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.
Mercury Fillings Removed
Posted by Ann (Timbucktoo) on 08/18/2019
★★★★★
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!!
Low Dose Naltrexone (LDN)
Posted by Rsw (Oh) on 08/06/2018
3mg. of LDN is often recommended for those with MS due to spasticity problems in some at 4.5 mg. If muscle cramping or spasms occurs at 4.5mg/day, reduce your dose to 3mg/day and see if you feel better. You will still reap the benefits of LDN.
Dave Thomas Protocol
Posted by Dave (Fountain Inn, Sc) on 05/20/2015
Hello Sameer,
Re the EC video post on my wife's MS;
The list is given on the video but I'll be happy to relist for you:
1. We had to get the mercury out of her system. There is evidence that MS is caused by a heavy metal combined with a virus. When tested she DID have mercury off the chart. She had just had amalgam fillings put in six months earlier. So chelation removed the mercury at large and one at a time using a "dam" the amalgams were replaced.
2. She took a lot of colloidal silver to kill the virus...that over a year... two times daily...about six tablespoons a day.
3. She took sphingolin daily to rebuild the myelin sheath. Can get on line. She took 3 tablets daily.
4. She took six tablets of AEP daily...vital.
5. Also she took 3 tablets Evening Primrose Oil daily which helps build cells. The western diet provides inferior oils... too much hydrogenated oils... deadly for the brain and causes dementia. By the way, this is why an extended low fat diet can be detrimental.
I was told aster her MRI that she would have to face a life of degenerating mobility. She was fine all her life after we got past the initial six months of turning her around.
Hydrogen Peroxide
Posted by Mark (Co) on 03/26/2014
★★★★★
I am taking hydrogen peroxide for my MS and find it very beneficial. :)
Dave's Remedies
Posted by Dave (Fountain Inn, Sc) on 10/06/2011
★★★★★
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.
Vaccinations
Posted by Joyce (Joelton, Tn.) on 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.
Hydrogen Peroxide
Posted by Rich (Niles, Trumbull) on 03/20/2008
★★★★★
I am trying HP added to distilled water to treat my wife who is disabled and unable walk. I am trying 35% hp in distilled water/6 drops per 6oz once per day. I would appreciate any recommendations. She seems to be more mentally alert and aware. Have been using for about a month and just recently increased from 3 to 6 drops.
Hydrogen Peroxide
Posted by Rich (Niles, Trumbull) on 03/20/2008
★★★★★
I am trying HP added to distilled water to treat my wife who is disabled and unable walk. I am trying 35% hp in distilled water/6 drops per 6oz once per day. I would appreciate any recommendations. She seems to be more mentally alert and aware. Have been using for about a month and just recently increased from 3 to 6 drops.
Colostrum
Posted by Isabel G (San Antonio, Tx) on 04/14/2009
★★★★★
I suffered from season allergies, anyone who has them knows hos miserable it can make you feel...I actually started with ____, which is the same thing as colostrum but more technical and scientific, I ended up changing to colostrum because of the price...anyhow when cedar comes along all i need is my colostrum pill and the symptoms are almost none...while before i was taking oral medicine, eye allergy drops and still feel terrible and what to say about all the side effects from them . I really swear by this product.
Copaxone
Posted by Dallas (San Diego, California USA) on 03/29/2007
★★★★★
Reader Question from Saint Clair Shores' asked if they could try other therapies along wtih Copaxone treatment. As Ted said, "YES". Copaxone is a complex amino acid chain that simply acts as a decoy and gives your immune system something to work on instead of attacking the myelin cover on the nerves.
Shared Solutions which helps patients manage their Copaxone therapy says that there's no drug or vitamin interaction with Copaxone so it's safe to take other meds and supplements. Once on Copaxone, do everything in your power to remain on the Copaxone therapy. Yeah it's a hassle with the daily injection but it's a small needle and much easier to deal with than Avaonex or Beta Seron. Usually the only problem could be an injection site reaction. I know people that took Beta Seron years ago before Copaxone came along and they had flu like symptons after taking the injection.
Even if you're not on Copaxone, go to the SharedSolutions.com web site and look at the info. Then give them a call and get signed up with them and they'll send you more info and keep you on their mailing list. Copaxone isn't cheap and you likely need insurance to offset most of the cost and Shared Solutions can possibly help with finding financial help.
But definately yes, try other natural therapies and adding supplements to your daily routine. Just as MS affects each of us differently, one thing might work for you while it doesn't work for the rest of us. Unless you're lucky enough to have an amazing Neurologist then it's up to you to educate yourself, network with group and individuals and sometimes be your own doctor to see what helps you.
And like others said here, plenty of sleep and a REGULAR schedule really helps most people suffering from MS. And here I am writing this at 4am :-) I can attest to having a mixed up sleep schedule and how it works against you.
Even though Copaxone has worked well for me and a good friend that takes it, I'd be interested in trying the Honey Bee Venon supplement. I'd seen a video years ago about people with MS getting together and doing group Honey Bee Venom therapy through actual Bee stings. It looked painful but it sure worked for many of the people.
I rambled on here quite a bit because if mentioning a single item here can point someone down the path to finding relief from MS, then I've done a good deed for the day. Be your own doctor, be your own researcher, be proactive and hopefully you too can find help.
May God Bless each of you.
Books of Interest
Posted by Jacqueline (Athlone, Westmeath, Ireland.) on 06/12/2011
Len from Chicago, "There is also medical treatment available from scientists who have put their products through all the rigorous trials required for a drug to be deemed both safe and efficacious.
Considering the well documented and severe side effects from a lot of pharmaceuticals medicines and their tendency to treat only the symptoms and not the underlying causes. Which can lead to a long term dependency and usually damage to the liver. I think there can be no harm in giving these natural remedies (which have been used for hundreds, sometimes thousands of years without strong side effects) a try.
Calcium, Magnesium, Vitamin D, Potassium and Chromium
Posted by Hope (Hannibal, Mo) on 11/29/2009
I am confused because I thought calcium was NOT to be taken at all -- because there is so much excess calcium in our systems from every direction. There is a hypothesis that excess calcium creates blockage by attaching to inflammation, and that blockages are causing back wash of blood into the brain, creating MS symptoms.
Low Dose Naltrexone (LDN)
Posted by Heather (Cincinnati, Oh) on 02/13/2017
★★★★★
I find LDN therapy for MS interesting. I have been on 2 mga twice a day everyday as it's in combination with my pain med. I actually notice more pain within 45 mins of taking it. I was diagnosed at 16 and I am now 32 so being so young and independent I sought out less acceptable ways of dealing with effects of MS. (i.e.) cocaine, which actually worked, I had no symptoms, amongst other dumb street drugs that numbed the depression and helped me block what was going on with my body.
Long story short when I wised up I found that the crap the docs gave me was making me worse so I sought out natural alternatives and I have felt much better without the injections and percocet and zoloft etc. I happened upon this H2O2 therapy and am going to try it along with all my supplements. The biggest thing through it all that I want to try and eliminate is the pain I experience so hopefully this helps and I can get rid of pain meds even with LDN altogether
Low Dose Naltrexone (LDN)
Posted by Serena (Clover Sc) on 02/17/2014
★★★★★
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.
MS Natural Treatments
Posted by Rsw (Uniontown, Oh) on 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!
Hydrogen Peroxide
Posted by Dave (Fountain Inn, Sc) on 03/08/2014
Pete, re your MS;
Also look into a substance that Dr Robert Adkins used as his number one go to for his MS patients that he would give to them in IV form, although the oral consumption I have seen is amazingly effective for the symptoms you describe; "Calcium AEP" and the "calcium" part is not the issue...it is the AEP part that is the miracle. You can google "Nutrition Review Calcium AEP" and find an amazing article on the 20 different things AEP can do to help the human body, To deal with leg symptoms, especially when stressed, up to eight tablets of AEP are needed.
Also, I have found Colloidal Silver to be effective in killing viral infections. It is theorized that MS has as a trigger a virus.
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.
Vitamins D and B12
Posted by Marina (Bristol, UK) on 07/20/2009
★★★★☆
I was diagnosed with MS 2 years ago, after several bladder infections and major dizzy spells. Several years previously I was diagnosed with very low levels of Vitamin D, a fallout from the anti sun campaign prevalent in Australia where I was living at the time. I dont know if any of you saw recently the Times headline about the link between low vit D and MS, I have been aware of this for some time, as there appears to be very low rate of MS near the equator, but I also agree with the previous posts re Turmeric and selenium both of which I use sporadically{ of course in India one would presumably have higher sun exposure too.}, I take cod liver oil capsules containing 25 to 50 ugs of vit D daily, depending on time of year ,sun exposure etc. The other thing that seems to help, sometimes quite radically is sub lingual B 12 which I also take every other day. I do think its important to take a complete B supplement as well [ or good multi vit] so that you dont imbalance your B groups. Oh and good quality fish oils are great, flax for vegetarians. I havent taken any medications and my symptoms are much much better. Sugar makes everything worse!
Dietary Changes
Posted by Andreka (Atlanta, GA) on 12/04/2008
★★★★★
My MS is well under control never took any MS Meds went to a VEGAN Vegetarian Diet -- no white flour Products no meats, no Dairy my DR. says I look 5 younger years later @ 33yrs.old I'm doing so much better From Severe Progreesive to thriving and loving it.
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.
Vaccinations
Posted by Leslie (Indianapolis, In) on 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.
Selenium
Posted by Dr. J (Bombay, Maharastra) on 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
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.
Low Dose Naltrexone (LDN)
Posted by David (Poole, UK) on 09/03/2007
★★★★★
Low Dose Naltrexone is being used by people with MS (and other conditions) to stop the progress of the disease. Regrettably it does not seem to work for absolutely everyone and does not give much if any improvement with existing symptoms. It does however give one a chance to try other possible solutions knowing you will not get worse as time goes on.
Copaxone
Posted by Barbara (Parkersburg, USA) on 01/26/2008
I read a
comment regarding the copaxone injections. Granted not every solution is for every person however, I was taking the daily copaxone shots and suffered at least twice a month, sometimes more often, of all over body pain and could not do anything that was close to my normal activity level. My suggestions are that only you know your body. Listen to it. I do feel that a more natural path is the way one should follow if they are looking for relief. Remember God didn't intend for us to live unaturally. FDA approved medicines are not always the best way to go and Doctors get paid wether you listen or not.
Low Dose Naltrexone (LDN)
Posted by Dudley (Virginia Beach, Va) on 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.
Low Dose Naltrexone (LDN)
Posted by Deb (Florida ) on 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!
Calcium, Magnesium, Vitamin D, Potassium and Chromium
Posted by Patrice (Uniontown, Pa.) on 02/08/2011
★★★★★
For MS holistic treatments, I have found that taking B6 [which helps with PMS and mood for me] and Bcomplex vitamin helps with the muscle shaking tremors which I get alot on using weight bearing or squeezing an item with hands or legs. Also helps immensely with energy boosting. Also take 2000 iu of D3, calcium, magnesium.
Calcium, Magnesium, Vitamin D, Potassium and Chromium
Posted by Mario (Dallas) on 12/10/2020
Dr. Terry Wahls protocol for MS.
Low Dose Naltrexone (LDN)
Posted by Rialc (Ireland) on 10/07/2023 7 posts
Hi
My partner has MS for a long time, his walking is deteriorating. He is taking Ampyra. I wonder if LDN would be a benefit for him.
We are living in Ireland but I don't know where to get LDN. Has anyone bought LDN in Ireland or Europe?
Inclined Bed Therapy
Posted by 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.
MS Natural Treatments
Posted by Just A Thinking Guy (Kansas) on 08/02/2013
Hydrogen Peroxide
Posted by Rsw (Uniontown, Oh) on 01/21/2012
I have some good news for you. Please look at this website, www.ldninfo.org. LDN is an inexpensive, FDA approved drug, which when taken in a very small dose can help with many autoimmune diseases, and is usually very effective in stopping progression of MS. Additionally, please join the Yahoo LDN group that has over 10,000 members, at least half of whom have MS. They will help you very willingly and with much understanding and experience. You are not alone and help is as close as your computer. Best wishes!
Hydrogen Peroxide
Posted by Laura (Denver, Co) on 02/01/2012
Hi Orshi, I have MS too, I have found oxygen therapy helpful. Hydrogen peroxide, and also Homozon. I did CCSVI treatment several times but while there were benefits they only last 6 months for me. I had it again and veins were open but symptoms came back. After lots of supplements, and continued progression, I tried stem cell therapy which stopped the progression and with exercise seems to be helping me get better. Went from wheelchair to walker outside the house. It's been 2 months.
Laura laura.laurapino[at]gmail[dot]com
Hydrogen Peroxide
Posted by LittleWing (Boston) on 05/26/2026
I know this post is super old, but I just read an NHI report that said you cannot get MS if you haven't had the Epstein-Barr virus. So virus-triggered it appears to be.
Nutrition, Electrotherapy
Posted by Wongoblly (San Diego, Ca, Us) on 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.
Dietary Changes
Posted by Jonathan (Asheville, North Carolina) on 05/21/2010
★★★★★
I like to learn from other people's experiences. Having been diagnosed with "it LOOKS like you MIGHT have ms", I wanted to do something immediately. I was going deaf in one ear, having trouble walking, etc. My indefatigable will to walk and not be crippled by this menace was effective but not good enough. Now I am Vegan, but I warn those with MS to stay the hell AWAY FROM SUGAR, ALCOHOL, CAFFEINE, GLUTEN, DAIRY, and any kind of FUNGI! DOING A CANDIDA CLEANSE WILL HELP. Also, take something with DHA and EPA combined, phosphatidyl serine, DHLA, and Gingko/ginseng. Now I am SUPERMAN! I feel great. (I also take LDN).
