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Fyi after I typed my second response, I developed a fever and then got sicker than I ever have in my entire life. No cough and got tested for covid. Even if it’s negative I’ll have my suspicions because this illness has been above and beyond anything I’ve ever had. On a slow mend now which means my goal today is a shower! BF has been taking care of me, lovely man.
I love surfing and cardio kickboxing and hiking, and go bananas if I don’t get outside. Getting back to playing trombone, fiddling with ukelele, and I do large scale chalk art and started making pastel paintings and taking online classes. Big crazy mutt and big cat at home too. Plenty of lovely things to do ( though chalk art was cancelled due to covid or smoke outside ) I want to have the peace of mind to do these things again!
What’s surprised me is, my mom is in a retirement community w/graduated care, I thought I had good boundaries, and certainly get/got enough exercise. I have a second simple phone with a number mom will never have, I keep the other one on silent most of the time. Maybe it’s the sheer length of time - years - of this constant grinding mom stress ...the tasks...the calls...being the ‘only one’...just the never ending ness of this high maintenance woman ...then throw in some wildfire drama and a medical emergency and voila! I’m cooked.
Thank you everyone for your wise words. My mom has some great qualities ( truly! ) but she is so relentless she eats people alive. If she was an absolute narcissist it’d be easier for me to deal with in some ways because I’d have no problem stepping waaaaay away. ( Have one in my family and I just totally avoid her )
Maybe I needed to hear from others it’s okay to step back further, not ‘be there’ for her every day and that doesn’t make me a terrible person. That’s the kind of thing I don’t hear from other family members or her care team.
I’m sorry you guys have gone through the same/similar experience, but thank you so much for sharing your stories. It makes me feel less alone in this reaction. Speaking of, the ‘cuckoo’ stands for something I was asked to write as a play some years ago, so it’s not a bad word :)
Excuse the long reply but your responses have been really dear! Plus rambling ...I am a bit loopy right now. Do not get covid or whatever this beast illness is!
Lastly I’ve sent a Hail Mary to the geriatric care manager and will take a hit to my savings, but she is helping co-ordinate the move. Still a lot to do but clearly I have to get well and that means stepping back from mom. Bless you all!
I also have IBS and although I work very hard to keep it under control, when I am stressed it flares up too.
I have mentioned in various posts being triggered by what may appear to others to be inconsequential things, but when a person has lived through trauma, it can be a simple thing that brings it all back.
As I said I now have very firm boundaries in place. I also have regular check ins with my therapist to keep me on an even keel.
My parents divorced 30+ years ago. I have gone no contact with both of them at various times in order to protect myself from their NP behaviours.
Madison, you are allowed to hang up on your Mum if she makes cruel comments. There is no law on the books that we have to continue to listen to their abuse. When she is cruel, you can restrict contact until you are ready to deal with her again
You also are allowed to block her phone number and tell the MC that you are not taking her calls for the next period of time. If there is an emergency they will have to handle it.
I won't go into detail, but years of CG for older relatives, friends, and mostly my DH has left me with hyper sensitivity to stress. I had cancer last year and the TX took me to my knees, emotionally. People kept telling me how strong I was. To only the few people close to me did I disclose that I was really almost suicidal--and wished I did not opt for TX. (I would have died within 6-9 months). I did do the full TX and achieved remission in time to get the shingles, then got through 6 weeks of that to have COVID roll in. (I have not gotten it, but it really does cut into our lives)
Panic attacks became the norm, and I was already dealing with those for years and years. I started having 2-4 hour panic attacks where my heart would pound and race at about 250 BPM. Horrifying and actually painful. I just thought 'great, one more thing to deal with' but I did bring it up to my PCP in a virtual visit. He had me do a 3 day heart monitor test--turns out I was throwing 'episodes' with my heart almost all day long, only the bad ones were making me miserable.
I'm on a beta blocker and it has helped. I have had to be a LOT tougher about DH's desire to argue politics all day--having him home is awful but I don't have a choice. I'm doing a follow up TX which makes me so tired and depressed. Yet, I have panic attacks all the time. They're better--and I know that once COVID is 'better' and DH can go back to work, things will be better.
My Dr. said my body/mind was simply overwhelmed with 'bad stuff'. A lot of family problems, which I will not go into--but I am trying to step away and not be involved any more.
Your body will have a limit. We all have one. Some people are amazingly calm and collected all the time. I used to be...years ago. But life happened--if I listed all the health issues my DH has been through and all the stuff with raising 5 kids--I am amazed I am still standing.
GET TO YOUR PCP and get something for the panic attacks. They are not to be left w/o treatment. List the issues in your life and try to cut out as many of the negative triggering ones as best you can.
I no longer speak to my MIL and I never will again. People think I'm horrible, but I just couldn't deal with her. I also don't see my own mother often and that's the way it has to be. I also leave the house if DH is home and working, which is very stressful--our home is small and he is loud. One of our kids has no spoken to me for 6 months--and doesn't respond to texts or calls. That hurts.
But you have to take care of you and I have to take care of me. I'd love for my DH to care for me, but he can't and won't. I am learning to not expect him for anything.
Good Luck. Don't ignore the PA's--they are legitimately awful and a good sign things aren't OK.
((Hugs))
That said. Are you POA? It seems you must be. They cannot force you to find a place in that short time. They have nowhere to discharge her to. Are there any organizations/businesses like A Place For Mom that can help you search memory care? The worst they can do is send her to hospital if she cannot safely be handled there, and then get the Social Worker there on it.
UTI recovery is tough. Keep on that. Ask for some mild anti anxiety med; talk with your doctor about all this right now. Remember Panic Attacks are giving us a message. It is fight or flight, and with us unable to get anywhere with any of that the body just paralyzes with fear and anxiety. Be easy on yourself. More people get panic attacks than you can even begin to imagine.
So sorry you are going through this. Remember, a day at a time. They cannot discharge her to your home and must make a safe discharge. Remember to take deep breathes often. Practice breathing in to slow count of 3, and out to count of four. Just the counting of it helps, as well as the breathing.
As to the answer to your question of the have we had the breakdown. Oh YES! And many years ago, not over parents, but over abusive husband. I am 78. I was about 22 at the time. Will never forget it. Talk about an out of body experience. Brief, and never had another, but it was the trip of a lifetime.
Madison, first I would mentally eliminate the "cuckoo" in your screenname, if only in your mind. I don't disagree that mental challenges present themselves to someone in your situation, but accepting them works against getting past them.
Personally, I think caregiving at any level affects someone, with varying degrees depending on the individuals, extent and length of care, and especially lack of support. I also think getting through and then past this was probably the biggest challenge of my life. I'm still working on it.
I know that time is scarce, but we do have to find some way to relax, redirect, and find resources to cope. Perhaps the hardest aspect is recognizing when boundaries need to be set, and doing so. Sometimes just explaining that you can't continue to provide support as you have been doing w/o some relief, and that works both ways, so you both need to find ways in which the arrangement can work is less stressful.
Sounds easy in writing, doesn't it? We know though that it's not. It's challenging; we feel guilty; our parents, perhaps in a panic we can't even begin to comprehend, feel abandoned. In some ways it's a negotiation. I approached it that way, and it helped me.
I also listened to music, a lot, wandered through my garden and sometimes at a local park, crafted or designed crafts that I didn't have time to make...I found that creative ideas sparked an otherwise dormant coping mechanism and helped me plan, more positively.
Perhaps all the good advice others have and will offer can help you realize you're not alone; I'm sure that many people face similar situations but don't share it. And many are fortunate to have family who help.
This is a challenge, and you will be stronger for it once you're able to begin putting distance between it and your life now and in the future. Yes, that's easier said than done, but it can be done. Each of us has to find the method that helps guide us through.
The "overwhelming" issue needs to be specially addressed. Prioritizing helps, making charts and lists helps, but they need to incorporate down time, even if it's only 5 minutes every hour.
What were your hobbies and pleasures before caregiving started? How can you now resurrect them, again, even if only in a planning stage, or for a few moments a day?
I always kept gardening magazines in my tote bags and relied on them heavily when sitting in the ER or hospital room. I also took a notepad and made sketches of different garden configurations, or just plans for the next season. The distraction helped immensely, especially while waiting for diagnoses.
Help us help you by telling us of your life before caregiving. What did you do? Were you working, involved in volunteer work? What hobbies did you have? Spent some time thinking about them and sharing them with us; I think it will really help.
Something else that helped me is keeping track of decisions and factors affecting them, what alternatives existed, how my parent and I handled them, and especially those that were successful. I can translate some of them into lessons learned for the rest of my life.
I also agree having "cuckoo" in her screenname just produces a disparaging thought against herself even if it's in the subconscious. We somehow need to become our own best allies in order to move forward productively. We get beat up enough through caregiving that we needn't do it to ourselves.
My counselor has helped me recognize what I need to do each day to stay healthy. For example sleep x hours, drink water and eat, pray, clear space/clean something, be creative, be in nature, and move my body. A big factor for me is sleep. What you are experiencing is normal, but not healthy. I hope you can make changes to avoid burn out.
Being outside helps too. Nature is so soothing.
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