Amyotrophic lateral sclerosis (ALS) is a severe progressive neurodegenerative disease in which motor neurons — the nerve cells that control muscle movement — die. As a result, muscles gradually weaken, atrophy, and lose their function.
ALS can lead to impairment of:
The disease has a steadily progressive course, but the rate of deterioration is individual and may change over time.
Even over just a few weeks, the following may change:
This helps to adjust:
Examinations every 2–3 months are not enough to understand the true dynamics of the condition.
Regular monitoring of ALS is key to timely treatment adjustments, improving quality of life, and creating a valuable data set for scientific research.