ALS, otherwise known as Amyotrophic Lateral Sclerosis, is a progressive neurodegenerative disease that affects the nerve cells in the brain and spinal cord. It is a progressive disease that can cause muscle weakness, difficulty speaking, difficulty swallowing, difficulty breathing, and eventually paralysis. The exact timeline for the progression of ALS varies greatly from person to person. For some, the progression of the disease is very rapid, while for others it may take years for symptoms to become evident.
The severity of ALS symptoms and the rate of progression will depend on the individual. In general, the disease will cause muscle weakness and atrophy, which can lead to difficulty speaking, swallowing, and breathing. As the disease progresses, it can cause paralysis, which can eventually lead to death.
In general, ALS can progress over a period of months to years, depending on the individual. Typically, the disease progresses faster in those who have a genetic form of ALS, although this is not always the case. The rate of progression can also be affected by other factors, such as age, overall health, and lifestyle.
In conclusion, there is no definitive answer as to how long it takes for ALS to get bad as it varies greatly from person to person. Depending on the individual’s age, overall health, and lifestyle, the progression of the disease can range from months to years.