May 2024

Do You Suffer From Amyotrophic Lateral Sclerosis?

Learn about ALS and how we can help.

ALS, or amyotrophic lateral sclerosis, is a progressive neurodegenerative disease that disrupt nerve cells in the central nervous system such as the brain and spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. The progressive degeneration of the motor neurons in ALS eventually leads to their atrophy. When the motor neurons die, the brain can no longer initiate and control muscle movement. When voluntary muscle action is progressively affected, devastating symptoms arise.

The motor nerves affected when you have ALS are the motor neurons that control voluntary movement and muscle management. For example, voluntary movement consists of the

conscious effort to reach for a beverage or dance to music. These actions are controlled by the muscles in the arms and legs.

 
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What are Signs & Symptoms of ALS?

Signs and Symptoms of ALS can be identified by early onset of

symptoms such as:

 

  • Muscle twitches in the arm, leg, shoulder, or tongue.

     

  • Muscle cramps tight and stiff muscles (spasticity).

     

  • As the disease progresses, muscle weakness and atrophy spread to other parts of the body. Individuals may develop problems with moving, swallowing (called dysphagia), speaking or forming words (dysarthria), and breathing (dyspnea).

Familial v. Sporadic ALS

The term "familial" ALS means that there is more than one occurrence of the disease in a family. The term "sporadic" applies when there is no known history of other family members with the disease. ALS is caused by interplay of various molecular pathways in motor neurons and an interaction with neighboring non-neuronal cells like microglia and astrocytes. 90% ALS are sporadic cases with no clear genetic linkage. However, the remaining 10% of cases show familial inheritance.

Stem Cell Research

for ALS

Photo credit given to the ALS Association.

Stem cells can be thought of as cells that are in the very early stages of development, before they become specialized (differentiated) to

perform specific roles in tissues. They may be precursors to a specific cell

types (such as muscle or nerve cells), or they may still retain pluripotency the ability to develop into any cell types. Stem cell research is an evolving field that may potentially benefit people affected by neuromuscular

disease. There are many different types of stem cells used in biological research.

How We Can Help

Some symptoms of Amyotrophic Lateral

Sclerosis can be reduced through

treatment by a Physical Therapist.

 

Physical therapy can help patients with ALS adjust

to their physical disabilities and lead more

fulfilling lives. Physical therapy can also

help relieve pain and delay the loss of

mobility. At Neuro Physical Therapy, our physical

therapists approach ALS by providing

moderate-intensity exercises, and

activities to improve balance and

coordination. We also focus on safety

precautions such as bracing to protect

injured nerves or to help you move safely

and provide patient education on how to

safely manage ALS.

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1840 North Dixie Highway Boca Raton, FL, 33432
(561) 961-4726

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