What is family caregiver burden? Caregiver burden is a term used to describe the overwhelming load of responsibility carried by caregivers all over the world. Family caregivers of individuals with Alzheimer’s disease and other dementias are more prone to feel the weight of caregiver burden than caregivers of other chronic diseases. This is because Alzheimer’s caregivers usually provide care over a longer period of time. Alzheimer’s caregivers average about 4 years or more of caregiving.
Being a caregiver for someone with Alzheimer’s requires the caregiver to put the care recipient first. This can often lead to problems for the caregiver’s health. Family caregivers are at a higher risk of developing their own health challenges when they are prevented from providing sufficient self-care.
Unfortunately, it is common for family caregivers to provide care without any support. It can be difficult to ask for help, especially for family caregivers who may feel like it is their sole duty to look after their loved one. Thankfully, there are resources available to support caregivers. Family, friends, and local and national resources can provide a wide range of help.
Are you a family caregiver? Our team at PAAD2 consider you a hero! Keep up the good work, but don’t forget to ask for help when you need it! Additionally, you may qualify to participate in the PAAD2 study — a research opportunity investigating the relationship between physical activity and Alzheimer’s disease.
Do you know a family caregiver? If you’re not a caregiver, but you know one, we encourage you to reach out to offer a helping hand where you can. Read our next article for ways you can support a caregiver.
Together as a community we can lighten each other’s loads in the fight against Alzheimer’s!