It is slowly becoming a reality that my mother will need some care at home. This is a concern because she is digging her heels in and stating that if she needs 24 hr care at home, she wants to remain in the home with round the clock care. She has some money, but paying for full time care will quickly deplete her funds.
I am not able to do any of her physical care due to health problems. I am able to take her to the doctor now and also do her grocery shopping.
What is the reality of round the clock care? Has anyone ever done this?
Hope you have control over how the caregiver's work is done. Not down to how to release the tape on the diaper, but what hours will she work, what duties will she perform, what products will she use, what activities and how they are done will most please mom.
Would you let this person into mom's house without training her or telling her what her responsibilities are? I doubt it. Would you have them bring the tools, diapers, etc used for the care? Or does mom and you prefer a specific brand? Caregivers are employees unless they work for an agency.
I was my mom's caregiver for four years and paid as an employee a minimal amount. All taxes withheld, Medicare paid, workmen's comp and all. It was legal according to the IRS, Department of Labor, multiple attorneys, a CPA and a geriatric care manager as well as a conservator.
A request for the future. It's easier to follow if we keep these posts all in the subthread discussing this topic. Top level posts for each response pollutes the main thread. Not everyone is interested in this so it's just noise they have to ignore.
I was using Visiting Angels 3 days a week, 3 hours day before this and then used them for 24 hour care. That cost about $13,000 a month. Two ladies alternated weeks. They did a good job, but I wanted something not so costly. I had found a memory care apartment for them in an assisted living facility and convinced the husband it was time to make the move in order to save money. The memory care apartment would be around $10,000 a month. The care there was excellent and the staff nurse guided me through her decline until hospice was necessary. They assured me they would never have to leave as they provide care to the very end. After 18 months of regular payment, if they ran out of money, the facility would accept whatever public financing was available. The husband has now been there over 5 years and we haven't run out of money yet. The wife only lasted another 5 months before passing away. The day of the move another friend came and took them out to breakfast in a nearby town, then to have their nails done. In the meantime, the movers and I were setting up their new apartment and made it look just like it was in their home--the same furniture arranged the same way, same pictures on the walls, etc. When they got there, the husband saw his favorite recliner and sat down with a sigh of relief and has been happy ever since. Only once has he expressed a desire to leave and that was in frustration in not being able to talk to anyone at meals because of how far they had declined. Since then, new people have come and he sits with them at every meal and they can talk to each other. They probably say the same things every meal, but that's o.k. He sees a doctor once a month to check his blood pressure, etc. I see the bills and drugs being used and if I see a change, I ask the staff nurse about it so I can keep up with things. I was so grateful for the help with his wife and the guidance I was being given as she declined since I had never done anything like this before. And as a bonus, the man who was in charge of leasing these apartments wanted to know why I was doing this for people who weren't even my relatives. I told him the story about how I met them 40 some years previously and how we quickly became friends and how when I had to change jobs, I ended up working in the same school as my friend, not knowing she was there when I was hired. We became closer friends as couples--worshipping together, vacationing together, etc. This man, JJ, and I became friends over the 2 1/2 years it took to get them to move in and left shortly after that to help care for his own father.
His wife encouraged him to get his real estate license and he did. It took me another 2 1/2 years to empty out their home and get it ready to sell and JJ became my realtor, giving me advice on how to prepare, what to fix, and guided me through the paperwork until the sale was complete. What a service! I am so thankful for the guidance and help I have received in taking on this responsibility. The sale of the town home provided another 2+ years of memory care costs, too.
Having the authority to make these decisions was key. Then finding the right place was a wonderful answer for their dilemma. The husband remains in good health--doesn't even need glasses at age 92--but the short term memory issues are worse than ever. But, the staff is there to guide him, give him his meds at the right time, etc. He is intelligent, too, just can't remember short term. We joke about being brothers of another color, as he is black and I am Swedish white. But that is the role I play--a brother.
I went into carry for my mom thinking it was temporary, her needs would change an someone else would be needed to take over, but there was only me. At 49, my son raised, and on his way, now I’m going to lose out on my life !
She passed, reflections of 17 yrs of everyday care, surprised and gladdened. I became life to someone loosing theirs.
it intensified any Love I understood, it made my faith stronger and clearer. I saw around me friends and family that despaired. The rewards of true love never cease.
if you can find love ones to pass around to help, encourage them, even after many complaints, the good ones grow.
when as a child I was lost, it was because I didn’t look close enough. In caring for someone it’s needed almost daily.
The physical part, lifting if needed, has remedies. Doctors, shopping, cooking, all important, but time spent with little conveniences and comfort rule the day.
Sounds like you really love your mom, your questioning Her needs and trying to resolve her worries. our relationships an needs change over time. Not what we usually thought.
This is probably one of the most feared times in life on both sides. But what better Love could you give a parent, even if you thought you were cheated. All the more reason to give.
now, I wouldn’t have changed things much. I feel and sense I could of done more, loss brings that guilt out. But then you'll realize it may have been the best thing for you both.
I learned to see the blind world she was falling into, I learned I’m more capable than thought. There is no “been their done that” examples, like Gods mercies, new everyday.
if you commit, you’ll carry a truth, few know, and a love even fewer will ever experience. Keep your sense of humor, oh there’s nasty stuff, but it’s the easiest to forget.
I put you in good thoughts, I think you know your choice.
I used this site over many of those years, not always for my issues, but in reading what others were struggling with too, the courage of love really conquers.
My only family was my sister, she’s spent the last 26 years
quadriplegic with MS. Trying to keep her close in with all of this was profound. Her mind has since slipped away.
Life. What do we know ? If we all looked at our heart first before we let our minds interfere. We’d see better.
Ive been caring for her for over 7 yrs now and it has not been an easy road. I’ve done my best, but it has gotten the better of me a few times. I can’t afford anymore stress.
I pray God is good to us both. This is what I can do now. Pray for the best. But at least I have more answers now than when I started worrying about her demands. I wish I wasn’t in the position to have to make these decisions, but my parents never took steps to take care of their needs when they reached their elder years. When my mother became dependent (with macular degeneration), both my sisters were still alive. I always thought they could help me. But they have both passed away during these 7 years and now it’s just me. Mom is 93 now. And she has heart failure and invasive skin cancer that is causing many problems.
Thanks you for your reply. I just say a lot of prayers for help. For her and for me. Xxoo
https://www.thebalance.com/household-employment-taxes-3192937?_ga=2.73734674.1096113486.1550540248-2092615929.1549630136
If you want to know more information about how to legally claim a caregiver as an employee, the Care.com site makes it really easy!
Nanny/Private Duty Nurse Tax by state: https://www.care.com/homepay/resource-center/requirements-by-state
Things to get filled out before you hire a caregiver:
1. I-9
2. Federal W-4
3. State W-4
(https://www.care.com/homepay/w-4-forms-for-nannies-and-caregivers-1304191931)
4. You will need to apply for an EIN number as well because you are an employer.
Hope this helps someone besides me!
I can now sleep at night, go out and not have to worry. I consider them part of our care team and not employees.
it is the best thing I ever did but it is expensive and no financial help is available.
Ifyou can afford it , by all means , do it.
It took a while to get over the intrusion of a third person in the home but is working out fine.
Why did you choose this over assisted living? Just wondering...
Hope you find the right person. Otherwise it could become a nightmare.
Saying that I deserve my retirement, I have worked hard all of my life, or that I am old and ill and deserve to be taken care of, might be true, but not when it becomes such a burden to society that people in their productive years are being punished – as well as their children.
You know it and I know it; sometime in the near future the load will get too great, medicine will not justify the cost, and countries around the world will have to consider a humane way of taking care of us – the problem.
Until that happens people like me will have to wait around till our cells wear out, we get one of the big three, and cause so much cost and effort to be wasted on us.
As John Wayne used to say “That’ll be the day!”.
I have two live in caretakers, one four days and the other three days. They take care of him so I can do housework, shop, cook, go out etc.
It is expensive but well worth it. My stress level is low now that I don’t have to be by his side every minute and get up at night with him.
If you can afford it, by all means do it...just check references. Insist on good hygiene for both caretaker and your loved one . Stress honesty and consider them a team member and not a worker.
Thank you all for your responses. All so informative!
Be kind to yourself during this time.