Signs of Caregiver Burnout

How Family Caregivers Can Recognize Their Own Depression

© Lisa C. DeLuca

May 1, 2008
Prevent Caregiver Burnout., Morguefile.com
If you have two or more symptoms of caregiver depression, it is time to get help. Read about the signs of burnout here.

Caregiver burnout, strain and depression are terms used to describe a physical and emotional condition experienced by people who are caring for ill family members. It is not a sign of weakness, it simply goes with the territory, though it is essential that those who give care take steps to prevent or ease burnout. If left untreated, serious consequences could result.

Warning Signs of Caregiver Depression

  • Harmful behavior toward the care recipient. (If this happens even once the caregiver should seek help for him or herself immediately.)
  • Unrelenting feelings of sadness or doom.
  • Feeling like your life is being stolen from you.
  • Crying frequently.
  • Being easily angered by, and constantly annoyed at the care recipient.
  • Sudden change in eating habits resulting in unwanted weight gain or loss.
  • Change in sleeping: inability to fall or stay asleep, or, wanting to stay in bed and sleeping too much.
  • Lack of desire to do anything.
  • Loss of interest in people and pleasurable activities.
  • Feeling worthless and guilty.
  • Feeling like nothing you do is good enough.
  • Thoughts of death or suicide. (Seek help immediately.)
  • Chronic physical symptoms: headache, back pain, etc.
  • Panic attacks or continual anxiety.
  • Feeling completely overwhelmed with worry about how you will manage.

If caregivers experience two or more of these symptoms, it’s time to take a look at the situation and to begin helping themselves.

Guilt often Prevents Family Caregivers from Getting Help for Burnout

If a person entered an occupation which required them to:

  • be on call 24 hours per day, seven days per week;
  • interrupted their sleep so they were never rested;
  • provided no training but tons of responsibility;
  • offered little or no pay and actually cost them money;
  • and prevented them from having any free time to themselves;

nobody would judge them as being weak if they suffered burnout, nor would they tell them to stop complaining and snap of it. Yet caregivers judge themselves this way. And they have the added burdens of being worried about their loved one and all of the consequences of illness in a family.

Why Suppressing Feelings Can Contribute to Caregiver Depression

The function of feelings is to alert people that something needs to be changed or addressed. Having guilt about feelings can interfere with this process. People caring for ill loved ones may feel like running away, but just because they feel that way doesn’t mean they should or would do it. Perhaps they would simply like to have a few hours off. People will be judged by their actions, not their feelings, so it is important for caregivers to not let guilt about feelings prevent them from understanding what their feelings are trying to tell them.

While it is true that wallowing in feelings is not helpful for family caregivers who must take action every day, suppressing and ignoring feelings can lead to caregiver burnout because their valuable message is ignored. Instead of wallowing or suppressing, people can think about interpreting their feelings and translating them into positive action that will help them cope with caregiving.

There is no magic cure for the pains of caring for a sick loved one. Chronic illness is indeed sad for the patient and the family members, there is no way to avoid this. Caregiving is extremely challenging and there is no way to deny that. Managing the situation in the healthiest way possible is all that a person can aim for. This includes being alert to the signs of caregiver burnout and seeking out support groups, mental health, or medical care as necessary.

This article is not meant to be personal medical or mental health advice. Anyone experiencing troubling symptoms or behaviors should consult in person with a medical or mental health professional.


The copyright of the article Signs of Caregiver Burnout in Caregiver Support is owned by Lisa C. DeLuca. Permission to republish Signs of Caregiver Burnout in print or online must be granted by the author in writing.


Prevent Caregiver Burnout., Morguefile.com
       


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Comments
Oct 9, 2009 8:55 AM
Guest :
Is anyone else fed up with being told how their parent, is there responsibility? These pressumptious people...they have no idea, not every parent was good, not all were the Cleavers or the Cunninghams like TV. If anything good comes of these pages, inform the public not every parent cared whether their child had a childhood. I for one am sick of being told to look after my mother. People started telling me that at 13 yrs old. No one seemed to worry I'd gone hungry, missed out on school activities, never did all sorts of functions because she spent the cash on herself and their was none for incidentals: meals, school pictures, dental work, health care, etc. PLEASE STOP PRESUMING THEY WERE ALL GREAT AND WE'RE JUST UNGRATEFUL WRETCHES. I have looked after her, til I'm fed up. She lies about money, her health and expenses to me, the last one helping her! She has no respect for others, we're all stupid.
Oct 9, 2009 9:06 AM
Lisa C. DeLuca :
I highly recommend that you seek professional counseling right away to help you address your anger. This article does not presume that all parents are great or that their children are ungrateful. Many children are severely neglected by self-centered or abusive parents. Their negative feelings toward the parent can be completely justified.

However, as an adult, you alone are responsible for how you handle your anger and the choices you make. This level of unresolved anger does not sound healthy. Most counties and states provide free counseling to family caregivers. Please, take advantage of it.
Oct 14, 2009 11:19 AM
Guest :
If a person entered an occupation which required them to:
* be on call 24 hours per day, seven days per week;
* interrupted their sleep so they were never rested;
* provided no training but tons of responsibility;
* offered little or no pay and actually cost them money;
* and prevented them from having any free time to themselves;
Thank you for reminding me of this... I have been taking care of my mother for 4 years now, and even with respite and hospice assistance, I am exhausted. I've gained weight, given up my profession (and lost income from not working for four years). The lack of sleep and stress exacerbated my fibromyalgia and I have zero privacy and no time for myself or a love life.
What is sad is that my Mother really has no quality of life except the minuscule connection with me(she's aphasic) and she is suffering in great pain. She never wanted this for herself or for me but I'm stuck until she dies and I feel guilty for even saying stuck. I love my mother, but after four years, I am finding it difficult to follow through with daily activities of caregiving. Where I once took care of my mother with great attentiveness to the detriment of myself, I find it a struggle to even want to get out of bed to get her meds.
Oct 26, 2009 2:45 AM
Guest :
Its the 21st century folks, no ones parent should be "suffering in great pain". Get her decent pain management. If your hospice is not doing their job and keeping her comfortable, fire them and get another one. My mother is dying, and her hospice works-she's quite comfortable, with sufficent meds to help control her pain, anxiety etc. Of course her medications have needed many adjustments as her condition progressed, and we've had a few hiccups-but no one should be in pain! Or suffering. At all. My Mother is going to have a peaceful, pain free death, just like my Father did. Thank God for Hospice.
Oct 27, 2009 1:59 PM
Guest :
Although I'm not a full time caregiver, I help my husband everyday with showering, dressing and getting his meals. Yet I have a full time job, an 18-year-old who has her own issues, and all financial responsibilities for the family. Everyday is the same. Make his breakfast, get his shower, get him dressed and then finally do the same thing for myself as I rush off to work almost late everyday. (making sure he has meals to eat while I'm gone). Do part time caregivers suffer from burn out too?
Oct 27, 2009 5:29 PM
Lisa C. DeLuca :
The most recent guest asked, "Can part-time caregivers get burnout?" From what you describe you are not a part-time caregiver and yes, you are at risk for burnout. I answered your question in more detail here: http://www.suite101.com/blog/lcdeluca/do_part_time_caregivers_get_burnout_t oo
6 Comments