I haven't blogged for a while because I was letting my reaction to some recent news sink in, feeling a bit confused and waiting to feel good about it. Last week saw some long awaited news and steps forward in our civil case. That woman's insurers have finally accepted primary liability and are making an interim payment that will enable us to buy a bigger home.
So why do I feel so deflated?
I know that some reading this will be wondering what my problem is and rightly so. I get it; we are unbelievably lucky to be able to claim compensation and there are many, many people in our position who don't have that opportunity.
The problem is the wood and the fact that I can now see it for the trees. The last 18 months have been all about the fight; Jake's fight to live, the fight to get him the right treatment and funding, the fight to get justice, the fight to secure our financial future and, frankly, the fight to stay sane.
Today Jake is back at home, he has a phenomenal rehab package in place through the NHS, we have found a property that can accommodate our changed needs, we have a justice of sorts and I know we have a fabulous legal team who will make sure we are OK in the future. I don't have to fight anymore.
There is no doubt that this is a good thing and I am certainly battle weary and in need of a rest, but I miss the fight. The fight is absorbing, a distraction. Deep in the fury and adrenaline of battle you don't have to face the reality of right now and right now I am scared.
I am scared because I am having to face the future and even though I have known it would be tough, that knowledge was an abstract, amorphous thing that I was vaguely aware of. Now I am no longer in the fight reality has been brought into sharp relief.
This breaks my heart, because if it is hard for me, I cannot imagine what it is like for my Jake.
Last night I woke at around midnight to find Jake trying to get comfortable in soaking wet bedding having had a horrendous night sweat. With fresh sheets on the bed and a reassured Jake we both went back to sleep. An hour later Jake got up to go to the loo which wakes me as I need to put the light on for him as he is sight impaired and so unsteady on his feet. A few seconds later I realised that Jake was sleep walking again and going to the toilet in the hallway, waking up and realising as he was doing it. Can you imagine how mortified he was? Now imagine feeling like that and not being able to express it. Imagine that you are so dyspraxic that you are unable to help clean it up and will have to sit on the edge of the bed watching whilst your wife cleans up after you have already watched her get up in the night to change the bedding. Imagine your frontal lobe damage means you can't manage or control your feelings of shame and upset. Now imagine you don't really understand why you are no longer a capable, reliable husband and find yourself helpless, standing in your own urine unable to do anything about it. My imagination certainly didn't let me go back to sleep.
This makes me want to weep. I am SO angry that this has happened to him, to us. I want to sweep him up and transport him away from this reality. I want to take all of his pain and confusion away and would gladly swap places with him in a heartbeat.
So you see, I miss the fight, it was keeping my heart whole.
Thursday, 25 April 2013
Tuesday, 9 April 2013
Good people
In a very weird way brain injury is both isolating and inclusive. All of the books tell you that after the initial acute phase people who have been very involved will become less present, often finding if difficult to know how to interact with the new person the survivor inevitably becomes. One hates to be a cliche, but that has definitely happened to us. That's not a dig by the way, it's just the way it is.
The compensation for this is the new network of virtual friends I have found through social networking. Both Twitter and the Headway health unlocked site have brought me into contact with good people who understand, would never judge and give me endless support and encouragement.
I think my favourite thing about the very good people on the Headway forum is the utter lack of bullshit; whether it is because of frontal lobe damage or just simply the honesty of people who have experienced true trauma, I know that what I read is real, unvarnished and truthful; even if that means sometimes it is a little blunt! I can count on one hand the number of people in my non-virtual life who are that genuine; wouldn't be great if everyone was? Apart from Jake obviously, I could REALLY do without some of his frontal lobe damage induced bluntness!
This life is far from easy, but the comradeship and acceptance of my virtual friends makes it easier to cope.
This life also makes you look at problems a little more creatively; when Jake sustained his severe injury 17 months ago he wasn't expected to survive and no one could have predicted that last weekend he would stand up next to his great friend Mike as his best man. With such a complex mix of cognitive and speech deficits the best man speech was always going to be a bit tricky, but with the help of my sister in law's colleague (and very good people) Andy Davies, we still managed to make everyone cry with this! The best man
The compensation for this is the new network of virtual friends I have found through social networking. Both Twitter and the Headway health unlocked site have brought me into contact with good people who understand, would never judge and give me endless support and encouragement.
I think my favourite thing about the very good people on the Headway forum is the utter lack of bullshit; whether it is because of frontal lobe damage or just simply the honesty of people who have experienced true trauma, I know that what I read is real, unvarnished and truthful; even if that means sometimes it is a little blunt! I can count on one hand the number of people in my non-virtual life who are that genuine; wouldn't be great if everyone was? Apart from Jake obviously, I could REALLY do without some of his frontal lobe damage induced bluntness!
This life is far from easy, but the comradeship and acceptance of my virtual friends makes it easier to cope.
This life also makes you look at problems a little more creatively; when Jake sustained his severe injury 17 months ago he wasn't expected to survive and no one could have predicted that last weekend he would stand up next to his great friend Mike as his best man. With such a complex mix of cognitive and speech deficits the best man speech was always going to be a bit tricky, but with the help of my sister in law's colleague (and very good people) Andy Davies, we still managed to make everyone cry with this! The best man
Monday, 1 April 2013
Here's hoping
Someone recently asked me if I was 'OK' because I seemed a 'bit up and down at the moment'. They were completely genuine in their question and I know it came from a place of caring.
Their choice of words made me smile inwardly in a sort of ironic way as the title of this blog is no accident; every stage of this journey has taken us up and down, like a twisted game of snakes and ladders.
In the early phases you career between the hope of a flickered eyelid and the terror of the 'when to withdraw treatment' conversations. As time moves on you are buffeted between the joy of small victories like the first few sips of thickened water and the pain of accepting what is lost. This develops into a focus on how much rather than if at all and still you undulate along the ups and downs, grateful to still be on the journey.
In a weird 'if I knew then what I know now' way the more acute, in-patient phase is not so bad; you have tangible, concrete things to focus on and a place to spend your hope. You can clearly chart the improvements and have no real responsibility for what happens in that environment. If it's not working, then 'they're' doing something wrong. The highs and lows are more immediate and visceral, but at least you can take comfort from knowing hope is likely to go up again soon.
No, the worst ups and downs are the ones that are so imperceptible as to hardly register. As progress slows and you begin to establish the new 'normal', everyday feels like an unremitting, featureless landscape and you find yourself compensating by experiencing every tiny thing, whether good or bad, to it's extreme, a bit like voluntary bi-polar. Trying to force the hope to do something, anything.
Add to this the constant feeling of failure you have from not being able to help, understand, mend it, or do the right thing in any situation and you start to feel as though you are truly running on empty. I have believed that I reached this point many times over the last 17 months only to be able to thankfully scrape some more reserves off the bottom of the barrel, I am sure I will do so again and be rewarded by an upward tilt soon.
So, if I seem a bit up and down it is because that is the nature of brain injury whatever the stage; hope goes up...hope goes down.
Their choice of words made me smile inwardly in a sort of ironic way as the title of this blog is no accident; every stage of this journey has taken us up and down, like a twisted game of snakes and ladders.
In the early phases you career between the hope of a flickered eyelid and the terror of the 'when to withdraw treatment' conversations. As time moves on you are buffeted between the joy of small victories like the first few sips of thickened water and the pain of accepting what is lost. This develops into a focus on how much rather than if at all and still you undulate along the ups and downs, grateful to still be on the journey.
In a weird 'if I knew then what I know now' way the more acute, in-patient phase is not so bad; you have tangible, concrete things to focus on and a place to spend your hope. You can clearly chart the improvements and have no real responsibility for what happens in that environment. If it's not working, then 'they're' doing something wrong. The highs and lows are more immediate and visceral, but at least you can take comfort from knowing hope is likely to go up again soon.
No, the worst ups and downs are the ones that are so imperceptible as to hardly register. As progress slows and you begin to establish the new 'normal', everyday feels like an unremitting, featureless landscape and you find yourself compensating by experiencing every tiny thing, whether good or bad, to it's extreme, a bit like voluntary bi-polar. Trying to force the hope to do something, anything.
Add to this the constant feeling of failure you have from not being able to help, understand, mend it, or do the right thing in any situation and you start to feel as though you are truly running on empty. I have believed that I reached this point many times over the last 17 months only to be able to thankfully scrape some more reserves off the bottom of the barrel, I am sure I will do so again and be rewarded by an upward tilt soon.
So, if I seem a bit up and down it is because that is the nature of brain injury whatever the stage; hope goes up...hope goes down.
Monday, 25 March 2013
Moving on up
Jake and I have just returned from a weekend of luxury and relaxation at a local spa hotel. It was fabulously indulgent, the staff were incredible and I can honestly say that a change of environment and a removal of stress has left us both feeling more relaxed than in a very, very long time. So much so that we've booked to go again in June!
We arrived home this morning to the icing on the cake; a message to say that our offer has been accepted on a new house.
The current Korving Towers was the perfect forever home when we moved here in August 2011; it is small but perfectly formed and had everything we needed; a big bedroom, office, two reception rooms, a lovely new kitchen, sunny south-west facing garden, a massive garage for the imp of doom, really close to my sister and her family in a good area on a quiet road and close to local amenities (and a nice pub!). If things had gone to plan I can honestly say we would have stayed here until they carried us off.
Sadly things haven't gone to plan and since Jake came home it has become increasingly obvious that the current KT is just too small. I am finding this particularly difficult as I literally have nowhere to go; I work from home and so for most of the day you can find me, Jake and a carer bumping into each other. Add to that the various therapists and related visitors and the house suddenly feels very small indeed. Jake's supported and carefully managed morning routine means that access to our bedroom and one bathroom is restricted until at least 10:00am and his need to rest regularly means that sometimes I have little or no choice as to where I go in my own home.
In fact I often find myself still in my PJ's at 10:30am with the door to our room closed as Jake has gone back to sleep!
The journey to finding a new property has been tricky as we have needed to balance getting a property that reflects our original needs, the new needs our situation adds and a budget that both sides can accept. The new Korving Towers feels perfect; with much more space, in an area we are happy to live in and still within a reasonable distance from my sister (and therefore the wine!).
There was a near miss that was judged as 'over provision' by the other side (easy for them to say, it's not going to be their home!), which has led to us being in the crappy position of having to go to court for the interim payment we'll need to purchase a new property. All I can do is trust that our legal team will manage this side of things for us and hopefully we'll be in the new Korving Towers before the end of the Summer.
We arrived home this morning to the icing on the cake; a message to say that our offer has been accepted on a new house.
The current Korving Towers was the perfect forever home when we moved here in August 2011; it is small but perfectly formed and had everything we needed; a big bedroom, office, two reception rooms, a lovely new kitchen, sunny south-west facing garden, a massive garage for the imp of doom, really close to my sister and her family in a good area on a quiet road and close to local amenities (and a nice pub!). If things had gone to plan I can honestly say we would have stayed here until they carried us off.
Sadly things haven't gone to plan and since Jake came home it has become increasingly obvious that the current KT is just too small. I am finding this particularly difficult as I literally have nowhere to go; I work from home and so for most of the day you can find me, Jake and a carer bumping into each other. Add to that the various therapists and related visitors and the house suddenly feels very small indeed. Jake's supported and carefully managed morning routine means that access to our bedroom and one bathroom is restricted until at least 10:00am and his need to rest regularly means that sometimes I have little or no choice as to where I go in my own home.
In fact I often find myself still in my PJ's at 10:30am with the door to our room closed as Jake has gone back to sleep!
The journey to finding a new property has been tricky as we have needed to balance getting a property that reflects our original needs, the new needs our situation adds and a budget that both sides can accept. The new Korving Towers feels perfect; with much more space, in an area we are happy to live in and still within a reasonable distance from my sister (and therefore the wine!).
There was a near miss that was judged as 'over provision' by the other side (easy for them to say, it's not going to be their home!), which has led to us being in the crappy position of having to go to court for the interim payment we'll need to purchase a new property. All I can do is trust that our legal team will manage this side of things for us and hopefully we'll be in the new Korving Towers before the end of the Summer.
Sunday, 17 March 2013
Grief
I don’t know why, but after 555 days suddenly I can’t breathe. I feel smothered by anger, sadness, confusion, responsibility and fatigue.
But it hurts, in a way I can’t even begin to explain. I am burning at the centre of my soul and I want to close my eyes and sleep forever so I don’t have to feel it anymore.
All I can think about is what is lost; all the experiences
we were going to share, the pride I know I would have felt watching him be an endlessly
amazing father and radiographer, the chance to be a mother, my career, my
social life, my future.
I spend all my time trying not to show Jake how broken I
feel, crying when he’s not there and closing myself off pretending to be
strong, positive and cheerful when he is.
He’s got a brain injury, but he’s not stupid; he knows.
I’m sitting here now on the sofa in the lounge with hot
tears splashing on my laptop, trying to bring myself back under control before
I climb into bed with my Jake.
I know this is grief, I know this is normal and necessary, I
know it will pass.But it hurts, in a way I can’t even begin to explain. I am burning at the centre of my soul and I want to close my eyes and sleep forever so I don’t have to feel it anymore.
But then my beautiful man would be all alone and that would be so much
worse.
So tomorrow is day 556 and I will get up and start again. Because I know this is grief and I know it
will pass.Thursday, 7 March 2013
Remember this
Our wedding in New York
Our honeymoon in California
Our beautiful new home
Our roles
Our rules
Our plans
Our secrets
Your degree
Your second career
Your colleagues
Your words
Your age
Your triumphs, trials, decisions and set-backs
My flaws
My quirks
My fears
My dreams
...my name
These memories may be lost to you my love, but they are just moments in time and I promise you we will make more.
So, if you remember nothing else remember this; my name doesn't matter because I will love you every day, forever; you are truly amazing and we have literally millions of new moments ahead together with which to make new, wonderful memories.
Lets start today.
Monday, 4 March 2013
A plea to the professionals
I don't want this post to be misunderstood, so I'd like to start by stating my intent; I genuinely believe that anyone who chooses to work in a field where there are such extraordinary personal and emotional stakes does so because they are fundamentally good people who want to do the right thing. The majority of our journey has been characterised by the provision of exceptional care, empathy, thoughtfulness and professionalism by these people...some of it has not.
The sad thing is that it is the little things that are overlooked, not considered or ignored that often have the most devastating impact and, I suspect, often without the offender being aware of this impact. That is what this post is about and it is intended as a positive call to action. So please read it in that context.
Cutting to the chase, YOUR PROCESS IS RUINING MY LIFE!
Jake and I are just two people, we're not particularly exceptional for anything apart from what happened at 7:25am on the 26th October 2011. We don't have access to limitless resources or medical knowledge; we're just doing what we can in a truly shitty situation.
Thankfully we are optimists and so are both attempting to make the best of it. This is difficult to sustain though when each corner we turn seems to lead us to a big, ugly and unresponsive process.
When your world has shifted so fundamentally that you are having to re imagine every plan, expectation and dream, the thoughtless proclamations of 'that's the process', 'it's not our policy', 'we have to wait for A to talk to B, who needs to check with C who is on holiday for the next 2 weeks', 'that's not in the guidance' or (a personal favourite), 'that's not my job' are breathtakingly stupid and unhelpful.
Before you go all indignant and defensive on me, I know that these are the facts of your job and probably true in that context, but do you really have to say it that way? Could you choose to look around the process and see the broken person behind it? Could you take the time to really listen and then explain why the process is there, how it will benefit me and what you are going to do to make my experience of the process a bit less painful?
Take a moment to consider where the process came from, who did 'they' have in mind when they designed it? I'm guessing it was originally meant to help people like us, not defeat us. If not, why not?
So, a simple plea; next time you're about to take out your process and brandish in the face of someone who is potentially crumbling under the pressure and terror of their situation, please think about why you do what you do, the way you are about to communicate and the impact you're about to have.
Thank you from me and my Jake for reading; we'll keep trying if you will.
The sad thing is that it is the little things that are overlooked, not considered or ignored that often have the most devastating impact and, I suspect, often without the offender being aware of this impact. That is what this post is about and it is intended as a positive call to action. So please read it in that context.
Cutting to the chase, YOUR PROCESS IS RUINING MY LIFE!
Jake and I are just two people, we're not particularly exceptional for anything apart from what happened at 7:25am on the 26th October 2011. We don't have access to limitless resources or medical knowledge; we're just doing what we can in a truly shitty situation.
Thankfully we are optimists and so are both attempting to make the best of it. This is difficult to sustain though when each corner we turn seems to lead us to a big, ugly and unresponsive process.
When your world has shifted so fundamentally that you are having to re imagine every plan, expectation and dream, the thoughtless proclamations of 'that's the process', 'it's not our policy', 'we have to wait for A to talk to B, who needs to check with C who is on holiday for the next 2 weeks', 'that's not in the guidance' or (a personal favourite), 'that's not my job' are breathtakingly stupid and unhelpful.
Before you go all indignant and defensive on me, I know that these are the facts of your job and probably true in that context, but do you really have to say it that way? Could you choose to look around the process and see the broken person behind it? Could you take the time to really listen and then explain why the process is there, how it will benefit me and what you are going to do to make my experience of the process a bit less painful?
Take a moment to consider where the process came from, who did 'they' have in mind when they designed it? I'm guessing it was originally meant to help people like us, not defeat us. If not, why not?
So, a simple plea; next time you're about to take out your process and brandish in the face of someone who is potentially crumbling under the pressure and terror of their situation, please think about why you do what you do, the way you are about to communicate and the impact you're about to have.
Thank you from me and my Jake for reading; we'll keep trying if you will.
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