Hospices refuge for families

Categories: Opinion.

The recent death of Tom Magliozzi, co-host of NPR’s “Car Talk,” from complications of Alzheimer’s disease, is a reminder that dementia is a terminal illness. While Alzheimer’s accounts for at least 60 to 80 percent of all dementia cases, according to the Alzheimer’s Association, people don’t often think of Alzheimer’s as a terminal condition. But it is a crippling affliction that slowly robs the brain of its ability to direct normal bodily function. The sixth leading cause of death in the U.S., it accounts for more than 500,000 deaths each year, more than breast cancer and prostate cancer combined.

An unfortunate consequence of not recognizing Alzheimer’s as a life-ending illness is the missed opportunity to tap into the strong resource of hospice care, designed specifically to assist patients facing terminal illnesses and their families.

Hospice is the model for compassionate care for people facing a life-limiting illness like Alzheimer’s. Hospice focuses on caring, not curing. Hospice is most often provided in the patient’s home, but it also can be provided in hospitals, nursing homes and other long-term care facilities. A family member or facility worker typically serves as the primary caregiver, and hospice staff make regular visits and are on call 24-7.

A growing number of older Americans in hospice care today suffer from Alzheimer’s and other dementias. In fact, for the first time, dementia is the leading non-cancer diagnosis for hospice patients. More than 15 percent of patients are admitted to hospice because they are dying from Alzheimer’s disease or dementia, according to the latest National Hospice and Palliative Care Organization’s Fact and Figures: “Hospice Care in America.”

Still, considering that Alzheimer’s deaths increased almost 70 percent between 2000 and 2010, too many caregivers are shouldering the burden alone. Either they don’t know that hospice care is available because a medical professional failed to suggest it, or they are so buried with responsibilities that they do not have the time or energy to figure out if hospice may be the answer.

While hospice is a good fit for most families caring for people with terminal illnesses, it can be a particularly good choice of care for Alzheimer’s and other patients with dementia. Family members of someone with dementia grieve not only the loss of the person they know, but ultimately the death of someone they don’t know. Hospice care teams understand this special loss, and they are available for a year after the death to help family members cope.

The topic of hospice care may be difficult to discuss, but it is important for family members to share their wishes long before it becomes a concern. Having this conversation early on can reduce stress when the time for hospice is needed. Receiving a diagnosis early means the conversation about end-of-life care can occur when the person is able to participate.

Hospice care may not be the right solution for every family, but it can lift a heavy burden off a caregiver’s shoulders and help someone who is dying enjoy peace, comfort and dignity.


Amy Tucci is President & CEO of Hospice Foundation of America. The mission of Hospice Foundation of America is to provide leadership in the development and application of hospice and its philosophy of care with the goal of enhancing the U.S. health care system and the role of hospice within it.

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