How to Reduce the Stress in your Life and Find Focus at Work

October 8th, 2009

By David A. Travland, Ph.D. and Rhonda Travland

 

While daily living can certainly be stressful, nothing compares to the level of stress faced on a daily basis by caregivers.  How can caregivers continue to give their best performance at work with caregiving chores are hanging over their heads before, during and after work?  How can caregivers concentrate on their jobs under all that pressure?

 

We know that stress adversely affects employee performance.  What we may not know is how things at home affect the ability of employees to concentrate on their work.  A family healthcare crisis can create enormous stress for employees, whether it be a sick child, an elderly parent or an ill spouse, especially if long-term or permanent care is required.  How does the average employee (or manager, for that matter) handle these health care situations?  Do they come to their supervisor, spell out the details of their domestic obligations and ask for help?  Not likely.  Most working Americans play their home lives pretty close to their chests.  Family matters are considered private.  In fact, one of the big frustrations of self-help organizations is that caregivers tend not to self-identify; that is, they don’t even define themselves as “caregivers” and thus are not motivated to attend support groups.  Outreach is a continuous challenge for such organizations which, in good faith, have the desire and capability to be of help.

 

Why is caregiving so stressful?  Those who volunteer to care for a beloved family member who has become chronically ill or disabled are indeed heroes. They deserve the respect and gratitude of extended family and the community at large. However, the very admirable qualities that make them dedicated and self-sacrificing are the reasons they are vulnerable to stress symptoms, and in extreme cases, burnout. They are compassionate to a fault. They are inclined to give their all at their own expense.

 

This kind of chronic caregiving is stressful for a variety of reasons:

  • Caregiving for someone chronically sick or disabled is often expensive, putting a strain on the family budget.
  • Caregiving takes an emotional toll.  The personal lives of caregivers are dominated by the elephant in the room; that is, there is no end to what needs to be done for the care recipient, so there is constant pressure.
  • The caregiver’s needs are not being met; there is no time for play, for rest, for happiness.
  • In the case of the ill spouse, the caregiver’s pal is not available so companionship and intimacy needs are not being met.
  • Caregivers tend to get minimal support from extended family.  Family and friends are happy they don’t have to make these sacrifices, so they often just stay away.
  • Sleep deprivation is very common among caregivers.  The needs of the care recipient don’t go away at bedtime.

 

Caregiver Stress Symptoms at Work

Caregivers are under siege all the time.  Those who know them well can readily see that something is wrong.  Caregiver stress can take the following forms on the job:

 

  • Wandering attention during meetings or conferences
  • Missing deadlines on more than one occasion
  • Periodic tardiness arriving at work
  • Time spent doing computer research on company time
  • Sad or depressed demeanor, diminished sense of humor
  • Slower than normal speech pattern
  • Unusual eagerness to leave work at the end of the day

 

If you are an employee and a caregiver, here are resources to look into: Caring for a loved one is admirable but typically caregivers put their own needs and comfort on hold in deference to the needs of the care recipient.  Before it is too late and burnout takes its toll, caregivers need to take inventory of the sacrifices they have made and the stress that is created because important needs (such as free time, reading, travel, companionship, etc.) are not being met.  Then they need to make a commitment to make the necessary changes in their routines and find more balance and time for themselves.

 

  • Caregivers need frequent breaks from caregiving duties.  Find a way to get relief, whether by prevailing on family members to fill in, day care programs with nursing homes, volunteer organizations, sitting services, or whatever can be arranged.  No excuses.  Do it today.
  • Find someone to confide in, such as a professional counselor.  You may tell yourself you don’t need to talk to someone, but that is baloney.  Caregivers need the kind of perspective that comes from opening up to someone.
  • Get more sleep.

 

What Should the Organization Do?

All organizations, large and small, private and public, are impacted by the caregiver stress problem.  It is estimated that there are in excess of 50 million caregivers – about half of these are caring for a spouse – in this country, so the odds are in favor of some significant percentage of your employees are caregivers.  Here are some steps to minimize the adverse impact of home caregiving responsibilities on employee productivity:

 

  • Top management should communicate to all employees that the organization understands that providing care to relatives, children, and spouses is part of being a responsible family member.  The company plans to provide whatever support is possible to help employees stay focused at work and live a balanced lifestyle.
  • Managers and supervisors should receive special training to spot symptoms of caregiver stress.  They should be taught how to initiate communication with these employees in a way that will encourage them to open up and talk.
  • Human resources managers should be given special instructions and training on how to create workable strategies for helping caregiver employees work out a program that will bring relief at home, and restore productivity at work.
  • Those at work may be the first to recognize the employee is suffering debilitating stress symptoms as a byproduct of caregiving.  If the organization has an Employee Assistance Program, care should be taken to ensure that program makes provision for supporting caregivers in distress.  A strategic alliance can be formed with existing self-help organizations, such as the Alzheimer’s Association or the M.S. Society.  They would welcome the opportunity to cooperate with your organization.

 

Trained employees are an organization’s most important asset, and should be treated accordingly.  Caregivers are characterized as charitable, goal-directed, hard-working and productive.  The qualities that make them good caregivers also make them wonderful employees.  It is in your organization’s long term economic interests to recognize caregiver stress, and respond constructively to that knowledge.

The Feeling Owed Syndrome (FOS): A Cautionary Tale for Caregivers

October 6th, 2009

Feeling Owed Syndrome: A Cautionary Tale for Caregivers

How could a man just take a gun into a crowded store and start shooting people? How could a mother drown her two children in a car? How could a drunk driver mow down a crowd during a street festival? Why would a successful executive commit suicide by jumping out of his office building window? How in the world can we explain this behavior in terms of normal motives and common, well-understood forces that are common to all of us?

And what does any of this have to do with caregiving?

The people who commit these horrific crimes are angry. Where does all this anger come from? These people are feeling put upon. In their minds, they have done for others and in return have gotten the shaft. They have succumbed to Feeling Owed Syndrome (FOS). Caregivers tend not to be potential criminals, but this kind of inequity is built into caregiving relationships, and with time and additional stress, it can turn into an explosively violent situation.

Caregiving relationships often suffer from inequity, where one person contributes more to the relationship than the other. Caregivers give, and give, and give, and then receive very little in return from the person receiving care. You might be tempted to observe, “Of course. The sick person can’t give much back. They are too sick.” And you would be correct. But understanding it does not make it go away.

Our society teaches us that this inequity shouldn’t make us angry, but it does. The fly in the ointment is the brain has a mind of its own. We all carry around an internal ledger that keeps track of what we are investing in any given relationship, and what we are getting back in return. For example, let’s say you are exiting a department store and someone with their arms full of packages is following you. As a courtesy you hold the door for them. We have all done this hundreds of times.

Now suppose that the person with the packages walks through the door, nose in the air, and does not even bother to acknowledge your presence. How does this make you feel? If you are normal, you are going to be at least a little annoyed. You won’t be hostile or depressed, but you are likely to be miffed. Why? Because you performed a service for that person, holding the door, and they did not bother to give you anything back, such as a “thanks” or a smile or a nod. You have just experienced an unbalanced relationship and you feel owed. That has resulted in a tiny amount of stress.

Multiply that situation by a thousand, as would be the case in the caregiver situation, and you are likely to be facing an accumulation of stress a thousand times more obvious. Behavioral scientists know stress is cumulative, one stressor just piles on top of the next one, and it gets worse and worse. As the relationship imbalance gets more and more pronounced, we gradually begin to identify we are feeling owed, that we are not getting nearly enough back from the person we are caring for to counterbalance what we are putting into the relationship. FOS is brought about by chronic imbalance in a relationship, any relationship. It is not only experienced by caregivers, but by anyone who feels they have been short-changed or denied an adequate return on their investment in others. The more they feel they are owed, the more extreme their reaction, whether it be stress translated into illness, or acting-out behavior taking revenge on an ungrateful world.

What can caregivers do about this? How can FOS be avoided?

  • Caregivers must admit they keep track like everyone else. They need to admit caregiving is extremely demanding, that it is often a thankless job, and that they are carrying around some resentments.
    The next step is caregivers must commit to finding a way to reduce the amount of inequity. They must find a way to limit what they invest because it is unlikely they can successfully demand more back from the patient.
  • Caregivers need to pay close attention to their own needs. Sacrificing too much for another person is a dangerous game, resulting in physical and emotional damage.
  • Caregivers should treat their own symptoms – anxiety, depression, escape fantasies, loneliness, anger – seriously and create an action plan to correct the imbalance in the caregiving relationship.
  • Caregivers need a confidant, someone to talk with who can understand caregiving frustrations. Normally another caregiver is the best choice; a mental health professional is another option. Those who don’t have any caregiving experience will often have a hard time relating or empathizing.
  • Caregivers need periodic breaks from the caregiving routine. Finding a substitute caregiver is crucial, whether a relative, friend, neighbor, or someone hired to sit with the patient.
  • Caregivers must distinguish between what the patient wants and what the patient needs. Compassionate caregivers have a tendency to treat wants and needs alike, and the patient’s wants can run caregivers ragged. The needs must be met, but not the wants, especially those that interfere with the caregiver’s needs.
  • Caregivers need to make every effort to arrange for a full night’s sleep every night. Sleep deprivation amplifies FOS and  may result in depression, anxiety and anger.

Caregivers must take care of their own needs or they will not be effective as caregivers. FOS causes caregivers to become indifferent to the needs of the patient, and if there is no relief in sight, the symptoms of depression, anxiety and anger can get out of hand. Caregivers make headlines occasionally by exhibiting violent behavior toward their loved ones and themselves. In these cases, FOS was not recognized early enough to head off disaster.

ABOUT

October 6th, 2009

Please check our bios at www.sickpartner.com

Dr Dave on the Radio!

September 30th, 2009

This brief radio interview was one of our best, to date….

David had lots of fun and the Radio Host was Jacqueline Marcell, author of Elder Rage.  What a lovely person and quite empathic on the needs informal caregivers put aside to care for loved ones.

Link to Radio Show

New Book Review

September 30th, 2009

I just came across a book review for our book (see link below).  While it was a surprise to me and David, the reviewer does not appreciate our writing style, or editing, she does still recommend the book for caregivers who have been living with the situation for an extended period of time.  Perfect!  That is actually our target audience.

 

We could not have asked for a better review!!  We want to extend our thanks for the review and our link is meant to create further awareness of the organization to which the reviewer is clearly a key participant. 

 

The truth is that we insert anecdotal stories to exemplify the help Dr. Travland provided to his therapy clients over nearly 40 years of private practice.  We do not footnote or reference techniques he fine tuned for specific reasons.

 

Too many people are suffering with illnesses, or disabilities, along with their primary caregivers. The other day on the radio, it was noted that when an individual is in chronic pain or ill, the whole family is experiencing the hardship.  Unless people have experienced this first hand, there is no way to make others understand how isolating it feels.  We are outsiders in the real world as caregivers to a loved one.

 

Sadly, this is a key component in the ongoing debates about health care reform.  Those who have not lost everything they have ever earned to cover the costs of health care have no idea why we must help all Americans obtain access to affordable health care.  Rhonda knows first-hand the perils of expensive medical needs.  She made choices – groceries or medicines – on a daily basis.  Just today in the local paper, a father of a terminally ill six year old child watches his family sell cupcakes to offset medical expenses.  All the while he wonders why and how in a country – as great as America – does it come down to a bake sale for cancer treatment?  

 

That is what we want to know, too.  Frankly, we want informal caregivers to be recognized for the efforts they put forth, for the financial hardships that are incurred.  It is not enough to offer words of encouragement, caregivers need real help, real suggestions and proactive plans for reclaiming some sense of normal without guilt or financial ruin out of love for a family member.

 

Thank you again for the book review.  We are all in the same business of raising awareness help for the ill, in pain, or disabled.

 

BOOK REVIEW

 

Caregiving and Finances by Rhonda Travland

August 5th, 2009

One of the most difficult parts about spousal caregiving is the financial burden. 

We attended a financial seminar today for an update on the situation.  We have been out of active caregiving for about 36 months and nothing much has changed. 

But, what the seminar did reinforce is the fact that many spousal caregivers become dependent financially on their social security income, social security disability, their pensions or their moderate investments to the point that they are scared.  Scared of the future, scared of living without their income, scared of having to spend every penny before they can qualify for help.  

So, what happens is that they do nothing.  They let the world take over, they do what they can to survive.  Thay pay the medical expenses they can, scrape together copays for meds and do without advice from experts.  Many people are so confused about insurance that they never look into alternatives.

Sadly, this is a mistake.  Anyone dealing with Chronic illness that is leading into disability, already qualifies for disability or is already over 65, receiving Medicare benefits and living on social security income MUST speak with a certified Elder Law Attorney and financial planner that specializes in elder care issues with investments.

Take it from me, I had no great amount of assests when my ex-husband got sick.  All we had was the house we owned with a mortgage on it with very little equity.  Ex was receiving disability benefits, but every penny went to his care and medications.  I paid his health insurance through work and paid all the other living expenses.  Even with little financial resources, it was necessary to obtain the services of an Elder Law attorney.  He helped me understand more than I knew about Medicaid & Medicare.  I learned what I could keep and how we qualified.

There is another Deadly Misconception that I have to add to the list……Nursing Home medicaid is not welfare…..It is an entitlement and every state has their own rules…FIND OUT WHAT THEY ARE & SEEK PROPER ADVICE.   Do not make the life changing mistake of hiding in fear until you really have no choice but complete impoverishment.

The struggle so many caregivers have could be eliminated by speaking with a pro.  Someone who can advise you about what your rights are, what can you do to still feed yourself and consider alternatives for nursing home placement.

Get help!  You do not have to lose everything you have worked for because someone you love got sick.

Caregiver Empowerment is the only way to survive.

Caregiver Survival & The Travlands in the News

August 4th, 2009

Today’s article…. www.tampabay.com/news/health/article1024481.ece

A brief moment in time captured in the local news….The problem is it only represents split second of a conversation with the reported.

While we stand behind the articles premiss- that we offer spousal caregivers an alternative view of life – especially in regard to sex within a caregiving marriage-  we do not spend the majority of  time talking about it in the book.  It is one chapter in a fourteen chapter book & has much more to do with relationship dynamics than sexual intimacy.  

Give it a chance.  We all need to understand how relationships work…….This book does it and put individuals in command of their own lives.

Rhonda Travland

Top 10 Ways to Defeat Caregiver Stress by Dr Dave & Rhonda Travland

July 20th, 2009

TOP TEN WAYS TO AVOID CAREGIVER BURNOUT

By Dr. David and Rhonda Travland

Authors, The Tough & Tender Caregiver, a Handbook for the Well Spouse

HERE ARE THE FACTS:

People who have never been a caregiver are clueless.

They seem to think caring for a loved one at home is a picnic. “After all, you get to be with him.” &    “You don’t have to work.” Most full time caregivers would give anything to have the opportunity to go back to work. Compared to caregiving, going to the office is more like recreation.

Most of the advice caregivers receive from these people is useless.

Meditate,” “spend time gardening,” “trust in the Lord”, “count your blessings,” and so forth. We believe caregivers should be given advice based on practical experience.  We want caregivers to receive advice that will make a real difference in the day-to-day lives.

As health care professionals and former caregivers, we believe there is a shortage of practical information available about what caregivers should be doing to minimize stress and avoid caregiver burnout. In our seminars caregivers ask us to summarize the most important caregiving tips we discuss in our book. Caregivers are hungry for advice that can help them find joy in their lives despite their caregiving responsibilities.

Below is our top ten list of ways to defeat caregiving stress:

No. 10. Ignore messages from our society that “It is wrong to be selfish.” They come in a variety of forms, such as “It is more blessed to give than receive.” These are dangerous messages that can encourage caregivers to sacrifice their own lives on the alter of a loved ones’ needs. Caregivers who believe it is wrong to think of themselves are flirting with burnout. Not only will they suffer, but their loved one may lose their caregiver, the one person in their lives who cares enough about them to provide care. The advice is this: you should pamper yourself at every opportunity.

No. 9. Avoid people who make you feel bad. Friends and family members who have not been caregivers are not tuned in to the daily grind of caregiving, and are likely to make remarks that are well-intended, but ignorant and hurtful. When possible, stay away from those people. Find people who are not inclined to offer unsolicited advice.

No. 8. Make a list of what help you need from others and keep it handy. Friends and extended family will tend to offer you the kind of help that will make them feel better, or help they find convenient and easy to give, whether or not it is what you need. Be prepared with your list so you can say, “I appreciate your offer, but here’s what I need instead. Could you mow my lawn? That would really help us.”

No. 7. Require your ill or disabled loved one do as much as possible for themselves. This not only helps the patient feel better about themselves, but it takes away some of your burden. It also discourages the kind of dependency that some chronically ill or disabled people fall into that handcuffs caregivers to their home. Also, insist that your ill or disabled loved one speak for themselves. For example, let the patient interact with their doctor. Do not act as the spokesman for the patient in the doctor’s office. If you do, the patient and his or her doctor will come to see you as completely responsible for all aspects of their care, which will intensify the patient’s dependency on you.

No. 6. Learn the symptoms of caregiver burnout so you will know when it is time to ask for help. Those symptoms include yelling at your loved one, difficulty sleeping (or waking up), eating too much “comfort food,” driving recklessly, spending money on useless trinkets, chronic sadness, new aches and pains without apparent cause, crying spells and so forth.

No. 5. You should provide care for your loved one at those times that are most convenient for you. This allows you to create a schedule that can leave blocks of time for your personal activities that serve as a break or respite from caregiving duties. These caregiver breaks should be scheduled several times every day to provide balance between your needs and the needs of your loved one.

No. 4. Protect your privacy. You do not owe your loved one a complete, detailed explanation of where you are going or what you are doing when you leave the house to “run errands.” Care recipients often fall into the trap of thinking they are entitled to exercise control over the comings and goings of their caregiver. You can spot this sense of entitlement when they insist on a detailed itinerary as you are about the leave the house. At times it is their anxiety about being left alone, but it is also frequently about power; they want to be in control of events. You must create boundaries around yourself and enforce them.

No. 3. Distinguish between your loved one’s needs and wants. See to it that the patient’s needs are met, but satisfying wants, such as recreational activities, videogames, board games, and so forth, are far less important than your need to be away from the patient on a regular basis to recharge your batteries. Satisfy the patient’s needs, and negotiate about the wants.

No. 2. As soon as it becomes clear that your loved one’s disease or disability is chronic, and that they won’t get better anytime soon, begin to scale back on the intensity of care you are providing. Our immediately burst of care when a loved one is first injured or becomes ill is fueled by adrenaline and cannot be sustained for the long haul. Acute care is like a 100 yard dash, but chronic care is a 26 mile marathon. Make sure you make the transition as soon as possible.

No. 1. Make arrangements for respite care, whether by hiring someone to sit with your loved one periodically, or enrolling the patient in a day care program. Our ill or disabled loved ones may resist having someone other than you care for them, but it is essential to make the arrangements before caregiver burnout becomes serious. In hiring someone to spend time in your home, make sure someone does a background check. Day care programs are a marketing strategy for reputable nursing home and assisted living facilities. This familiarizes patients and their families with the facilities for when placement becomes necessary or desirable.

Top Ten Reasons to Buy “The Tough & Tender Caregiver” by David & Rhonda Travland

July 10th, 2009

Top Ten Reasons to Read

“The Tough & Tender Caregiver: A Handbook for the Well Spouse”

 

10.     Your caregiving misery is not cosmic punishment for anything you have done.                

9.      The authors have experienced personal caregiving situations that lasted decades, but have the professional credentials to support their “Caregiver Survival Strategies”.                                                                                                                                 

8.      You will learn that all relationships are contracts with identifiable provisions.                  

7.      The book advocates caregivers take good care of their health & sexual needs.                  

6.      Caregivers who neglect themselves can no longer give good care ~ thus, potentially harming the one person they are trying to protect.                                        

5.      We all have an “Internal Ledger” keeping track of our investment in others & what we get back.  If the ledger is out of balance, we suffer from F.O.S. (Feeling-Owed-Syndrome)                                                                                                         

4.      “Relationship Boundary Errors” are a leading cause of caregiver burnout.  Dr Travland has created a simplified way to understand the boundary error concepts to improving relationships.                                                                                                                           

3.      “Enlightened Self Interest” keeps us from exploiting others, but gets our needs met.                                                                                                                                          

2.      It serves as a “support group” without leaving home.

                                       

1.      It’s cheaper than counseling.

 

 

 

Caregiving in the home ~ Survival Suggestions by Rhonda Travland

July 10th, 2009

We are working on a variety of Caregiver Survival Presentations that are coming over the next six months.  As we complete the various tasks, we are reminded, again, of promises, wedding vows &Compassion-Run-Amok” (Travland, 2009. p 34)  

 

For caregivers, we get stuck in a limbo between love & obligation.  How did we end up in this situation and how much are we willing to give up for the sake of our partner or our family member?  For some, there is no question in the matter ~ they will never quit providing hands on care.  For others, they were unhappily involved in the relationship before illness or disability invaded regardless of the type of relationship.  Some adult children seem to think caregiving will provide them with the long overdue “I love you” or “Thank You” from the parent.  Some will provide care seeking some type of absolution from past actions toward their loved one.  Some spouses will be trying to repair a marriage that had seen better days by being a devoted assistant.  It does not really matter why the caregiver keeps going, they just do it without much regard for their own well-being.

 

Those duty-bound caregivers will take no action because they feel guilty…. or simply do not know how to find relief.

 

 

For all caregivers, though, here are some suggestions from our list we give to clients to survive caregiving in the home:

 

  • Communicate openly what you are willing to do and what you are not willing to do. We call it “Renegotiation of the Relationship Contract”    We suggest using it with your LO, but they may not be able to participate due to mental status, but it can still be used.  Renegotiate with yourself.  Be honest about the areas that are draining you and work towards seeking resolution.  CSI can help fill those gaps with suggestions by evaluating your resources.

 

  • We think we can do it all, but we cannot.  Ask for help and take all offers of help no matter how your ego resists the offer.  We always suggest asking a friend or family member have a “Caregiver Shower” before the L.O. moves in, if possible, or when the sudden onset of a change happens to a loved one.   Actually, there is no reason not to have a ”Caregiver Shower” right now…No matter how long you have been caregiving.                                                                                                

 

We have bridal showers & baby showers for those life altering events…Why not a “Caregiver Shower”?  Caregiving is expensive and requires very similar equipment,      clothing & assistive devices as a new baby or a new home.  If you have chosen the role of  caregiver to an adult…You need the support systems in your life to provide you with a ”shower”.  It will minimize your stress & bring the family together to witness the             strenuous needs. 

 

We at CSI can help caregivers create a “Caregiver Shower Gift List” & it helps create a little  brighter view of the caregiving duties.  It is also a time where the family & friends can be educated on how to interact with the ill or disabled LO which will help lessen the chances that they will slowly stop checking in and offering to help.

 

  • If you cannot immediately think of what you need, then let them know you will take the offer in an “I Owe You” form with no expiration date.  Lee Woodruff refers to this as a “chit” system to call in favors as she helps her family recover from her husband’s TBI.

 

  • When you have an opportunity to let your LO participate in therapies, or there is an offer for “free respite care” so that you can attend a caregiver workshop or seminar….GO.

      Even if you do not like the subject matter, GO, take advantage of the “free respite”.  Use the time to recoup, sit in the back and read a book, snooze, or whatever you can do with    your mind for an hour or so.  Many times these marketing seminars are designed     precisely for you & your LO to get a glimpse of the facility incase their services are  needed in the future.  DO not feel guilty for using it…they are created for that very reason.

 

For example, we wrote in our book that my former husband was prescribed “Anger Management” educational classes early in his disease process. 

 

Did I think it would help? NO. 

 

Did I enjoy the fact that for 30 days in a row (M – F) 8:30 a.m. until 12 p.m. he was not my responsibility or that I had respite?  YES.

 

My point is, be creative & look constantly for ways to make the most out of opportunities that are presented even if they are not ideal.  If they do not put your LO at risk and you get some type of relief…Go for it!

© 2009 Travland Consulting &Caregiver Survival Institute, All Rights Reserved