Being the primary caregiver for a loved one with ALS can be stressful — not only are you on call 24/7, but you may have additional outside responsibilities, like working a full- or part-time job. Often, caregivers are so busy supporting their loved ones that their own physical or mental health takes second priority.
But as a caregiver, it’s important that you get the support and assistance you need so you can care for your loved one to the best of your abilities.
That’s why we make it a priority to provide resources, such as education and support groups, for caregivers of ALS patients, and we do our best to alleviate the burden of ALS for patients and their families.
Nearly 66 million people in the United States provide care to a chronically ill, disabled, or aging family member or friend during any given year.
Caregivers spend an average of 20 hours per week providing care for their loved one.
66% of all caregivers in the United States are female, and the average age of a caregiver is 48.
78% of adults who need long-term care depend on family and friends as their only source of help.
The value of the services family caregivers provide for “free” is estimated to be $375 billion a year. That’s almost twice as much as is actually spent on home care and nursing home services combined ($158 billion).
All data, unless otherwise cited, is from the National Alliance for Caregiving and AARP’s CAREGIVING IN THE US SURVEY.