Lou Gehrigs Disease

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Lou Gehrigs Disease (ALS)

Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease, is a motor neuron disease that was first described in 1869 by the French neurologist Jean-Martin Charcot.  ALS is a degenerative neuro-disease that typically attacks both the lower and upper motor neurons and interferes with the brains messages to the muscles. It causes degeneration throughout the spinal cord and the brain.  Essentially, ALS makes you lose control of your voluntary muscles.  Early symptoms include a painless weakening of a hand, foot, arm, leg and speech, swallowing or walking difficulty.

It is still not completely understood what causes ALS.  Right now, there is only one known cause of ALS.  That cause is a mutation of a specific gene, the SOD1 gene and this mutation only account for 1 or 2 percent of all ALS cases, or 20% of the familial or inherited cases.  This mutated gene makes a defective protein that is toxic to motor nerve cells. 

Familial ALS makes up for 5-10% off of the cases.  The remaining cases come on spontaneously and without explanation which means that these random attacks on otherwise healthy adults could happen to anyone, anytime. 

More On ALS 

Amyotrophic lateral sclerosis is a form of motor neurone disease. ALS, sometimes called Maladie de Charcot, is a progressive, fatal, neurodegenerative disease caused by the degeneration of motor neurons, the nerve cells in the central nervous system that control voluntary muscle movement. The condition is often called 'Lou Gehrigs Disease''' in North America, after the New York Yankees baseball icon who was diagnosed with the disease in 1939 and died from it in 1941, at age thirty-seven. Today, renowned physicist Stephen Hawking and guitar virtuoso Jason Becker are likely the best-known living ALS patients. The disorder causes muscle weakness and atrophy throughout the body as both the upper and lower motor neurons degenerate, ceasing to send messages to muscles. Unable to function, the muscles gradually weaken, develop fasciculations (twitches) because of denervation, and eventually atrophy because of that denervation. The patient may ultimately lose the ability to initiate and control all voluntary movement; bladder and bowel sphincters and the muscles responsible for eye movement are usually (but not always) spared.

Cognitive function is generally spared except in certain situations such as when ALS is associated with frontotemporal dementia. However, there are reports of more subtle cognitive changes of the frontotemporal type in many patients when detailed neuropsychological testing is employed. Sensory nerves and the autonomic nervous system, which controls functions like sweating, generally remain functional.

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ALS Nutritional Protocol 

ALS Nutritional Protocol

A comprehensive nutritional protocol designed to assist the body from a nutritional perspective in combating ALS. This protocol works on the bodies nutritional needs through vitamins, whole foods, enzymes, minerals and trace minerals. The ALS Nutritional Protocol also helps in easing inflammation of the muscles and nerves and helping to support memory and in protection from degenerative diseases of the brain.*
*These statements have not been approved by the FDA.

ALS, Lou Gehrigs Disease Explained 

ALS Lou Gehrig's Disease Bay Area Chapter

I directed/edited this video for the ALS foundation greater bay area chapter. ALS "Lou Gehrig's Disease attacks the nerve cells causing the body to waste away. The average life span when diagnosed is 3-5 years.There is no known cause and no known cure. To learn more or donate go to http://www.als.org

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Les Turner ALS Foundation 

Help Fight ALS

The Les Turner ALS Foundation is the only independent publicly supported non-profit organization in the Chicago-area devoted solely to the treatment and elimination of amyotrophic lateral sclerosis (ALS), better known as Lou Gehrig's disease.

The Foundation is affiliated with Northwestern University Feinberg School of Medicine - where it funds medical research at the Les Turner ALS Research Laboratory and a patient service program at the Lois Insolia ALS Center - and is also a member of Community Health Charities of Illinois and the International Alliance of ALS/MND Associations.

One Man's Struggles With ALS 

Jack Orchard ALS Foundation

Jack Orchard Foundation, Extra Hands ALS is a national voluntary service charity assisting people with ALS, also called Lou Gehrig's disease. Extra Hands is expanding nationally and now operates in many cities in the United States.

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Books On Lou Gehrigs Disease 

Als-Lou Gehrig's Disease (Diseases and People)

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Walking Through the Valley - Dealing with the Prospects of Death with Bulbar A.L.S. (Lou Gehrig's Disease)

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Amytrophic Lateral Sclerosis

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Diseases and Disorders - Lou Gehrig's Disease (Diseases and Disorders)

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Lou Gehrig's Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References

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Share Your ALS Experience 

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  • Reply
    JerryB JerryB Nov 5, 2009 @ 12:49 pm
    Very helpfull lens! Five! I'm finding out that there are quite a few diseases that most people know very little about. Squidoo is a great place to spread the word. My unknown disease (not by choice) is Ormond's Disease. Stop by and learn about it if you have a few minutes.
    http://www.squidoo.com/ormonds-disease
  • Reply
    DeboraR DeboraR Jul 29, 2009 @ 1:28 am
    Good lens on this subject matter. A friend of mine's husband lived 7 yrs with this disease.
  • Reply
    dhyana dhyana Mar 10, 2009 @ 1:53 pm
    My father had ALS for three years before he passed away last July. I've given support to ALS-TDI, a research group working solely for further information about this disease. Please check them out and help raise awareness of this and all other neuro-degenerative diseases. Thanks for the lens.
  • Reply
    promolife promolife Oct 21, 2008 @ 9:39 am
    Thanks for making another lens about ALS. The more we get people to know about it, the better.
  • Reply
    flaminglacer flaminglacer Nov 25, 2007 @ 3:03 am
    Excellent lens - found it most informative. Squid Angel Blessing.....

Blog Posts on ALS 

The Role of Copy Number Variation in Susceptibility to Amyotrophic ...
Background The genetic contribution to sporadic amyotrophic lateral sclerosis (ALS) has not been fully elucidated. There are increasing efforts to characterise the role of copy number variants (CNVs)... [[ This is a content summary only ...
Amyotrophic Lateral Sclerosis Clinical Trial: Memantine Therapy in ...
Tau, a protein in the cerebrospinal fluid CSF is believed to be elevated in amyotrophic lateral sclerosis (ALS) patients. The investigators believe that Tau is...
Peer Professional Workgroup Profile: Amyotrophic Lateral Sclerosis ...
The ALS Workgroup was one of eight peer professional workgroups formed by national program office staff to bring medical leaders together to generate new ideas for their fields.
Metal-free Superoxide Dismutase-1 and Three Different Amyotrophic ...
The structure and unfolding of metal-free (apo) human wild-type SOD1 and three pathogenic variants of SOD1 (A4V, G93R, and H48Q) that cause familial amyotrophic lateral sclerosis have been studied with amide hydrogen/deuterium exchange ...

by jeffwend

Hello everyone.  I have been working as a holistic nutritional consutlant for 10 years. I wrote this lens to help those with ALS or Lou Gehrigs D...

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