How can I pay for Home Modifications?

How can I pay for Home Modifications?

Many minor home modifications and repairs can be done for about $150-$2,000. For bigger projects, some financing options may be available. For instance, many home remodeling contractors offer reduced rates and charge sliding-scale fees based on a senior’s income and ability to pay or the homeowner may be able to obtain a modest loan to cover urgent needs. Other possible sources of public and private financial assistance include the following:

* Home modification and repair funds from Title III of the Older Americans Act-These funds are distributed by your local area agency on aging (AAA). To contact your local AAA, call the U.S. Administration on Aging’s Eldercare Locator (1-800-677-1116) or visit the Eldercare Locator website at www.eldercare.gov
* Rebuilding Together, Inc., a national volunteer organization, through its local affiliates, is able to assist some low-income seniors with home modification efforts. To obtain more information contact your local area agency on aging or contact Rebuilding Together at 1-800-4-REHAB-9 of visit the website at: http://rebuildingtogether.org/home_modifications
* Investment capital from the U.S. Department of Energy’s Low-Income Home Energy Assistance Program (LIHEAP) and the Weatherization Assistance Program (WAP)-Both of these programs are run by local energy and social services departments.
* Medicare and Medicaid funds-Although these programs usually cover only items that are used for medical purposes and ordered by a doctor, some types of home modifications may qualify. To find out if Medicare will help to cover the cost of a home modification ordered by a doctor, call 1-800-MEDICARE (1-800-633-4227 or
* TTY/TDD 1-877-486-2048). You can also find answers to your questions by visiting the website at http://www.medicare.gov/ on the Internet.
* Community development block grants-Many cities and towns make grant funds available through the local department of community development.
* Home equity conversion mortgages-Local banks may allow a homeowner to borrow money against the value of his or her home and pay for needed improvements. The homeowner then repays the loan as part or his or her regular mortgage.
* In fact, your local AAA can tell you more about whether you are eligible for any of these forms of financial aid or refer you to the agency that can answer your questions.
* Seniors may also choose to bypass public assistance programs and hire a contractor to do their home modifications or even do the job by him or herself. Keep in mind these points if you want to have a professional contractor come into your home to work on a large project:
* Ask for a written agreement that includes only a small down payment and specifies exactly what work will be done and how much it will cost (with the balance of payment to be made when the job is finished).
* Check with your local Better Business Bureau and Chamber of Commerce to see if any complaints have been filed against the contractor.
* Make sure that the contractor has insurance and is licensed to do the work required.
* Talk with your family and friends to get recommendations based on their experiences with the contractors they have hired. This step may actually be the most important one; because contractors with a good reputation can usually be counted on to do a good job.
* The National Resource Center on Supportive Housing and Home Modifications has a guide with useful information on home modification resources across the country. Go to the center’s website at http://www.homemods.org and click on the link to “The National Directory of Home Modification and Repair Programs” for a listing of what is available in the state where you live.

Where can I learn more

* NRCSHHM USC Andrus Gerontology Center       http://www.homemods.org/
* NAHB Research Center, Inc.       http://www.nahbrc.org/
* Rebuilding Together       http://rebuildingtogether.org/home_modifications

For more information

AoA recognizes the importance of making information readily available to consumers, professionals, researchers, and students. Our website provides information for and about older persons, their families, and professionals involved in aging programs and services. For more information about AoA, please contact: US Dept of Health and Human Services.

Source: Administration on Aging, www.aoa.gov

Provided by: The Staff at www.RetirementConnection.com
Copyright © 2008 RetirementConnection.com. All rights reserved.

Providing Senior Care in the Non-Traditional Family

Providing Senior Care in the Non-Traditional Family

Caring for a senior in a non-traditional family can be complicated, but it also represents an opportunity for single parents and blended families.

Both the senior population and non-traditional families are on the rise. According to the U.S. Census Bureau, by 2030, nearly 70 million people will be over the age of 65. At the same time, the number of households that fall into the “non-traditional” family category has increased 23 percent since 1990 from 27.4 million to 33.7 million. When the two trends intersect in the same family, effective management of senior care issues is important as well as rewarding.

The communication of expectations is the key to managing senior care in a non-traditional family. When family members know their roles and responsibilities, providing care to a senior can be easily accomplished.

Single parents who care for a loved one can enlist the help of older children or an in-home care provider such as Right at Home, to assist a senior with shopping, laundry and medication reminders. Also, having younger children read to or with a senior can occupy both children and seniors.

In a blended family, caring for a senior can be a great way for step-children to get to know their new grandparent. Seniors may feel confused about their role as a step-grandparent, but an emphasis on communication is the key in any blended family, specifically those who care for seniors.

Any home that cares for a senior should make it a family affair. Non-traditional families are no exception. There are opportunities for all family members to get involved.

Source:  Right at Home Managing Director
For more information: www.RAHcares.com, 503-574-3674

Copyright © 2008 RetirementConnection.com. All rights reserved.

Respite: What Caregivers Need Most

Respite: What Caregivers Need Most

Family caregivers of chronically ill older persons or those with disabilities are generous, compassionate individuals. They care for loved ones in the familiar surroundings of their own home or community. These caregivers are “on call” 24-hours a day, 7 days a week because they want to see their loved one remain in the comfort and security of their own environment. But at some point, even the caregiver needs a break, a rest, or a breather. The caregiver needs respite. Respite provides informal caregivers – usually relatives a break from their daily responsibilities.

Family caregivers save federal, state and local governments, which are faced with the challenge of covering health and long term care expenses of persons who are ill and have chronic disabilities, a great deal of money. If the work of caregivers had to be replaced by paid home care staff, the estimated cost would be $45 – $94 billion per year. In response to and in recognition of the distinct needs of caregivers, the Administration on Aging (AoA) of the U.S. Department of Health and Human Services is implementing a program that will soon begin to offer respite and other services to some caregivers who so desperately need a break.

The National Family Caregiver Support Program Offers Respite

The enactment of the Older Americans Act Amendments of 2000 (Public Law 106-501) established an important program, the National Family Caregiver Support Program (NFCSP). Funded at $125 million in fiscal year 2001, approximately $113 million has been allocated to states to work in partnership with area agencies on aging and local and community service providers to put into place multi-faceted systems of support for family caregivers. A specific component of these systems is respite. That could include, for example, respite care provided in a home, an adult day-care center or over a weekend in a nursing home or an assisted living.

Research has confirmed the benefits of respite. A paper compiled by Drs. Dale Lund and Scott Wright – experts in the field of caregiving analysis — states that respite benefits both caregivers and their loved ones. It further states that to be most effective, caregivers should consider accessing services early in their caregiving experience. Lund and Wright have found that caregivers need sufficient and regular amounts of respite, and it is important that the caregiver give sufficient thought as to how he or she wants to use that freed-up time, when and if it becomes available.

Respite can cover a wide range of services based upon the unique needs of the caregiver. It might involve medical or social adult day care and/or a short-term stay in a nursing home or assisted living facility for the loved one; a home health aide or home health companion; a private duty nurse or adult foster care.

For the caregiver, personal respite varies as much as the individual and could mean, for example: giving the caregiver a short break to attend a doctor’s appointment or to go shopping; allowing the caregiver the opportunity to nap, bathe, or otherwise rejuvenate him or herself; attending a church service or seeing a movie; taking a much-needed vacation; pampering oneself with a hair appointment or manicure; scheduling elective surgery; or simply visiting friends or relatives.

Listening to the Caregivers

In developing the NFCSP, AoA conducted a series of roundtable discussions with caregivers of older persons who have chronic illnesses or disabilities. These discussions were held in more than 30 cities across the United States, and allowed AoA to gain a more complete understanding of the day-to-day challenges faced by families caring for their older relatives, and to obtain additional insights into the types of services and supports that would respond to the needs of these and other caregivers. It was clear after listening to these caregivers that respite is a necessity. Here’s what some of the caregivers told AoA:

“I took a vow when we got married 54-years ago, and I intend to carry it out. My only fear is that I will die from exhaustion before she does, and who will care for her then?”
— Caregiver husband; Chicago, IL

“It has been a challenge going through this alone. To be able to have someone help me . . . for just one-half hour or one hour to put her [mother] in bed, or get her up in the morning . . . this would be helpful.”
— Caregiver daughter; San Francisco, CA

“Respite is my number one need. I’ve been caring for Mom for seven years . . . in that time, I have had one vacation for 3 days.”– Caregiver daughter; Milwaukee, WI

Many caregivers noted hardships and problems including physical and mental strain and feeling burned out or overwhelmed. Some felt they did not have enough time or energy to meet the demands facing them and that caregiving takes away from their personal lives. AoA, through the state and area agencies on aging (AAA), adult day care centers, and some community- and faith-based organizations, offers respite services to caregivers. The degree and types of respite services offered are discretionary in each state and often vary widely from state to state.

The National Aging Network

Under the authority of the Older Americans Act, AoA leads a national aging network to plan, coordinate, and provide home and community and faith-based services to meet the unique needs of older persons and their caregivers. AoA’s aging network includes: 56 State Units on Aging, 655 Area Agencies on Aging, 236Tribal and native organizations representing 300 American Indian and Alaska Native Tribal organizations and 2 organizations serving Native Hawaiians, plus thousands of service providers, adult care centers, caregivers, and volunteers.

Who to Contact for Help

Local AAA is one of the first resources a caregiver should contact when help is needed. Almost every state has one or more AAA, which serve local communities, older residents, and their families. (In a few states, the State Unit or Office on Aging serves as the AAA.) Local AAA’s are generally listed in the city or county government sections of the telephone directory under “Aging” or “Social Services.”

The Eldercare Locator

AoA supports a nationwide, toll-free information and assistance directory called the Eldercare Locator, which can locate the appropriate AAA to help an individual needing assistance for their loved ones, relatives, or friends. Older persons and caregivers can call the Eldercare Locator at 1-800-677-1116, Monday through Friday, 9:00 a.m. to 8:00 p.m. Eastern Time.

“Taking time out, away from the care of an impaired person, is one of the single most important things that you can do to make it possible for you to continue to care for someone.” – Mace and Robins, The 36 Hour Day.

* Many caregivers experience immense stress and feelings of burden, high rates of depression, and feelings of anger and anxiety.
* Caregiving can adversely affect one’s physical health and ability to continue providing care leaving two impaired persons, rather than one.
* The emotional and physical strain of caring for a frail older relative is often exacerbated by worries over paying for care, particularly for nursing homes.

Research has shown that some caregivers must quit their jobs to give care, while others experience increased absenteeism, lower productivity at work, lost career opportunities, and loss of future earnings.

American Society on Aging

A unique feature of respite care is the help it offers to both the caregiver and the care recipient.

Respite care can allow time to go to the doctor or the grocery store, participate in a support group, or attend a class to learn caregiving skills.

Researchers have suggested that respite care can relieve the burden of the caregiving situation and allow families to continue to care for loved ones who would otherwise be placed in a nursing home.

For More Information

Working in close partnership with its sister agencies in the U.S. Department of Health and Human Services, the AoA is the official Federal agency dedicated to policy development, planning and the delivery of supportive home and community-based services to older persons and their caregivers. The AoA works through the national aging network of 56 State Units on Aging, 655 Area Agencies on Aging, 236 Tribal and Native organizations representing 300 American Indian and Alaska Native Tribal organizations, and two organizations serving Native Hawaiians, plus thousands of service providers, adult care centers, caregivers, and volunteers. For more information about the AoA, please contact:

U.S. Administration on Aging
http://www.aoa.gov
Eldercare Locator: 1-800-677-1116, Monday — Friday, 9 a.m. to 8 p.m. ET

Source: www.aoa.dhhs.gov

Provided by: The Staff at www.RetirementConnection.com
Copyright © 2008 RetirementConnection.com. All rights reserved.

Restraints Have Risks, Make the Right Choice

Restraints Have Risks — Make the Right Choice

From childhood on, one of the most important impulses is to maintain independence through movement. As people age, their ability to move is compromised by the natural processes of aging. For people who reside in nursing homes, it was thought for many years that using “restraints” – devices that prevent people from moving around – would ensure safety from falls and other dangers.

Today, restraints are used much less frequently because studies have shown they can be dangerous. Nursing homes and health care agencies are working hard to reduce the use of restraints. Inside is information we would like you to consider.

What Is a Physical Restraint?

A physical restraint is anything near or on the body which restricts movement. Some examples of physical restraints are:

* Lap buddies, belts, “geri” chairs, vests, or trays, which keep the body immobile in a wheelchair,
* Bed rails or belts, which keep people confined to their beds, and
* Door alarms, which prevent people from walking beyond a set point

What Are Chemical Restraints?

A chemical restraint is a medication given to control behavior such as striking out or yelling. Chemical restraints include sedatives and antipsychotic drugs. These have many appropriate uses as prescribed by a physician to treat specific conditions caused by mental illness. Using these drugs for problems like pacing, wandering, restlessness, or uncooperative behavior is often inappropriate.

Restraints May Be Used to:

* Prevent falls
* Reduce wandering
* Minimize behavior problems
* Respond to medical necessity

The restraints question is not an “all or nothing” issue. Some devices can be used appropriately to enable the individual to maintain certain functions. For example, a lap buddy can be used as a tray for reading or other activities. When restraints must be used, the least restrictive device that promotes the highest level of functioning for the individual should be chosen.

Dangers Associated with Restraints

Possible physical effects of the inability to move freely include:

* Decreased bone/muscle strength
* Decreased appetite and malnutrition
* Dehydration
* Pneumonia
* Urinary tract infections
* Constipation
* Incontinence
* Pressure sores and/or bruising
* Death by asphyxiation

Possible mental or emotional effects of using restraints include:

* Agitation
* Depression/withdrawal
* Loss of dignity
* Sleeping problems
* Humiliation

Bed Rails Can Be a Risk

* Bed rails can increase the risk of injury to the elderly. People must be appropriately assessed to ensure correct use of bed rails.
* Bed rails do not prevent all falls. People sometimes climb over their rails, often to get to the toilet. When people climb over their bed rails and fall, the height of the fall is greater and, therefore, so is the risk of injury.
* Elderly people with decreased strength can become trapped between their bed rail and their mattress.
* Before using bed rails, consider alternatives such as lowered beds, futons, or waterbeds.

If You or a Relative Live in a Nursing Home…

* Know that restraints may only be used to treat specific medical symptoms
* Participate in care planning and ask how the restraint, if being considered, will help the resident function.
* Be involved when decisions are made regarding the use of restraints.
* When deciding whether restraint use is appropriate, consider the alternatives first and ask questions of health care providers and nursing home staff.

Here are some options for you and the nursing home to consider prior to using restraints:

* Try non-restraining positioning devices
* Increase social opportunities
* Provide physical and massage therapy
* Conduct medication review
* Lower beds
* Encourage family/volunteer involvement
* Provide entertaining activities
* Continuously assess individual needs

The Benefits of Keeping People Mobile Longer:

* Preservation of dignity
* Greater sense of well-being and independence
* Greater muscle strength
* Independence with regard to eating, toileting, dressing, and walking
* Greater self-esteem
* Ability to interact with environment

Things you can do to prevent falls in the home:

Because falls are a major cause of nursing home admissions, consider modifying the home environment to decrease the risk of falling. A few suggestions include:

* Remove throw rugs, electrical cords, and other items that can cause an elderly person to trip and fall.
* Install railing and/or hand grips to help seniors move around safely.
* Determine whether poor vision or side effects of medications may be putting an elderly person at increased risk for falling.
* Provide shoes that fit properly.
* Ensure adequate lighting in all rooms.
* Avoid wet or slippery floors.

For a home risk assessment, contact a public health nurse or your county health department. If you are using a home health agency, contact that agency for a home risk assessment.

Source: Colorado Department of Public Health and Environment, Health Facilities and Emergency Medical Services Division, Colorado Long Term Care Ombudsman Program and Colorado Foundation for Medical Care. www.cdphe.state.co.us
Provided by: The Staff at www.RetirementConnection.com
For more information: www.cdphe.state.co.us

Copyright © 2008 RetirementConnection.com. All rights reserved.

Home Safety for People with Alzheimer’s Disease

Home Safety for People with Alzheimer’s Disease

Caring for a person with Alzheimer’s disease (AD) is a challenge that calls upon the patience, creativity, knowledge, and skills of each caregiver. We hope that this booklet will help you cope with some of these challenges and develop creative solutions to increase the security and freedom of the person with AD in your home, as well as your own peace of mind.

This booklet is for those who provide in-home care for people with AD or related disorders. Our goal is to improve home safety by identifying potential problems in the home and offering possible solutions to help prevent accidents.

We begin with a checklist to help you make each room in your home a safer environment for the person with AD. Next, we hope to increase awareness of the ways specific impairments associated with the disease can create particular safety hazards in the home. Specific home safety tips are listed to help you cope with some of the more hazardous behaviors that may occur as the disease advances. We also include tips for managing driving and planning for natural disaster safety. The booklet ends with a list of resources for family caregivers.

What is Alzheimer’s Disease?

Alzheimer’s disease is a progressive, irreversible disease that affects brain cells and produces memory loss and intellectual impairment in as many as 4.5 million American adults. This disease affects people of all racial, economic, and educational backgrounds.

AD is the most common cause of dementia in adults. Dementia is defined as loss of memory and intellect that interferes with routine personal, social, or occupational activities. Dementia is not a disease; rather, it is a group of symptoms that may accompany certain diseases or conditions. Other symptoms include changes in personality, mood, or behavior.

Although AD primarily affects people age 65 or older, it also may affect people in their 50s and, although rarely, even younger. Other causes of irreversible dementia include multi-infarct dementia (a series of minor strokes resulting in widespread death of brain tissue), Pick’s disease, Binswanger’s disease, Parkinson’s disease, Huntington’s disease, Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis (Lou Gehrig’s disease), multiple sclerosis, and alcohol abuse. The recommendations in this booklet deal primarily with common problems in AD, but they also may apply to any of the related dementing disorders.

What are the Symptoms of AD?

There is no “typical” person with Alzheimer’s. There is tremendous variability among people with AD in their behaviors and symptoms. At present, there is no way to predict how quickly the disease will progress in any one person, nor to predict the exact changes that will occur. We do know, however, that many of these changes will present problems for caregivers. Therefore, knowledge and prevention are critical to safety.

People with AD have memory problems and cognitive impairment (difficulties with thinking and reasoning), and eventually they will not be able to care for themselves. They may experience confusion, loss of judgment, and difficulty finding words, finishing thoughts, or following directions. They also may experience personality and behavior changes. For example, they may become agitated, irritable, or very passive. Some may wander from home and become lost. They may not be able to tell the difference between day and night, and they may wake up, get dressed, and start to leave the house in the middle of the night thinking that the day has just started. They may suffer from losses that affect vision, smell, or taste.

These disabilities are very difficult, not only for the person with AD, but for the caregiver, family, and other loved ones as well. Caregivers need resources and reassurance to know that while the challenges are great, there are specific actions to take to reduce some of the safety concerns that accompany Alzheimer’s disease.

General Safety Concerns

People with AD become increasingly unable to take care of themselves. However, individuals will move through the disease in their own unique manner. As a caregiver, you face the ongoing challenge of adapting to each change in the person’s behavior and functioning. The following general principles may be helpful.

Think prevention. It is very difficult to predict what a person with AD might do. Just because something has not yet occurred, does not mean it should not be cause for concern. Even with the best-laid plans, accidents can happen. Therefore, checking the safety of your home will help you take control of some of the potential problems that may create hazardous situations.

Adapt the environment. It is more effective to change the environment than to change most behaviors. While some AD behaviors can be managed with special medications prescribed by a doctor, many cannot. You can make changes in an environment to decrease the hazards and stressors that accompany these behavioral and functional changes.

Minimize danger. By minimizing danger, you can maximize independence. A safe environment can be a less restrictive environment where the person with AD can experience increased security and more mobility.

Is it Safe to Leave the Person With AD Alone?

This issue needs careful evaluation and is certainly a safety concern. The following points may help you decide. Does the person with AD:

* become confused or unpredictable under stress?
* recognize a dangerous situation; for example, fire?
* know how to use the telephone in an emergency?
* know how to get help?
* stay content within the home?
* wander and become disoriented?
* show signs of agitation, depression, or withdrawal when left alone for any period of time?
* attempt to pursue former interests or hobbies that might now warrant supervision such as cooking, appliance repair, or woodworking?

You may want to seek input and advice from a health care professional to assist you in these considerations. As Alzheimer’s disease progresses, these questions will need ongoing evaluation.

Home Safety Room-By-Room

Prevention begins with a safety check of every room in your home. Use the following room-by-room checklist to alert you to potential hazards and to record any changes you need to make. You can buy products or gadgets necessary for home safety at stores carrying hardware, electronics, medical supplies, and children’s items.

Keep in mind that it may not be necessary to make all of the suggested changes. This booklet covers a wide range of safety concerns that may arise, and some modifications may never be needed. It is important, however, to re-evaluate home safety periodically as behavior and abilities change.

Your home is a personal and precious environment. As you go through this checklist, some of the changes you make may impact your surroundings positively, and some may affect you in ways that may be inconvenient or undesirable. It is possible, however, to strike a balance. Caregivers can make adaptations that modify and simplify without severely disrupting the home. You may want to consider setting aside a special area for yourself, a space off-limits to anyone else and arranged exactly as you like. Everyone needs private, quiet time, and as a caregiver, this becomes especially crucial.
A safe home can be a less stressful home for the person with AD, the caregiver, and family members. You don’t have to make these changes alone. You may want to enlist the help of a friend, professional, or community service such as the Alzheimer’s Association.

Throughout the Home

* Display emergency numbers and your home address near all telephones.
* Use an answering machine when you cannot answer phone calls, and set it to turn on after the fewest number of rings possible. A person with AD often may be unable to take messages or could become a victim of telephone exploitation. Turn ringers on low to avoid distraction and confusion. Put all portable and cell phones and equipment in a safe place so that they will not be easily lost.
* Install smoke alarms near all bedrooms and carbon monoxide detectors in appropriate places; check their functioning and batteries frequently.
* Avoid the use of flammable and volatile compounds near gas water heaters. Do not store these materials in an area where a gas pilot light is used.
* Install secure locks on all outside doors and windows.
* Hide a spare house key outside in case the person with AD locks you out of the house.
* Avoid the use of extension cords if possible by placing lamps and appliances close to electrical outlets. Tack extension cords to the baseboards of a room to avoid tripping.
* Cover unused outlets with childproof plugs.
* Place red tape around floor vents, radiators, and other heating devices to deter the person with AD from standing on or touching a hot grid.
* Check all rooms for adequate lighting.
* Place light switches at the top and the bottom of stairs.
* Stairways should have at least one handrail that extends beyond the first and last steps. If possible, stairways should be carpeted or have safety grip strips.
* Keep all medications (prescription and over-the-counter) locked. Each bottle of prescription medicine should be clearly labeled with the patient’s name, name of the drug, drug strength, dosage frequency, and expiration date. Child-resistant caps are available if needed.
* Keep all alcohol in a locked cabinet or out of reach of the person with AD. Drinking alcohol can increase confusion.
* If smoking is permitted, monitor the person with AD whilehe or she is smoking. Remove matches, lighters, ashtrays, cigarettes, and other means of smoking from view. This reduces potential fire hazards, and with these reminders out of sight, the person may forget the desire to smoke.
* Avoid clutter, which can create confusion and danger. Throw out/recycle newspapers and magazines regularly. Keep all walk areas free of furniture.
* Keep plastic bags out of reach. A person with AD may choke or suffocate.
* Remove all guns or other weapons from the home, or safety proof them by installing safety locks or by removing ammunition and firing pins.
* Lock all power tools and machinery in the garage, workroom, or basement.
* Remove all poisonous plants from the home. Check with local nurseries or poison control centers for a list of poisonous plants.
* Make sure all computer equipment and accessories, including electrical cords, are kept out of the way. If valuable documents or materials are stored on a home computer, protect the files with passwords. Password protect access to the Internet also, and restrict the amount of online time without supervision. Consider monitoring the person with AD’s computer use, and installing software that screens for objectionable or offensive material on the Internet.
* Keep fish tanks out of reach. The combination of glass, water, electrical pumps, and potentially poisonous aquatic life could be harmful to a curious person with AD.

Outside Approaches to the House

* Keep steps sturdy and textured to prevent falls in wet or icy weather.
* Mark the edges of steps with bright or reflective tape.
* Consider a ramp with handrails into the home rather than steps.
* Eliminate uneven surfaces or walkways, hoses, or other objects that may cause a person to trip.
* Restrict access to a swimming pool by fencing it off with a locked gate, covering it, and keeping it closely supervised when in use.
* In the patio area, remove the fuel source and fire starters from any grills when not in use, and supervise use when the person with AD is present.
* Place a small bench or table by the entry door to hold parcels while unlocking the door.
* Make sure outside lighting is adequate. Light sensors that turn on lights automatically as you approach the house are available and may be useful. They also may be used in other parts of the home.
* Prune bushes and foliage well away from walkways and doorways.
* Consider a NO SOLICITING sign for the front gate or door.

Entryway

* Remove scatter rugs and throw rugs.
* Use textured strips or nonskid wax on hardwood floors to prevent slipping.

Kitchen

* Install childproof door latches on storage cabinets and drawers designated for breakable or dangerous items. Lock away all household cleaning products, matches, knives, scissors, blades, small appliances, and anything valuable.
* If prescription or nonprescription drugs are kept in the kitchen, store them in a locked cabinet.
* Remove scatter rugs and foam pads from the floor.
* Remove knobs from the stove, or install an automatic shut-off switch.
* Do not use or store flammable liquids in the kitchen. Lock them in the garage or in an outside storage unit.
* Keep a night-light in the kitchen.
* Remove or secure the family “junk drawer.” A person with AD may eat small items such as matches, hardware, erasers, plastics, etc.
* Remove artificial fruits and vegetables or food-shaped kitchen magnets, which might appear to be edible.
* Insert a drain trap in the kitchen sink to catch anything that may otherwise become lost or clog the plumbing.
* Consider dismantling the garbage disposal. People with AD may place objects or their own hands in the disposal.

Bedroom

* Anticipate the reasons a person with AD might get out of bed, such as hunger, thirst, going to the bathroom, restlessness, and pain, and try to meet these needs by offering food and fluids, and scheduling ample toileting.
* Use a night-light.
* Use an intercom device (often used for infants) to alert you to any noises indicating falls or a need for help. This also is an effective device for bathrooms.
* Remove scatter rugs.
* Remove portable space heaters. If you use portable fans, be sure that objects cannot be placed in the blades.
* Be cautious when using electric mattress pads, electric blankets, electric sheets, and heating pads, all of which can cause burns. Keep controls out of reach.
* When the person with AD is at risk of falling out of bed, place mats next to the bed, as long as this does not create a greater risk of accident.
* Use transfer or mobility aids.
* If you are considering using a hospital-type bed with rails and/or wheels, understand that many people can sleep safely without bed rails, and reassess the need for using bed rails on a regular basis:
* Use beds that can be raised and lowered close to the floor to accommodate both the person with AD and your needs.
* Keep the bed in the lowest position with wheels locked.
* Use a proper size mattress or mattress with raised foam edges to prevent the person from being trapped between the mattress and rail.
* Reduce the gaps between the mattress and side rails.
* Monitor the person with AD frequently.

Bathroom

* Do not leave a severely impaired person with AD alone in the bathroom.
* Remove the lock from the bathroom door to prevent the person with AD from getting locked inside.
* Place nonskid adhesive strips, decals, or mats in the tub and shower. If the bathroom is uncarpeted, consider placing these strips next to the tub, toilet, and sink.
* Use washable wall-to-wall bathroom carpeting to prevent slipping on wet tile floors.
* Use an extended toilet seat with handrails, or install grab bars beside the toilet.
* Install grab bars in the tub/shower. A grab bar in contrasting color to the wall is easier to see.
* Use a foam rubber faucet cover (often used for small children) in the tub to prevent serious injury should the person with AD fall.
* Use plastic shower stools and a hand-held showerhead to make bathing easier.
* In the shower, tub, and sink, use a single faucet that mixes hot and cold water to avoid burns.
* Adjust the water heater to 120 degrees to avoid scalding tap water.
* Insert drain traps in sinks to catch small items that may be lost or flushed down the drain.
* Store medications (prescription and nonprescription) in a locked cabinet. Check medication dates and throw away outdated medications.
* Remove cleaning products from under the sink, or lock them away.
* Use a night-light.
* Remove small electrical appliances from the bathroom. Cover electrical outlets. If men use electric razors, have them use a mirror outside the bathroom to avoid water contact.

Living Room

* Clear all walk areas of electrical cords.
* Remove scatter rugs or throw rugs. Repair or replace torn carpet.
* Place decals at eye level on sliding glass doors, picture windows, or furniture with large glass panels to identify the glass pane.
* Do not leave the person with AD alone with an open fire in the fireplace. Consider alternative heating sources. Remove matches and cigarette lighters.
* Keep the controls for cable or satellite TV, VCR, and stereo system out of sight.

Laundry Room

* Keep the door to the laundry room locked if possible.
* Lock all laundry products in a cabinet.
* Remove large knobs from the washer and dryer if the person with AD tampers with machinery.
* Close and latch the doors and lids to the washer and dryer to prevent objects from being placed in the machines.
* Garage/Shed/Basement
* Lock access to all garages, sheds, and basements if possible.
* Inside a garage or shed, keep all potentially dangerous items, such as tools, tackle, machines, and sporting equipment either locked away in cabinets or in appropriate boxes/cases.
* Secure and lock all motor vehicles and keep them out of sight if possible. Consider covering those vehicles, including bikes, which are not frequently used. This may reduce an AD person’s thoughts of leaving.
* Keep all toxic materials, such as paint, fertilizers, gasoline, or cleaning supplies out of view. Put them either in a high, dry place, or lock them in a cabinet.
* If a person with AD is permitted in a garage, shed, or basement, preferably with supervision, make sure the area is well lit and that stairs have a handrail and are safe to walk up and down. Keep walkways clear of debris and clutter, and place overhanging items out of reach.

Home Safety Behavior-By-Behavior

* Although a number of behavior and sensory problems may accompany Alzheimer’s disease, not every person will experience the disease in exactly the same way.
* As the disease progresses, particular behavioral changes can create safety problems. The person with AD may or may not have these symptoms. However, should these behaviors occur, the following safety recommendations may help reduce risks.

Wandering

* Remove clutter and clear the pathways from room to room to allow the person with AD to move about more freely.
* Make sure floors provide good traction for walking or pacing. Use nonskid floor wax or leave floors unpolished. Secure all rug edges, eliminate throw rugs, or install nonskid strips. The person with AD should wear nonskid shoes or sneakers.
* Place locks on exit doors high or low on the door out of direct sight. Consider double locks that require a key. Keep a key for yourself and hide one near the door for emergency exit purposes.
* Use loosely fitting doorknob covers so that the cover turns instead of the actual knob. Due to the potential hazard they could cause if an emergency exit is needed, locked doors and doorknob covers should be used only when a caregiver is present.
* Install safety devices found in hardware stores to limit the distance that windows can be opened.
* If possible, secure the yard with fencing and a locked gate. Use door alarms such as loose bells above the door or devices that ring when the doorknob is touched or the door is opened.
* Divert the attention of the person with AD away from using the door by placing small scenic posters on the door; placing removable gates, curtains, or brightly colored streamers across the door; or wallpapering the door to match any adjoining walls.
* Place STOP, DO NOT ENTER, or CLOSED signs in strategic areas on doors.
* Reduce clues that symbolize departure such as shoes, keys, suitcases, coats, or hats.
* Obtain a medical identification bracelet for the person with AD with the words “memory loss” inscribed along with an emergency telephone number. Place the bracelet on the person’s dominant hand to limit the possibility of removal, or solder the bracelet closed. Check with the local Alzheimer’s Association about the Safe Return program.
* Place labels in garments to aid in identification.
* Keep an article of the person’s worn, unwashed clothing in a plastic bag to aid in finding someone with the use of dogs.
* Notify neighbors of the person’s potential to wander or become lost. Alert them to contact you or the police immediately if the individual is seen alone and on the move.
* Give local police, neighbors, and relatives a recent picture, along with the name and pertinent information about the person with AD, as a precaution should he or she become lost. Keep extra pictures on hand.
* Consider making an up-to-date home video of the person with AD.
* Do not leave a person with AD who has a history of wandering unattended.

Rummaging/Hiding Things

* Lock up all dangerous or toxic products, or place them out of the person’s reach.
* Remove all old or spoiled food from the refrigerator and cupboards. A person with AD may rummage for snacks but may lack the judgment or taste to rule out spoiled foods.
* Simplify the environment by removing clutter or valuable items that could be misplaced, lost, or hidden by the person with AD. These include important papers, checkbooks, charge cards, and jewelry.
* If your yard has a fence with a locked gate, place the mailbox outside the gate. People with AD often hide, lose, or throw away mail. If this is a serious problem, consider obtaining a post office box.
* Create a special place for the person with AD to rummage freely or sort (for example, a chest of drawers, a bag of selected objects, or a basket of clothing to fold or unfold). Often, safety problems occur when the person with AD becomes bored or does not know what to do.
* Provide the person with AD a safe box, treasure chest, or cupboard to store special objects.
* Close access to unused rooms, thereby limiting the opportunity for rummaging and hiding things.
* Search the house periodically to discover hiding places. Once found, these hiding places can be discreetly and frequently checked.
* Keep all trashcans covered or out of sight. The person with AD may not remember the purpose of the container or may rummage through it.
* Check trash containers before emptying them in case something has been hidden there or accidentally thrown away.

Hallucinations, Illusions, and Delusions

Due to the complex changes occurring in the brain, people with AD may see or hear things that have no basis in reality. Hallucinations come from within the brain and involve hearing, seeing, or feeling things that are not really there. For example, a person with AD may see children playing in the living room when no children exist. Illusions differ from hallucinations because the person with AD is misinterpreting something that actually does exist. Shadows on the wall may look like people, for example. Delusions are persistent thoughts that the person with AD believes are true but in reality, are not. Often, stealing is suspected, for example, but cannot be verified.

* It is important to seek medical evaluation if a person with AD has ongoing disturbing hallucinations, illusions, or delusions. Often, these symptoms can be treated with medication or behavior management techniques. With all of the above symptoms, the following environmental adaptations also may be helpful.
* Paint walls a light color to reflect more light. Use solid colors, which are less confusing to an impaired person than a patterned wall. Large, bold prints (for example, florals in wallpaper or drapes) may cause confusing illusions.
* Make sure there is adequate lighting, and keep extra bulbs handy in a secured place. Dimly lit areas may produce confusing shadows or difficulty with interpreting everyday objects.
* Reduce glare by using soft light or frosted bulbs, partially closing blinds or curtains, and maintaining adequate globes or shades on light fixtures.
* Remove or cover mirrors if they cause the person with AD to become confused or frightened.
* Ask if the person can point to a specific area that is producing confusion. Perhaps one particular aspect of the environment is being misinterpreted.
* Vary the home environment as little as possible to minimize the potential for visual confusion. Keep furniture in the same place.
* Avoid violent or disturbing television programs. The person with AD may believe the story is real.
* Do not confront the person with AD who becomes aggressive. Withdraw and make sure you have access to an exit as needed.

Special Occasions/Gatherings/Holidays

When celebrations, special events, or holidays include large numbers of people, remember that it is possible that large groups may cause a person with AD some confusion and anxiety. The person with AD may find some situations easier and more pleasurable than others.

* Large gatherings, weddings, family reunions, or picnics may be cause for anxiety. Consider having a more intimate gathering with only a few people in your home. Think about having friends and family visit in small groups rather than all at once. If you are hosting a large group, remember to prepare the person with AD ahead of time. Try to have a space available where they can rest, be by themselves, or spend some time with a smaller number of people, if needed.
* Consider simplifying your holidays around the home and remember that you already may have more responsibilities than in previous years. For example, rather than cooking an elaborate dinner at Thanksgiving or Christmas, invite family and friends for a potluck dinner. Instead of elaborate decorations, consider choosing a few select items to celebrate holidays. Make sure holiday decorations do not significantly alter the environment, which might confuse the person with AD.
* Holiday decorations, such as Christmas trees, lights, or menorahs, should be secured so that they do not fall or catch on fire. Anything flammable should be monitored at all times, and extra precautions should be taken so that lights or anything breakable are fixed firmly, correctly, and out of the way of those with AD.
* As suggested by most manufacturers, candles of any size should never be lit without supervision. When not in use, they should be put away.
* Try to avoid clutter in general, especially in walkways, during the holidays.

Impairment of the Senses

* Alzheimer’s disease can cause changes in the ability to interpret what a person can see, hear, taste, feel, or smell, even though his or her sense organs may still be intact.
* The person with AD should be evaluated periodically by a physician for any such changes that may be correctable with glasses, dentures, hearing aids, or other treatments.

Vision

People with AD may experience a number of changes in visual abilities. For example, they may lose their ability to comprehend visual images. Although there is nothing physically wrong with their eyes, people with AD may no longer be able to interpret accurately what they see due to changes in their brain. Also, their sense of perception and depth may be altered. These changes can cause safety concerns.

* Create color contrast between floors and walls to help the person see depth. Floor coverings are less visually confusing if they are a solid color.
* Use dishes and placemats in contrasting colors for easier identification.
* Mark the edges of steps with brightly colored strips of tape to outline changes in elevation.
* Place brightly colored signs or simple pictures on important rooms (the bathroom, for example) for easier identification.
* Be aware that a small pet that blends in with the floor or lies in walkways may be a hazard. The person with AD may trip over a small pet.

Smell

* A loss or decrease in smell often accompanies Alzheimer’s disease.
* Install good quality smoke detectors and check them frequently. The person with AD may not smell smoke or may not associate it with danger.
* Keep refrigerators clear of spoiled foods.

Touch

People with AD may experience loss of sensation or may no longer be able to interpret feelings of heat, cold, or discomfort.

* Adjust water heaters to 120 degrees to avoid scalding tap water. Most hot water heaters are set at 150 degrees, which can cause burns.
* Color code separate water faucet handles, with red for hot and blue for cold.
* Place a sign on the oven, coffee maker, toaster, crock-pot, iron, or other potentially hot appliances that says DO NOT TOUCH or STOP! VERY HOT. The person with AD should not use appliances without supervision. Unplug appliances when not in use.
* Use a thermometer to tell you whether the water in the bathtub is too hot or too cold.
* Remove furniture or other objects with sharp corners or pad them to reduce potential for injury.

Taste

People with AD may lose taste sensitivity. As their judgment declines, they also may place dangerous or inappropriate things in their mouth.

* If possible, keep a spare set of dentures. If the person keeps removing dentures, check for correct fit.
* Keep all condiments such as salt, sugar, or spices away from easy access if you see the person with AD using excess amounts. Too much salt, sugar, or spice can be irritating to the stomach or cause other health problems.
* Remove or lock up medicine cabinet items such as toothpaste, perfume, lotions, shampoos, rubbing alcohol, or soap, which may look and smell like edible items to the person with AD.
* Consider a childproof latch on the refrigerator, if necessary.
* Keep the poison control number by the telephone. Keep a bottle of Ipecac (vomit inducing) available, but use only with instructions from poison control or 911.
* Keep pet litter boxes inaccessible to the person with AD. Do not store pet food in the refrigerator.
* Learn the Heimlich maneuver or other techniques to use in case of choking. Check with your local Red Cross chapter for more information and instruction.

Hearing

People with AD may have normal hearing, but they may lose their ability to interpret what they hear accurately. This may result in confusion or over-stimulation.

* Avoid excessive noise in the home such as having the stereo and the TV on at the same time.
* Be sensitive to the amount of noise going on outside, and close windows or doors, if necessary.
* Avoid large gatherings of people in the home if the person with AD shows signs of agitation or distress in crowds.
* Check hearing aid batteries and functioning frequently.

Driving

Driving is a complex activity that demands quick reactions, alert senses, and split-second decision-making. For a person with AD, driving becomes increasingly more difficult. Memory loss, impaired judgment, disorientation, impaired visual and spatial perception, slow reaction time, certain medications, diminished attention span, inability to recognize cues such as stop signs and traffic lights can make driving particularly hazardous.

* People with AD who continue to drive can be a danger to themselves, their passengers, and the community at large.
* As the disease progresses, they lose driving skills and must stop driving. Unfortunately, people with AD often cannot recognize when they should no longer drive. This is a tremendous safety concern.
* It is extremely important to have the impaired person’s driving abilities carefully evaluated.

Warning Signs of Unsafe Driving

Often, it is the caregiver, a family member, neighbor, or friend who becomes aware of the safety hazards. If a person with AD experiences one of more of the following problems, it may be time to limit or stop driving.

* Does the person with AD: get lost while driving in a familiar location? fail to observe traffic signals? drive at an inappropriate speed? become angry, frustrated, or confused while driving? make slow or poor decisions? Please do not wait for an accident to happen. Take action immediately!
* Explaining to the person with AD that he or she can no longer drive can be extremely difficult. Loss of driving privileges may represent a tremendous loss of independence, freedom, and identity. It is a significant concern for the person with AD and the caregiver. The issue of not driving may produce anger, denial, and grief in the person with AD, as well as guilt and anxiety in the caregiver. Family and concerned professionals need to be both sensitive and firm. Above all, they should be persistent and consistent.
* The doctor of a person with AD can assist the family with the task of restricting driving. Talk with the doctor about your concerns. Most people will listen to their doctor. Ask the doctor to advise the person with AD to reduce his or her driving, go for a driving evaluation or test, or stop driving altogether. An increasing number of States have laws requiring physicians to report AD and related disorders to the Department of Motor Vehicles. The Department of Motor Vehicles then is responsible for retesting the at-risk driver. Testing should occur regularly, at least yearly.
* When dementia impairs driving and the person with AD continues to insist on driving, a number of different approaches may be necessary.
* Work as a team with family, friends, and professionals, and use a single, simple explanation for the loss of driving ability such as: “You have a memory problem, and it is no longer safe to drive.” “You cannot drive because you are on medication.” or “The doctor has prescribed that you no longer drive.”
* Ask the doctor to write on a prescription pad DO NOT DRIVE. Ask the doctor to write to the Department of Motor Vehicles or Department of Public Safety saying this person should no longer drive. Show the letter to the person with AD as evidence.
* Offer to drive.
* Walk when possible, and make these outings special events.
* Use public transportation or any special transportation provided by community organizations. Ask about senior discounts or transportation coupons. The person with AD should not take public transportation unsupervised.
* Park the car at a friend’s home.
* Hide the car keys.
* Exchange car keys with a set of unusable keys. Some people with AD are in the habit of carrying keys.
* Place a large note under the car hood requesting that any mechanic call you before doing work requested by the person with AD.
* Have a mechanic install a “kill switch” or alarm system that disengages the fuel line to prevent the car from starting.
* Consider selling the car and putting aside the money saved from insurance, repairs, and gasoline for taxi funds.
* Do not leave a person with AD alone in a parked car.

Natural Disaster Safety

Natural disasters come in many forms and degrees of severity. They seldom give warning, and they call upon good judgment and ability to follow through with crisis plans. People with AD are at a serious disadvantage. Their impairments in memory and reasoning severely limit their ability to act appropriately in crises.

* It is always important to have a plan of action in case of fire, earthquake, flood, tornado, or other disasters. Specific home safety precautions may apply and environmental changes may be needed. The American Red Cross is an excellent resource for general safety information and preparedness guides for comprehensive planning. If there is a person with AD in the home, the following precautions apply:
* Get to know your neighbors, and identify specific individuals who would be willing to help in a crisis. Formulate a plan of action with them should the person with AD be unattended during a crisis.
* Give neighbors a list of emergency numbers of caregivers, family members, and primary medical resources.
* Educate neighbors beforehand about the person’s specific disabilities, including inability to follow complex instructions, memory loss, impaired judgment, and probable disorientation and confusion. Give examples of some of the simple one-step instructions that the person may be able to follow.
* Have regular emergency drills so that each member of the household has a specific task. Realize that the person with AD cannot be expected to hold any responsibility in the crisis plan and that someone will need to take primary responsibility for supervising the individual.
* Always have at least an extra week’s supply of any medical or personal hygiene items critical to the person’s welfare, such as: food and water, medications, incontinence undergarments, hearing aid batteries, glasses.
* Be sure that the person with AD wears an identification bracelet stating “memory loss” should he or she become lost or disoriented during the crisis. Contact your local Alzheimer’s Association chapter and enroll the person in the Safe Return program.
* Under no circumstances should a person with AD be left alone following a natural disaster. Do not count on the individual to stay in one place while you go to get help. Provide plenty of reassurance.

Who Would Take Care of the Person with AD if Something Happened to You?

It is important to have a plan in case of your own illness, disability, or death.

* Consult a lawyer regarding a living trust, durable power of attorney for health care and finances, and other estate planning tools.
* Consult with family and close friends to decide who will take responsibility for the person with AD. You also may want to seek information about your local public guardian’s office, mental health conservator’s office, adult protective services, or other case management services. These organizations may have programs to assist the person with AD in your absence.
* Maintain a notebook for the responsible person who will be assuming caregiving. Such a notebook should contain the following information:
* It is important to have a plan in case of your own illness, disability, or death.
* Consult a lawyer regarding a living trust, durable power of attorney for health care and finances, and other estate planning tools.
* Consult with family and close friends to decide who will take responsibility for the person with AD. You also may want to seek information about your local public guardian’s office, mental health conservator’s office, adult protective services, or other case management services. These organizations may have programs to assist the person with AD in your absence.
* Maintain a notebook for the responsible person who will be assuming caregiving. Such a notebook should contain the following information: emergency numbers , current problem behaviors and possible solutions, ways to calm the person with AD , assistance needed with toileting, feeding, or grooming, favorite activities or food.
* Preview board and care or long-term care facilities in your community and select a few as possibilities. If the person with AD is no longer able to live at home, the responsible person will be better able to carry out your wishes for long-term care.

Conclusion

Home safety takes many forms. This booklet focuses on the physical environment and specific safety concerns. But the home environment also involves the needs, feelings, and lifestyles of the occupants, of you the caregiver, your family, and the person with AD. Disability affects all family members, and it is crucial to maintain your emotional and physical welfare in addition to a safe environment.

We encourage you to make sure you have quiet time, time out, time to take part in something you enjoy. Protect your own emotional and physical health. Your local Alzheimer’s Association chapter can help you with the support and information you may need as you address this very significant checkpoint in your home safety list. You are extremely valuable and as you take on a commitment to care for a person with AD, please take on the equally important commitment to care for yourself.

Additional Resources

Alzheimer’s Disease Education and Referral (ADEAR) Center www.alzheimers.nia.nih.gov

Alzheimer’s Association www.alz.org

Ageless Design www.agelessdesign.com

American Red Cross www.redcross.org

Children of Aging Parents www.caps4caregivers.org

Eldercare Locator www.eldercare.gov

Elder Care Online www.ec-online.net

Family Caregiver Alliance www.caregiver.org

Well Spouse Association www.wellspouse.org

Article Source: The National Institute on Aging, Alzheimer’s Disease Research Center at the University of California, San Diego, and the Alzheimer’s Association of San Diego, U.S. Department of Health and Human Services, Public Health Service, National Institutes of Health, National Institute on Aging, Alzheimer’s Disease Education and Referral (ADEAR) Center. www.nia.nih.gov
Provided by: The Staff at www.RetirementConnection.com
For more information: www.nia.nih.gov
Copyright © 2008 RetirementConnection.com. All rights reserved.

Saving Money on Your Medications

Saving Money on Your Medications

There are strategies you can use to save money on your medications. The strategy you use depends on whether you have prescription drug coverage and your income. Regardless of income, consider asking your doctor if the dosage can be doubled, then the pill scored and cut into halves. This will not work for all medications because of the chemical make-up or if there are coatings on the medications. These directions should be on the label from the pharmacy. If you pay co-pay, this can cut down on the amount you pay. Sometimes, if you pay cash, you may also save a great deal as well.

Additionally, you can check with your doctor and pharmacist to see if there are any rebates and/or coupons for your medications. You may be able to get a free one-month supply of medication by simply verifying if that medication is offering a rebate or coupon. These are offered regardless of income. Also, some companies offer rebates/coupons to people paying co-pays. Read the conditions before attempting to utilize this strategy.

If you need to mail order generic medications, there are two possible options for lower co-pays. Both these companies have income guidelines that are generous. They do not ask about insurance coverage. Some of the co-pays are as low as $20.00 for a three month supply of medication. Verify drug costs before you order. The two companies I recommend are www.rxoutreach.com and www.xubex.com.

Did you know you could possibly get your medications FREE?

Some drug manufacturers give away medications to people who can’t afford them. The bad news is that not all medications are available. Also, there are income guidelines and you cannot have traditional prescription coverage. So, if you are uninsured and can’t afford your medications, this might be a viable option for you. Most of the forms require your doctor’s assistance. Each company has different guidelines and requirements for proof of income. To do these forms yourself, you can look them up at www.pparx.org. Case management assistance is available for a nominal fee as well.

Provided by: The Staff at www.RetirementConnection.com

Copyright © 2008 RetirementConnection.com. All rights reserved.

Services and Support to Help the Family Caregiver

Services to Help the Family Caregiver

Families, not social service agencies, nursing homes, or government programs, are the mainstay underpinning long-term care (LTC) for older persons in the United States. More than 22.4 million persons are informal caregivers-providing unpaid help to older persons who live in the community and have at least one limitation on their activities of daily living. These caregivers include spouses, adult children, and other relatives and friends. The degree of caregiver involvement has remained fairly constant for more than a decade, bearing witness to the remarkable resilience of the American family in taking care of its older persons. This is despite increased geographic separation, greater numbers of women in the workforce, and other changes in family life. Thus, family caregiving has been a blessing in many respects. It has been a budget-saver to governments faced annually with the challenge of covering the health and long-term care expenses of persons who are ill and have chronic disabilities. The economic value of our nation’s family and informal caregivers has been estimated at $257 billion annually.

The National Family Caregiver Support Program

The enactment of the Older Americans Act Amendments of 2000 established an important new program, the National Family Caregiver Support Program (NFCSP). The program calls for all states, working in partnership with area agencies on aging and local community-service providers, to have five basic services for family caregivers.

These services include:

• Information to caregivers about available services;

• Assistance to caregivers in gaining access to services;

• Individual counseling, organization of support groups, and caregiver training to caregivers to assist the caregivers in making decisions and solving problems relating to their caregiving roles;

• Respite care to enable caregivers to be temporarily relieved from their caregiving responsibilities; and

• Supplemental services, on a limited basis, to complement the care provided by caregivers. Currently funded at $155.2 million, this program has served more than 275 thousand caregivers nationwide. Efforts regarding NFCSP have resulted in new partnerships, improved access to services, outreach to special populations, and provision of services to respond to the unique needs of families.

Eligible Populations

• Family caregivers of older adults

• Grandparents and relative caregivers, age 60 years or older, of children no older than age 18 (including grandparents who are sole caregivers of grandchildren and those individuals who are affected by mental retardation or who have developmental disabilities)

Family Caregiving Resources

U.S. Department of Health and Human Services, Administration on Aging (AoA),
www.aoa.gov

Who to Contact for Help

AoA supports a nationwide, toll-free information and assistance directory and the Eldercare Locator, which can connect older persons and their caregivers with the National Aging Services Network. Older persons and caregivers can call the Eldercare Locator toll-free at 1-800-677-1116 or visit www.eldercare.gov.

Source: www.aoa.dhhs.gov

Provided by: The Staff at www.RetirementConnection.com
For more information: www.aoa.gov
Copyright © 2008 RetirementConnection.com. All rights reserved.

Six Steps to a Safe Wheelchair Transfer

Six Steps to a Safe Wheelchair Transfer

Some patients who use wheelchairs can transfer themselves into the dental chair, but others need assistance. The extent of your involvement will depend on the patient’s or caregiver’s ability to help. Most people can be transferred safely from wheelchair to dental chair and back by using the two-person method. The following outline describes a safe transfer with a minimum of apprehension for the patient and clinician. Practice these steps before doing an actual patient transfer.

Six Steps to A Safe Wheelchair Transfer

STEP 1: Determine the patient’s needs

* Ask the patient or caregiver about:

o preferred transfer method

o patient’s ability to help

o use of special padding or a device for collecting urine

o probability of spasms
* Reduce the patient’s anxiety by announcing each step of the transfer before it begins.

STEP 2: Prepare the dental operatory

* Remove the dental chair armrest or move it out of the transfer area.
* Relocate the hoses, foot controls, operatory light, and bracket table from the transfer path.
* Position the dental chair at the same height as the wheelchair or slightly lower. Transferring to a lower level minimizes the amount of strength necessary during the lift.

STEP 3: Perform the two-person transfer

* Support the patient while detaching the safety belt.
* Transfer any special padding or equipment from the wheelchair to the dental chair.
* First clinician: Stand behind the patient. Help the patient cross his arms across his chest. Place your arms under the patient’s upper arms and grasp his wrists.
* Second clinician: Place both hands under the patient’s lower thighs. Initiate and lead the lift at a prearranged count (1-2-3-lift).
* Both clinicians: Using your leg and arm muscles while bending your back as little as possible, gently lift the patient’s torso and legs at the same time.
* Securely position the patient in the dental chair and replace the armrest.

STEP 4: Position the patient after the transfer

* Center the patient in the dental chair.
* Reposition the special padding and safety belt as needed for the patient’s comfort.
* If a urine-collecting device is used, straighten the tubing and place the bag below the level of the bladder.

STEP 5: Transfer from the dental chair to the wheelchair

* Position the wheelchair close to and parallel to the dental chair.
* Lock the wheels in place, turn the casters forward, and remove the armrest.
* Raise the dental chair until it is slightly higher than the wheelchair and remove the armrest.
* Transfer any special padding.
* Transfer the patient using the two-person transfer (see step 3).
* Reposition the patient in the wheelchair.
* Attach the safety belt and check the tubing of the urine-collecting device, if there is one, and reposition the bag.
* Replace the armrest and footrests.

This information can make a difference in your efforts to provide oral health care for patients who use a wheelchair. A skilled and sensitive dental staff can instill confidence during the transfer and encourage the patient to maintain a regular appointment schedule.

Source: www.nidcr.nih.gov, National Institute of Dental and Craniofacial Research
Acknowledgments: The National Institute of Dental and Craniofacial Research thanks the oral health professionals and caregivers who contributed their time and expertise to reviewing and pretesting the Practical Oral Care series.
Expert Review Panel:
Mae Chin, RDH, University of Washington, Seattle, WA
Sanford J. Fenton, DDS, University of Tennessee, Memphis, TN
Ray Lyons, DDS, New Mexico Department of Health, Los Lunas, NM
Christine Miller, RDH, University of the Pacific, San Francisco, CA
Steven P. Perlman, DDS, Special Olympics Special Smiles, Lynn, MA
David Tesini, DMD, Natick, MA

Provided by: The Staff at www.RetirementConnection.com
For more information: www.nidcr.nih.gov
Copyright © 2008 RetirementConnection.com. All rights reserved.

Social Security has Online Services

Social Security has Online Services

Social Security has launched enhanced online services on their website. Known as Social Security Online the website lets you do the following tasks online:

* Apply for Social Security retirement or spouse’s benefits
Note: If you’re an Advocate, Attorney or Third Party Representative, we need additional information from you on the application.
* Apply for Social Security disability benefits (includes the Adult Disability Report).
Note: If you’re an Advocate, Attorney or Third Party Representative, we need additional information from you on the application.

Begin or continue the Adult Disability and Work History Report.
When you apply for any type of disability benefits, we need information about your medical, work, and education history to help us decide if you are disabled.

* Apply for extra help with your Medicare prescription drug costs.
* Check the status of your online application.
If you applied online for Social Security Retirement, Spouse’s, or Disability benefits you can check the status of your application.
* Appeal our recent medical decision about your disability claim or continue the appeal you already started.

Do you qualify for benefits?

* Find out what benefits you can apply for.
Use our screening tool to help identify all the different Social Security programs for which you may be eligible.
* Find out if you can get extra help with your Medicare prescription drug costs.

Estimate your future benefits

* Use our benefit planners to calculate your retirement, disability and survivors benefits. (You can do this any time.)
* Request a Social Security Statement
Get your personal earnings report and benefit estimates by mail.
This service is available (Eastern Time):
Weekdays – All Day (except 2 AM – 3 AM),
Saturday 5 AM – 11 PM,
Sunday 8 AM – 10 PM,
Holidays 5 AM – 11 PM.

If you get benefits, you can

* Change your address or telephone number.
* Get a replacement Medicare Card.
* Request a Proof of Income letter.
Get a letter that verifies your Social Security benefit information.
* Get a Form 1099/1042S — Social Security Benefit Statement. (Available February 1, 2008.)
Replace the lost, damaged, or missing tax summary of your Social Security benefits for 2007. (not available for SSI).
* Get a password when:

o You want password access to information about your benefits.

o You lost, forgot, or do not have your password or password request code.

o Your password request code has expired.
* Block online and automated telephone access to your personal information.

If you have a password, you can

* Check your information and benefits.
See the contact, direct deposit, Medicare and payment information we have on file for you.
* Change your address or telephone number.
* Start or change direct deposit.
* Choose your password.
If you received a letter from us about password services, you can choose your password or block access to your personal information.
* Change your password.

Other things you can do online

Find out if you qualify for …

* Social Security, Supplemental Security Income (SSI), or other benefits
* Extra help with your Medicare prescription drug costs

Estimate your future benefits

Request a Social Security Statement if you get benefits …

* Change your address/phone number
* Get a replacement Medicare Card

Source: http://www.socialsecurity.gov/onlineservices/

Provided by: The Staff at www.RetirementConnection.com
For more information: www.SocialSecurity.gov/onlineservices/
Copyright © 2008 RetirementConnection.com. All rights reserved.

Statistics Show Senior Care Continues to Increase Locally and Nationwide

Statistics Show Senior Care Continues to Increase Locally qnd  Nationwide

If you provide care for an aging loved one, or plan to offer care for one in the future, national statistics show you are not alone. As adults live longer and Baby Boomers approach older ages, the number of Americans who need in-home care, or will require such care in the coming years, continues to rise.

National numbers are showing that Americans are living longer lives. Because of this, in-home care is quickly becoming a necessity. However, many American families can easily feel alone when they find themselves in a senior care situation. They don’t always know where to turn for help.

Besides living longer, aging adults often find themselves living alone after the loss of a spouse. Oftentimes, their children have moved out of the area or state as society becomes increasingly mobile. When these and similar situations occur, aging adults are often in need of additional care, either from the family or an outside provider.

In-home care continues to increase, for example, due to the number of chronic disease patients. According to the Center on an Aging Society at Georgetown University, nearly 100 million Americans have chronic conditions.

An increase in elder care also has resulted from the number of Americans living with Alzheimer’s disease. According to the Alzheimer’s Association, 6 million Americans will be diagnosed with Alzheimer’s disease by 2010. That number is expected to jump to 10 million by 2035.

When adult children find themselves in these situations with aging loved ones, they often need to make a decision about the best care available for that person. In several cases, the care comes from a family member on a full-time basis or from an in-home care provider. The adult in need of care, however, does not want to become a burden to their family members. They seek a high quality of life that allows them to remain independent and living at home as long as possible.

Source: Right at Home,  503-574-3674
For more information: www.RAHcares.com, 503-574-3674

Copyright © 2008 RetirementConnection.com. All rights reserved.