ALS (amyotrophic lateral sclerosis), also known as Lou Gehrig's disease, is a serious neurodegenerative disease that affects motor neurons in the brain and spinal cord. The disease is characterized by progressive muscle weakness, loss of motor function and, ultimately, paralysis. ALS is a rare disease, but its consequences are devastating for those affected.

The exact cause of the disease is not yet fully understood, but there are certain genetic and environmental factors that may play a role. It is important to note that ALS is not contagious.

ALS affects each individual differently, but the most common symptoms include muscle weakness, muscle cramps, difficulty speaking and swallowing, and loss of coordination. As the disease progresses, it becomes increasingly difficult for patients to perform everyday activities such as eating, walking or breathing, which can lead to a very challenging life situation.

Unfortunately, there is currently no cure for ALS, but treatment methods and medications can help alleviate symptoms and improve the quality of life for those affected. Support from caregivers, family and friends is also essential in managing the disease.

Research into ALS is going on intensively all over the world, and there is hope of finding effective treatment methods and a cure for this terrible disease in the future. At the same time, it is important to raise awareness of ALS, support those affected and their families, and contribute to research efforts to improve the understanding and treatment of this disease.


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