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Natural Remedies for ALS

Last Modified on Jan 25, 2016

A particularly progressive and debilitating condition, amyotrophic lateral sclerosis or ALS is a particularly aggressive condition. While doctors normally don’t give very positive prognoses to individuals diagnosed with the disease, natural treatments can help improve the quality of life for individuals with the condition. In addition to traditional treatment, we suggest that you try vitamins and supplements including vitamin C, vitamin B complex, and vitamin E to better support your ALS treatment plan.

What Is ALS?

ALS, also called Lou Gehrig’s disease, is a disease that targets the central nerve cells in the brain and spinal cord. The condition causes the slow demise of these cells which typically leads to diminished physical and mental functioning as the specific cells involved in the condition are the motor neurons.

While the progression of the condition varies slightly for different individuals, ALS causes the gradual disabling of anyone affected. Over time, common tasks including walking, speaking, eating, swallowing, and even breathing becomes difficult for individuals.

How is Lou Gehrig’s Disease Usually Treated?

An ALS diagnosis can be very scary for anyone, but the good news is there are often a variety of treatment options provided. While some of the “typical” treatments for the disease are more invasive, many involve holistic practices. Physical and occupational therapy are common, as is speech therapy. Additionally, many individuals are provided with supportive devices and equipment to help them cope with everyday tasks more easily. Other more aggressive treatments include medication, feeding tubes, and breathing devices; however, these options are generally for more developed cases of the condition.

Are There Any Natural Remedies I Can Try?

We believe a balanced approach to treating this condition is best – one that utilizes traditional treatments paired with natural supplements to support overall health. That being said, a few of the most effective natural treatment supports include vitamin C, vitamin B complex, and vitamin E.

1. Vitamin C

As ALS effects the functioning of the entire body, vitamin C is a particularly important treatment support. Vitamin C helps strengthen the immune system as well as the connective tissue in the body to prevent deterioration.

2. B Complex

Vitamin B complex is a combination of the essential B vitamins. This complex helps support energy levels as well as muscle and nerve function.

3. Vitamin E

Vitamin E is another important supplement as it helps support muscle and nerve function as well. Taken as a daily supplement, vitamin E also helps prevent deterioration of the muscle function.

While nutritional supplements are an important support to ALS treatment, a variety of other natural treatments help as well. Read below to gain additional information from our readers as well as one of our regular contributors, Ted from Bangkok, Thailand.

Remedies for Lou Gehrig's Disease

The Popularity of Lou Gehrig's Disease Remedies - Full List

Alphabetical Popularity Recent Post
Coconut Oil02013-02-02
Dietary Changes, Supplements12015-02-02
Hyaluronic acid02015-01-04
Medication Combination Warning02009-10-22
Rhinacanthus Root Powder02014-01-14
Ted's Remedies02014-03-01

Coconut Oil  

Posted by Jacques (St-georges, P.Quebec / Canada) on 02/02/2013

TO MR TED, I am treating a case ALS presently and I found at many sites on the web the coconut oil ( or MCT OIL) are very helpfull with many positives results. You write on your pages to do not us ANY OIL ??

What do you think about theses very good results and are you encouraged to use it ?? Your opinion will be very appreciated.

Also from all informations you put on yours pages in regard with the colitis ulcerous , please be informed I treated 4 cases with 100% success without any recidive. Thank a lot to you.

Waiting yours comments,

Jacques from Canada

Replied by Marge
Daytona Beach, FL
My friend makes us coconut cream it cures many things. I have trouble with stomach disorders so try it. It is a great detox which is the cause on many disorders.
Replied by Medicineman
Harrisburg, PA
Coconut oil is fine. What you want is an overall healthy diet of real foods. No processed, no farmed fish. As wholesome and close to the land as possible. It should be a lifestyle.

The biggest contributor to mucus is dairy. Eliminating dairy from the diet, would be my first go-to.

Run with this iodine and vitamin C (and take a multi for safe measure)

You need to detox. Iodine will detox heavy metals and help get systems back online. Vitamin C acts as like a shuttle service for the iodine going in as well as the toxins going out.

My father died of als years ago and suffice it to say - you'll get nowhere with standard medical procedure. Rilutek is a joke.

ALS is caused by toxicity, stress and degredation of the stystems. All of which can be brought back to working order, I believe.

Dosage wise take 1-2 grams of vitamin C every 1-2 hours. Maybe stop closer to bed time as it can keep you up at night and rest is important.

Iodine you'll want to aim for around 1000 mcg. Gauge yourself at maybe half that or less. Iodine will produce detox effects that are flu like and depression.

If you're getting heavy detox symtoms just dial it back a while or take a day off.

Iodine is about the long game, it can take a year for it to do its work fully.

I like kelp as a source, because it's in its natural form with other companion nutrients that will help absorbtion. Sea weeds also have addictional detoxifying elements in them ontop of iodine.

But that's the gist of it. Health is a natural, organic process. It doesn't happen overnight and won't come from a pharmaceutical drug.

We come from nature and our road to wellness is a natural one.

Namaste', C

Replied by Nm
For Neurological diseases, ALS, MS, etc... try Plumbum homeopathic 30 or 200, Causticum is a huge central nervous system remedy, Calcarea Carb, Arsenicum in some cases... Bryonia is another... Main ones to try though are the first two... Search "homeopathy +als or ms and read the descriptions of each remedy and find the one that fits your symptoms... I got great assist from plumbum & causticum... Calc Carb also helped.. Try to be happy because mood can affect these diseases as well.
Replied by Nmx
Along with Plumbum or Causticum homeopathic - The Carnicom Institute who is working on Morgellons which I think might be involved in ALS - has found that Vit C and N Acetyl Cysteine (which helps create Glutathione - the chief antioxidant of all) are halting growth of Morgellons in the body - Morgs leaches iron and amino acids - which could cause your muscle weakness.., try these

Dietary Changes, Supplements  

5 star (1) 

Posted by Alon Shomer N.d. (Jerusalem, Israel) on 02/02/2015
5 out of 5 stars

I treated a person that came to me several years ago.

He complained that he is progressively losing control over his legs making it difficult to walk, and that he has lots of muscle twitching in his left shoulder.

Since I believe that most of the CNS diseases are caused by funguses, I treated him for candida:

Mainly - no sweet beverages or drinks of any sort ( including fruit juices) at any time.
Large amount of probiotics. Very little sugars including fruits.

Diet: as much as he wanted vegetable salad with olive oil.
Semi hard yellow cheese or camembert (made with rennet and bacteria). Green drinks (green vegetables with one carrot only). Rice (small portion). Meat that was cooked or grilled for about two hours (moderate amounts). Eggs - two to four a week. Almonds soaked in water over night. Miso soup with wakame. Nuts and seeds

Supplements: (5-6 days a week all supplements) multivitamin and minerals. + zinc picolinate 10 mg + fish oil (3 times more EPA then DHA) 300 to 500 mg + vitamin E 200 mg mix tocopherols +1000 mg lecithin + B12 (4000 microgram a week) + vitamin C 500 mg + probiotics several strains, 2 capsules 4 times a day.

(He was instructed to wear copper bracelet, but today I will replace it by using on top of the one mg of copper in the multi, 3 mg of copper twice a week separated from any other supplement).

Exercises - at least 20 minutes a day, whatever he wanted to do in order to burn up calories, preferably before going to sleep.

In few months all his symptoms disappeared and all functions became normal.

I am unable to say for sure that it was the beginning of ALS but it is definitely worth the try.

Hyaluronic acid  

Posted by Reflectivegypsy (Sicklerville, New Jersey) on 01/04/2015

Hi, Ted. I was diagnosed with ALS almost two years ago and I'm trying to find things to help me get better. I have a few questions about hyaluronic acid. On 6/6/14, you told one poster that you recommend "a small amount of hyaluronic acid .5 grams to 500 cc to water mix with sea salt 5 grams also." Did you mean to say we should use 5 grams of hyaluronic acid, not .5 grams? And how many times a day should this be taken? Thanks!

Medication Combination Warning  

3 star (1) 
1 star (1) 

Posted by Heather (Sudbury, Ontario, Canada) on 10/22/2009
1 out of 5 stars

Many people who are on a combination of diabetic medications and cholesterol medication find that they develop symptoms that mimic Lou Gehrig's Disease. I know of at least 5 women in my town who have been mis-diagnosed by their doctors. One had gotten to the point of all her muscles collapsing and her lungs and heart were stopping working. Luckily, a new young surgeon at the hospital's emerg. department realized what was happening and took her off the cholesterol medication. She went from almost comatose to up in a wheelchair in 3 days, and walking by day 5. Apparently diabetic medications or cholesterol medications by themselves are fine, it's the combination that's terrible.

Replied by Meghan
Brooklyn, Ny
My father was recently diagnosed with ALS. I still have that hope that it might not be true. He takes both diabetic medicines and cholesterol meds. Can you by any chance find out what her medications were that she was taking? And how they figured out that the combo of meds were doing it to her body?
Replied by Syed
Ontario, Canada
3 out of 5 stars

Better But With Side Effects:
ALS - lost my right hand movements ( called motor skill), was taking 40mg of Lipitor for quite some time.

Replied by Rsw
Hi Syed,

I am sorry to hear of your probably unreported "adverse reaction" to statin drugs. For up to date information on the newest findings about how statins affect the human body, see Dr. Duane Graveline's Facebook page here:

There is also a Yahoo "Stopped Our Statin Group" you can join to feel some connectiveness, research data and awareness of the thousands of statin victims out there.

Dr. Graveline is currently doing a study on Dolichols that are blocked along the mevalonate pathway along with CoQ10 and other pathways and functions essential to repairing DNA. Cholesterol is needed by every part of our bodies, especially the heart and brain. It is inflammation that we don't want.

We would like to see the statin drug companies use some of those enormous profits to fund research to help the thousands of people like you, in fact about 25% of people taking statins, to regain functions that were lost, sometimes permanently and progressively even after statins have been discontinued, after short-term/long term statin drug use. You are not alone and every person's experience and thoughts are important in finding a solution. Take care.

Rhinacanthus Root Powder  

Posted by Mr Don (Gold Coast Australia) on 01/14/2014

My 70 year old wife has ALS for at least 8 months she is finding it hard to talk now and has trouble eating and sometimes breathing She is also losing strength in her arms She has herpes virus for many years. What can you suggest as a treatment I have been told that rhinacanthus root powder can reduce the amount of glutamate your body produces. Is this correct? Where can I purchase this product? It is widely used in the Bangkok uni. Regards Mr Don

Replied by Dave Donate

Fountain Inn, Sc
Hello Mr Don from Gold Coast,

If you google search "ALS herpes simplex" you'll find a number of articles on the possible connection. "Pub Med" has one such article. That article has connect with a specific type of ALS. You said that your wife did indeed have the virus long prior to the ALS onset.

The point is, if I were suffering from ALS I'd consider the possibility of a virus as either a trigger or the underlying cause of the ALS and would at least try to rid the body of the infection. I use a number of anti viruses, my favorite being Colloidal Silver; also Echinacea, tea tree oil... lots of "go to virus killers."

On the CS, I'd take orally three tablespoons daily for three months. I'd also do the CS as a nasal irrigation

I know your wife must be very frightened. Encourage her never, never to lose hope. Same for you, "Mr Don." This is a terrifying disease to combat and I'll be praying for you to have wisdom and strength through it all.

Your friend here in America,


Ted's Remedies  

1 star (1) 

Posted by Anupam (Poland) on 03/01/2014

Dear Ted, my father is diagnosis ALS. He is 68 lives in India .now he is unable to walk and talk. Doctors says there is no treatment of ALS. Pls help us

Replied by Mike62
Anupam: Ingredients need to be organic. Eat raw fruits and vegetables from Organic India. Make smoothies with a blender from the leaves and peels. Most of the nutrients are in the leaves and peels. For oil and protein eat soaked nuts and seeds raw. Keep fat below 5%/g of carbs. Take 1/2 saturated fat and 1/2 unsaturated. Get some omega 3's from plants. Make home brewed water kefir with whole sugars or/and whole flours, 60g carbs/quart. Put 4oz papaya, 1tsp papaya seeds, some chili, and 4oz pineapple in a blender with some water, grind up, and drink. Do this 4x/day. Include the peel, core, and stem.
Replied by Dave Donate

Fountain Inn, Sc
Hello Anupam,

I see you ask Ted about ALS and I'm not Ted nor even close to his expertise but if you will allow me, I'll give you my own approach to ALS.

I believe there is evidence that ALS has at its root a viral infection in the spine, cousins to the Polio virus. The Polio virus is a "specialty" virus and in theory so is ALS. Cadaver studies were performed on ALS corpses and (as I can recall) about 80 percent of those had the virus in the horns of the spinal vertebra.

In theory, then if I suspected a spinal infection, I would use a 50/50 mix of DMSO (see Earth Clinic under Remedies) and Colloidal Silver (see Earth Clinic again under Remedies). I'd apply with a white cloth as a poultice to spinal column for thirty minutes three times a week. After a month if I'd improved at all, I'd continue for six months. I'd also drink CS daily, three tablespoons on empty stomach daily for six months to kill the virus in the rest of the body. The DMSO will carry the Silver atoms into the skin and DMSO is also an anti viral so it too will help.

This combo has worked for me for numerous "below skin" infections and, yes, it will penetrate bone. If the combo is applied to base of skull it will penetrate into the brain. If I thought I had any infection in brain I would try this combination three times a week for at least a month and judge results.

Your father is very far advanced; you said he could not walk or talk; so the approach is a long shot....but if this were me...I'd try anything at this time.

Replied by Prioris
Fl, Usa
Ted's email address is parhatsathid(at)gmail(dot)com
Replied by Musibul
Hi Dave,

You mention you have apply white cloth as a poultice to spinal column. Please tell me the quantity for one time and you mention drink cs daily it means Colloidal Silver ?

Can you little elaborate how to apply?

Replied by Dave Donate

Fountain Inn, Sc
Hello Musibul,

I hope I spelled your name correctly....

but you ask a few questions on how I apply colloidal silver to myself. If I want to get CS into my spinal area I use a 50/50 mix of CS plus DMSO. The DMSO is a solvent and carrier. So the DMSO will penetrate my skin and spinal column carrying the CS with it.

I also will drink two tablespoons of CS daily to kill infections in the body.

Replied by Robert Henry
Ten Mile , Tn
HI U DAVE, , , , , , , , , , , boy you telling me something because I do the same thing, but use sto bought liniment. Does this relieve your pain?

If so, I'll give it a try. =====ORH=======

Replied by Dave Donate

Fountaiin Inn, Sc
Hello Musibul,

And you also asked how to apply....a poultice is just the wet cloth laid onto the skin and let absorb for twenty minutes.

Use about two cups with a light white cloth for poultices. Enough to have the cloth very wet without being too drippy.

Replied by Dave Donate

Fountain Inn, Sc


However you spell that ... and what ever a patoot is...

I do use store bought liniments. I don't use colloidal silver for relief of pain...but it could have that effect IF the pain were the secondary result of infection. I believe of course that CS is killing the infection. I have a liniment I bought at the old Feed and Seed store out in the country that seems to work well on inflammation issues... called Bigeloil. That has worked to reduce inflamation in a few cases.

I am a big fan of poultices for both pulling out toxins and putting in wanted ingredients. I use charcoal for the former and DMSO for the latter.

Replied by Robert Henry
Ten Mile , Tn
HI U DAVE, , , , , , , , , , , yep, you using liniment that was concocted for horses. I found it on the internet.

Dr. Jacobs , the father of DMSO, says that horses don't know about double blind studies so if they feel good then they run, otherwise, they don't. Our medical field is so stupid , it's not funny any longer.

I congratulate you on your contribution to common folks health. I know you not suppose to call folks, common, but we got got a bunch in this country. I now think my job is to keep folks entertained so they will read and help themselves.

I'm pretty smart , but not in the league with you and others.


Replied by Robert Henry
Ten Mile , Tn
HI U DAVE, , , , , , , , , I have used this term all my life and really did not know what it meant . I have researched and it originally was a term of endearment and that's how I use it. Just like when I call you my buddy.

Of late, it means something else. I will stick to the old version and hope all think likewise. Lordy, how folks are revising our history!!!!!


Replied by Liz
Boston, Ma
My Canadian-born and raised mom used that word often. I never knew what it meant either, but it was always used as a term of endearment.
Replied by Robert Henry
Ten Mile, Tn.
HI U LIZ, , , , , , , , , , thanks for coming to my rescue. I need all the help I can get.


Replied by Liz
Boston, Ma
HA! :) You're welcome! My pleasure.
Replied by Roger
Charleston, Wv
My brother was diagnosed with ALS in June. What r some of the treatments that u make and how to use them, ie colloidal Silver and what is DMSO, if any other. I have been told about the coconut oil.. How does that work, do u drink it or put it on your skin. Thank u anything to help him PLEASE
Replied by Bill Donate

San Fernando, Philippines

1230 Posts
Hi Roger...Here is Ted from Bangkok's protocol for late stage ALS. ALS, according to Ted, appears to be caused by adenovirus. Here is the remedy that he used:

"There is a lot of things you can do. The most important is the mucus and toxins. N acetyl cysteine 4000 mg 6 times a day and taurine 1000 mg 4 times a day. This will remove toxins. Methylene blue 0.1% 20 drops morning lunch and dinner. Adenovirus can be protected with poly lysine 1000 mg 3 times a day to kill it.


The child was in late stage ALS and in coma when he was put on Ted's regimen. When the parents took him out of hospital the doctors gave the boy 24 hrs to live. but the boy came out of coma and improved.

You can read all about his treatment here:

So, for adults, Ted's protocol would be thus:

N-Acetyl Cysteine -- 4000 mgs 6 times a day

0.1% Methylene Blue -- 20 drops mixed with 1000 mgs vitamin C in a half glass of water -- take this morning, lunch and dinner.

Taurine and Lysine each at 1000 mgs 4 times a day. Take them together dissolved in or with water.

Other useful remedies from Ted wrt ALS:

Rubbing ACV or vinegar directly on the back of the neck with help to kill the virus in the neck and brain regions.

Use 2% Lugol's Iodine mixed 50%-50% with DMSO. Apply this topically once a day along the whole length of the backbone and neck. DMSO will help the iodine to penetrate the bone to help kill ALS virus hiding in the synovial fluids there. Povidone Iodine is well known to kill adenovirus through research so lugol's iodine will do the same. Povidone Iodine cannot be ingested or used internally -- which is why you must only use the lugols iodine form(which can be ingested or used internally). Colloidal silver + DMSO could also perhaps be used like this with similar beneficial effects.

Rubbing drops of clove oil + aloe vera oil along the whole length of the backbone and neck area will also help to chase out the virus from the synovial fluids in the bone into the blood where the immune system can more easily kill it.

Take Lithium Carbonate 1.5 to 5 mgs per day.

You can buy most of the above nutrients from the health shop or internet vendors. You can purchase Methylene Blue at any aqua-culture shop that deals with fish tanks and fish for display. Methylene Blue is used in aqua-culture to help kill bacteria and fungus on the fish. MB is normally sold at 2.3% strength so you may have to dilute it down to 0.1% strength for use as Ted advises.

Replied by Vaso
Hello Dave,

I am from Georgia and my father was diagnosed with ALS. He can't rise with hands heavy things. and fingers are loosing strength. he can talk and walk normally. but he is loosing weight few years long. and he is sweating higher then normal. he was a handball player. Can you advise me what can we do to help him? Doctors prescribed rilutek. thanks in advance for any help or advise

Posted by Steve (Pittsburgh, Pa) on 06/10/2013

Has any with ALS followed Ted's protocols for ALS? If so, what level of success? Thanks, Steve

Replied by Steve
Pittsburgh, Pa
This was my question from 2-1/2 years I'm guessing no one has had any luck...if you have had luck with Ted's treatments, I would like to hear about it...Thanks, Steve

Posted by Nancy (Englewood, Fl) on 04/14/2013

Hi, Interested in starting the Lysine/Threonine regimen with my 59 year old friend with ALS. I haven't yet seen this question addresses, but my friend is NPO (nothing by mouth) and with a PEG tube. Can these be safely put into her PEG tube?

Replied by Nancy
Englewood, Fl
Dear Ted, thanks for your recent response informing me that Lithium and zinc are supplements needed to help stop the ALS progression. I could use some help in locating the lithium though.

Posted by Sarah (Carlyle, Illinois ) on 04/10/2013

My father-n-law has recently been diagnosed with ALS. We are having a really hard time to figure out what to do to help him. His progression is coming way to fast he is really having a tough time sleeping, problems with saliva, constipation and he is also very depressed. He has doctor appointment this Friday at the ALS clinic in St Louis. Ted, I need your help.

Replied by Timh Donate

Louisville, Ky, USA
Sarah: I'm not Ted and cannot offer any specific recommendations, BUT I just watched an ihealthtube video of Professor Garth Nicholson of the Institute of Molecular Medicine speaking of his successes treating degenerative and chronic diseases with Lipid Replacement Therapy (LRT). He mentioned only recently using LRT in degenerative neurological diseases with success.

Posted by Angela (Modesto, Ca) on 04/05/2013

Hello all! This question is for Ted

It's been a while since I posted, I have been busy with the care of my dad who is healing from als. He is being called the 'new' miracle man. Ted has been of major and effective assistance in this arena and my family and I continue to be grateful for his contributions. I wanted to ask Ted if he knew of any side effects of branch chained amino acids for someone like my dad who is not on any medications - except for acid reflux and constipation which are both PRN. He breathes room air (never been on oxygen) and continues to seek natural ways to help his muscles repair and rebuld themselves. What is your opinion on BCAA's positive and not-so positive?

Replied by Tonya
San Diego, Ca
Hi Angela -- Can you tell me what worked and didn't work with the treatment for your "new miracle man" father? :) My mother has been recently diagnosed with ALS. Thanks in advance!
Replied by Sara
Hi Angela,

Your posting gives me hope for my mom who has ALS. I have my mom on the Deanna Protocol and she is also on Rilutek. She is getting so much weaker in her arms. She has drop foot and has a hard time getting up. She also coughs alot and has trouble projecting her voice. Could you please tell me what regime worked for your dad? This site has useful information but it seems Ted has recommended slightly different doseages and supplements for everyone with ALS. So Ted if you read this, I would appreciate if you would be able to otherwise recommend a regime for my mom, my best friend.

Thank you very much, Sara

Posted by Carolyn (Simpsonville, South Carolina) on 12/22/2012

Dear Ted I was diagnosed with als in January 2012, right now all I have is severe weakning of the legs and arms is there anything I can do to help the weakness. And the vitamin D3 for muscle atrophy is it 20, 000 IU a day for a month or 20, 000IU in one month look forward to hearing from you

Posted by Janice H (Eastaboga, Alabama, Usa) on 10/10/2012

Ted, I followed your guidelines on the mixture of enzymes for my brother-in-law who was recently diagnosed with ALS after a process of elimination for other causes of MND. He said his kidneys seem to be overactive and after 5 days of treatment he was exhausted from sleep deprivation due to trips to the bathroom all night and day. He was drinking fluids yet still feels dehydrated. Is this normal when starting enzyme-treatment? Other concerns: He was water skiing (on one/two ski) this time last year, and rode his bicycle 500 miles in Jan (2012) when he had lower back pain & knee pain; his doctor recommended a regimine of 3 epidurals beginning in Feb (2012). Immediately after the first epidural he had severe muscle cramps and pain; his doctor recommended potassium and continued with the other 2 epidurals. Soon after he began to stumble and fall; loose strength and use of his hands. He continues to have pain in limbs, and recently fell injuring his shoulder; so he doesn't have paralysis; he just can't control his limbs. He has no problems eating or talking. His doctor refused to connect the epidurals with his sudden loss of control of his limbs. Recently there has been a recall of medication used in epidurals for back pain due to contamination resulting in "fungal miningitis epidemic" in the USA. NO DOCTOR WILL ADDRESS THIS ISSUE WITH MY BROTHER-IN-LAW; he has always felt this sudden onset of MND is related to the epidurals. What would you suggest his next approach in this matter? Thanks so much, I read all you material! Janice H

Posted by Mahesh Thapa (Kathmandu, Nepal) on 08/26/2012

Hello Ted, I am Mahesh Thapa from Kathmandu, Nepal. I was diagnosed MND 10 years ago when I was 25. Actually I have 11 years of history. I used Vitamin B complex, Vitamin E & Calcium for few years but there was lots of wounds like bigger pimples came to face because of its side effect & I stopped it. I used other available alternative treatments for 2 years & since then I haven't used any treatment and medicine except using free homeopathic medicine from a government hospital. I haven't checked up for 7 years.

I can stand for few minutes & few steps on my own but need support to walk, can't speak properly (unclear & nasal voice), fasciculation & cramping on muscles in most part of body, muscle loss in hand & shoulder resulting minimal movement in both hands, I use on screen keyboard to type. I need support to use toilet & bathroom but I strongly believe that I can overcome this disease. doctors had given me around three years of prognosis & asked that I will have to use feeding tube within 6 months but it didn't happen.

Now I don't have any problem in respiration, lungs & heart. I can eat normally & use all types of food as normal person & don't have digestive problem. I can sleep well. I can sit & work on computer for hours. I have good memory. I am good player of chess at national level, have got FIDE chess rating 3 months ago.

Please suggest me your remedy in detail. is it MND or I am misdiagnosed? Is there any pathological test needed before using your remedy?

Thanks, Mahesh mthapa9(at)

Posted by Stephen (Sydney, Australia) on 08/05/2012

Hi Ted, I read your coments and sugestions with interest re. this disease, which my wife suffers from, and we are keen to start trying the suggested treatment, a couple of questions re. some of the products, Firstly, humic acid seems hard to find except for agricultural use, will keep trying to source it. Also I have only found threanine in an amino acid complex, is it ok to use this until I can locate some? Thanks Ted, Stephen.

Posted by Chris (Pueblo, Co) on 06/09/2012
1 out of 5 stars

I have been helping a friend with ALS/Lou Gehrig's through the treatment recommended starting with the Lysine and Threonine as foundation. The Threonine dramatically increased mucous production in my friend and her breathing, which was strong before, had suddenly become labored. I did some more research on the Threonine and discovered on the WebMD site's description of Threonine side effects stating:

"Amyotrophic lateral sclerosis (Lou Gehrig's disease): There is some concern that threonine might decrease lung function in patients with ALS. In one study, ALS patients taking 4 grams of threonine per day had significantly reduced lung function compared to patients who did not receive threonine..."

And this is exactly what we saw. With all the symptoms of ALS she showed, the reduced lung function has not yet been one of them. But the introduction of Threonine directly coincided with a dramatic affect on her breathing. She said it felt like an elephant sitting on her chest.

On the positive, she previously had a clenched feeling in her throat that was pinching and really wearing her down. Since taking the Threonine, this has noticably relaxed and made it much easier to bear. But the thick mucous increase and belabored breathing is a bit scary, especially since many ALS sufferers die from this aspect. We are stopping the Threonine in hopes that her breathing will return to normal. If it doesn't I may counteract it with arginine, but I know this supports the possible viral function that we are attacking with Lysine. So I want to be careful and take it one day at a time.

I just felt it important to share this experince in case it is of help to anyone else out there.

Replied by Chris
Pueblo, Co
An update on my friend who stopped Threonine due to a dramatic reduction in breathing capacity. Within 48 hours of stopping the Threonine, her breathing capacity has improved. She said this morning that she is feeling about 90% recovered to the state she was at before starting the Lysine/Threonine. The annoying mucous production has also subsided and she is feeling comfortable.

She has a relative that is a massage therapist and has been using clove oil, as suggested, in working it into the back of her neck and spine. It is helping her be a lot more comfortable, whether its the massage, the oil or both, we don't know, but she has been free of the cramping, spasms and pain she previously struggled with.