We specialize in providing our clients with the equipment and products they need to recover, rejunevate and live life to its fullest in the comfort of their own homes.
Tycon Medical has put together an extensive resource center of information for patients & caregivers.
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Health Issues - below are some of the most common health issues. Please feel free to read the information we have collected. Some of this information includes risks, tips, explanations, and prevention tips for patients and caregivers.
Safety: Steps to Enhancing Your Home
With some creativity, flexibility and problem-solving, the home can be adapted to support these changes. This article provides simple steps to make the home safe and supportive for the individual with Alzheimer's. Before modifying your home, consider the following: Focus on adapting rather than teaching. Avoid reteaching the person with Alzheimer's about safety issues. Instead, identify potential risks and take the appropriate precautions. Simplify the activities. Most accidents, especially in the area of personal care, occur when the person with Alzheimer's is rushed. Break activities into simple, step-by-step tasks allowing her plenty of time to complete them. Giving extra assistance, such as laying out clothes in the order that they are put on, will also help her with simple tasks that have become hard to do. Support the person's needs. Try not to create an environment that is too restrictive. The home should encourage independence, social interaction and activities that are meaningful. Be realistic about what you can do. You will never be able to prevent every problem. Rely on your common sense while paying close attention to objects or activities that could be dangerous.
MAKE POTENTIALLY DANGEROUS PLACES LESS ACCESSIBLE Lock or disguise hazardous areas. Cover doors and locks with a painted mural or cloth. Use "Dutch" doors, swinging doors or folding doors to hide entrances to the kitchen, stairwell, workroom and storage areas. TIPS FOR CREATING A SAFE AND SUPPORTIVE ENVIRONMENT
Bathroom
Bedroom
Garage
Throughout the home
Outdoors
<<Back to Top>>Safety: Steps to Ensuring SafetyPreventing Wandering and Getting LostWhen someone with Alzheimer's disease wanders and becomes lost, it is a frightening experience that puts that person at risk for serious or fatal injury. This article offers ways to prevent unsafe wandering and to prepare for an emergency situation. | Wandering can be aimless or purposeful roaming that can cause a person to become lost, leave a safe environment, or intrude in inappropriate places. Wandering is one of the most frequent and challenging problems that caregivers face. Seven of every ten people with dementia will wander and become lost during the course of the disease, and most will do so repeatedly. Someone with Alzheimer's disease may not only wander by foot but also by car or other mode of transportation. Understanding Wandering Wandering may be triggered when a person with Alzheimer's:
Preventing Wandering Structure the Day Making Your Home Safe
Talk to Your Neighbors Involve Your Local Police Survey the Neighborhood Be Prepared For A Wandering Incident Having reliable and accurate information will help those involved in a search:
Register in the Safe Return Program Safe Return provides:
To register:
Additional Resources The following materials are available from your local chapter or the national office of the Alzheimer's Association:
The Alzheimer's Association is the only national voluntary organization dedicated to conquering Alzheimer's disease through research and to providing information and support to people with Alzheimer's disease, their families, and caregivers. <<Top of Page>>How to Be a Long-Distance CaregiverI am miles away.If you are caring for someone who lives far away, you are not alone. Currently, more than six million Americans are long-distance caregivers. Long-distance caregiving for someone with Alzheimer's disease can be especially difficult. Concerns about your loved one's safety, nutrition, health and care may seem overwhelming. You may also feel guilty and anxious because you cannot be there every day to see how the person is doing. However, with the right mix of services, ongoing coordination and support, long-distance caregiving can work. How can I help? How do I know what services are needed? Visit the person with Alzheimer's disease to determine what kind of assistance he or she may need. Make the following observation:
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Tips for Family Caregivers from Doctors
Care Management Techniques You Can Use
Did you ever wish you could just pick up the phone and call someone who would take stock of your situation, help you access the right services, counsel you and your family to help resolve some of your differences, then monitor your progress with an eye toward channeling your energy and abilities as effectively as possible? If your answer is “yes,” you’re not alone. Having the help of a care coordinator (often called a care manager) could make all of our lives easier and less lonesome, and help us be more capable family caregivers. While most of us may not have access to a care coordinator, we can all learn how to think and act like one, thereby reaping numerous benefits for our loved ones and ourselves.
What Is Care Coordination?Although every case is different, the care coordination approach usually involves:
Unfortunately, an assessment of your abilities and needs is not necessarily a standard part of the process, but it should be. A complete view of the situation cannot be gained without one. An objective analysis of your health, emotional state, other commitments, etc., are key elements in determining how much you can and cannot do yourself, and what type of outside support is needed to ensure your loved one’s health and safety.
Become Your Own Care Coordinator By learning and applying at least some of the care coordination techniques and ideas that follow, you’ll be in a much better position to develop an organized course of action that will, hopefully, make you feel more confident and in control — a goal well worth working toward.
Educate yourself on the nature of the disease or disability with which you’re dealing. Reliable information is available from the health agency that deals with your loved one’s condition and the National Institutes of Health. When using the Internet, stick with well-known medical sites. Understanding what is happening to your care recipient will provide you with the core knowledge you need to go forward. It will also make you a better advocate when talking with healthcare professionals.
Write down your observations of the present situation including:This assessment will help you come to a realistic view of the situation. It will let you know the questions to which you need answers. It can be a handy baseline for charting your caregiving journey and reminding you just how much you’ve learned along the way.
Hold a family conference. At least everyone in the immediate family should be told what’s going on. A meeting can set the stage for divvying up responsibilities so that there are fewer misunderstandings down the road when lots of help may be needed. A member of the clergy, a professional care coordinator, or even a trusted friend can serve as an impartial moderator. A family meeting is a good way to let everyone know they can play a role, even if they are a thousand miles away. It can help you, the primary family caregiver, from bearing the brunt of all the work all of the time.
Keep good records of emergency numbers, doctors, daily medications, special diets, back-up people, and other pertinent information relating to your loved one’s care. Update as necessary. This record will be invaluable if something happens to you, or if you need to make a trip to the ER. If you can maintain a computer-based record, that will make updating all that much easier and it might even allow you to provide the medical team with direct access to the information.
Join a support group, or find another caregiver with whom to converse. In addition to emotional support, you’ll likely pick up practical tips as well. Professionals network with each other all the time to get emotional support and find answers to problems or situations they face. Why shouldn’t family caregivers?
Start advance planning for difficult decisions that may lie ahead. It’s never too early to discuss wills, advance directives, and powers of attorney, but there comes a time when it is too late. It is also vital that you and your loved one think through what to do if you should be incapacitated, or, worse, die first. It can happen.
Develop a care team to help out during emergencies, or over time if your situation is very difficult. In an ideal world there will be lots of people who want to help. More likely you’ll be able to find one or two people to call on in an emergency or to help with small chores. The critical thing is to be willing to tell others what you need and to accept their help.
Establish a family regimen. When things are difficult to begin with, keeping a straightforward daily routine can be a stabilizer, especially for people who find change upsetting and confusing.
Approach some of your hardest caregiving duties like a professional. It’s extraordinarily difficult to separate your family role from your caregiving role, to lock your emotions up in a box while you focus on practical chores and decisions. But it is not impossible to gain some distance some of the time. It requires an almost single-minded approach to getting the job at hand done as efficiently and effectively as possible. It takes practice, but is definitely worth the effort.
©National Family Caregivers Association | www.nfcacares.org | Phone: 800/896-3650
<<Back to Top>>Seating & Mobility As a caregiver, you need to be very understanding to the individual's needs. This is a very hard time as they are being told they need to start living their life in a different manor than they had done so previously. It will be most beneficial to educate them, either with a professional, or through a support group. By becoming involved in different activities with others in the same condition, the individual will be able to make the transition much easier. As far as the actual device, you will want to make sure that the individual is fully capable of performing all the operations of the mobility device and can do so in a comfortable manner. Areas to pay close attention to include an adjustable backrest, a suspension system, a fore-and-aft track adjustment, an up-and-down seat adjustment, an armrest and/or footrest, and lumbar region support.
How do you care for your mobility device? The most important areas that you need to pay attention to are referred to as the 3 B’s…Bad batteries, bent wheel rims and failed bearings. If you notice something that doesn’t seem right, but it isn’t all too annoying, you should still get it looked at right away. This could prevent a more severe accident from happening. So as the saying goes “it’s better to be safe than sorry”.
When a wheelchair is purchased, you will want to make sure that all the correct adjustments and modifications are made. This needs to be done by a professional and should take up to a couple of hours if done correctly. As long as the proper measures are taken initially, the work of maintaining the device will be substantially easier.
<<Back to Top>>Additional Resources It's always wise to find out what your county and state have to offer in the way of services, even if you think you won't qualify for them. Check the blue pages of your phone book for the numbers, or go on line. Counties and states all have web sites. Type the name of your state or county and state into any major search engine i.e. Iowa, or Montgomery County, PA. Navigate from there to locate the Department of Health and Human Services and the specific office most relevant to your needs, such as office on disabilities, elder affairs, or maternal and child health.
Other good sources of information include your local hospital or clinic (social work department), area adult day centers, social service and faith-based agencies, and/or the local chapter of the health agency that focuses on your loved one's condition. It is by no means certain that any of these will offer caregiver support services, but they are good places to check, and they are good sources for information about services to directly support your loved one.
National Family Caregivers Association 10400 Connecticut Avenue, Suite 500 Kensington, MD 20895 800-896-3650 Web site: http://www.thefamilycaregiver.org :: e-mail: info@thefamilycaregiver.org
The National Family Caregivers Association (NFCA) is a grassroots organization created to educate, support, empower, and advocate for the millions of Americans who care for chronically ill, aged, or disabled loved ones. NFCA is the only constituency organization that reaches across the boundaries of different diagnoses, different relationships, and different life stages to address the common needs and concerns of all family caregivers. NFCA serves as a public voice for family caregivers to the press, to Congress and the general public. NFCA offers publications, information, referral services, caregiver support, and advocacy.
Caregiver-Specific Web Sites There are a variety of Web sites that offer information and support for family caregivers, in addition to those from specific organizations.
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