I have been taking care of Mom in her small 1 bedroom condo in Florida for the last three and a half years. I have my own place in New York where my children still reside and I miss them dearly. My mom can no longer travel with me as she used to.
Her dementia has become pretty severe she's losing control of her bladder and bowels she will yell and not make any sense she needs to be coaxed to eat and have her food cut up. I am seriously at the my end of my rope . I desperately need to go home for a few weeks to take care of my place and be around my two children they are grown but they are my everything.
My question is do I need a doctor's referral to find a place for her for a few weeks as I can get some much much much needed change of scenery. Even if she was able to travel our last trip in May of 2018 for two weeks ended up to be a catastrophe. It was more work for me than it was worth. Mom is 84 and has been diagnosed with dementia in the last 5 years. I am 64 and I am currently on disability for severe arthritis and I have since put on 20 lb which is insane considering I can barely walk. As it is I'm just rambling on because I need someone to speak with desperately when I speak with my children about this they tell me it's time for her to go into a nursing home that breaks my heart but I feel like I am dying here everyday is the same there is no life for me here except cooking and cleaning up after her. It feels like I have a set of twin toddlers but they're not growing and learning things it's the reverse and it's very exhausting.
I already mourned my mother about two years ago when she became unable to complete a sentence or understand a simple request. I'm starting to become resentful because I feel like I'm taking care of a total stranger and there's no hope for recovery. Perhaps my children are right and I should look into putting her into some kind of memory care facility. Please excuse my rambling I just needed to vent. These last two weeks have been extremely difficult and I find myself crying everyday. I fear that I may be falling into a depression. Even while I'm asleep I'm jolted awake by hearing her scream and yell and when I check on her she's sleeping so she's entering my dreams.
And don't bother to suggest that I request family members to assist BECAUSE THEY DON'T. My children will come down here every few months and give me much needed relief from the unbearable redundant monotony. Just writing this I realize I need to go see a therapist soon but that would entail finding someone to come in to watch her once or twice a week for a few hours I also need to start attending Weight Watchers. I don't like how I have become emotionally and physically . Thanks for listening
Just a thought. I’m going to try it for my mom.
SNAP, YOU GO GIRL!
You are one of many of us who have siblings who just don't give a rat's butt when it comes the time in their/our lives to take CARE OF OUR PARENTS! My husband and I had to place my Mother/step-father in an assisted living group home because my older sister moved out of Mom's house after 10 yrs living scott free, didn't tell anyone.
Long story short, EVERYTHING was dumped in my lap (Same sister convinced the others I was the Witch of the West and cut me off). I dropped everything and drove back home to find the bills were once again so delinquent the City was ready to place a lien on Mom's house and turn off services! It took me A MONTH to get the bills up to date. THEN step-siblings learned that Daddy wasn't getting anything should Mom pass first because the State is Community property! They, especially the oldest, feel that Daddy should get everything i.e. the house which is Mom's sole/separate should this happen. I just had to have the house furnishing inventoried as well as hers/his/theirs. It was funny when the appraisers said it'd be easier to go thru the house and just tell them what is his, what is community🤣🤣. The oldest step-sister "stole" $40.000 from Mom's checking by having Daddy (authorized signer) write out an internal bank debit/deposit in the joint acct she opened with Daddy. THEN she made on-line transfer (she did not have any legal right to have access) $8.800, deposit to said joint acct so the check she sent to pay the 1st month "rent" 4 our parents to show she paid from Daddy's funds. I opened a POA account for Mom and paid the non refundable deposit from that acct so I told her that she would pay from the money she took. DO NOT MESS WITH A FORMER BANKER WHO HAD TO DO RESEARCH FOR CUSTOMERS REGARDING ACCT THEFT ETC.
She/her attorney petitioned the Court to be considered an interested party when I had my hearing to be appointed Mom's guardian/conservator, she isn't according to the Law, I objected so the Judge told her (telecommed) she couldn't say ANYTHING no matter what is said. He asked me about the $$$, I explained EVERYTHING and how anybody with 1/2 a brain could read a statement and find a lot of stuff from that. She also feels that since nothing will be Daddy's then he doesn't owe anything on the bills, COMMUNITY LAW SWEETIE! He is responsible for 50% for everything during the marriage. I took her/attorney/appointed Fiduciary/Judge to school. I was appointed, her attorney wanted her to be able to use her Durable POA....Judge told both that her POA MEANS NOTHING, I HAVE ALL THE POWER! She'd planned to take Daddy back to MI to live...NOPE she and the others HAVE TO GET MY PERMISSION FOR ANYTHING/EVERYTHING!
STICK TO YOUR GUNS, YES FIND A THERAPIST (I've had 1 for 7 yrs because of my siblings treatment with Mom). Get help from everyone you can. Medicare/Medicaid should help with respite, need a vaca place her in a rehab for a week (this is done all of the time). Keep track of all your expenses, you're acting as guardian/conservator and you are allowed to charge a fee or recover the $$ once Mom passes. Don't tell your siblings because the shock for them will be priceless! Conservator is paid 1st just like in a BK, and you still get your portion of whatever Mom leaves to you. That is going to cut into what they think they're getting. You can claim your rent for your apt, plan tickets; you HAVE TO KEEP ALL RECEIPTS WITH A RECORD KEEPING SYSTEM/EXPLANATION. I have an excel spreadsheet that is EXTREMELY detailed as well as the $$ owed for community debt and EVERY PENNY "she" used or took from Mom's account. My attorney is preparing for that case, I'll be there if I can because she'll have to be present in Court in AZ🤗🤗 FRAUD BEACH! She'll also have to pay my atty's fees/court costs.🤑🤑🤑
As far as the respite referral, I don't know, but I would start with asking the dr. office and get a few answers from different sources.
Good luck to you and your parent!
P.S. I was under the impression Medicaid had a 5 year look back?
I am 72 years old and I speak from experience of what you are going through. My answer is simple.
1) Listen to your own heart. You raised your children well be close to them, relocate to where they are to bring JOY to their lives.
2) Move your mom with you or to a care facility where you will be living. Florida has served its PURPOSE it is time to move ON to where your HEART wants to go.
Emi
HOWEVER .. You should listen to your kids - this is your cry for help & we all have been there is some way or another - when she is invading your dreams then your own subconcious is telling you that now is the time
On top of that I very highly recommend that you bring her to near your home - don't listen about the weather being nicer in Fla. because unless she goes outside often then she could be anywhere - the NH is always the same temperature inside year round - my mom is now 4 minutes away [used to be 40 min] & that is fantastic - I see her more often but for shorter time periods as her dementia is also severe
If you found somewhere close enough to walk on nice days that would get your exercise upped too & kill 2 birds with 1 stone - when you visit often & at different times of the day then they don't know when/if you will come so she will be optimized all the time -
Time to take back your life for you & it sounds like she needs more help than you can do physically anymore - congrats for your effort but it looks like it is time for the professionals to come on board
The doctor can also help with suggestions for places more capable to handle your Mother's particular issues
1. Is she wheelchair bound
2. Bed bound
3. Nursing home v assisted living group home
She will need to be tested both physically and mentally to help determine the type of care she needs.
You will need this also to provide to Medicare/Medicaid or any other extended insurance benefits she may have.
I am so sorry for what you are going through. It does sound like you need a break. My expérience is that you do NOT need a referral from a doctor. But, if you want her care to continue with her current doctor you may want to ask him/her which nursing homes he/she actually visits. I was lucky to get a referral from my mother's MD. And, for the most part, I did find that he visited reasonably regularly. He had other patients in the same facility.
When you place someone in a nursing home - even for respite care - they will require a lot of information. My expérience is that they also required payment in full for the respite stay. My situation was different than yours because I lived in the same city as my parents. Therefore, I was able to visit daily. This could be a good opportunity for you to "try out" nursing home care.
I guess my advice to you is to discuss your concerns with your mom's MD. I find that doctors who care for geriatric patients do have some valuable insights. I always looked for nursing homes that were near major hospitals so that I knew where my mother would be taken in the event of an emergency.
One thought occurs to me. If you would be happier to return home on a permanent basis, have you considered moving your mother near your home. I did find that my parents "did not know where they were anymore" after a period of time.
I have been through all of the things that you described. Understand, that the burden always seems to fall on the shoulders of one family member. The others can manufacture all kinds of excuses for why they can't do more. My parents have both passed and now I am left with many feelings of ressentment towards my brother and his children who rarely managed to visit my mother. I am trying very hard to forgive this because it is not healthy, it does not accomplish anything, and it is not what my faith teaches me to do. My mother has been gone for over a year, and I still have dreams of her calling me for help. I still remember her facial expressions when she was in pain and when she was angry because I could not help her.
You have been good and dévoted to your mother. Acknowledge that you need and deserve help. Reach out to others who may be able to provide you with good information. That will give you some peace of mind. I know that you are exhausted. Find the help that you need as soon as you can. You will be able to make better long - term décisions after you get a little rest.
Many of us have been where you are and understand how difficult it is. I hope my words have been helpful.
Is your mother on HomeHealthCare? If so, they can arranged for respite care for you.
As for respite care, you don't need a doctor's approval but the site you use may request medical information such as last physical, flu shot and other details.
Each center is different. PLEASE pick a site with a memory center. Memory Center patients are kept in a separated, and locked area. They eat together and easily managed when they are together. They may ask if you the room locked or unlocked. MAKE IT LOCKED. Too often patients float from room to room and just make themselves at home.
Don't take anything of value for them and don't take any original pictures or identification(color copies are fine for most areas).
As much as would like to dress them in clothes they like please don't. Buy sweat pants. They are easier to take off and put on.
Buy plastic gloves, and body wipes. Don't fill a new prescription prior to entering them into respite care. Many sites will not take the bottle. They have back deals with a local pharmacy to package the medication in a sheet(be prepared to pay for it and to take it home with you).
Be prepared to have your loved not showered everyday. Most respite care centers for dementia have a schedule for showering. Your loved one may shower twice or three times a week.
Also be aware of any suggested medication the site may offer. If your loved one is too much of a hassle, they may suggest a medication to "calm" them down. They may have even give it to them without your consent and call you later just to report an issue and slide in they are giving them an additional medication.
Please know you are not alone.
But if you are placing her in a facility, rather than having someone come in to care for her I am sure you will also need a note from the doctor that she is in good health as well as current prescription medications. And you will need them in the original prescription bottles with current refill info. You will also need a TB skin test (unless she has tested positive in the past)
May I also suggest that while she is in respite that you choose a place that she will transition to. She may do very well and you need your life back. I am sure if you two spoke about this 30 years ago she probably would not have wanted you to give up your life, your family to care for her.
We don't know where you are in Florida. But the Council on Aging locally can advise you on your options and also provide referrals. At least they do here in Indiana.
Try contacting them. https://fcoa.org/Resources
I agree that you should look in your home state as well.
It is time to get back your life while you still can.
https://medicare.com/coverage/does-medicare-cover-nursing-home-care/
Medicare Part A covers the hospitalization; Medicare Part B does not pay for custodial care (feeding, bathing, toileting, etc).
If you get her on hospice, which needs a doctor's order, you can have 5 days of respite care (or whatever the facility dictates).
IF she is on MEDICAID -- you can put her in a nursing home and it sounds like you need to do that permanently since you have health issues yourself and caregiving gets much, much worse as she ages. See her doctor to get that order. If she is not on Medicaid see your eldercare attorney about getting her Medicaid prepared.
You’re on disability, you can barely walk, you’ve been uprooted from your home, you miss your children, you get no help or support, your mother can no longer interact with you AND you’re a full time caretaker of a virtual stranger!
If you were not depressed it would indicate to me that you’re just a machine, which you are not. You need something positive in your life to keep going because you are HUMAN! You have needs of you’re own and the top of the list is some kind of JOY to counter the burden of your life.
I cant answer your question but I say do everything in your power to make a change before your own body breaks down more than just gaining weight!
i can already tell you have symptoms of ptsd hearing her cry out when she’s sleeping.
If now is not the time to move her to a care home when will it be? It sounds as if she doesn’t even recognize you. Why are you killing yourself? Is this what she would’ve wanted when she was clearheaded? For you to sacrifice yourself while she is practically in vegetative state?
i wonder if it would be easier for you to place her in your home state so you can have easier access to her.
just wondering, because I have no experience here except for being a full time caretaker and my mom is fully cognitive and can still do a lot for herself. As a matter of fact, that is what I require of her as I have had no medical or geriatric training and I only have the strength of a gnat so I won’t be much help when she becomes incapacitated. Actually, I can’t even get her to do anything without a struggle. Not motivated by me at all.
Thats my world and I complain. Can you believe it? My life must sound like a dream to you. Go get yours back...RUN!
Good luck!
Charlotte
Have doc test for TB, it is required by law prior to entering a facility even if on a temporary basis.
XO XO XO
Went thru the EXACT SAME THING 9mo ago! Dad's Lewy Body dementia was EXHAUSTING!!!
It got so bad that at one time I was walking w/ my Boyfriend in the winter when dad had fallen asleep for 20mins and I asked him "Am I still alive or is this a nightmare?"
The toddler analogy you refereed to is spot on ~ It NEVER EVER EVER stopped.
I couldn't turn my back on him w/o something horrible happening.
I did finally put him in respite for me to get some rest and he passed away the second day. I knew I was just keeping him alive from hour to hour towards the end ~ And I have a disability also ~ Amputee from cancer ~ so it was EXHAUSTING!!! So I can relate.
Do yourself a kindness and put her in care where they are trained and have the manpower to help w/ this phase of her life. I waited way too long.
Besides that ~ The memories of his last months still haunt me daily ~
I should've,
Why didn't I,
Maybe if I could've ~~~
You're gonna be ok ~ Much love J
Don’t let your mother’s decline in health break your own heart. You have already mourned this, so you need to accept the reality and its consequences. Your mother definitely needs more care than you can reasonable provide, from what you say. You need to know that she is safe, and you need your own life back. There are lots of posts on this site about ‘promises’ that I will never let you go into a nursing home, will care for you forever, etc, and how they simply cannot bind you forever when circumstances change. Any more than marriage vows bind you forever when things go seriously pear shaped. Start looking for a good nursing home.
Go Home! Use the air fares to visit your mother as often as you can, and get your own life back!
I am more worried about you at this point than I am your mom. You sound like you are at the breaking point and you need to do something NOW!
I remember feeling that way when I could no longer take it. I have lost hair from stress, gotten diverticulitis, insomnia, and felt like I was mentally cracking. If she didn't leave when she did, I don't know what my body would have done next.
Can she get to her doctor? I'm sure you'll get a referral.
If worst comes to worst, drop her at the Emergency Room and say she lives alone but you have been coming in to care for her. Tell them you need to go back home and there is no one is no one else to care for her. They will apply for emergency placement and start the application process for Medicaid.
Like Popeye said, "It's all I can stands and I can't stands no more."
Definitely seek therapy for yourself when you get back home. This doesn't go away over night.