Taking care of someone with ALS (amyotrophic lateral sclerosis) takes more than just helping them every day. It also takes knowledge, strength, and emotional strength. As the disease gets worse, the right caregiver needs to aid with both emotional and physical requirements. This is because ALS makes it hard to breathe, talk, and move muscles. An ALS caregiver helps with everyday duties, moving around, devices for communication, and breathing requirements. They also give comfort during moments of insecurity. Even if it's only part-time, having an experienced caregiver makes life much safer and better. Families typically feel better when they know that their loved one is getting reliable ALS care at home.
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