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“Beyond Driving with Dignity; The workbook for older drivers ”is now available in Raleigh, NC

May 20, 2013 - RALEIGH, N.C. – Raleigh Geriatric Care Management http://www.rgcmgmt.com is pleased to announce that they have partnered with Keeping Us Safe http://www.keepingussafe.org and are now an authorized distributor for the nationally-recognized “Beyond Driving with Dignity; The workbook for older drivers and their families”.

The workbook was specifically designed to help families by providing a “roadmap to success” in their quest to overcome the challenges of an older driver’s safety.  It is designed to be used by families as a tool to meet the demands of a potential problem (tragedy) as they become suspect of a loved-one’s ability to remain a safe driver.

The workbook is quickly gaining popularity across both the United States and Canada as an invaluable tool in helping families (and geriatric professionals) deal with what can be a very emotionally charged and daunting family concern.

Timely and appropriate use of this workbook and of all available resources will help keep families from making many of the common mistakes encountered by others as they move toward a possible driving retirement for their loved one.

Lauren Watral, Certified “Beyond Driving with Dignity” Professional and owner of Raleigh Geriatric Care Management, explains that “Working through this instrument will help your family make driving-related decisions that are not only in the best interest of the older driver, but decisions that simultaneously find themselves in the best interest of highway safety in general.  The workbook was designed to be used by your family in the confidence and comfort of your own home, most likely seated right at your family’s kitchen table.”

Keeping Us Safe is an international organization that provides practical, real-life solutions to older drivers and their families.  Their programs are designed to save lives while simultaneously helping to ease the burden of the family as they find themselves faced with this very challenging issue.

To learn more about the workbook or to place an order, contact Lauren Watral (lwatral@rgcmgmt.com) at 919-803-8025 or visit the Raleigh Geriatric Care Management website at http://www.rgcmgmt.com/.

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Is it time for Assisted Living?

by Paula Spencer Scott

The decision to help an aging adult move out of a current home is a complex one — both emotionally and practically. Above all, you want the person to be safe and well. How can you all feel more confident about whether circumstances suggest that your loved one should no longer be living alone?

1. Big-picture signs it might be time for assisted living

Keep the big red flags in mind. Certain situations make it more obvious that it’s wise to start thinking about alternate living arrangements.

Look for:

  • Recent accidents or close calls. Did your loved one take a fall, have a medical scare, or get in a fender bender (or worse)? Who responded and how long did it take? Accidents do happen, but as people get older, the odds rise of them happening again.
  • A slow recovery. How did the person you’re caring for weather the most recent illness (for example, a flu or bad cold)? Was he or she able and willing to seek medical care when needed, or did last winter’s cold develop into untreated bronchitis?
  • A chronic health condition that’s worsening. Progressive problems such as COPD, dementia, and congestive heart failure can decline gradually or precipitously, but either way, their presence means your loved one will increasingly need help.
  • Increasing difficulty managing the activities of daily living (ADLs) and instrumental activities of daily living (IADLs). ADLs and IADLs are the skills needed to live independently — dressing, shopping, cooking, doing laundry, managing medications, and so on. Doctors, social workers, and other geriatric experts evaluate them as part of a functional assessment, which is one way to get an expert’s view of the situation. Difficulties with ADLs and IADLs can sometimes be remedied by bringing in more in-home help.

2. Up-close signs it might be time for assisted living

Give your loved one a big hug. Clues aren’t always visible from a distance; especially when you don’t see the person every day, you might learn more through touch.

Look for:

  • Noticeable weight loss. Does the person feel thinner? Are clothes loose, or has he added notches to his belt? Many conditions, from depression to cancer, can cause weight loss. A person who is having trouble getting out to shop or remembering how to cook (or to eat) can lose weight; check the fridge and watch meal-prep skills.
  • Seeming more frail. Do you feel anything “different” about the person’s strength and stature when you hug? Can your loved one rise easily from a chair? Does she or he seem unsteady or unable to balance? Compare these observations to the last time you were together.
  • Noticeable weight gain. Common causes include an injury slowing the person down,diabetes, and dementia (when someone doesn’t remember eating, he or she may indulge in meals and snacks all day long). Someone with money troubles may choose fewer fresh foods and more packaged goods or dried pasta and bread.
  • Strange body odor. Unfortunately, a close hug can also reveal changes in personal hygiene habits. Causes range from memory trouble to depression to other physical ailments.
  • Changes in appearance. Does the person’s hair and makeup look all right? Are clothes clean? Someone known for crisply ironed shirts who’s now in a stained sweatshirt may lack the dexterity for buttons or may have lost the strength for managing an ironing board and iron. A formerly clean-shaven man with an unkempt beard may be forgetting to shave (or forgetting how to shave).

3. Social signs it might be time for assisted living

Think realistically about the person’s social connections. Social circles tend to shrink with age, which can have health and safety implications.

Look for:

  • Signs of active friendships. Does your loved one still get together for lunches or outings with friends or visits with neighbors, or participate in religious activities or other group events? Does he or she talk about others or keep a calendar of appointments? Lack of companionship is associated with depression and heart problems in older adults. If friends have died or moved away, moving to a place where other people are around could be lifesaving.
  • Signs that your loved one has cut back on activities and interests. Is a hobby area abandoned? Has a club membership been given up? A library card gone unused? There are many reasons people cut back, but dropping out of everything and showing interest in almost nothing is a red flag for depression.
  • Days spent without leaving the house. This sometimes happens because the person can no longer drive or is afraid to take public transportation alone and lacks a companion to come along. While many older adults fear being “locked away” in a retirement home, many such facilities offer regular outings that may keep them more mobile and active, not less.
  • Someone who checks in on a regular basis. If not you or another family member, who does this? Is your loved one willing to consider a home-safety alarm system, a personal alarm system, or a daily calling service?
  • A plan for a worst-case scenario. If there’s a fire, earthquake, flood, or other disaster, is someone on standby to assist? Does your loved one understand the plan?

4. Money signs it might be time for assisted living

Riffle through the mail. Your loved one’s mail can offer an often-overlooked clue to how he or she is managing money, a common early warning sign of cognitive trouble.

Look for:

  • Snowdrifts of mail in various places. Finding lots of mail scattered around raises concern about how bills, insurance, and other matters are being managed. (Piles of mail are also a potential tripping hazard.)
  • Unopened personal mail. Everybody skips junk mail, but few of us can ignore a good old-fashioned, hand-addressed letter.
  • Unopened bills. This can indicate that your loved one is having difficulty managing finances — one of the most common first signs of dementia.
  • Letters from banks, creditors, or insurers. Routine business letters aren’t worrisome. But it’s alarming if they’re referring to overdue payments, overdrawn balances, recent accidents, or other concerning events.
  • Thank-you messages from charities. Older adults are often vulnerable to scammers. Even those who have always been fiscally prudent are vulnerable if they’re having trouble with thinking skills (a common sign of Alzheimer’s disease). Some charities hit up givers over and over, and your loved one may not remember having donating the first time.
  • Lots of crisp, unread magazines. The person may unknowingly have repeat-renewal subscriptions he or she doesn’t need.

5. Driving signs it might be time for assisted living

Take a drive — with your loved one behind the wheel, if he or she is still driving. Living independently in our culture often depends on the ability to drive (or the arrangement of alternate transportation options).

Look for:

  • Nicks or dents on the car. Notice the car body as you get in and out. Damage marks can be signs of careless driving.
  • Whether the person promptly fastens his or her seatbelt. Even people with mild dementia usually follow the rote basics of driving. It’s worrisome if he or she is forgetting this step.
  • • Tension, preoccupation, or being easily distracted. The person may turn off the radio, for example, or be unwilling to engage in conversation while driving. He or she may avoid certain routes, highway driving, or driving at night and in rain — a safe kind of self-policing but also signals of changing ability.
  • Signs of dangerous driving. People whose driving ability is impaired are more likely to tailgate, drift from their lane, go below the speed limit, react slowly to lights or other cars, and mix up gas and brake pedals. See 8 ways to assess someone’s driving.
  • Warning lights. Check out the dashboard as you ride along. Does the car have sufficient oil, gas, antifreeze, windshield-wiper fluid?

6. Kitchen signs it might be signs for assisted living

Go through the kitchen, from fridge to cupboards to oven. Because people spend so much time in this room, you can learn a lot.

Look for:

  • Stale or expired foods. We all buy more than we need. Look for signs that food is not only old but that this is unnoticed — mold, sour milk that’s still used, or expiration dates well past due, for example.
  • Multiples of the same item. Ten bottles of ketchup? More cereal than can be eaten in a year? Multiples often reveal that the shopper can’t remember from one store trip to the next what’s in stock at home.
  • A freezer full of TV dinners. Your loved one may buy them for convenience sake, but frozen dinners tend not to make healthy diet. If there’s not much fresh food in the house (because it’s too hard to for the person to procure or cook), your loved one might be ready to have help with meal prep or delivery services.
  • Broken appliances. Check them all: microwave, coffeemaker, toaster, washer, and dryer — any device you know your loved one uses (or used to use) routinely.
  • Signs of fire. Are stove knobs charred? Pot bottoms singed badly (or thrown out)? Do any potholders have burned edges? Also look for a discharged fire extinguisher, smoke detectors that have been disassembled, or boxes of baking soda near the stove. Accidents happen; ask for the story behind what you see. Accidental fires are a common home danger for older adults.
  • Increased use of takeout or simpler cooking. A change in physical or mental abilities might explain a downshift to simpler recipes or food choices.

7. Around-the-house signs it might be time for assisted living

Look around the living areas. Sometimes the most obvious sign is hard to see because we become so used to it.

Look for:

  • Lots of clutter. An inability to throw anything away may be a sign of a neurological or physical issue. Obviously it’s more worrisome in a neatnik than in a chronic slob. Papers or pet toys all over the floor represent a tripping hazard.
  • Signs of lax housekeeping. Spills that haven’t been cleaned up are a common sign of dementia — the person lacks the follow-through to tidy. Keep an eye out for cobwebs, bathroom mold, thick dust, or other signs of slackness. Physical limitations can mean your loved one needs housekeeping help or a living situation where this is taken care of for him or her.
  • Bathroom grime and clutter. A common scenario: Your loved one makes an effort to tidy up living areas but overlooks the bathroom. Or the guest bath is clean, but not the one the person uses all the time (the one off a bedroom, for example). Here you may see a truer picture of how your loved one is keeping up.

8. Pet-care and plant-care signs it might be time for assisted living

Be sure to check out how the other living things are faring. An ability to take care of pets and plants goes along with self-care.

Look for:

  • Plants that are dying, dead, or just gone. Most of us have seen plants go brown sometimes. Keep an eye out for chronic neglect, especially in a former plant-lover’s home.
  • Animals that don’t seem well tended. Common problems: dogs with long nails, cat litter boxes that haven’t been changed lately, or dead fish in the fish tank. Poor grooming, overfeeding, and underfeeding are other red flags.

9. Home-maintenance signs it might be time for assisted living

Walk around the yard. Yard maintenance — or lack of it — can yield clues that your loved one isn’t faring as well at home alone anymore.

Look for:

  • Signs of neglect. Look for discolored siding or ceilings that might indicate a leak, gutters choked with leaves, broken windows or fences, dirty windows.
  • Newspapers in the bushes. Are papers being delivered but ignored? Sometimes people pick up those they can see on a driveway but not those that go off into the yard.
  • Mail piled up in the mailbox. Go out and check — it’s an indication that your loved one doesn’t even retrieve it regularly.

10. Get help looking for signs it might be time for assisted living

Get the input of others who know your loved one in order to collect a fuller picture of reality. Gently probing about what others think isn’t nosy; you’re being loving, concerned, and proactive.

Look for:

  • Input from those in your loved one’s circle. Talk to old friends and close relatives to get their sense of how the person is faring. Listen for stories that hint that the person doesn’t get out much (“She doesn’t come over anymore.” “She quit book club.”). Pay attention to comments that indicate ongoing concerns (“Has he had that heart test yet?” “We were worried the day the ambulance came.”).
  • Medical insight. With appropriate permission, your loved one’s primary doctor may share your concerns about his or her patient’s safety at home — or may be able to alleviate those concerns or suggest where to get a home assessment.
  • A second opinion. A social worker or professional geriatric care manager visits older adults’ homes and does informal evaluations. While your loved one may initially resist the notion of a “total stranger” checking on them, try pitching it as a professional (and neutral) second opinion, or ask the doctor to “prescribe” it. Some people wind up sharing doubts or vulnerabilities with a sympathetic, experienced stranger that they’re loathe to admit to their own children or family.

11. Caregivers’ signs it might be time for assisted living

Finally, realize that some of the information you collect is intangible — it has to do with feelings and emotions, and the stress levels of everyone involved.

Look for:

  • How you’re doing. While this decision to remain in one’s home is not primarily about you — the son, daughter, grandchild, caregiver — your own exhaustion can be a good gauge of a decline in older adults’ ability to care for themselves. Keeping someone at home can require lots of hands-on support or care coordination, and this is time-consuming. If your loved one’s need for care is just plain wearing you out, or if a spouse or children are feeling the collective strain of your caregiving activities, these are major signs that it’s time to start looking at other options.
  • Your loved one’s emotional state. Safety is crucial, of course, but so is emotional well-being. If someone living alone is riddled with anxieties or increasingly lonely, then that may tip the scales toward a move not solely based on health and safety reasons.

If your loved one has a full life, a close neighborhood and community connections, and seems to be thriving, it’s worth exploring as many in-home care options as possible before raising stress levels by pressing a move from a beloved home.

If, on the other hand, your loved one is showing signs that living alone is a strain, it may be time for a talk. Broach the subject of where to live in a neutral way and you may find that your loved one harbors the same fears for current and future safety and security that you do. Find out what your loved one fears most about moving and about staying before launching into your own worries and what you think ought to be done.

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Dealing With Verbal Abuse

Abuse of any kind is difficult to deal with, even if the abuser has Alzheimer’s disease and you know he can’t control it.

First of all, you have to work at not taking it personally. If this is an extension of his previous personality, you know it’s just the way he is. If this is a personality change, it will be a shock. You will have to mourn the fact that he has changed dramatically, and get to the point of acceptance.

Give the primary caregiver a break – whether that’s you or someone else. Maybe it means hiring someone to come in, taking your loved one to an adult day center, or having family members take turns, the primary caregiver needs a break. Chances are he will act differently with non-family members. If he does verbally abuse staff you have brought in or at the adult day center, it becomes a bigger problem. At that point, you may want to get your loved one’s doctor involved. Let the doctor know what is going on and see if he has any suggestions. He may want to try something for anxiety or depression. Many times individuals with Alzheimer’s are acting out because of an underlying problem such as anxiety, depression, or even physical pain.

Another way to deal with this situation is with humor. You can’t control how he is acting, so you have to control how you respond. At one adult day care center, when patients would say harsh things or become verbally abusive, the staff refers to it as “terms of endearment.”

Validating your loved one’s feelings may help decrease his frustration. Many times individuals with Alzheimer’s are so frustrated that they act out through this type of behavior. He has lost much of his independence and now he has both of you telling him what to do. Be sure when you are trying to get him to do something or avoid something, that you ask in a non-threatening way. If he resists, stop and go back later. Give him time to calm down, and then try again. Also try not to talk down to him. He is still an adult with a life history of success and independence. He will sense it if he is being treated differently.

Finally, join a support group. Many times others in the group will have experienced the same behavior with their loved ones. Group members may be able to counsel you on how they coped or dealt with it. Journal your feelings and frustrations about his behavior. Dealing with your feelings will help you deal with his behavior more effectively.
 

Thank you to Jackie Bedard, Carolina Estate Planning in Raleigh, NC for this article.

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The 5 Wishes Document

What is Five Wishes and why is it so popular?

 Five Wishes is an advance directive that allows all adults to make important healthcare decisions before a serious illness. It is used to give instructions to your family, friends, and healthcare providers about the types of medical treatments you would want, or not want, if you become seriously ill and can no longer speak for yourself. The concept of an advance directive has been around for decades, but most Americans have not filled one out. Five Wishes is different, and popular, for several reasons:

  • It’s easy to understand. Many advance directives were written by well-meaning legislators, attorneys, and doctors. The documents answered many important questions, but they were very hard for most people without medical or legal training to understand. Five Wishes set a new standard by “translating” the medical and legal jargon into a form that is more understandable and user friendly.

  • It includes important personal preferences. Again, the first generation of advance directives — most of the documents written in state statutes — were created to answer the questions that were most important to doctors and lawyers. Five Wishes is different because it aims to answer the questions that are most important to the person who is seriously ill and his or her caregivers. For example, when people are asked to list the things that would be most important if they knew they were near the end of life, people responded: I want to be at home, I don’t want to be in pain, I want to be prayed for, I want my family to know that I love them, I want my loved ones to be at peace with each other. Five Wishes is the only widely available advance directive that meets the legal requirements in most states and also includes these issues identified as “most important” by the majority of people.

  • It helps communication. It is broadly agreed that talking about your advance directive — explaining your thoughts and decisions to your loved ones and healthcare providers — is just about as important as signing the legal document. But imagine taking a typical legal document (let’s say the forms you sign when you buy a house) or medical paperwork (let’s say the forms you sign when you’re admitted to a hospital) and trying to summarize these documents clearly to your grandparents, parents, siblings, friends, or adult children. Hard to imagine? You’re not alone. And that’s why many people who completed a legally valid advance directive many years ago did so, and didn’t tell anyone about it! Five Wishes puts advance care planning on your turf in terms that are comfortable. We may not all know the legal and medical nuances, but we know what it means to maintain our dignity at the end of life. Five Wishes helps us express these thoughts.

 

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Dare To Care

A fellow collegue, Cheryl Carmichael, of Phoenix, Arizona, recently published her book, Dare To Care, after experiencing first hand caregiving for her mother, grandfather, and grandmother.  The book is an excellent resource for information about caring for elders and how to keep them living in their own homes as they age for a longer period of time.  It’s a basic “cookbook” for new or existing adult non professional caregivers in an easy to read fashion. The book is  considered to be a readily, useful handy reference complete with information on supervisory and personal care, caring for people with memory loss, and palliative care.

I highly recommend this book for any caregivers library.  It is one of the most complete and comprehensive resource manuals for caregivers that I’ve read.

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How to Grieve/5 Myths That Hurt

by Paula Spencer Scott

Grief is a natural response to loss, and it can unfold in many ways. Unfortunately, well-intentioned onlookers — dubbed “grief police” by grief expert Robert Neimeyer, professor of psychology at the University of Memphis — often say things that mistakenly imply to the bereaved that there’s a “right” way to grieve.

Consider these all-too-common grief myths:

Myth #1: It’s possible to cry too much.

Everyone grieves differently. There’s no single correct way to express the pain, sorrow, yearning, and other aspects of the transition of adjusting to the death of a loved one. Intense responses are sometimes seen as “losing control,” when in fact they’re simply how that person is actively (and productively) processing the loss.

Myth #2: If you don’t cry now, it’ll be worse later.

Some people never cry. Tears or outward expressions of anguish simply aren’t everyone’s grieving style, says psychologist Neimeyer. This doesn’t mean they’re grieving less intensely than a visibly shaken individual, or that they loved the person who died any less. Nor does a lack of obvious emotion mean the griever has an emotional block or problem or will face a longer, more difficult adjustment to the loss.

Myth #3: Grief is something you “get over.”

Most people never stop grieving a death; they learn to live with it. Grief is a response, not a straight line with an endpoint. Many psychologists bristle at words such as “acceptance” or “resolution” or “healed” as a final stage of grief. The real stages of grief involve tasks of processing and adjustment that one returns to all through life.

Myth #4: Time heals slowly but steadily.

Time is the commodity through which a grieving person sorts through the effects and meaning of a loss. But that process isn’t a steady fade-out, like a photograph left in the sun. Grief is a chaotic roller coaster — a mix of ups, downs, steady straight lines, and the occasional slam. Periods of intense sadness and pain can flare and fade for years or decades.

Myth #5: Grieving should end after a set amount of time.

Ignore oft-quoted rules of thumb that purport to predict how long certain types of grief should last. A downside to six-week or eight-week bereavement groups, says Sherry E. Showalter, a psychotherapist specializing in grief and the author of Healing Heartaches: Stories of Loss and Life, is that at the end of the sessions, people mistakenly expect to be “better” (or their friends expect this). “Everyone tells me the same story: ‘I failed Grief 101,’ because they still feel pain,” Showalter says. “We grieve for a lifetime, because we’re forever working to incorporate the death into our own tapestry of life.”

Learning how to grieve is ultimately part instinct, part stumbling along, part slogging along — a bit like learning how to live.

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6 New Year Resolutions

~Paula Spencer

If there’s someone with Alzheimer’s disease or another dementia in your life, the last thing you need to ring in the new year is more nudges toward self improvement. You may already be thinking, Forget resolutions about losing weight and giving up alcohol – I just need to figure out how to survive the stress (not to mention the economy) in the new year.

Fear not. This list of resolutions is meant to help you. How? By making taking care of someone with dementia easier. It’s stuff you may already know — what I’m asking is that you consider it through a fresh lens. Make it your ultimate resolution to see tough situations as opportunities to make life better for yourself.

So as a new year begins, why not vow to:

  • Bite my tongue rather than say the dreaded words, “You just asked me that!”There’s an old saying, If you want to get along, go along. Losing patience or quarreling lets you vent — but actually makes the situation worse, since the person with dementia is apt to grow frightened or agitated.

    Learn little tricks for smoother communication. For example, when repetition is a problem and your patience is fried, try moving to a different room to redirect the conversation around new, different stimuli.

  • Move out of my comfort zone to find fresh ways to help my loved one stay occupied and connected. True, it’s work to think up meaningful activities for someone with dementia to do. But in the long run you save time by making the person feel more content. Staying busy provides a fortifying sense of purpose, even if it’s folding (and refolding) towels or organizing (and reorganizing) a tool box.

    One starting point: Music. Because of the way the brain is organized, music can reach even those who never showed the slightest artistic inclination.

  • Have a weekly date night — with myself. Couples with young babies often receive the advice to have a standing evening out to stay in touch with their relationship as partners, not just as parents. Similarly, you need to preserve a sense of yourself as an individual, not just a care partner. The trick is to set a regular appointment with regular care coverage — whether it’s to exercise, to meet a friend for coffee, or just to go “Wal-Marting,” idly pushing a cart down the aisle with nobody else to worry about.

    Then ink this regular appointment in your datebook like a doctor’s appointment. You wouldn’t skip that, would you?

  • Let it go, let it go, let it go.When you catch yourself second-guessing yourself (Oh why didn’t I realize Dad would be hungry . . . OMG it’s my fault I let that bedsore develop!) take a deep breath and just quit. Nobody is a perfect caregiver…because nobody’s perfect.
  • Be open to advice — but toss out what doesn’t fit.There’s a saying, When you’ve seen one person with Alzheimer’s…you’ve seen one person with Alzheimer’s. Each person’s disorder manifests uniquely. So do snarf up all the info you can find on day-to-day life with dementia, but realize that it won’t all apply to your situation. Don’t waste a second feeling isolated or like you’re doing something “wrong” if a certain approach doesn’t work. There are many approaches.
  • Draw yourself a support circle.Can’t get out of the house often enough for regular meetings? No excuse nowadays. Like-minded people with big hearts and lots of ideas are only clicks away. And believe me, we all need them.

One final resolution: Tear up those this-year’s self-improvement lists! A whole year is too much to plan for. If you’re caring for someone with dementia, all you can do is take it one day at a time.

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Caring For The Caregiver

Being a caregiver is a stressful and demanding job. There is usually very little, if any opportunity to prepare for a new caregiving situation. The well-being of the caregiver requires priority consideration. Thought must be given to the fate of the care recipient if the caregiver becomes unable to continue with caregiving responsibilities.  Caregivers are susceptible to depression, illness, physical exhaustion and emotional exhaustion. Any of these conditions will easily interfere with a person’s ability to be an effective caregiver.

The following are suggestions for maintaining caregiver well-being:

  • Become informed about the care recipient’s health issues and any expected changes in behavior.
  • Accept the facts and deal with your situation the best that you can.
  • Seek professional help whenever necessary.
  • Share the burden of caring and caregiving with family members and other interested persons.
  • Talk about your problems with a trusted person.
  • Don’t be too shy, proud, or afraid to seek help with caregiving.
  • Become aware of the limits of your caregiving abilities.
  • Maintain social activities and important relationships.
  • Get away from the responsibilities from time to time.
  • Pace yourself. You may be responsible for caregiving for many years.
  • Work off anger with physical activity.
  • Plan ahead to avoid crises where possible.
  • Live one day at a time.
  • Recognize the worst-case scenario, but hope for the best.
  • Join a family support group.
  • Keep your sense of humor.

Taken from: “Understanding and caring for the person with Alzheimer’s Disease” A practical Guide prepared by the Atlanta Area Chapter of the Alzheimer’s Association.

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Fall Risks for Older Adults

 

Activities that take place in the bathroom, such as showering and bathing, are a simple part of most peoples’ daily routine. Yet, slips in the tub and falls in the shower or from the toilet may cause serious injuries.

New CDC Research

According to a new CDC study published in the Morbidity and Mortality Weekly Report (MMWR), an estimated 234,000 people ages 15 and older were treated in U.S. emergency departments (ED) in 2008 for injuries that occurred in bathrooms. Four out of 5 of these injuries were caused by falls—which can have especially serious consequences for older adults.
 
Almost one-third (30 percent) of adults aged 65 and above who were injured in bathrooms were diagnosed with fractures. Among adults aged 85 and older, 38 percent were hospitalized as a result of their injuries. 

Steps for Safety in the Bathroom

Certain home safety measures may reduce the risk for all household members of being injured in the bathroom. Some prevention strategies include: 

  • Adding non-slip surfaces and grab bars inside and outside the tub or shower to reduce slips and falls.
  • Installing grab bars next to the toilet for added support, 
    if needed.

Preventing Falls Among Older Adults

Four out of five injuries that took place in bathrooms in 2008 were the result of falls. Falls can be especially dangerous for adults ages 65 and older. 

Older adults can take steps to make falls less likely. If you are 65 or older, take the following steps to reduce your risk of falling:

Get some exercise: Lack of exercise can lead to weak legs, which increases the chance of falling. Exercise programs like Tai Chi can increase strength as well as improve balance, making falls less likely for aging adults.
 
Be mindful of medications: Some medicines—or combinations of medicines— can have side effects like dizziness or drowsiness. This can make falls more likely. Having a doctor or pharmacist review all your medications can help reduce the chance of risky side effects and drug interactions.
 
Keep your vision sharp:  Poor vision can make it harder to get around safely. To help make sure you’re seeing clearly, have your eyes checked every year and wear glasses or contact lenses with the right prescription strength.
 
Eliminate hazards at home: About half of all falls happen at home. A home safety check can help identify fall hazards, like clutter and poor lighting that should be removed or changed.

 

caregiver.com

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October 23, 2012 · 2:00 PM

Fighting Caregiver Fatigue

Kristine Dwyer, caring.com

Calvin’s day begins before 5 A.M. He knows another exhausting day lies ahead. He allows himself only enough time to have a cup of coffee and read the paper before lying back down by his wife’s side until 6 A.M. when the daily routine begins again; toileting, showering, dressing, wheelchair transfers, laundry, meal preparation, housekeeping, correspondence, paperwork, yard work, personal care. Soon its time for a doctor appointment; more wheelchair transfers, a trip to the pharmacy, grocery shopping, and then, finally, a return home to continue the care routine. No time to rest during the day. Bedtime planning takes an hour so he begins by 9 P.M. Calvin is physically and emotionally exhausted by 10 P.M. and falls asleep quickly. But he is awakened and out of bed at least three times during the night, tending to his wife’s needs, taking her to the toilet, or changing wet sheets. He attempts to return to bed and finds he cannot fall asleep. His mind is active, he feels anxious and has relentless thoughts that swirl in his mind. Daybreak seems to come too quickly and the schedule begins once again. Caregiving consumes 24 hours of the day and sleep deprivation and fatigue are the common denominators.

Caregiver fatigue cannot be understated. According to Webster’s dictionary, fatigue means “physical or mental exhaustion; weariness.” Spouses, adult children and family members alike are susceptible to caregiver fatigue whether they are providing care twenty-four hours a day or caregiving from a distance. The sandwich generation faces particular challenges as they attempt to provide care to elderly parents while juggling the demands of young families and fulltime careers. Whether caregivers are losing actual sleep or simply wearing down from the constant worry and obligations, help is needed before feelings of resentment and guilt set in or the caregivers’ health is compromised.

Sleep is absolutely necessary to live; however, it is often a low priority in the whole caregiver scenario. As an adult, our bodies need six to nine hours of sleep and after age 65, we need six to eight hours per night. The American Association of Retired Persons (AARP) likens the need for caregivers to take care of themselves to performing regular maintenance on a car. Without regular attention, even the finest cars and caregivers will soon deteriorate. Rest must be a priority. The brain’s frontal lobe especially relies on sleep to effectively function. Without adequate rest, the brain’s ability to access memory, control speech and resolve problems, is greatly hampered.

Family caregivers truly are at risk of physical and emotional problems of their own while they are providing care to a loved one. Fatigue contributes to an increased vulnerability to illness and it is prevalent in nearly all caregivers, yet unseen by most. The results of fatigue creep in over time, robbing the energy and focus of a caregiver. They often become so immersed in their role that they are unable to see their own health decline ‘right before their eyes’. According to one home care director, by the time many care providers realize they have become caregivers, they are already suffering from the symptoms of caregiver fatigue and are headed for burnout!

Lack of sleep can affect emotional as well as physical health. It can produce anxiety, anger, irritability, affect concentration and task performance, impair judgment to the point of danger (driving, using machinery and administering medications), and impact job performance. Sleep deprivation can lead to mental distress, memory loss, and depression. One male caregiver reported that the emotional fatigue was greater for him than the physical exhaustion. He explained that his wife’s behaviors (for example, false accusations, memory loss, hallucinations, and repetitive statements) often lead to daily arguments and disrupted routines that drained his emotions. He finally learned, over time, that he had to train himself to ‘pick his battles’ in order to avoid arguing as well as ignore some of his wife’s peculiar responses and redirect their daily conversations.

The physical consequences of sleep deprivation can include changes in appetite (weight gain or loss), frequent infections, addictions to alcohol or prescription drugs, problems with focusing, droopy eyelids and increased sensitivity to pain. In addition, lack of sleep can interfere with the body’s ability to regulate insulin production and the metabolism of sugar, putting caregivers at a higher risk of developing diabetes.

There are several ways that caregivers can take steps to fight fatigue and improve their physical and mental health.

1. Recognize that fatigue is present and that it is negatively affecting daily life.
2. Seek solutions to alleviate fatigue and sleep loss.
3. Carry out these solutions with the help of family, friends or hired services.

One caregiver in a support group shared that she actually used respite care in her home to get a much-needed nap three times a week. Another woman asked family members to stay overnight once or twice a week to allow her a full night of rest. An important consideration is for caregivers to step back, set personal limits and encourage the care receiver to perform some of their own self-care activities. As time goes on, it can be easy to over-help and invite greater dependence by the care receiver. Others found, when they finally accepted outside help, they experienced a strong sense of relief. Most caregivers wished they had taken the help much sooner. In some cases, when 24-hour care is no longer achievable, moving a loved one to an assisted living facility or to a nursing home is the best solution.

Caregivers, as well as care receivers, need a well-balanced diet and adequate hydration during the day to stave off fatigue and vulnerability to illness. Try to avoid large meals, high fat foods and the drinking of fluids before bedtime. Taking vitamins, eating proteins, grains and fresh produce and decreasing sugar, caffeine, and alcohol can also promote wellness. Caffeine is a mild stimulant and consuming it before bedtime can affect sleep. It is also a diuretic and will result in an increased need to urinate during the night. Alcohol is a depressant by classification; however, it does cause a person to sleep lighter and awaken more frequently.

Fortunately, there are many things that can help to decrease weariness and promote a good night’s sleep:

Regular exercise can have a positive effect on improving sleeping habits as well as decreasing stress, depression and anxiety.
Try to maintain a daily routine for naps and sleep so that the body can adjust to a rhythmic pattern.
Listen to positive sounds to promote relaxation before sleep. Music or nature sounds, such as waves, can be soothing to the soul. Avoid watching stimulating television shows right before bed as this may bring alarming news that unsettles our mood and disrupts our ability to rest
Meditation, prayer, and deep breathing exercises are also options to use for calming our minds and bodies so that we can sleep. These can also be done if one awakens during the night.
Try drinking warm milk, taking a relaxing bath, reading something pleasant and perhaps journal some thoughts prior to bedtime.
If insomnia is prevalent, discuss medication options with a physician.
Caregivers must take time for themselves and focus on their own needs (both physical and emotional) to avoid depleting their strength and energy. Keeping a daily log of sleeping habits can be a “wake up call” to caregivers and a helpful tool for the doctor to determine recommended solutions. Record the quality of sleep as well as the frequency. Record also the foods eaten and the use of medication, caffeine and alcohol. Note the activities engaged in during the day as well as the emotions. After several weeks, trends may appear that offer great insight into the toll of caregiving and the decisions that need to be made to decrease fatigue and increase energy.

After years of sleep deprivation, fatigue can become a chronic state. The body’s biological clocks are disrupted and symptoms of aging seem to accelerate. One adult daughter, who cared for her mother daily for three years, felt she herself had aged ten years and gained over 50 pounds. Three months after her mother was able to move to an assisted living facility, the daughter appeared physically transformed and actually looked younger than before she became a caregiver. She attributed it to finally being able to sleep normally and to focus on her own daily care needs now that her mother’s needs were being met by a caring staff.

It can clearly be seen that fatigue and sleep deprivation strongly impact the caregiver’s ability to provide the best possible care to their loved one. Family caregivers are at risk and must open their eyes to their own needs and solutions that may be available to them. Asking for help is a sign of strength, not weakness! When someone else takes over the caregiving responsibilities, even for a short time, caregivers can step back, focus on themselves, rest and get recharged.

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