) Good luck


Turmeric


Posted by CORAGA (Milwaukee, WI) on 09/26/2007
★★★★★

I was diagnosed with MS in 2001 and it been a living nightmare. I did some research and I found Turmeric on the internet. I went to Outpost health store in Milwaukee. I am really shocked at my symptoms. They are not as bad as they were before. I am working out everyday and not having as many relapses as before. I feel better then every. I though a few months ago I was heading for a wheelchair. I take it with Organic Carrot Juice in the morning and occassionally I have it in some bottle water a few days a week. It works.

Replied by Kim
(Atlanta, Ga)
03/21/2011

HOW MUCH OF THIS DID YOU USE IN YOUR CARROT JUICE? AND WAS IT THE KIND YOU BUY IN THE GROCERY STORE - POWDERED?

Replied by Coraga
(Milwaukee, , Wi)
05/18/2011

I use about one tablespoon. I stopped taking it a few years ago. But I started back as my MS has progressed, and I am eating a lot of healthy food every day.


Vaccinations


Posted by Mary (Southaven, MS) on 05/18/2008
★★★★★

This is so strange; I found this site while researching about my dog's bad reaction to vaccination. I watched the video on You-Tube in the above link, thinking it was about animals. It was about human vaccinations. In the information, it mentioned persons getting auto-immune diseases, such as multiple sclerosis, after routine vaccinations. My husband got MS 8 years ago when he was 48 -- after taking his very first-ever flu shot, and had received a tetnus booster just a month or so before. Coincidence???.... I can see I have some more research to do. As for my chihuahua, after reading all the stories on here, she will NEVER receive another vaccination of any kind. She is strictly an indoor dog and I no longer see the need for it.

EC: The post Mary is referring to is from our Pet Vaccinations Side Effects page:

05/11/2008: Sherri from Atlanta, GA replies: "You may want to sit down and take a deep breath before you watch this disturbing video on vaccines. http://www.youtube.com/watch?v=ELx2eX_kM-w"

Replied by Joyce
(Joelton, Tn.)
05/18/2008
★★★★★

To Mary from South Haven 5/18/08 - Could very well be connected to his first ever flu shot, but you're not likely to ever convince the FDA of this (or his doctor). Knowing that they are now putting monosodium glutamate into vaccines, if they are calling it a preservative, they might also be putting it into the nasal spray ones which would give the MSG a direct route to the brain through the olfactory nerve. MSG is a well-known neurotoxin to the brain. Also the Gulf Storm veterans are still battling to prove that something in the vaccine they were given as a prophylactic caused their Gulf Storm Syndrome and the last I heard the government was trying to say there is no Gulf War Syndrome, that it is all in their heads (fancy word is psychosomatic). One doctor found squalene in GS veterans blood samples that she checked that she said caused. But the argument is still alive! Another known neurotoxin called sodium fluoride in our water supply is also implicated in multiple scherosis. Any toxin that you can eliminate won't hurt and probably will help.

Replied by Leslie
(Indianapolis, In)
10/23/2009
★★★★★

It is possible his vaccination contained a preservative called Thimerosol which is mercury-containing. Mercury is highly toxic to the human body. I have had bad reactions after vaccinations. Mercury is also present in "silver" dental amalgam fillings of the teeth and has been implicated as a possible contributor towards MS. It could be a heavy metals issue or that the vaccination was the impetus for an immune response that triggered the MS. FYI.


Vitamin D3


Posted by Phyl (Ocklawaha, Fl) on 08/26/2009
★★★★★

Research has now shown that the cause of MS is the lack of vitamin D3. On the web site patientslikeme.com a group of patients have been keeping a journal. All the research that is being done in the world says the you can take up to 40,000 iu of D3 a day and it is not toxic. There is alot of info to read. In my own research, John Hopkins told the FDA years ago that people were deficient in Vitamin D3 and there would be more diseases because of it. I have MS and I am not able to walk without a cane, walker or I use a wheelchair. I am on Copaxone and have no trouble with it. There is a new drug going for FDA approval in Oct., it is call Fampridine. It is suppose to help with walking ability. I live one day at a time.

Replied by Jen
(Eureka, Mt, Usa)
01/18/2011

Phyl mentions Fampridine (also called Ampyra) for MS. Please research this carefully before using -

"The non-sustained release form of fampridine (i.e. , 4-Aminopyridine Or 4-AP) is used as a bird poison to excite the nerve cells so much so that birds get seizure and die. In the process of neuronal excitation, a few individual members of a flock of birds, who have ingested the poison on the roof of a federal building, become hyperactive and utter distress calls which signal other birds to leave the site. The compound is highly poisonous to mammals. It has in fact been known to cause severe poisoning, and in some cases, death, in adult humans. "

I looked into this at my mother-in-law's request, as she has been dealing with MS for about 15 years. This drug is not only dangerous, but in the control studies, people's ability to walk a distance of 25 feet was only increased by .8 seconds. Not even a full second, so is it worth the risk for next to no pay-off?

Replied by Wendy
(Mississippi)
04/09/2015

Hi David, your post, by far, has been very enlightening and has opened my eyes to things that I've been missing in regards to treating my MS. When you discuss the Primrose oil, how much should I be taking daily or more than once a day and do I take it with something else or do I just drink it doesn't come in a capsule? Also, in regards to Dr. Atkins book Vita nutrients does the title also include something about all the other drugs. I have had MS for 10 years and I have been a doctor of pharmacy for 20+ years but I no longer work but instead I do consults from home. You have given me hope and truly means more than anything else. Thank you for the information. I hope this text makes it to you and know it was written a few years back and I hope you are doing well. Thanks for the info and I look forward to hearing from you. God bless

Replied by Greg
(Port Alberni BC Canada)
12/10/2024
★★★★★

My wife woke up 5 years ago and was in complete body pain. Found out she had the autoimmune disease rheumatoid arthritis. They put her on 4 drugs. She took herself off 2 right away because of sickness. Then we did research and decided to try natural. She started taking 200,000iu's of vitamin D3 along with K2, magnesium, turmeric and moringa. Every month she got her blood checked. By September she had reduced herself to half of one drug. By December her blood test came back saying it didn't register RA. She cut herself back to 30,000 iu's a day and it's Dec 2024 and she's doing amazing. She had a flareup in July and cutout sugar and carbs and has been feeling better then she ever has. She had some bumps on her hands before July but they're all gone as well and she's lost 30lbs and is about 130lbs and feels great. So keep your vitamin D high with vitamin K2, magnesium and tumeric and drink at least half a gallon of water a day and things will be great. The key is patience, it takes time for your body to recover and build the nutrient supply.

Todd
(Philly)
12/11/2024

Thank you for sharing. Can I ask what brand of vit d3 with k2 you used?



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