Travel for Alzheimer’s Patients
#1: Flying
- Realize that even someone with early dementia shouldn’t travel alone.
- Stay together in the airport at all times.
- Remain calm and don’t rush the person in security lines. Some airports offer family-friendly lanes — they’re not just for people traveling with children.
- Schedule flights early in the day, when the person may be in the best spirits and you’re less likely to be marooned overnight in case of bad weather or other delays. It’s worth the extra price to fly nonstop. Allow plenty of time for connections.
- Don’t place medication in checked bags. Your carry-on should also contain everything the person would need if luggage is lost or a flight is delayed overnight: pajamas, toiletry items, change of clothing, medical contact-us information, and legal papers (power of attorney, insurance).
- Pack snacks and provide water, since dehydration is a risk for seniors. Use the bathroom just before the flight to help avoid the need for the person to do so on the airplane.
- Bring something for the person to do with his hands: a puzzle book, a photo album, knitting, a textured rubbery ball to hold, playing cards.
- Carry a blanket and small pillow for comfort’s sake, as they may not be available on the flight.
#2: Car Trips
- Stop often, but stay with the person at gas stations and restaurants. New places invite confusion.
- Play the person’s favorite music in the car, or find a radio station playing holiday classics.
- If you must stay in a hotel, remain with the person at all times. Get one large room with two beds rather than separate or adjoining rooms.
#3: Frenzy at Home
- Preserve, as much as possible, the person’s daily routine regarding times for meals, exercise, activities, and so on.
- Don’t think you have to make the holiday exactly as it always was. Emphasize a few favorite traditions and let go of the rest.
- Adapt longstanding traditions to the person’s present abilities. If Mom always decorated the tree, help her attach ornaments rather than completely taking the job over. If Dad carved the turkey, let him sit in his customary seat but bring the bird to the table already sliced, and let him help fill plates.
- Keep the person’s hands busy while you handle holiday chores. Some ideas: decorating sugar cookies, kneading dough, stirring a pot, sorting through a box of unbreakable ornaments, stringing popcorn or cranberries, looking at Christmas cards.
- Safety-proof: Avoid candles (fire hazard), artificial fruit (a choking hazard if mistaken for real), gingerbread houses (if made of inedible items), blinking lights (disorienting), garlands that obscure railings on stairs.
- Take advantage of the powerful sensory memories of this time of year. Whether it’s playing in the background or sung in the form of carols or hymns, holiday music taps into deep emotional memories and usually brings a great deal of pleasure to someone with dementia. Expose the person to familiar holiday smells, such as clove-studded oranges, evergreens, cinnamon, and peppermint.
- Reminisce by bringing out photo albums or telling old family stories. But don’t make it feel like a quiz by asking, “Do you remember…?” Just start the story.
#4: Parties
- Invite small groups to visit the person at home. A few friends at a time may be more manageable — and therefore more enjoyable — than one large party.
- If you’re hosting, keep the gathering small. Make it a brunch or luncheon if sundown syndrome is a risk.
- If you’re a caregiver invited to a party, consider having someone stay at home with the person who has dementia rather than bringing her with you. You both may enjoy this arrangement better.
- Designate someone to stay at the person’s side throughout an event to provide a continuous, calming presence and to prevent wandering. Noise and new faces can overwhelm.
- Introduce those who approach the person with dementia, no matter how close a friend or relative they may be: “And here’s your niece, Susan!” Don’t draw attention to the fact that they were introduced just ten minutes earlier.
- Invite the person with Alzheimer’s or dementia to join activities such as opening gifts or watching a sports game — but don’t insist that he participate.
- Withdraw as needed to a quiet corner or room where the person can feel relaxed and safe, away from loud kids or a cocktail-party crowd. Walk outside, weather permitting.
- Monitor the person’s intake of alcohol, as he may not be able to remember and track it himself.
- Watch for cues that the person has had enough: increased impatience or fretfulness, pulling at clothes, withdrawal. Don’t wait until he’s overtired.
#5: Shopping
- Avoid shopping just for tradition’s sake. A drive to look at holiday lights is less likely to confuse and upset than a visit to a crowded shopping mall.
- If you shop, do so early in the day when it’s less crowded.
- Visit one store, not a whole mall-full at once. Another reason to avoid malls: The vast parking lots can be disorienting.
- If you plan on making lots of purchases, it’s easy to become distracted, so consider bringing a third person along who can stay with and focus on the person who has dementia.
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Skin Cancer
Ground Water.
Power Outage Preparation
There are a lot of people still without power and another storm approaching. Please make sure you are prepared.
- Bottled Water
- Batteries
- Candles
- Matches
- Put gas in your cars
- make sure your carbon monoxide detectors have new batteries
- charge cell phones
- get coolers ready and have plenty of ice on hand to help food not go bad
- first aid kits stocked and handy
- make sure there is enough food that does not need to be refrigerated or cooked
For a more comprehensive list check this out from the Red Cross:
https://www.redcross.org/images/MEDIA_CustomProductCatalog/m4340180_PowerOutage.pdf
Stay safe out there!
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SuperAgers
Duchenne Muscular Dystrophy Care Considerations
“Families who care for people with Duchenne muscular dystrophy (DMD) face questions like these every day. DMD is a form of muscular dystrophy, a rare genetic (inherited) disease with muscle weakness that gets worse over time and ultimately affects the heart and lungs. Living with DMD provides challenges for families and caregivers: Activities of daily living (for example, getting dressed or eating on your own) can be challenging. Care for a person with DMD involves different kinds of doctors, which makes coordinating care difficult. The quality and type of care that patients with DMD receive may vary from one treatment facility to another.”
Read more here: https://www.linkedin.com/organization-guest/company/ameribest-home-care?challengeId=AQGGqU14rU0JjAAAAXKeutHoTqDI-q657ky0hcWeXBbRPKSSVeENaMwoX0_Ugk-x8KsEKUVCC5d5K5k3vxQHY3N_aMLa3LruJg&submissionId=9e570f1a-8636-1716-5a07-5b8e2363e265
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