Lou Gehrig Disease also known as Amyotrophic lateral sclerosis (ALS), is a progressive disease of the nervous system. Nerve cells, called neurons, are located in the spinal cord and brain and normally give signals to muscles.
ALS causes these neurons to degenerate, or break down. So, when neurons stop sending signals to muscles, the muscles atrophy, which means they weaken and shrink. This may progress to paralysis. Spasticity is increased muscle tone that can make it hard to coordinate movement, and it may also develop as a result of ALS.

There is no effective treatment for ALS. The drug riluzole may add 3 months to life expectancy. Creatine may help improve strength. Physical, occupational, and speech therapy are helpful. Baclofen, tizanidine, and diazepam may help to relax spastic muscles. Feeding tubes are often needed in the end stages of the disease. A ventilator, or breathing machine, can be used to prolong the life of someone with ALS. However, most people with ALS prefer not to use a ventilator to prolong their lives.

What are the side effects of the treatments?
There are very few side effects from the medicines used for people with ALS. Sedation is probably the most common side effect.

What happens after treatment for the disease?
Treatment usually does not extend life. It can ease pain or discomfort and spasticity and help with general care.

How is the disease monitored?
The disease is monitored by a healthcare provider.