bullying aged person – Shrinking Horizons

Another day……..

…….. and another with each day slipping seamlessly into the next with little to distinguish one from the other. I fight some mornings to even remember what day it is because apart from having to eat, there is no structure to our time. The LSO and I have slipped into a routine that revolves around mealtimes with the inevitable question after breakfast of ‘what will we eat tonight’? I am sure this is echoed in many homes around the country.

We are both feeling rather demotivated which, I guess is inevitable. At least we don’t have the AP living with us anymore so the stress factors are minimal and I really do think it is just a case of getting on and ‘doing’. I still have the weekly telephone call to the AP which can vary from being quite pleasantly normal to demanding and difficult. I cannot believe that we put up with over five years of utter misery; life with the AP was dreadful starting from day one. We spoke to a friend from Surrey whom we hadn’t heard from for a long time, who had decided to bring his mother to live with him and his wife. They lasted twelve weeks until they were forced to put her in a home and could not believe that we had put up with the AP for so long.

I know that we shouldn’t dwell too much on the past but it’s impossible to completely forget the daily stresses and strains we endured on a daily basis and how desperate we became. I was the punch bag, focal point of all my mother’s nastiness which was unbelievably hurtful and damaging and when she couldn’t get the reaction she wanted from me she turned on the LSO. Lockdown has, in a strange way, brought a great deal of it back. We were trapped in our own home then but with an old woman who was rude, inconsiderate, unkind, controlling and utterly divisive and that’s being quite mild about the situation. She certainly bore little resemblance to the person I thought of as my mother.

They say time is a great healer and perhaps it is, but the LSO and I have more years behind us than ahead of us. I just hope that this virus runs its course and we can have some semblance of a normal life back. I do find it hard to be motivated at the moment. Before the arrival of the AP it was never a problem; life was delightfully busy and interesting.

Now I just fight feelings of negativity telling myself to just get on with it, make the best of the situation and look on the bright side, at least the AP is in a care home and no longer living with us.

A brief return to the darkness.

It’s one of those days when I would just love to go to sleep and wake up to find everything is back to the way it was before this virus appeared. Sad really, I have no doubt many people feel the same way but it is a feeling that must be dealt with or it will take over. The LSO is experiencing much the same emotions so we need to help each other over this feeling of depression. We have managed really well with the lockdown until now but I know exactly what triggered all this off; I rang the AP yesterday and whereas the last few calls have been relatively pleasant, if not a little bizarre, yesterday it was a return to the old unpleasant, blackmailing, demanding and controlling person who almost destroyed us.

During this lockdown I had actually managed to feel a tiny element of liking for the AP which had surprised me after the hell she put us through for over five years. But as the LSO said, never let your guard down, she will never change and he’s right because all that happens is you set yourself up for a fall. I have in previous posts explained why I began writing this blog, to somehow cope with the immense emotional stress that she inflicted on me and it did make a difference. It was a bit like counselling, but I had hoped never to feel like this again nor to need to write about the black hole it put me in. Should I be surprised by this, probably not but I guess I live in hope that things might have changed but the LSO is right in what he said, a leopard never changes its spots although this one managed to disguise hers for decades.

Looking on the bright side, at least the AP doesn’t live with us anymore and I need only to telephone, thanks to the lockdown, so there is a plus point to the whole situation!

I did question yesterday why do I bother? Well I guess, simply put, I never, never want to be like the AP.

Keep on smiling.

There is no doubt that laughter is the best medicine and some hysterically funny jokes, videos and stories have emerged from this lockdown. They certainly take the mind off the seriousness of what is happening here and around the world.

We try not to watch too much news on TV but inevitably the late afternoon briefing has become compulsive viewing which is no doubt the same for many thousands of people. The AP is tucked up safely in the Care Home and can’t seem to get a handle on this pandemic and according to her no-one is taking it seriously anyway. When I spoke to her this week she asked why had I not been to see her so I explained again that no visitors are allowed. This elicited the response that she had heard me outside in the corridor on several occasions recently and she gets quite distressed and upset when I don’t go to see her. I explained that one of the Care Assistants must have a similar voice because I haven’t been to see her for over three weeks because of the lockdown.

The whole situation left me feeling a little bemused and then of course I realised that she was just reverting to type and it was the old ‘trying to control me’ bullying technique coming into play. Had I really forgotten the dreadful years the LSO and I suffered looking after her? Her utter determination to control and manipulate us whilst telling everyone how wonderful we were. No, I guess that will take many years and it may be that I will never have fond memories of my mother but lately has been easier in that we cannot visit so that dread has gone. Mind you it isn’t something to be thankful for since it is because of the coronavirus that I feel the way I do which is ironic to say the least.

It is interesting to note that for the LSO and myself being tied to the house is not too much of a problem. We had up until last August been forced to socially distance for over five years, unable to go anywhere or do anything for most of that time. So although we had begun to really enjoy our freedom, we equally have been able to settle back into a routine that had been a habit but at least we don’t have the AP causing us grief. She really was a huge black cloud hanging over us, definitely a large bat in the attic.

I am thoroughly enjoying cooking and baking again and have managed a couple of inches of my sweater while the LSO has produced some wonderful lino prints which is good to see again. The AP slowly ground us down, knocking any sense of creativity or love of life out of both of us as we fought to survive her vindictive and malevolent nature. This was something we never saw at all until she came to live with us but bit by bit our love and appreciation of life is returning along with a sense of humour which has always been a huge part of our relationship.

Although I am not lighter I feel lighter but just have to endeavour not to end up being rolled sideways out of the house when some form of normality eventually returns.

It was inevitable.

Indeed it was inevitable. My visit to the Diabetic Nurse this week revealed what I had already guessed; I am back to having Type 2 Diabetes although not as high a blood glucose count as last time.

A mixed blessing in some ways as it makes it even more important that I lose the excess weight again and the fear of the consequences that can occur because of it certainly focusses the mind.

Last time the LCHF diet worked well for me in the beginning but as I have said before, no diets are sustainable in the long term. No matter how often you say to yourself that you don’t miss the things you can’t have the inevitable happens and you do. So this time I will do some mixing and matching; a couple of months on this one then have a rest and continue dieting using the 800 5:2 diet. It’s not hugely different but allows a bit more flexibility.

I am trying not to be stressed as the years of being in a continual state of fight or flight mode because of the AP have taken a massive toll on my health never mind happiness. But I do feel much calmer as long as I don’t dwell too much on the past and the lost years. Visiting her still tends to be stressful but at least she is not living with us anymore.

An added bonus is that my love of cooking has returned and I am experimenting with a variety of vegetable, meat and fish dishes. The LSO is definitely still the long suffering one because to a greater extent he is having to eat the same meals as me but so far he seems to be enjoying them. So that’s a bonus.

I just need to get moving again once Storm Ciara passes and what a storm it is. I am writing this with the rain lashing the windows and the wind singing in the guttering and whistling in the chimney.

The aftermath.

I haven’t written a blog for about seven weeks which can only be a good sign as far as my emotional and mental health is concerned. For almost four years this blog has stood firmly between me and insanity of that I have no doubt; I have been able to keep things in perspective by writing down my feelings and my responses to intolerable situations. The inevitable run up to the Christmas festivities is partly responsible for the radio silence and now that the AP is in a care home the stress factors have vanished almost completely. I say almost because we still have to visit her once a week. This does nothing for our peace of mind because her behaviour with us is often aggressive, demanding and thoroughly unpleasant. We go out of a sense of duty but often come away feeling very down having listened to a string of moans about nothing in particular. We try to steer the conversation to lighthearted things but the AP can and does think only of herself. She is rude about the other residents, calling them thick and is convinced someone has stolen a pink bag she had in there. She probably took it to the dining room with her and forgot about it. The staff party all night too, shades of the hospital! I bet they wish they could.

None of this is new as she was horrid to us when she was living here but now we are seeing much, much less of her we have a much clearer picture of the AP and it isn’t flattering. She still tries to play her controlling games with us but now we can walk away from it all and we do, thank goodness. It is a completely different story when others go to visit her in the home and just like before she makes a huge effort and plays the sweet, slightly dotty old woman.

Christmas will be an interesting experience because the AP will be spending hers in the care home. She will not be coming back here not only because we don’t actually want her malign presence casting it’s long shadow over us but we cannot get her back in the same day. She cannot sleep here as the AP is unable to get up and down the stairs and her room is not habitable now, we are slowly regaining our space back. But, in truth she could no longer cope with the general noise and hubbub of the day. She is in a care home for a reason, we can no longer look after her and nor do we wish too. The five and a half miserable years of looking after her have taken their toll on both the LSO and myself at a time in our lives when we should have been free. I am now seventy four and cannot have that time back but what is so very frustrating and what makes me still very angry is the fact that all the AP had to do was be pleasant, accept and enjoy what we had to offer with some grace and we could have rubbed along well. What we endured was the polar opposite. My anger lessens as time goes by but I have no liking for the AP who tried to drive a wedge between the LSO and myself whilst being controlling, conniving, devious and thoroughly unpleasant.

In the meanwhile I have been dealing with the aches and pains that have woken me continually during the nights. I put aside the need to lose weight in order to concentrate on the niggling but nevertheless debilitating minor problems which taken as a whole were becoming a much bigger issue. There has been some success in that area thanks to CBD oil and a ten milligram dose of Amyltriptiline a day which apparently can help nerve pain in some people. It would appear to be the case for me and the pain in my lower back has all but gone which is a massive relief. The CBD oil took a while to have an effect but I generally am improving which is great because I can now look to losing some weight. At the moment I am eating smaller portions, keeping carbs low and endeavouring to not drink alcohol from Monday to Thursday. Is it working? Well not as much as I had hoped but the direction is downwards, just slowly.

Hopefully Christmas won’t cause too much damage but we have our family descending on us and for the first time in some years I am looking forward to it all.

Wavering resolve.

Oh dear, my ability to stick to a dieting regime is severely compromised at the moment. I must stop wavering and prevaricating and get on with it. I am sure this must sound familiar to many people who like me, struggle with their weight.

Our trip to Essex was a delight and so was the meal at the restaurant but I am sure it broke all the rules of my diet. Also and much to my surprise the AP was on her best behaviour which was a surprise after the week before but then she has always managed to con this particular grandson and would not want to spoil his belief in his dear, sweet grandmother. Is he conned by her? I really don’t know but my daughter-in-law has few illusions but maybe that is because she is female and more astute. It’s a curious set-up really but one I find myself watching with interest.

Our next onslaught of visitors is this coming week and it is only one ex-colleague of the AP’s coming from Australia who actually married the AP’s boss. She is a particularly pleasant person but those high up in the world of academe have always brought the true snobbery out in the AP and this particular visitor is a Professor Emeritus.

Fortunately the LSO and I really like her and find her pleasant company so we don’t find the ‘below stairs’ activity too onerous but we will only have one lunch out to break up a day of burbling from the AP. I am still feeling a bit bruised and battered from her behaviour during our last set of visitors so have decided to cook. At least it gives me an excuse to be in the kitchen and I would like to think I will have more control over the food I consume. Did I say that? I spend most of my waking day in there, that is, when I’m not writing another blog!

Anyway I shall endeavour to stick to a low carb regime and try to resist the new potatoes grown and harvested daily by a neighbouring farmer although I feel my resolve will waver when I see them coated in a dollop of fresh butter, some sea salt and freshly ground black pepper.

On the edge of reason.

This last astonishing session with the AP has taken an emotional toll both on the LSO and myself. I have just spent a day with my own thoughts because the LSO has had a rare few hours away fishing with a friend, something he doesn’t do enough of these days.

There was a time pre AP time when we were both hugely busy and happily doing things and it isn’t important what these ‘things’ were, it was just the sheer pleasure of being retired and finally after a lifetime of working being able to use the time available to do what we wanted. In reality we still have that time but the constant battling with the selfishness, changeability and malevolence of the AP has taken away the joy we both had in life itself.

We feel trapped in our lovely home and have to battle with ourselves to do anything at all. I found myself today struggling to just prepare lunch. I used to love cooking and experimenting with lots of flavours, baking and bread making, pickling and jam making were a regular occurrence but now the will is vanishing and instead is being replaced with a sense of futility and frustration. The AP’s constant wittering has ground us down both physically and emotionally. I teeter on the edge of reason most days.

This whole situation is having a devastating effect on my need to lose weight and in fact I have put some pounds back on and am trying desperately to find a way back to my former determination. I cannot afford to go back to being diabetic but that will happen if I cannot reverse this situation. Another rather frightening aspect of this stress, because it certainly is very stressful looking after the AP, is that the LSO and myself use alcohol as an anaesthetic. We don’t drink to excess but do tend to drink each evening to soften the feeling of emotional distress we are permanently in and of course, that is another reason for the steady weight gain.

It is a fact that when you lose the will to live and you merely exist, you lose the will to overcome obstacles. It is simpler to have another glass of wine and relax; simpler but extremely dangerous and we need to pull back from this particular precipice sooner rather than later.

On than very serious note I will take another sip of my rhubarb and apple gin and contemplate starting a new regime tomorrow. It’s bit like giving up any addiction, you just have to keep on giving up not giving in.

…….a thankless task indeed.

Well, just as we think our situation can’t get much worse or depressing, it does.

My lovely cousins from Scotland have just departed after a four day stay with us and the AP. It should have been a great visit but the weather was awful, wet and chilly but that shouldn’t have made much difference, what did was the complete dominance of the AP. She was determined to be sitting in the living room, receiving as if she was the Queen, her acolytes circling around her whilst she burbled non-stop for three days; most of it was made up, mixed up or just completely incorrect. It was impossible to enjoy anything or even sit for long in the room because she just talked over everything. The LSO and I began to lose the will to live. Fortunately my cousin is a natural comedian and in between these times we did manage to have a good and much needed laugh.

In itself, the AP’s attempted dominance although irritating, shouldn’t have been a problem but when I overheard her saying that I was a bully it hurt. I am not a bully and never have been, the bully is the AP. Yes, I am firm about some things but they are for her benefit not mine and I also cannot allow her to completely wreck our lives although, in truth, she is doing a fine job of it at the moment.

When we went out for dinner last evening the AP called the LSO and I ‘pains’ and proceeded to lie about what she had said but it was in front of my cousin and his wife. Liz has no illusions about how unpleasant the AP can be and has been on the receiving end of it in the past when she has stayed with them but my cousin is never present when those moments have occurred so last night came as a bit of a shock. But enough is enough and I firmly told her what I thought of her comment which was absolutely uncalled for and just typical when she feels she is not getting her own way.

Unsurprisingly there was no remorse but she is cunning and when she came down this morning she was clingy and holding his hand like a child, trying to make a point no doubt but for me it was a case of ‘get me a bucket’. We have a carer coming soon to take her out until 6pm, but sadly it will continue to emphasise the problems for us as she will be fawned over and unnecessarily cosseted. She will play the sweet little old lady which she can manage for that length of time, then return to us and revert to the unpleasant and selfish person she really is.

My cousin has said she needs to go into a home and he is right but I did say we would get through the summer and reassess the situation and I will keep my word. He even suggested to the LSO, a care home in Scotland but I don’t think that he understands the full ramifications of that situation, or maybe he was just being kind. Fortunately his wife does understand and the LSO says there was a firm veto issued. No, if it’s a home it will be here but we will see what the future brings, the AP still has to have the basal cell carcinoma on her nose removed and we are just waiting for the appointment.

That sinking feeling.

You really would think that things should get better as time goes by. I even tell people when they ask how things are that they are all good, hoping I guess that they will improve, that life in our ‘care home’ is rolling along nicely but the truth is just the opposite. It’s rolling along but not necessarily nicely.

I wake up in the mornings with a sinking feeling that we have another day with the claustrophobic presence of the AP living with us. I take her breakfast up to her room and always have to take a deep breath before producing a cheery ‘Good Morning’ in a rather desperate attempt to start the day off in the right direction. Most times it works but not this damp and rather dreary Monday morning. I find the AP slumped in her chair staring at the ‘no satellite’ image on the TV, and when I make a comment she says she has just put it on and is waiting for the programmes to come up. I explain she needs to press the Sky control and this prompts a nasty and unpleasant response that she was just going to do that, that she always does that. All lies of course, she had forgotten that part of the process and just hates being caught out so her immediate reaction is one of attack. Unfortunately my response is extremely terse as I leave her room feeling a sense of utter despair sweep over me.

This is no way to start the day or even the week and just to add to everything we have my cousin from Scotland and his wife coming to stay until Friday. We will have to witness the AP alternating between being gushingly sweet to moaning about her health which in truth, for her age is extremely good. Fortunately they do know what she can be like and are both good company so we will just sit back and enjoy the charade that is, of course, in between our ‘below stairs’ activities. There will be a sudden attack of good manners, seldom apparent when it is just the LSO and myself here, the comments will abound about how wonderful we are and how well she is looked after. OK, the last comment is actually correct but we know she doesn’t really feel that way herself because she still makes vain attempts to dominate us and is completely delusional about how much she is capable of doing.

As I have said before, looking after this ungrateful, self opinionated and vain old woman is a thoroughly thankless task.

An unreasonable sense of anger.

When I first began this blog is was to help dispel the terrible angst that had built up over the first years of looking after the AP. The shock that this person was a stranger to me has been with me since the day she moved in with us, up until then she was my mother. Writing the blog certainly helped and somehow I found a kind of limbo that helped me get through the days, the weeks and the months. We are now in the sixth year of being carers and it doesn’t get any easier and although we have recognised that this would be the case, nothing prepared us for the reality.

I wake up every morning now realising that the years are slipping by and we are not getting any younger, both of us are in our early seventies. The AP, who lives in a bubble is apparently unaware of any of this, thinking only of herself and continuing to sail onwards unscathed and uncaring. We had wanted to spend the latter years of our retirement touring this lovely island of ours, never dreaming that we would end up shackled to a one hundred and one year old woman. In our naivety we thought she would be open to allowing us space and time together, dear God, how wrong could we have been.

There is a small light on the horizon. We finally have found someone who will help her shower once a week, take her out for lunch and spend some quality time in the afternoon basically entertaining her, this is also giving us a short break. It was thought of as an alternative to a care home and at first seemed the ideal answer but like everything to do with dealing with the AP there is a downside. The lady carer and her husband are lovely and genuinely like the AP who for the time she is with them is capable of playing the sweet little old lady. We have said nothing about the five years of misery looking after her and in the short term they may never know. The contrast with our business-like approach to everything to do with caring for her and the short day with someone else who makes a huge fuss of her couldn’t be more different. Unfortunately this has meant that the AP has slipped back into making demands, trying once again to manipulate and control us which is not leading to a relationship made in heaven. She seems to resent bitterly the fact that we have some time alone but she is also jealous that we also get on well with this new couple.

In the meantime the AP continues to make up stories. I heard her on the telephone telling someone that she fell and banged her head which has left her feeling fuzzy. This is not true but what’s the point in saying anything. The whole situation leaves me swinging from an unreasonable sense of anger to utter despair with a short respite in the middle where I try to find some peace but sadly in the back of my mind I hear a small voice saying ‘how much longer can this go on?’