
HOW TO MANAGE AMYOTROPIC LATERAL SCLEROSIS
How to manage amyotropic lateral sclerosis. Amyotrophic lateral sclerosis is a neurodegenerative disease that impairs nerve cell-muscle communication. Over time, it causes muscle weakness that worsens. The symptoms may impact your speech, breathing, and movement. Treatment for ALS involves both medication and therapy to control symptoms and slow the disease’s progression.
HOW TO MANAGE AMYOTROPIC LATERAL SCLEROSIS
Amyotrophic lateral sclerosis, is a neurodegenerative condition that damages the brain and spinal cord’s nerve cells, or neurons. Your motor neurons are the goal. These control your voluntary breathing and muscular movements, such as the ones you use to chew, talk, and move your arms and legs. While there isn’t a cure for ALS, new medicines are being developed all the time. The disease’s course can be slowed and your quality of life enhanced with the correct combination of treatments.
Symptoms

ALS symptoms include: • Weakness in the arms, legs, and neck muscles. Muscle cramps. • Fasciculations, or twitches, in your tongue, hands, feet, and/or shoulders. • Stiff muscles. • Speech difficulties, such as slurred or difficult-to-form words. • drooling. • Uncontrollable emotional reactions, such as sobbing or laughing. • Exhaustion. • Dysphagia, or trouble swallowing. These symptoms worsen after beginning mildly. Each person experiences symptoms at a different rate.
Risk Factors
Among the risk factors for ALS are: • Age: Symptoms are more likely to appear between the ages of 55 and 75. •
1. Race and ethnicity
ALS is more common in white (non-Hispanic) individuals.
2. Sex
Men are more vulnerable to incidents that happen before the age of 55.
3. Veterans
Veterans of the armed forces may be more vulnerable. According to researchers, it may result from physical trauma or exposure to poisons or pesticides in the environment.
Treatment

Damage to motor neurons cannot be repaired. However, receiving treatment can help you live a better life and slow the progression of your symptoms. The ALS treatments listed below may be suggested by your care team: • Drugs. • Rehabilitative therapies. • Assistance with nutrition. • Assistance with breathing. As the illness worsens, you could require more or other forms of treatment. To help you live as comfortably and independently as possible for as long as feasible, supportive care is also provided to match your needs.
Physical treatment: Improving your safety and independence is the aim of physical therapy for ALS. Walking or swimming are examples of mild aerobic exercise that can build muscle and enhance overall health.
Occupational therapy: This field gives you methods and approaches to get through the day. This is beneficial if you require assistance technology, such as braces, a wheelchair, or a walker. You can learn how to utilize these gadgets and move without feeling worn out with the assistance of occupational therapists.
Speech therapy: Communication training helps you keep talking for as long as possible, and speech therapy offers techniques for safer swallowing. You can learn nonverbal communication techniques from speech therapists as well. Nonverbal communication saves energy, even if you can still communicate verbally.
Prevention

There isn’t a known way to stop ALS. To help develop future preventative strategies, research is being conducted to better understand the causes and risk factors.
Summary
When someone is diagnosed with ALS (amyotrophic lateral sclerosis), many questions and feelings may arise. Being unable to perform daily tasks as well as you once could, such as brushing your hair, eating, or conversing with loved ones, can even leave you feeling overburdened and irritated. Depression and anxiety may result from this, particularly when symptoms gradually worsen.