People with Alzheimer’s disease may not see, smell, touch, hear and/or taste things as they used to. Make life safer around the house by:
- Checking foods in the refrigerator often. Throw out anything that has gone bad.
- Put away or lock up things like toothpaste, lotions, shampoos, rubbing alcohol, soap, or perfume. They may look and smell like food to a person with Alzheimer’s.
- If the person wears a hearing aid, check the batteries and settings often.
Remember to re-evaluate the safety of the person’s home as behavior and abilities change.
Learn more about home safety for people with Alzheimer’s.
Caregivers, please talk to your doctor about getting the vaccinations you need. Also, make sure that the person with Alzheimer’s is also current on the following immunizations:
• Pneumococcal Disease
• Tetanus and Diphtheria
• Measles, Mumps, and Rubella
Learn more about vaccinations for older adults in the AgePage Shots for Safety. And don’t forget to schedule updates for your own immunizations!
Caregivers—get helpful resources delivered straight to your inbox! Sign up for the NIA for Caregivers list and receive biweekly e-mails with information and tips about:
• Alzheimer’s caregiving
• Long-distance caregiving
• Caregiver health, and more!
Caregivers play an important role in helping people with mid-to-late stage Alzheimer’s communicate with their doctors.
Make the most out of your time with the doctor with these tips:
• Make a list of what you and the person with Alzheimer’s want to discuss.
• Prioritize your concerns so you talk about the most important issues first.
• Plan to update the doctor on any changes in health, behavior, or medication side effects.
• Take lists of all medications for the doctor to review. This includes prescription drugs, over-the-counter medicines, vitamins, and herbal remedies or supplements.
Learn more about getting the most out of doctor’s appointments.
Caregivers—remember that you need regular check-ups, too! Book your annual doctor’s visit today.
Caring for someone in the final stage of life is always hard. It may be even harder when the person has Alzheimer’s disease.
Palliative care provides comfort care, along with any medical treatments a person might be receiving for a life-threatening illness. When a person is near the end of life, hospice care gives family members needed support and help with their grief, both before and after the person with Alzheimer’s dies.
Learn more about end-of-life care and Alzheimer’s disease by downloading the 2-page Caregiving Tips document from the Alzheimer’s Disease Education and Referral (ADEAR) Center.
Personality and behavior changes are common with a dementia syndrome. Such changes are a common cause for concern for caregivers. The Alzheimer’s Disease Education and Referral Center (ADEAR) of the National Institute on Aging has created the following 2 page tip sheet to describe common personality and behavior changes along with providing some potential suggestions for how caregivers should manage the changes. Please click the link below to access the tip sheet.
The following infographic by the National Institute on Aging shares ways caregivers can take care of themselves.