For most caregivers, time isn’t the only thing demanded of them. The person who steps in to offer care to an ill family member usually also takes on the financial burden of looking after the person. The cost of giving care is tremendous physically and emotionally for the caregiver, but it can also be overwhelming financially. Medical care is extremely expensive, and most insurance plans do not cover the many of the expenses associated with long term care of a patient.

What are some of the costs that a caregiver frequently has to cope with? Obviously, the first, and usually the largest cost are the medical bills themselves. Doctor’s visits, prescriptions, hospital stays – the person who requires the care typically only has Medicare coverage that is often inadequate to meet their needs, and the caregiver often has to step in to make up the difference. There are many other costs that may enter the picture as well, however. There is the expensive of hiring home help, adult day care, or any other supplemental care that the patient might require. There is the cost of buying any medical equipment or making changes to the home that the patient may need or that may make caring for them easier. Also important to calculate in here is the lost earnings of the caregiver. Frequently, the caregiver either has to give up their job completely, take a new job that is less demanding or move to part time work, causing a marked loss in income, all while they are having to spend more.

What can you do if this sounds like the situation you are facing? First and foremost is that you must speak up and ask for help. Although it is easy for caregivers to feel resentful of family members who are not helping with the care of a sick relative, in many cases, they are uninvolved in the care because they don’t know what to do or believe you have it all covered. Sometimes, asking for help may be all that is required – you may find that other relatives are willing and able to chip in and help take the financial burden off of you.

Of course, not all families are in the position to provide this kind of help. If yours is not, there are still some resources out there for you. First, check and see what you employer has to offer. You may be surprised to find out that many employers have programs in place to help their employees meet the costs associated with providing care, like adult day care programs and home help workers. The insurance program you receive through your job might also have some benefits that you can tap into to see you through this time.

If there aren’t any benefits at work, you may be eligible to receive aid from the state. Some states “pay” people who provide care fulltime, and some states offer grants that let you hire in extra help without any cost to you.

To receive this kind of help, however, obviously you have to know where to find it. One good place to start is to seek out the local caregivers support group in your area. There is one of these groups in almost every town, and they can give you all of the info you need about the resources available to you. If you can’t find one of these groups, ask the doctor of the person you care for if they can recommend any help, or turn to the net. There is plenty of help out there, and putting in the time do some research can relieve your emotional and financial burden.

Caregiving is incredibly stressful at the best of times, but the holiday season can really add to the burden caregivers are carrying. There are many reasons the holiday season is usually not seen as a reason to celebrate for many caretakers. For one, the holidays can bring extra responsibilities, like shopping for gifts, hosting meals or parties, and the pressure to attend other holiday events. It can also be a time for increased emotional distress. The holidays generally mean that families come together – those same family members that have been unwilling to help you manage the caregiving burden throughout the rest of the year. Your caregiving responsibilities may mean that you don’t have the time you’d like to have to spend with other friends or attending holiday parties. Last but not least, it might be especially hard to cope with your loved one’s illness during the holidays, a time that is usually filled with memories of happier days.

If this sounds like the way you view the holidays as a caregiver, you should know that there are choices you can make to help the holiday season run a little more smoothly for you and to help you actually get some time to enjoy the season yourself. It all comes down to you being assertive about your needs and deciding how you’ll deal with the situations that arise. You can choose to have a happy holiday this year.

The first thing you have to come to terms with is seeing your family members that you might have some resentful feelings about. You probably want to confront them and insist that give you more help and show you some appreciation for the work you are doing. The holidays might make a handy time to have these conversations since everyone is gathered together, but you have to decide if the confrontation is worth the stress that it will cause you. If you know that it will cause a big blow up and you don’t want it hanging in the air, then choose to bite your tongue for now, enjoy your holiday, and confront your family after the season passes.

Next, you have to come up with some realistic idea of how much extra work you can put in over the holidays. Even if you are the usual host of the family holiday events – and it’s very common for the family member who has stepped up as caretaker to be the one who has stepped up for these kinds of events in the past – speak up and say that you simply can’t manage this year. If you must have the gathering in your home, ask other people to bring food so you don’t have the extra work to do. Likewise, be realistic about how much time you can spend attending holiday events yourself. Don’t feel obligated to accept every invitation, and don’t feel obligated to stay longer than you feel like when you do attend events. Make the decision not to take on the extra stress.

Last but not least, make sure to take some time out for you and your patient to enjoy some quiet time together on the holidays. Although you may be together all of the time, that may not be real, quality time. Even patients with dementia tend to hold on to their long term memories, so they may be very able to reminisce with you about holidays past. The holidays can be a special time for you as a caregiver to simply enjoy and remember the relationship you have with the person you care for – which may not always be easy to do when you care for them day in and day you.

The bottom line is that the holidays are what you make them. Decide to preserve your own needs, and you can enjoy the season as well.

Acting as a caregiver is never an easy task, but if the patient you are looking after has dementia, it becomes an even more difficult burden. Patients with dementia often cannot be left alone, and you have to worry not only about taking care of their health but also their safety. Plus, as the dementia worsens, the patient will become and more and more difficult to communicate with, and their mood swings can be distressing. If you find yourself in the position of caring for someone with dementia, learning to understand their condition and how to communicate with them as effectively as possible is critical for both of you. This will help the patient get what they need and will help lighten the load that you are carrying. Here are some tips to keep in mind when you are faced with a loved one with dementia.

First, know that the unspoken communication signals you use are as important as the words you choose. Sometimes, a patient with dementia may have a difficult time understanding your exact meaning, which can be alarming to them. However, if you use a calm tone of voice and maintain a friendly expression, even if your message is not getting across, the fact that you’re trying to be helpful and positive will. Losing your temper and raising your voice will escalate a bad situation and can be extremely unnerving for the patient – not to mention the fact that you will feel guilty afterwards. If you don’t think you can maintain your composure at any given moment, wait until later to deliver the message you need to deliver.

Of course, if you want to be understood, it helps if there is nothing else competing for the patient’s attention. Focus is a tremendous issue with dementia, and if you are trying to talk to the patient while you are also watching TV, playing music or anything else distracting, you are unlikely to be able to get your point across. Keep things calm and quiet to make talking easier.

When the patient tries to respond to you, keep an eye on their nonverbal communication. It’s very common for a person with dementia to mix up their words, or to struggle to come up with any words at all, but you may be able to help them get their own point across if you pay attention to their behavior. Do they seem alarmed? If you’ve asked them to make a decision about something, can they point at what they want? Do everything you can to help them make themselves understood.

Your response also matters. If you’ve asked a question, if the patient can’t answer you or if they give you an answer that doesn’t make sense in relation to the question that you have asked, be calm. Judge the situation and decide if you should ask another way or wait until later. Never argue with a person who has dementia. Physical affection is important here as well. A hug can calm a patient down, let them know they are safe, and in turn help them communicate better.

Last but not least, remember to keep it simple and clear. You may need to find a new way of talking when you’re dealing with a patient with dementia. It is in our nature to pepper our sentences with pronouns and slang terms, but this can confuse a person suffering from dementia. Call everyone and everything but its proper name so the patient is not left guessing and use visual aids and clues when possible. Communication will always be a challenge for caregivers and dementia patients, but the right approach can make a potentially extremely stressful prospect much easier to manage.

Making the decision to move an elderly parent in with you is not one to jump into lightly. There are many things to consider including how your parent feels about the whole situation. You would be making drastic changes to your lifestyle as would your family. The family dynamic and roles will change causing tension and worry.

The decision to be your parent’s caregiver inside your own home is not always clear cut. First of all, you need to decide (with your parent) whether or not there are intermediate steps to take before making the big leap. Could you afford a caregiver to live with your parent? Can your parent even live alone safely? How comfortable do you feel with the role reversal? There are many things to consider first. Here are some questions that may crop up in the course of making that caregiving decision:

The Family Dynamic

First of all, many aging parents may feel they do not need any help and might resist moving in with you. How are you planning to talk with them about it? You need to be prepared with a list of reasons why they can no longer live alone. Also, your family will be changed as well if a parent moves in with you. How will your ailing parent integrate with your family? How will your spouse and kids feel and in what way will their lives change? You will need to talk with your family to even see if moving your parent in is the right thing for everyone involved.

You need your own personal time and space but how will you get them with a parent to take care of in your home? What would your limits be in caring for your ailing parent before a nursing becomes the better choice? How dependent will the parent be on you beyond the food and shelter and can you fulfill those responsibilities? Will any siblings feel resentful if you are the one taking care of your parent?

Modifying your Living Space

When the decision to move a parent in to your home comes into play, do you have any idea where to put them? Will one of your family members be displaced from their room and cause resentment? Can a spare room, home office or den be converted successfully for your parent? Would building an addition to the home be possible so no one loses their personal space? How about home modifications for any assistive devices? Would you have to build a wheelchair ramp, install special door knobs or railings?

Consider the “baggage” your parent will be bringing with them. Can you handle their yapping lap dog or precious kitty? Could you handle questionable personal behaviors such as smoking or drinking? What about having friends over? Can you handle your parent’s many friends coming over to visit?

Time and Money

Time and money are other aspects to consider when your parent moves in so you can care for them. How do you handle your finances as well as theirs? Should they offer to pay some rent or contribute to groceries? What should be the division of expenses? How will other family members such as your siblings feel about the financial aspect? Will you have to change jobs, reduce your work hours or quit all together to serve as caregiver to your parent?

If you do have to work, how will your parent care for themselves during the day? Will you hire a companion? Do you have any inkling on how you plan to juggle your needs, that of your spouse and kids in addition to your parent? How will the division of labor be spread out?

Other Considerations

Some parental caregiving may require with personal issues. Could you handle spoon feeding your parent? What about bathing them or changing their diaper should they have incontinence? Do you know what to expect in regards to your parent’s health and what to do in an emergency? Would you be able to take care of yourself so that you do not burn out serving as caregiver? If you need time to yourself, are you willing to hire a nurse or someone for respite care?

You have got to look before you leap into any situation regarding proving parental caregiving in your own home. There is not just one party (your parent) to think of but many, so delving into all of those questions above will help you make your decision.

Today is a BIG day for me, my e-Book called “Todays Caregivers Guide: A Guide for the Preparation of the Inevitable” has set a new record in sales. Not only that, but I got a lot of positive feedback from YOU, which made me so happy.
Now I would like to thank you with today’s little article, hope you will benefit from it:

No one ever knows how hard acting as a caregiver is until they have actually had to do it themselves. Once you become a caregiver, your life is no longer your own. It is certainly very much like having a child, but it also brings with it the extra stress. You are often watching a loved one deteriorate physically and mentally before your eyes. The toll it takes on you is physical as well as emotional, and most caregivers find that they carry the entire burden of the caregiving themselves. To provide good care for your loved, however, you need to be good to yourself and try to make the caring process as stress-free as possible. These tips and helpful hints will guide you in making the caring process go as smoothly as it can, do you can look after yourself and your patient.

There are two main sets of tips for caregivers – those that make the actual caring easier and those that help caregivers get a little bit of relaxation and a much needed break. In terms of making the caring process easier, think about the things that you do for your patient that you might be able to empower them to do for themselves. If the patient needs help finding their personal items and then has no idea where to put them away, you can consider labeling drawers and cabinets with little notes that tell where everything is. Your patient will relish the chance to be independent enough to not have to ask for your help, and the note may also encourage them to put things away easily so you don’t have to go behind them and clean up. If your patient is bedridden, keep a selection of things they may need close to them, including books, TV remote, tissues, and more. That way they have the ability to get some of what they need and want without your help.

If you frequently take your patient out in the car with you, make sure you care is stocked with everything you may need. Incontinence is a frequent problem with patients who need care, so make sure all of the materials you need to deal with an accident are in your car, so you can deal with the problem swiftly and with as little discomfort to the patient as possible. Likewise, keep important phone numbers and backups of any medications in your car just in case.

Caring for yourself is as important as caring for your patient – if you’re not operating at 100%, you won’t be giving them 100% care. But carving out the time you need to relax and recharge when you’re the primary caregiver can be next to impossible. To make sure you get some time, first, look for the little bits of time you can steal to yourself daily. If your patient is napping, instead of running around doing the cleaning, take some time to read a book or watch a favorite TV show. After your patient goes to bed at night, develop a relaxing routine like taking a bath or unwinding with some of your favorite music.

When you need a longer break, don’t be afraid to reach out for help. If there are no family members or friends around to step in and help you, then investigate adult day care services or home health care services. You need to get away for your own emotional and physical wellbeing, so don’t be afraid to ask for the help you need. If you don’t know where to start, check out your local caregivers’ support group for advice on the resources that are available in your area.

Caregiving is extremely expensive for the caregiver – that cannot be denied. Usually, the primary caregiver also has to shoulder the burden for expenses like doctor visits, prescription costs, medical equipment, home help, adult day care, and any other need the patient has. There is also the matter that most caregivers see their income decrease as their loved ones become more and more dependant.

They may not be able to work anymore, or they may have to reduce their work hours to part time. The financial burden of caretaking is enormous, but there are other costs associated with acting as a caregiver that have to be counted as well. These costs aren’t as easy to show on a bottom line, but they are every bit as important as the financial costs – if not more so. Before you become a caregiver, or if you know someone who provides care, consider these additional burdens.

One of the biggest costs of caregiving can be the health of the caregiver. While they are busy looking after the health of their loved one, their own health may be deteriorating. Caretaking is extremely stressful and extremely time consuming, all of which can take an enormous toll on the emotional, physical, mental and spiritual wellbeing of the caretaker. As a caretaker, you may not have the time to exercise and eat properly, which of course is a burden on your physical health. But the stress itself of looking after a loved one and watching them deteriorate, while experiencing the isolation associated with being a primary caregiver can be very damaging. It is not uncommon to experience headaches, stomach problems, sleep trouble, weight changes, extreme fatigue and more. You may become depressed, feel withdrawn, feel angry, and feel alone. You may also experience forgetfulness or confusion yourself from the stress, which can be particularly troublesome when you are caring for someone with dementia.

Another cost to you as a caregiver may be personal. Acting as a primary caregiver is extremely time consuming. You will likely end up missing a lot of time with family and friends and may find it impossible to have a social life. Most caregivers have to withdraw from their careers, and if your career was very important to you, giving this up can be an enormous blow. Your world will grow smaller as a caregiver, which of course can have a tremendous impact on your overall well being.

How can you avoid these costs? Well, the honest answer is that it may be impossible to avoid them entirely. By nature, caregiving is stressful and a huge responsibility. Watching a loved one suffer is never easy, and putting your life on hold will bring on a host of emotions. But there are things you can do to mitigate your costs.

First and foremost, ask for help when you need it! Most caregivers think asking for help means they have failed. It really means just the opposite. You have to recognize that protecting your own health is something important that you do for the person you care for – if you can’t take care of them, who will? Share the burden. Ask family and friends to stop in. If they can’t, then seek out local support groups, adult day cares, and home health care services. Get a break when you need one.

Also, give yourself a break. The laundry can wait for one night. You can order a pizza instead of cooking a meal. Prioritize what you need to do, and don’t sweat the small stuff.

Caregiving costs financially and in other ways. You have to take charge of the costs so you can afford to pay the bill.

Being the primary caregiver for an aging adult can be a very stressful experience; luckily, there are lots of ways to reduce this stress and to bring your life back under control if the stress has already become a bit of a problem in your life.  Some of the best ways to cope with the stress include options for taking care of your own physical and mental health, while other options concern the care of the person for whom you are a caregiver.

The most important thing that most caregivers for aging adults sometimes forget is that a caregiver has their own emotions and life to deal with even while they are such a strong source of support for a sick loved one.  This feeling of wanting to be able to do absolutely everything can lead to very detrimental results.  Instead of trying to take care of everyone and everything 24 hours a day, remember that you have to take care of yourself in order to be useful as a caregiver for your loved one.  The best ways to ensure that you are taking good care of yourself are to keep your life in balance and to keep sleeping, exercising and eating well enough to be full of energy and in good spirits.

If your mind is too occupied with the impending loss of a terminally ill loved one, or you are feeling angry or guilty, sad or in doubt, it’s a good idea to consult your doctor.  If your symptoms include loss of sleep and being worried, you should contact your doctor right away.  Of course, it’s normal to worry about a loved one who is sick. If thoughts of how you will support yourself after your loved one is gone have you awake at night, you should tackle the worry straight on instead of letting it get the better of you.

Your doctor can suggest healthcare providers according to your needs.  If stress has resulted in back pain, it might be time for a trip to the physical therapist; likewise, if you’re so worried that your stomach is unable to handle any solid foods, a trip to a therapist may well be the best idea.  In addition to healthcare providers, there is also the valuable option of joining support groups for caregivers of the elderly.  Such groups exist both for in-person meetings as well as there being online support groups.

Joining a support group can offer valuable support from knowing that there are lots of other people out there in your community or out in the whole world who are dealing with similar issues to what you are dealing with in your own life.  It’s not just with the logistics of being a caregiver that having some support is beneficial; it is also extremely positive to share the burden of thoughts and emotions with other caregivers who are going through the same emotions as you are.

Take time for yourself: watch your favorite television shows or rent comedy movies to lighten your spirits.  Don’t let yourself become isolated; especially if the person for whom you are caring is not fully present mentally; make sure to invite others into the home or to leave the house periodically so that you can interact with other people on a regular basis.  There are lots of people in the world who can help you through the caregiving process; some of these people, like friends, family and church members or coworkers are already in your life.  There are a lot of other people out there though who are willing and able to help you if you take the time to seek them out.  Don’t be scared to ask for help…everyone needs some help, especially when it comes to something as physically and emotionally demanding as being a full-time caregiver.

Emergencies can crop up regarding a loved one, particularly if there is a sudden illness or health issue that renders that loved one incapable of caring for themselves. While you may not need to quit your job to set up caregiving for your loved one, you will likely need some time off to initially care for your loved one, assess the situation and make plans accordingly. You might feel concerned about your job and whether you cannot take off for any length of time.

The good news is that the United States government passed the Family and Medical Leave Act (FMLA) back in 1993 which provide employees who find themselves in a caregiving role the assistance they need to juggle not only their livelihood but also the care of their loved ones. The FMLA basically ensures that you cannot lose your job based on the need to care for a loved one. Of course, this act does not work to save your job forever but allows employees to take up to 12 weeks of leave unpaid from the hob without fear of repercussions.

Please note that the FMLA does not guarantee any pay during these 12 weeks and it is between you and the employer about whether or not you receive any pay. It may be based on the amount of sick leave, vacation time and/or personal time off (PTO) hours you may have accrued. If you have any of these built up, it could end up providing you with some income during your time off. Again, the payment arrangement is solely between you and your employers as the FMLA only guarantees that you cannot lose your job due to taking off to take care of a loved one.

With all good deeds like the FMLA, there is a down side to it as well. It does not protect all employees in the country. Therefore, not everyone has the opportunity to take advantage of it. Employers who are bound by the FMLA must be an entity affecting or conducting business or commerce. They must have at least 50 employees working at any given time during the course of a normal business week and also during the previous 20 plus calendared working business weeks. Subsidiaries or entities that are smaller than 50 employees but are affiliated or part of a larger entity also fall under the auspices of the FMLA.

There are some exceptions to entities with fewer than 50 employees and they include any public, local, state or government office and public as well as private secondary and elementary schools. If you do not fall within any of these scenarios, you may not be covered to take off from work with a guarantee to return to a job. Small business owners under 50 employees are not bound by the FMLA so you might have to negotiate with them in order to receive time off for caregiving.

Other things of note to consider with the FMLA is how an employer determines a 12-month period since the act states you can request up to 12 weeks of unpaid leave during one 12-month time. An employer can simply follow a 12 month calendar year which is the simplest or even follow their company’s fiscal 12 month year or even a 12 month period starting on your anniversary date. In addition, the 12-month period could be on the first day of when your FMLA leave period starts or even based on a rolling 12 month time frame that is gauged by counting backward from the date you use the leave for FMLA.

As you can see, there are quite a few things to check so do not always assume you fall within the guidelines. While you may not be able to put off your caregiving duties, at least by knowing your eligibility, you can negotiate with your employer about the necessary time off you need to care for your loved one.

The caregiver role can be quite rewarding yet it is also a challenging experience that not only tries you physically and mentally but emotionally as well. And when the caregiving lasts over a long period of time, the result is stress and a lot of it. You will feel all of these conflicting emotions that you feel guilty for experiencing especially when you have experienced such positive aspects in your caregiving relationship with your ailing loved one.

Of all the experiences you derive from caregiving, the emotional demands are perhaps the most draining. With stress held within the body physically, you can experience some relief with a hot bath or massage but what about the stress that resides in your emotions? You have to find some type of relief that touches your soul so you can rest at night and feel refreshed for the caregiving day ahead.

Each person needs something different when it comes to assuaging those emotional issues that builds up during your caregiving experience. Here are some problems you may experience along with some suggestions to consider for emotional relief:

1. Caregiving can tend to bring on a sense of isolation because your friends and family are out in the world while you are inside tending to your ill loved one.

Break that sense of isolation by getting out and taking a walk or a drive. If you have no one to relieve you at that moment, bundle up your loved in a wheelchair and roll them around the neighborhood park or take them for a drive in the country. Even a trip to the grocery store with your loved one in a motorized chair or wheelchair should help.

2. You might lack the time to engage in personal hobbies and relaxation time is hard to come by during your caregiving duties.

No one said that you should be the sole person caring for your loved one. If you are married, prevail on your spouse or even an older child to sit with your loved one and spend some time with them. You can then leave the house, meet a friend or do whatever you want. And best of all, other people are connecting to your loved one which means that they feel as if they are in the loop of activity and not isolated either.

3. You may feel that you have no one to turn to or that no one understands what you are going through. Overburdened is a natural effect of caregiving and you may also feel that you have no control over your life.

The bottom line is that you need to seek help for these feelings. Turn to a trusted friend, minister or counselor and talk about what you’re feeling. You need affirmation that it is ok to feel angry, sad, resentful and even guilty. Consider joining a support group for caregivers, others who have walking in the same overburdened shoes you are.

You have got to be realistic about the demands of caregiving and know up front that you are not going to be everything to everybody unless you get some help. Before you sign on as caregiver to your sick loved one, examine your home atmosphere, schedule and other aspects of your life. What would caregiving interrupt? How can you work around it? Who can you enlist to help when needed? Outlining some of the sources of potential emotional distress in advance means that you can work hard to avoid them during your caregiving tenure. That is not to say that you won’t ever experience stress but that you will recognize it for what it is and react accordingly before it morphs into a more serious problem.

Caregiving is a rewarding experience as well as being a whole lot of work and being extremely stressful at times. Many people only hear about the negative aspects of being a caregiver for a family member; the positive impact of being a caregiver is seldom a focus of the media and general conversations about caregiving.

Most full-time caregivers are caring for either an elderly parent or an aging spouse. In the case of parents who are aging, significant areas of stress in the situation include the time needed in order to properly care for an elderly person at home as well as the financial and organizational efforts needed to coordinate care. Many family disputes arise when siblings are in disagreement about what the proper route of care should be. In this sort of family situation, there is often a lot of stress between siblings and spouses; however, the benefits of caring for an aging parent are usually quite apparent.

Grown adults who take care of their elderly parents often forge new relationships with their parents and gain a whole new perspective on their family’s past through the experience of reversing the caregiver—dependent party relationship. Another common area where a lot of benefits are found is that spending so much time with an aging parent means incredible powers of bonding in many situations.

These positive benefits enjoyed by the grown children of elderly parents are sometimes the same benefits enjoyed by a spouse who becomes the caregiver of their husband or wife. In other situations, these same benefits are not found in this different caregiving situation. For some couples, a new implicit understanding develops between them when they spend their entire day together. In other situations, these two aging partners, one with significant need of help and the other being the source of that help, it can be the case that these two partners grow angry and hostile with each other instead of finding a new peace and understanding in their relationship.

Even if this is the case, there is a silver lining to be found if the caregiver gets enough support for him or herself. An important thing to emphasize is that the stresses and concerns of an adult caregiver are 100% real. The physical demands of being responsible for another person (who is potentially as physically large as you) are significant. In addition to the physical demands, the amount of time needed is substantial and the amount of patience and understanding that is needed can be overwhelming, especially in cases where the mind of the other person is deteriorating. An important thing to remember is that the caregiver has to have a support network, time to him or herself, and a healthy lifestyle in order to be a successful caregiver.

Some adult caregivers find a new respect for their own well-being through the experience of taking care of someone else. The doctor of a caregiver, as well as his or her friends and family will tell them often to take care of themselves, both in terms of physical health and mental health. Caregivers need full nights of sleep and a well-balanced diet, not to mention sufficient exercise and a stable mental life. Caregivers often see this demand to take care of their own life in order to be capable of taking care of their spouse as one of the most positive results of being a caregiver. Not only do you spend time and energy on the person you love, but you also have to take the time and energy to keep yourself well. This makes both members of a couple happier and healthier in the long run, which is what caregiving is all about.