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The East Central Florida Memory Clinic Newsletter Caring for the Caregiver As individuals who work with patients dealing with Alzheimer’s disease or other dementing disorders know, they are devastating disorders for those who are experiencing them. But these disorders are farther reaching, as they also impact the patients’ families, who often feel either financially or emotionally compelled to care for their family members. On top of being forced to watch helplessly as the unpredictable nature of these disorders ravages the minds and lives of their loved ones, they frequently must do so in a world that has little understanding for the requirements and difficulties of their circumstances. As
the result of the strain of living with and caring for an Alzheimer’s
patient, family members and caregivers commonly experience the following:
These
feelings may be more or less present at various stages in the progression
of a dementing disorder. Nevertheless,
many of these issues will present themselves at some point in the caregiver’s
life. By recognizing the
potential negative impact that these feelings and experiences can have
on themselves and their loved ones, caregivers can then take the following
steps to deal with their experiences more effectively:
Caregivers have an incredible burden and loss with which to cope, along with feelings of guilt and loneliness. However, caregivers will help their loved ones most by taking care of themselves. The long-term negative health effects of stress have been well-documented, and if you are bedridden, hospitalized, or worse as the result of illness, you can be of little help to your loved one. It is far kinder to him or her to do all you can to keep yourself well as a caregiver and share some of the caregiving responsibility, than to be ever-present but ineffectual or ill as a result of stress. by Jason Webb East Central Florida Memory Clinic |