Dr Jekyll Mr Hyde

EverreadyCyn

New member
Feb 6, 2024
1
0
Hello. I am new here and this is my first post. I am somewhat reluctant to share my thoughts, feelings and experiences and would much rather read others experiences, but in all fairness, I will share, rather than observe. My Mum was recently diagnosed with vascular dementia, she is 86, living on her own, widowed for 10 years. (Dad had Alzheimer’s and Mum put him in a care facility within the 1st year of his disease as it “wasn’t something she signed up for”)

I am an only child and she has been co-dependent on me for my entire life. We have been close, probably too close in hindsight. Her dementia has been evident for at least the last 3 years but had progressed rapidly in the last 6 months. Short term memory non-existent. She has a split personality with her dementia which rears its ugly head every 4 days or so and she becomes Mr Hyde! Aggressive, violent, angry, paranoid, says vile and cruel things. She gets on the phone and calls neighbours and friends about her paranoia (the paranoia is always about me, and how I am “out to get her”, “trying to steal her money or her house, or she dreamed my husband was trying to kill her, etc etc). During these episodes, she writes it all down so she can remember the next day. I go to where she has it written and remove the pages from her little book. Then alas, the next day, or at times, the next 2 hours, she is back to being kind, loving and sweet and telephones me to ask “how was your day honey?”

Needless to say, I am exhausted, emotionally. This has caused me, most recently, to develop an ulcerated stomach which is very painful to say the least. I won’t even mention what it is doing to my family life, my marriage, even visiting my treasured grandchildren.

I see her every single day to bring meals, do her morning and evening meds, pay her bills etc., groceries, household items, social interactions and then come home to do the same in my own home….and of course SMILE! We wouldn’t want too much negativity now would we? Grrrrrrr.

I am the Every Ready Battery whose batteries are beginning a slow death right before my very eyes. I care so deeply, and yet I am worn to the bone.

How does one separate themselves emotionally to recharge without someone having to suffer for it? “No”, in-home care for her is not an option as she refuses and home support is aware of her personality switches and they will not enter a home if the patient has aggressive tendencies. “No”, a care facility is not an option as she refuses.

Yikes! It’s a proverbial emotional rollercoaster of emotions and I fear she will easily outlive me as the stress is monumental and wreaking havoc on my health.

My apologies as this was more of a rant rather than a question! PS. She drinks her “happy hour” in large quantities each day foregoing the nutritious meals I bring. I generally toss them out after a day or two as they go untouched in her fridge. Just a losing, and very difficult battle.
 

special 1

Registered User
Oct 16, 2023
135
0
Hi there. You made me laugh when you said Mr Hyde comes out. On the other issues you mentioned I have virtually the same with my Husband who is 78 and I am 72. Our lives have been taken away from us both through the dementia and becoming a full time carer. Take care.🤐🤐🤐
 

Lawson58

Registered User
Aug 1, 2014
4,453
0
Victoria, Australia
Hi and a big welcome.

Don’t be afraid to vent here as we are a pretty non judgmental lot and will give advice if we are able.

All I really want to say is that you cannot keep going as you are. Remember that old saying that you can’t light a fire under yourself to keep someone else warm. You are spreading yourself way too thin and the people who will suffer and are suffering are your family as well as yourself.

The paranoia is very common in people with dementia and the target always seems to be the person who cares for them most.

My first thoughts are that as she is still living alone, there are lots of things you can do to reduce your load. You can order groceries online for either delivery or click and collect. Bills can be paid by direct debit or on line and perhaps you can control the alcohol intake. How does she get it by the way?

I also think that you need to get some help for her to deal with the medication and others will have to advise you as to assessments and procedures.

You are obviously putting your own health at risk so the hard part is to step back and get some rest. I understand about being close to your mum but she doesn’t and shouldn’t be the focus of your life.

Time to reconnect with your family and let mum cruise on her own for a little while. But you knew all this!

😊😊😊
 

dq79

Registered User
Oct 23, 2022
47
0
Hi there, hope things pick up for you very soon. I can only echo the posts above - take a break for you, even if that's a few hours or a day or two, do whatever you can in advance, online , enlisting other people if able, and then have a breather. If your mum's GP or memory team are aware there may or may not be things they can do or suggest around her mental health and paranoia. The dementia support line and Admiral nurses helpline too. Sending love x
 

Izzy

Volunteer Moderator
Aug 31, 2003
75,480
0
73
Dundee
Welcome to the forum @EverreadyCyn.

I’m so sorry to read about your situation You sound at the end of your tether. No need for apologies. This is the place to come and have a rant if your need it. There will always someone here to listen and to understand.

I agree with other posters that you need support from others. You sound as if you’re heading for carer breakdown. The Admiral Nurse helpline and the Alzheimer Society Dementia Support Line have been mention. Here are the links -



Do you have any support from outside carers? If not then I think you should consider getting an assessment of care needs done -


You mention violence and aggression in your post. Please keep yourself safe. Try to keep your mobile phone on you so that you can get to another room and phone the police if you feel you are in danger.

I’m glad you’ve shared here.
 

upsanddownsdays

Registered User
Jun 14, 2023
49
0
Hello , I read your post with interest and sadness as I recognise the same in my own situation .
My mum had regular meltdowns of anger with me when she was at home . I would do all I could for her as you have done too . When she caught covid , she gave it to my family , but it was me who had to keep getting out of bed to care for her.

But don't let it get to a crisis , someone said that to me , I had noone to share the care with , have you ? A family member to draw up a rota with and share the burden ?
My mum would ring me late at night and shout at me and then put the phone down . I'd hold the phone away as I'd no idea what she was saying . She never once did this to any other member of my family . So is that selective ? Are Alzheimer rages able to be switched off and on ?
It came to a crisis when like you I had health issues and I knew we couldn't go on. It was a house of cards ready to fall .
My mum had a fall early one morning , again I rushed over and found her . That was it I knew I couldn't leave her again .
I moved in , too much , so hard and exhausting. So she went for respite and has stayed in care .
Now they have the meltdowns and anger . I see it too there sometimes , but the majority of the time I have nice times with my mum again .

I believe it takes a team to care for someone with dementia , you have night staff to watch over them , day staff to help them wash and dress , activities to socialise ,and a chef to cook nutrious meals . You can't possibly do that.

Don't wait for the crisis , start looking at carehomes now is my advice . If that is too much to cope with , have a back up plan , don't make yourself ill . You have your own family to think of too . Sending love xx
 

DeeCee7

Registered User
Oct 13, 2023
338
0
Hello @EverreadyCyn , it’s interesting that your mother chose to place your father in a care home within the year, as “ she hadn’t signed up for this”. Nor have you, but you have soldiered on for all this time , 3 years and counting. Do you think it’s time for her to go into care? Hardly anyone chooses to go into care, those with dementia cannot decide for themselves, but her needs now far outweigh her wants. Time to start the ball rolling by investigating options. You owe it to yourself and your own family. Take care.
 

SeaSwallow

Volunteer Moderator
Oct 28, 2019
6,837
0
Hello @EverreadyCyn and welcome from me also. I would agree with the other posters - you cannot go on like this, especially as it is effecting your health and your family life.
From what you have said i think that you might be based either in the US or Canada so I have attached the relevant links and would encourage you to contact them urgently for help and advice. It is time to look after yourself.
 

Kristo

Registered User
Apr 10, 2023
126
0
Really feel for you, please rest assured that each stage does pass and a new one comes in its place, with different challenges; some easier, some harder to manage.

My dad was very paranoid and verbally aggressive at times. This has eased, although Mr Hyde still pops up from time to time!

He was extremely resistant to any mention of care, befrienders, anything like that because “there’s nothing wrong with ME”. Unfortunately my mum supported his views in this somewhat, despite the fact that she bears the brunt of all his care needs, as otherwise she had to deal with his anger and frustration. However, I did persist as I could see how exhausted she was, and my thoughts were to just give it a go because at least then we had tried something. If he really hated it then we could try again at a later date.

I’m pleased (and still a bit amazed) that the most stubborn man in the world now has a befriender coming in once a week and he goes to daycare once a week too. We don’t ask him, don’t tell him where he is going and don’t ask him about it afterwards. And he is fine!

I still felt like I was betraying him (and my mum) every single time I spoke to an agency about him, and I have cancelled a tour of the local care home 3 times now!! I k ow we will need to do it at some point, but the current respite seems to be working which is keeping him at home for longer, for now.

It’s about what he needs, not what he wants - and if he were in his right mind he would never want to cause all the distress that the family have been going through on his behalf.

It’s so hard to know what to do for the best, you just need to do what you think is right for her, and acknowledge that Mr Hyde is NOT the person that you know and love.

Good luck x