ALS Basics
Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative condition that affects nerve cells in the brain and spinal cord, leading to the loss of muscle control. People with ALS often experience muscle weakness, difficulty breathing, difficulty swallowing, and even paralysis.
Care and Support
People living with ALS need access to comprehensive medical care, including physical and occupational therapy, behavioral health services, and supportive services. Additionally, they need access to education and resources about the disease, including information about the latest treatments and clinical trials.
Mobility Aids
People with ALS often require mobility aids such as wheelchairs, walkers, and other assistive devices to help them stay mobile and independent. Additionally, they may need ramps, lifts, and other home modifications to help them access their homes and get around.
Adaptive Equipment
People with ALS often require adaptive equipment, such as adapted forks and spoons, voice-recognition software, and switches and buttons that allow them to control their environment. Additionally, they may need computers, tablets, and other technology to help them stay connected with family and friends.
Assistive Caregivers
People with ALS may need assistance from family members, friends, and other caregivers to help with tasks such as cooking, cleaning, and personal care. Additionally, they may need help with activities such as transportation, exercise, and leisure activities.
Financial Support
People with ALS may need financial support to help pay for medical care, assistive devices, adaptive equipment, and other necessities. Additionally, they may need help navigating insurance and other financial resources.