Amyotrophic Lateral Sclerosis

ALS

Amyotrophic Lateral Sclerosis Overview

Amyotrophic lateral sclerosis (ALS) is a neurological and rare disease that progressively affects the nerve cells that manage voluntary muscle movements such as speaking, walking, eating, and even breathing.


ALS is part of a much broader group of medical conditions referred to as motor neuron diseases (MND); these diseases gradually deteriorate motor neurons until they eventually die. Motor neurons are the cellular nerves that stretch from the brain and onto the spinal cord and then to the muscles.


These motor neurons transmit vital signals from the brain to the voluntary muscles. ALS causes the neurons to degenerate which halts the communication between the brain and the muscles; this process ultimately reduces the strength of muscular fibers.



As the muscles progressively become weaker, they begin to twitch and then wither away until the brain loses all control of voluntary movements. Because of impaired muscle action, people with ALS may lose their ability to move, talk, eat, or breathe.




What Are The Types Of ALS

There are two general types of ALS:


Sporadic ALS occurs randomly with no defined risk factors or family history of the disorder; it also comprises nearly 90 percent of all reported cases of ALS.


Familial ALS is genetic, and the affected individual most likely inherited the disorder from their parents. Only one parent needs to carry the required gene for ALS, but several abnormal genes that can initiate familial ALS.


At any given moment, nearly 16,000 Americans are living with ALS, and approximately 6,000 Americans become diagnosed with ALS every year. It can affect people from any race or ethnic background; however, it’s more common to develop among Caucasians and non-Hispanics.


Men may have a slightly higher chance to develop ALS than women, but that probability gradually decreases when both genders become older. And even though it is possible for ALS to occur at any age, symptoms usually appear between 55 and 75.


Some of the medical research implies that military veterans are up to twice as likely to develop ALS than the general public. And there is no identifiable cause as to why, but the risk factors for veterans lean towards significant exposure to environmental toxins.


People with ALS typically survive within 3-to-5 years from when their symptoms start to appear, and only 10 percent of individuals living with ALS may continue to survive for 10 years or more. ALS-related mortalities generally result from respiratory failure.


What Are The Symptoms Of ALS

During the first stages of ALS development, symptoms may occur subtly and go unnoticed, but they gradually become more severe and cause more atrophy and weakness.


People with ALS typically experience muscle cramps, twitches in their legs, arms, tongue or shoulders; stiff and tightened muscles, difficulties with swallowing or chewing, and nasal or garbled speech.


Symptoms may usually start with the arms and hands; easy tasks like writing or fastening a button become increasingly difficult. In some cases, the legs become affected first which could create challenges when running or walking.


Speech and swallowing issue may also serve as prelimenary signs of ALS.


No matter where the symptoms may start from, the muscle atrophy and weakness will begin to spread causing several other health issues common with ALS. The order of symptoms and the progression of ALS will vary with each person. But eventually, the individual will lose most of their motor function.


By having extreme difficulties with eating, people living with ALS are at a higher risk of choking; they may not even bother to eat at all which typically results in faster weight loss and eventually to malnourishment.


Individuals with ALS generally retain their intelligence; however, the awareness of their progressive loss of movement may cause severe depression or anxiety. ALS may rarely affect a person’s cognitive abilities similar to a composition of dementia.


When symptoms become worse, the muscles found in the respiratory system will weaken. A person with ALS eventually lose their ability to breathe naturally and will need to use a ventilator; the risk of pneumonia at this later stage of ALS becomes substantially increased.


A proper diagnosis of ALS relies on a physical examination, the precise history of the individual’s symptoms, and a sequence of tests to eliminate the possibility of any other health complications with similar signs.


ALS has no cure, and there are no treatments currently available that can reverse or stop the progression of the neurological degeneration. Nearly everyone who develops ALS eventually ends up receiving palliative care from a hospice facility or from inside their home if they choose.


CBD For ALS – How It Helps

CBD is an organic compound found in Cannabis sativa plants; it’s also the most researched cannabinoid extracted from cannabis because of its highly valuable properties. Hemp-based CBD is from industrial hemp which has less than 0.3% THC, so it cannot produce any high or intoxicating effects.


CBD works together with the cannabinoid receptors that span through the human body and make up the endocannabinoid system (ECS). When CBD molecules interact with the ECS, it reinforces homeostasis – the natural ability to manage and balance bodily functions from abnormal changes.


Researchers have examined how the therapeutic properties of CBD could help restrict the progression of ALS and ease common symptoms. With models affected by ALS, the results depict CBD helping to release neuroprotective elements that improve the rehabilitation of muscular nerves and dramatically hinder ALS to spread.


Other findings suggest the possibility of CBD to induce anti-inflammatory, neuroprotective, and antioxidant properties that could help prolong the life of damaged nerve cells and prevent motor neurons from becoming worse, if not injured at all.


CBD Dosage For ALS

CBD oil products offer various methods of getting CBD into your system; however, receiving the best amount of CBD for ALS will be different for everyone.


The most reliable dose to take is based on individual assessments of mental and physical conditions and how severe the symptoms occur. You should talk with your primary doctor before starting or changing a health care routine.


Summary

ALS is a rare, neurological disorder that modifies the nervous system and dramatically impairs physical mobility; it progressively deteriorates nerve cells until they die which results in the muscles becoming weaker.


There are two different types of ALS, but both have the same symptoms involving muscular pain and stiffness in the arms, legs, shoulders, and tongue. The exact cause of ALS is unknown; however, experts suggest that genetics and environmental substances may influence ALS development.


Through laboratory observations, researchers recorded the effects of CBD helping to restore neuroprotective responses that could prohibit the gradual progression of ALS and prevent degraded nerve cells from becoming worse.


The right amount of CBD is different for all individuals. It’s recommended to use a small amount at first, but then increase the amount little by little until you find your correct dosage; this method may help reach the best results.