Lou Gehrigs Disease (ALS)

 

Symptoms

Amyotrophic lateral sclerosis (ALS) is a rare neurological disorder that became better known when the American baseball player Lou Gehrig became ill with this disease and died in 1939. ALS is a progressive degeneration of the nerve cells in the brain and spinal cord that control the voluntary muscles. The symptoms vary according to the part of the nervous system most affected. The disease generally occurs after age forty and is more common in males.

In most cases, muscular weakness and wasting (atrophy) begin in the hands and spread to the forearms and legs. Throat muscles may be affected, making speech and feeding difficult. From there, it spreads, affecting muscles randomly throughout the body and causing paralysis. In over half of all ALS patients, survival is not longer than a few years though, in other cases, progression is slow and can persist over decades. There is no effective medical treatment, except physiotherapy, to help slow down muscle deterioration. All current drugs and injections are experimental and the risk of the side-effects must be weighed with the possible benefit in each case.

Lou Gehrigs Disease (ALS) Causes

The cause of ALS is unknown. There are many theories, including one that suggests that it is viral in origin. Studies indicate that there are biochemical imbalances in ALS patients. These include both amino acid and mineral imbalances. Another study concluded that those with ALS have a defective glutamic acid metabolism. A defective gene prevents the body's natural ability to eliminate cell damage causing free radicals. Excess glutamate causes brain cells to fire neurotransmitters too often and die, eventually causing paralysis and death. One double-blind study showed that supplementing the diet with branch-chain amino acids (valine, leucine and isoleucine) for one year, significantly prevented muscle deterioration and maintained strength in the extremity muscles, and so prolonged the ability to walk.

Toxic and heavy-metal poisoning is a likely cause, particularly the mercury from silver-colored amalgam dental fillings. Mercury is a lethal substance that has been associated with hundreds of serious nervous and immune system problems. In 1991, the use of mercury in dental fillings was banned in Sweden. Aluminum toxicity should also be considered. Aluminum is ingested when cooking with aluminum pots. It is also found in many antacids and other medications. Toxic metals coupled with inadequate calcium and magnesium also possibly lead to ALS.

All patients suffering from this disease are diabetics. ALS, like diabetes, is caused by an abundance of ammonia in the body. People deficient in certain substances, such as manganese or arginine, do not process ammonia correctly. A high level of ammonia begins to kill off nerves in the brain and spinal cord. The muscle tissues then waste away because the nerves that stimulated them are gone.

Lou Gehrigs Disease (ALS) Nutrition

Emphasize foods containing magnesium and calcium, as ALS patients are often low in these minerals. Green, leafy vegetables and raw, unhomogenized and unpasteurized dairy foods such as quark, natural cheeses and yogurt are good calcium sources. Figs, almonds and green, leafy vegetables provide magnesium. Ammonia is counteracted by vitamin C, so the person suffering from this condition should supplement the diet with rose hips, black currants and acerola cherries, which are high in vitamin C. Glutathione is an amino acid which fights free-radical damage. Boost your intake of this essential nutrient by eating asparagus, avocado, grapefruit, orange, potato, tomato and broccoli.

Lou Gehrigs Disease (ALS) Nutritional Supplements

Vitamin C is essential for the maintenance of normal, healthy body functions. Taken in huge doses, this vitamin will also effectively neutralize various toxins in the system, speed healing and prevent the degenerative processes by strengthening collagen and the connective tissues. Because ALS patients also have high levels of manganese, mercury and aluminum in their systems and low levels of calcium and magnesium, adequate doses of calcium and magnesium help prevent the toxic effects of aluminum and mercury. Magnesium is often lacking in persons affected by toxic levels of aluminum. Vitamins E and B1 also help in the treatment of ALS. Vitamins B and E are important for muscle and nerve function.

Daily dosages:

Vitamin C, with bioflavonoids, 1,000 mg, up to bowel tolerance (For more information, see Section 6, Nutritional Supplements)

Calcium, 1,200 mg

Magnesium, 600 mg

Vitamin B complex, 100 mg

Vitamin E, with mixed tocopherols, 400 IU

Lou Gehrigs Disease (ALS) Herbal Remedies

For relief of specific symptoms, see appropriate sections.

Lou Gehrigs Disease (ALS) Homeopathy

Due to the seriousness of this condition, consultation with an experienced homeopath is recommended.

Lou Gehrigs Disease (ALS) Tissue Salts

See cramps and muscle weakness for tissue salt remedies.

Lou Gehrigs Disease (ALS) External/Physical Therapies

Physiotherapy helps slow down muscle deterioration.

Lou Gehrigs Disease (ALS) Other Suggestions

In order to make the necessary adjustments in diet supplementation, a blood, urine and hair mineral analysis can help determine the body's mineral balance.

A fasting plasma amino-acid analysis and allergy testing are also strongly recommended. (For more information, see Appendix 1.)

Lou Gehrigs Disease (ALS) Available Brand Name Products

Nutritional Supplements

Ascorbate/Non-acidic Vitamin C (Ester-C)

E 400 IU Mixed Tocopherol 100% Natural (Natural Factors)

Hi Potency Multi (Natural Factors)

Super Multi Plus (Natural Factors)

Ultra Multi Plus (Natural Factors)

Vitamin A (Natural Factors)



Comments

Add NewSearch


Roy Zimmerman Says:
Sep 09, 2009 @ 2:27 pm
 
 
It appears from the comments of many of the readers who have first hand experience with ALS, that diabetes is not a factor in their illness. It appears as though Mr. Gursche is off the mark in his book; I wonder what else is incorrect?
 
 
Neal M Waite Says:
Sep 03, 2009 @ 5:38 pm
 
 
My name is Neal M Waite. I believe I am
in the final stages of ALS. I haven't been
able to swallow for some time. My bodyweight is down to almost nothing.
Everything I take has to go through the
feeding tube. However, being a Christian
ALS doesn't scare me in the least. I feel
like a child waiting to go to Disneyworld.
May God bless you all.
Neal
 
 
meagan perry Says:
Aug 17, 2009 @ 10:49 pm
 
 
I just found out this morning that I have als.I was hoping that after the tests came back it would all be ok.I am the first in my family to ever have it and Im 20 years old.I havnt told my husband yet or any of my family for that matter.How long could I wait to tell them?I just dont know how my husband is going to take it.I dont want people sitting around having a pitty party for me.Am I being cruel by feeling that way?I am so confused someone please help...
 
 
Gayle Says:
Aug 11, 2009 @ 1:43 pm
 
 
My only sister was diagnoised in August og 2008, now 68 and her husband is 79. He says she has more bad days than good, now. She is not diabetic. It is very devastating to everyone involved!!!
 
 
hunter harshbarger Says:
Jan 15, 2009 @ 6:55 am
 
 
lou gehrigs is a terrible disorder that can kill
 
 
eddie Says:
Nov 10, 2008 @ 2:25 pm
 
 
I meet a special woman and she has Lou Gehrigs's Disease. She has had not i think 5 years now. She is still in the early stages. Walking is assisted by walker. She is eating health and it seems to have slowed it down. I am doing research on my end to know what i have to watch for. If anyone has a good site for more info please post so that i can know more. Thank you
 
 
carie Says:
Oct 07, 2008 @ 9:03 am
 
 
my grandmother also has ALS. We are wondering the same thing. her vision has become very blurry
 
 
Jane Says:
Sep 29, 2008 @ 10:44 pm
 
 
I have all the symptons you have an it's Lyme disease!
Jane
 
 
Sandy Keberlein Says:
Sep 13, 2008 @ 4:17 pm
 
 
Hi Dottie,

We just began a new Fund-raiser for Lou Gehrig's Disease in honor of a coworker of mine. If you are still interested in making a donation, please visit our group.

http://health.groups.yahoo.com/group/hurricanelougehrig/
 
 
Sandy Keberlein Says:
Sep 13, 2008 @ 4:14 pm
 
 
Nancy,

We just started a new fundraiser for Lou Gehrig's Disease in honor of a coworker. If you are still interested in making a donation, please visit our group.

http://health.groups.yahoo.com/group/hurricanelougehrig/
 
 
kathy Says:
Sep 08, 2008 @ 7:52 am
 
 
my dad was recently diagnosed with als and he is not diabetic either. they should fix that comment and i'm leary of the rest of the article now. i want to know what percentage of people is this hereditary in? my dad almost never drank bottled water and no mercury fillings in his mouth that i know of but he was a welder and worked with lots of metals. connection to this maybe? who knows.
 
 
Faye Says:
Sep 02, 2008 @ 2:17 pm
 
 
I have a friend who for the pass year has had trouble swallowing and eating. She has lived off soups and shakes for this pass year. She was just in the hospital to have a tube put in her stomach.
But they still don't know why she can't swallow. Could this have anything to do with Lou gerhigs Disease. Thank you
 
 
Joanne, Newfoundland, Canada Says:
Aug 22, 2008 @ 3:08 pm
 
 
A friend of ours passed away early this morning of ALS. Her late mother, 2 brothers, and a sister are diabetic, but she wasn't. I think this, like other diseases, needs to be researched further.
 
 
Cindy Says:
Aug 21, 2008 @ 3:54 pm
 
 
Hi, my name is Cindy. I had a mother and sister that both passed from ALS. Both got before the age of 35. neither one of them were diabeticts. Both lived very normal lives. WHERE dose it come from AND WHY?
 
 
Cindy Says:
Aug 21, 2008 @ 3:35 pm
 
 
Hi Laurie, my name is Cindy. I have had to deal with ALS since 1988 when my mother got it, passed in 1993. My sister also got it and passed in May of 2008. wow talk about the odds. However I know what you are going threw.... SCARED dosent seem to say enough. To sit day after day and watch with nothing you can do is unbareable sometimes.. But know you have GOD with you! and i9f you ask for help he will guide you. keep a smile on your face, and alwasy remind your brother you love. remember the good times. JUST BE STRONG!! i know its HARD. if you need a friend please email me. alvarci@msn.com
 
 
Dottie Morisette Says:
Aug 14, 2008 @ 5:04 pm
 
 
I want to donate in behalf of my friend who died of ALS recently. I have searched all your sites and cannot find where to send a donation. Plus, I could not find a Los Angeles phone number. Please email me or call me - 951-301-5677. Thank you very much.
 
 
Dawn Says:
Aug 12, 2008 @ 1:00 pm
 
 
I have a husband with als. He refuses to discuss the disease with me. He says that he dosn't want to burden me with what might happen. I know that in a year he has managed to completely remove himself from a wheelchair and cain and walk on his own. He will not ask anyone for help he still works 40hrs a week. what should I look for as to symptoms to worsing progress we have only been married for 1year and his family says it was because of me that he walks again. Please give your insight
 
 
Shirley Ann Watts Says:
Aug 11, 2008 @ 7:49 am
 
 
I am having pain in my thigh. The muscle is tight like a cramp and the outer side skin is numb. The top skin and inside leg skin feels really sensitive, like a sunburn. Then there are these stabbing pain in the muscle. What is going on? The neurologist is having me take MRIs (fixing to take 3rd one) right now and has me on 75 mg. Lyrica. He hasn't diagnosed me yet. Anybody have any ideas about stopping the pain. It really hurts so bad!
 
 
Mary J Laabs Says:
Jul 28, 2008 @ 8:16 pm
 
 
My husband has ALS and is not a diabetic.
 
 
steph Says:
Jul 25, 2008 @ 8:07 pm
 
 
I am a 35yr mom. Have been have some medical problems that are unexplained.I ahve seen a naturepath as well as a Nero. The only things confirmed are my levels. I dont hold cal or mag and my mercury and cooper are on the higher end. I do have carpoltunnel as well as barium which is the biggest isssue of concern. I have been having trouble with my muscles in my legs getting tight,and unexplained pain as if i had sprained my ankles. The tast of lead in my mouth. I have been ask by my other healthcare providers have you been check for ms als lymes disease. my engery for sport has been slowing down. I also get a taste of lead in my mouth. Should als be something i should be thinking of.
 
 
Nancy Barry Says:
Jul 14, 2008 @ 7:59 am
 
 
Were can I make a donation?
 
 
Lois Wallace Says:
Jun 09, 2008 @ 11:02 pm
 
 
There are ALS offices everywhere that can answer most all of the questions i have read. I will be calling in the am to our office to ask my question as well.
 
 
Lois Wallace Says:
Jun 09, 2008 @ 10:59 pm
 
 
Hello, I lost my sister to ALS on May 29th 2007. She was a very vibrant person who loved life and sports. She was never a diabetic. I learn today that an acquaintenance was just diagnosed. Most everyone else iv'e known was Athletic he was not but was a Landscaper who drank a lot of water. I am curious if anyone has ever checked in to this heavy (Bottle) water drinking as my sister definitely did as well as most any athlete. It is a thought?
 
 
gypsy134 Says:
Jun 05, 2008 @ 1:31 pm
 
 
does anyone know if owning a small dog has any relationship to developing ALS, or is this just a myth.
 
 
M.Quinny Says:
May 19, 2008 @ 5:57 pm
 
 
My boyfriend was a cabinet maker. We were wondering if this profession has any relationship to him developing als.
 
 
M.Quinny Says:
May 19, 2008 @ 5:52 pm
 
 
I have afriend who was diagnosed with als in Oct, he also is not diabetic, however I am and I tested his blood sugars and he has normal blood sugars.
 
 
Marian Says:
May 18, 2008 @ 8:26 am
 
 
Hello,

I am curious if anyone has researched nutritional solutions for ALS. My grandmother has been receiving deep tissue massages and seems to be responding well to that. Please let me know if you've read or heard of anything nutrition/food based. Thank you.
 
 
Lenora Says:
May 14, 2008 @ 8:23 pm
 
 
I am new with this ALS my mother inlaw after 5 months and six different Doctors has been told she has it! her balance has been off for a long time one step forward two steps back almost as if she was drunk,leg cramps and one hand is curling like a claw. she cannot dress her self and cant pick up her feet to get her into the car.
what stage would this be? please we really need to know!
 
 
Concerned Says:
Apr 28, 2008 @ 5:54 am
 
 
Try seeing a Homeopath. They have amazing remedies that might help with the progression of the Disease and maybe even halt it in it's tracks.
You can call a homeopathic school near you and find an alumni of the school. Make sure that you are looking for a homeopath who practices Classical Homeopathy. Good Luck.
 
 
Judy Ruffing Says:
Apr 26, 2008 @ 9:39 am
 
 
My Husband has been treated for memory problems since 9-07 and a month ago developed pain in his arms. The last week or so he has unbearable pain in his arms and cannot lift them past his shoulders. His hips are starting to hurt also. His brother died of ALS in his early 40's and his 1st Cousin died of ALS in her 60's. He is being treated by a Neurologist for memory. We are beside ourselves. My Husband has always been strong and vital.
 
 
Claudette Dee Says:
Apr 24, 2008 @ 6:05 pm
 
 
"Eric is Winning" is a book written by Eric Edly. He has survived over 14 years with ALS. You can order the book at www.evenbetternow.com
 
 
sue comstock Says:
Apr 22, 2008 @ 6:25 pm
 
 
My brother died of ALS at 53 in 2000. From diagnosis to death was a little over 18 months. Each stage came quickly and left just as fast. It began when he had triuble with his left leg being stiff. Eventually he lost his ability to speak and was on a respirator. He never had diabetis.
 
 
Claudette Dee Says:
Apr 18, 2008 @ 9:41 pm
 
 
I just read this fabulous article and thought that you should get this book and try saving your loved one.

Sincerely,

Claudette


Lou Gehrig's Disease, otherwise known as Amyotrophic Lateral Sclerosis and commonly referred to as ALS or Motor Neuron Disease (MND), is a serious neuromuscular illness affecting approximately 30,000 people in the United States. There are about 5,000 new cases diagnosed each year. Since 50 percent of all Lou Gehrig's disease patients die within 18 months after diagnosis and only 10 percent live longer than 10 years, ALS is considered to be an incurable fatal illness. However, there have been reports of several people outliving their diagnosis, halting the progression of the disease, and even reversing some of their symptoms.
This web page provides information on the suspected causes of Lou Gehrig's disease, the symptoms of Lou Gehrig's disease, genetic testing, diagnosing ALS, ALS organizations, and most importantly, the book Eric is Winning by Eri...
 
 
lavada Says:
Apr 17, 2008 @ 6:03 pm
 
 
could you tell me if blindness is one of the effects of als
 
 
lavada Says:
Apr 17, 2008 @ 6:01 pm
 
 
i am dealing with a family member who has the last stages of als. we would like to know if blindness is one of the stages of als.
 
 
lovely5007 Says:
Apr 13, 2008 @ 8:33 am
 
 
My sister lives in Tn and have been sick for a couple of months but recently have gotten worse, she has been to sevral doctors but know one knows anything.She is 40yrs old , she has lost some function in her arm and hand and has begain to sleep constantly. She used tobe the average soccer mom but she can't hold her eyes open if someone have
answers e-mail me.
 
 
PAT COPE Says:
Apr 09, 2008 @ 8:37 pm
 
 
I HAVE A DEAR FRIEND WHO WAS DIAGNOSED ABOUT 3 MONTHS AGO AND HE IS NOT DIABETIC. IN READING THE ABOVE COMMENTS. MANY WERE NOT. HE HAS ALREADY LOST ABOUT 50 POUNDS AND HAS A GREY COLOR. HE CANNOT OPEN JARS AND ETC. SHUFFLE CARDS OR EVEN CRACK PECANS. IS ALL THIS NORMAL. I READ ABOUT THE SUPPLEMENTS THAT MIGHT HELP. I WOULD LIKE TO HEAR FROM ANYONE WHO CAN TELL ME MORE. THANK YOU.
 
 
Destiny Says:
Apr 09, 2008 @ 6:57 pm
 
 
Thats sad I hope all your family gets better and rests in peace!
 
 
Destiny Says:
Apr 09, 2008 @ 6:56 pm
 
 
thats sad I hope all their family gets better
 
 
patricia van leeuwen Says:
Apr 06, 2008 @ 7:10 am
 
 
My mother died of ALS, she was not a diabetic, but did live in rural region in Iowa and Arkansas and drank well water.
 
 
suzanne michaud Says:
Mar 28, 2008 @ 7:55 pm
 
 
hi laurie, my sister is 46 and was diagnosed with bulbar als just over 1 year ago..onset similar to your brother.
we (my familly) have found our way, mostly on our own, and have overcome some problems . i could share my experience if you are interrested....i understand your feelings ...we are suffering alongside her as well and have some guidance for you.
hope to hear from you,
i am from sudbury ontario, canada
 
 
L. mcneil Says:
Mar 15, 2008 @ 6:41 pm
 
 
my dad passed away in 2006 and was never a diabetic but tested very high in mercury.
 
 
LAURIE WESTFALL Says:
Mar 15, 2008 @ 4:25 pm
 
 
Hello ,My name is Laurie & my 45 yr old brother has ALS & it is breaking all our hearts,hes about 5-6 months into it & it is taking him fast,speech,left arm.90% right arm,50% legs & now swallowing.we don't know were to go for help & how to help him.He lives in apt.w/my Mother who won't be able to take care of him & we really need some guidence please help with some we are all so hurt & scared.Thank You .
 
 
CHRISTI Says:
Mar 10, 2008 @ 12:04 am
 
 
MY FATHER JUST PASSED AWAY THIS JANUARY OF ALS AND HE WAS NEVER A DIABETIC.
 
 
Martha Murphy Says:
Mar 01, 2008 @ 1:42 pm
 
 
My morther-in-law died of Lou Gehrigs in 1993. She was never a diabetic.
 
 
Marian Says:
Jan 25, 2008 @ 5:36 am
 
 
Hello,

I was reading your article and would like to respond to the following:

All patients suffering from this disease are diabetics.

My grandmother was recently diagnosed with ALS and is not diabetic. Just thought I'd let you know.
Thanks for posting your article.
Marian