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By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington. Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services. APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid. We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour. APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment. You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints. Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights. APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.I agree that: A.I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information"). B.APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink. C.APFM may send all communications to me electronically via e-mail or by access to an APFM web site. D.If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records. E.This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year. F.You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
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Caregivers always seem to get the short end of the stick, if you ask me. The "poor elders" are so sweet and helpless, and all that nonsense, while we slave away unacknowledged and often criticized by the armchair critics for what we're not doing or doing wrong, in their opinion. Resentment goes with the territory for the vast majority of caregivers willing to admit the truth!
You DO NOT "kinda just have to suck it up. Be Happy for your mom." Don't buy into that nonsense at all! There are always alternatives to giving hands-on/in home care for an elder, so I suggest you look into it before YOUR health suffers from stress and burn out. Give YOURSELF the gifts nobody else is giving you, that you deserve too. Hire in home care with mom/dad's money, or explore placement with Medicaid if finances are an issue.
I don’t think it’s wrong to feel resentful, but it’s important to take steps - even teeny tiny ones - to extricate oneself from being totally stuck in the situation.
I’m not a hand’s on caregiver for my mom because A) literally impossible B) it would kill me. But I have done everything else, still do, and have a philosophy that POA stands for, ‘Person of Aggravation’. Meaning, once you’re POA you have a big target on your back for complaints, unwanted opinions, and all manner of aggravating requests from the LO and everyone else who has NO CLUE what your experience is like.
I’ve delegated as much as I can, and play music, pet dogs, whatever, to alleviate feelings and have a life. As a Person Of Aggravation, I also get my own aggravation out on a full size martial arts bag I’ve nicknamed, The Therapist. My ‘Therapist’ keeps my feelings a secret, plus the more I see this therapist the better shape I get into, so I totally recommend this kind of therapy if your joints can take it.
Since I announced my cancer diagnosis, 3 people have accused me of being a shitty caregiver.
One of them accused me of not taking my father to a parade. I'd never heard of the parade before that moment and when I told my father to talk to the guy, he got pissed off at me.
One of them accused me of not putting my father in a senior living center. My father wouldn't go and I couldn't force him.
The last one probably didn't care for his father for more than 15 minutes but decided I was a poor caregiver.
My father is loved, I'm hated, literally, my family won't talk to me. My aunt called me to ask where to toss my body when I died and that's been our only communication in months. I had really bad thrush, couldn't eat, lost 20 pounds, no one cared even a little bit in my family. In fact, I was being chewed out over something that literally didn't matter.
I'd tell you to not do this job. If I could go back in time, I'd have walked away and left my father and his shitty relatives behind and never have looked back. I have literally not received one iota of compassion from my extended family.
I'm so sorry for what you're going through. It's terrible and the way you describe how your family treats you, absolutely disgusting.
I would tell such a family to stick it where the sun don't shine and cut them out of my life.
You with a cancer diagnosis have to be the top priority in your own life. Screw your family. Any family that would behave as you say yours does does not deserve your love, time or respect.
Honestly being a hands on caregiver is not a good experience, there are no benefits.
Me, I would never do it, I have 2 in a facility, one on AL the other in MC. I am not willing to give up my life, my mental well-being for another, makes zero sense to me.
There are other ways to handle this, like placing your parent. Because he doesn't want to go is his choice, as long as he is mentally competent to make this decision. As long as you keep him propped up he will always think he is independent.
You do not have to care for him. That is your choice, so with that, there is an acceptance level as no matter what you do, you will be criticized.
We can all debate if feeling resentful is right or wrong, but perhaps the bigger question is where does resentment get a person? It brings on stress, possible emotional and physical health consequences, and does nothing to change the situation. Validating your emotion goes only so far. Maybe it’s time to consider changing the dynamics that cause resentment before the consequences become too much
I do so agree with you. This is like an anger at bottom of SELF in that we are grownups. We make our choices. When we take on this care it has consequences and they are OUR consequences. I think it is well and good to validate our emotions, as we've little thought as to what pops into our heads; but it is not OK to marinate in it. We weaken ourselves thereby. It keeps us from addressing what in our present daily lives needs to be addressed.
Caregiving for a family member is a thankless job. More often than not the caregiver is disrespected, berated, belittled, and even villified by the "loved one" (I use this term very loosely) they're taking care of. These family members (usually seniors)many times literally cannot wipe their own asses successfully on their own, yet will treat the person who does them this service with less regard than a bag of garbage thrown on the side of a highway.
When you do it for a living like I did for 25 years, it's usually just as bad. Clients and their families more often than not think that the caregiver is a slave who works for the whole family that they can treat anyway they like.
I'm in the business end of homecare now and my long experience is useful in this business. I will tell you this truth, my friend. I would rather make my living walking the streets than work at hands-on caregiving again.
You have a choice though. If the resentment is setting in, you can choose to walk away from it and you should.
Why would you stay with a parent, caring for said parent, when you feel this resentful, Roger? I don't understand. It may help us to get a picture of your situation if you fill out your profile and/or tell us a bit about your parent, his or her diagnosis and prognosis, whether you live with said parent in his/her home, or he/she lives with you.
On the face of it, and with so little information from you I will only say that when we move from being a son/daughter/sister/brother to being a CAREGIVER we have voluntarily given up the former positions for the latter. We become "caregivers". The responsible ones. The ones who make the decision and the rules and are resented for said rules and decisions. This just naturally happens.
If you have decided that caregiving isn't for you, then slowly you will have to disintangle yourself from it with honesty, and with, undoubtedly, no little trouble. You are an adult and took this on. Now it doesn't suit, and when that is the case it is time to reclaim your own life.
I wish you well, and hope you will tell us more about your situation.
Caregiving is a thanks less job...you might as well get use to that now. No one is going to through a parade in your honor.. You can choose to do it or not. Bring resentful is normal, but very useless and a waste of energy.
I think most caregivers don't care if they're being thanked for something or getting flowers and hugs as shows of gratitude.
I think what a family caregiver wants most from the family member they take care of is just basic respect. Also time off from that person is important.
(When I say 'you' in the following comments I do not literally mean you as in yourself)
Basic respect as in not treating that person like they are worthless garbage with nothing postive to contribute to human society. Basic respect as in not making up lies about the family caregiver who literally wipes your a$$ and works like a slave day in and day out so you can "age in place". Also, not villifying them to others because you're bored and want more attention. Basic respect in that you do not behave like an entitled, ingrate senior brat who's doing their family member a favor by "allowing" them to serve them. Basic respect in that you don't "lash out" at the one who does for you because you want to hurt someone, or are in the mood to fight, or just want to complain and bring somebody down.
This is really what most caregivers really want. Not gratitude, not praise and gifts. Just basic respect from their "loved one".
By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington.
Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services.
APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid.
We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour.
APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment.
You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints.
Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights.
APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.
I agree that:
A.
I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information").
B.
APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink.
C.
APFM may send all communications to me electronically via e-mail or by access to an APFM web site.
D.
If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records.
E.
This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year.
F.
You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
You DO NOT "kinda just have to suck it up. Be Happy for your mom." Don't buy into that nonsense at all! There are always alternatives to giving hands-on/in home care for an elder, so I suggest you look into it before YOUR health suffers from stress and burn out. Give YOURSELF the gifts nobody else is giving you, that you deserve too. Hire in home care with mom/dad's money, or explore placement with Medicaid if finances are an issue.
Best of luck to you.
I’m not a hand’s on caregiver for my mom because A) literally impossible B) it would kill me. But I have done everything else, still do, and have a philosophy that POA stands for, ‘Person of Aggravation’. Meaning, once you’re POA you have a big target on your back for complaints, unwanted opinions, and all manner of aggravating requests from the LO and everyone else who has NO CLUE what your experience is like.
I’ve delegated as much as I can, and play music, pet dogs, whatever, to alleviate feelings and have a life. As a Person Of Aggravation, I also get my own aggravation out on a full size martial arts bag I’ve nicknamed, The Therapist. My ‘Therapist’ keeps my feelings a secret, plus the more I see this therapist the better shape I get into, so I totally recommend this kind of therapy if your joints can take it.
Best to you!
One of them accused me of not taking my father to a parade. I'd never heard of the parade before that moment and when I told my father to talk to the guy, he got pissed off at me.
One of them accused me of not putting my father in a senior living center. My father wouldn't go and I couldn't force him.
The last one probably didn't care for his father for more than 15 minutes but decided I was a poor caregiver.
My father is loved, I'm hated, literally, my family won't talk to me. My aunt called me to ask where to toss my body when I died and that's been our only communication in months. I had really bad thrush, couldn't eat, lost 20 pounds, no one cared even a little bit in my family. In fact, I was being chewed out over something that literally didn't matter.
I'd tell you to not do this job. If I could go back in time, I'd have walked away and left my father and his shitty relatives behind and never have looked back. I have literally not received one iota of compassion from my extended family.
I'm so sorry for what you're going through. It's terrible and the way you describe how your family treats you, absolutely disgusting.
I would tell such a family to stick it where the sun don't shine and cut them out of my life.
You with a cancer diagnosis have to be the top priority in your own life. Screw your family. Any family that would behave as you say yours does does not deserve your love, time or respect.
Honestly being a hands on caregiver is not a good experience, there are no benefits.
Me, I would never do it, I have 2 in a facility, one on AL the other in MC. I am not willing to give up my life, my mental well-being for another, makes zero sense to me.
There are other ways to handle this, like placing your parent. Because he doesn't want to go is his choice, as long as he is mentally competent to make this decision. As long as you keep him propped up he will always think he is independent.
You do not have to care for him. That is your choice, so with that, there is an acceptance level as no matter what you do, you will be criticized.
Might be time to reassess the entire arrangement.
When you do it for a living like I did for 25 years, it's usually just as bad. Clients and their families more often than not think that the caregiver is a slave who works for the whole family that they can treat anyway they like.
I'm in the business end of homecare now and my long experience is useful in this business. I will tell you this truth, my friend. I would rather make my living walking the streets than work at hands-on caregiving again.
You have a choice though. If the resentment is setting in, you can choose to walk away from it and you should.
It may help us to get a picture of your situation if you fill out your profile and/or tell us a bit about your parent, his or her diagnosis and prognosis, whether you live with said parent in his/her home, or he/she lives with you.
On the face of it, and with so little information from you I will only say that when we move from being a son/daughter/sister/brother to being a CAREGIVER we have voluntarily given up the former positions for the latter. We become "caregivers". The responsible ones. The ones who make the decision and the rules and are resented for said rules and decisions. This just naturally happens.
If you have decided that caregiving isn't for you, then slowly you will have to disintangle yourself from it with honesty, and with, undoubtedly, no little trouble.
You are an adult and took this on. Now it doesn't suit, and when that is the case it is time to reclaim your own life.
I wish you well, and hope you will tell us more about your situation.
Or just a thankyou now & then?
Start with your parent. Hand his/her a cup of tea & if no thankyou, say 'Thankyou Roger' yourself - outloud.
Sometimes you get taken for granted but a little prompt is all you need. To retrain. Even if they cannot speak, a kind look means the same.
Or is it other family, other people you would like a thankyou from? To be acknowledged & appreciated.
I think most caregivers don't care if they're being thanked for something or getting flowers and hugs as shows of gratitude.
I think what a family caregiver wants most from the family member they take care of is just basic respect. Also time off from that person is important.
(When I say 'you' in the following comments I do not literally mean you as in yourself)
Basic respect as in not treating that person like they are worthless garbage with nothing postive to contribute to human society.
Basic respect as in not making up lies about the family caregiver who literally wipes your a$$ and works like a slave day in and day out so you can "age in place". Also, not villifying them to others because you're bored and want more attention.
Basic respect in that you do not behave like an entitled, ingrate senior brat who's doing their family member a favor by "allowing" them to serve them.
Basic respect in that you don't "lash out" at the one who does for you because you want to hurt someone, or are in the mood to fight, or just want to complain and bring somebody down.
This is really what most caregivers really want. Not gratitude, not praise and gifts. Just basic respect from their "loved one".