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The Madness That Is My Life…..a blog about my life

~ The madness that is my life…my thoughts, feelings and experiences as I go through life

The Madness That Is My Life…..a blog about my life

Tag Archives: dying

Sticking plasters

29 Monday Feb 2016

Posted by themadnessthatismylife in cold, Emotions, Life, Uncategorized

≈ 1 Comment

Tags

ambulance, blog, blogging, death, dying, emergency, help, homeless, nhs, proud, society

  
I love the NHS. I pretty much live and breathe it. I work full time for the NHS and at weekends I work as a contractor for NHS Trusts on front line ambulances.  When I have a day off I am often to be found at the doctors or the dentists with one of the kids.  The NHS is awesome, always there when you need it.  Anyone who has been ill abroad will tell you that the NHS is something to be proud of.  If I am ill , I don’t have to think about whether I can afford to go to the hospital or the GP,  I can just go.  I might have to wait, the hospital or GP surgery may be a bit tired looking, but I know that I will be looked after. 
However good the NHS is though, it is not a lot of things; it isn’t social care, it isn’t a hotel and it most certainly isn’t a miracle worker.  Much as those who work in it would like to work miracles and cure each and every person who walks through the door. 

The NHS is stretched to breaking point everyday. There are a lot of reasons for this but some of them are easy to see. I’ve lost count of the number of times that I have been called to patients who aren’t really patients at all. They are desperately in need of help,  but not medical help. They need social care. Or social housing. They need their basic needs to be met,  but they do not really need an ambulance,  it’s just that there is no one else that they can call on a Sunday afternoon when they are at the end of their tether. When the loneliness hits hard and the prospect of not seeing a friendly face for another week is more than they can bear.  Or when caring for their loved one just becomes too heavy a burden to carry for another day, another night.  When they are desperate for a little bit of respite from the ceaseless pressure of responsibility for an old or dying loved one.

In the past this would have been dealt with, perhaps, by ringing another family member, or by a carer or a respite centre to give the family a break.  These days though, families are spread far apart and so with cuts to Local Authority budgets meaning that social care has been decimated,  there is no one to call. There is no relief, no respite in sight for a lot of these people; and so, in desperation, they call an ambulance.  And, in turn, because the ambulance crew can see that the family cannot cope, that it’s just too much,  we have no choice. We take them to hospital in the hope that given a few hours of space the family feel better, more able to continue in the thankless task of caring. We put a sticking plaster over society’s failure. 

And so there goes a hospital bed. A nurse,  a doctor, all of who’s time is taken up, instead of looking after the sick. And there goes that ‘protected’ NHS budget. The one that the government has pledged to increase. Only it’s not really an increase or protected at all, because now, instead of the money being spent on social care, and coming out of local authority budgets, it is coming out of the NHS one. The one that we hold so dear. And all the while the NHS covers up this deficit elsewhere, the worse it will get.

Then there are the lost souls. Those who drift, who sofa surf or sleep on park benches. Many of them mentally unwell but not acutely so; they don’t need a hospital, they just need somewhere to be warm; to be safe. Again there is no reason for them to be taken to hospital, but where else is there for them to go?  It takes a cold hearted person to leave a person on a park bench when you know they have nowhere else to go and it is minus 3 centigrade outside. And so yet again we, the ambulance crew, paid for by the NHS spend our time and your money phoning around charities, forgotten contacts in our patients phone, in the hope that we can find them a warm bed for the night. And if not, due to cuts in social housing, there being by no easy access hostels, we take them to the warm waiting room of the hospital.  And as we sit there sticking plasters on the plight of the homeless, another cardiac arrest call goes unanswered. Another person dies. 

Other patients are just too old; their bodies far too weak.  Sometimes it happens slowly, other times it is quick.  I recently went to a patient who was nearly 100 years old and barely lucid.  Struggling to even open his eyes; despite that, there was nothing significantly wrong with him; if I had to hazard a guess (and as I am helping to treat we have to do an educated one), I’d probably say it was just his time to go.  His body was just worn out.  He was nearly 100! But his daughter insisted he had been fine until he got pneumonia previously and was taken in hospital for a month.  Obviously the hospital had made him ill; before that he had been fine. Before that he had lived alone; was fine. There was no point telling her that maybe it was just his time to go.  That he had lived longer than most people, that the hospital that she was blaming by for the state of her father, probably was to blame, only not in the way that she thought; because years ago, her dad wouldn’t have been taken to hospital to be treated for the pneumonia, that nearly killed him. He would likely have just died. At home. Peacefully in his bed. Instead we dragged him off to A & E,  for more interventions. To prolong his life further such that it is.  And when he isn’t restored back to full health, no doubt his daughter will claim that the hospital killed him.  Because blame, it would seem is easier than the truth; that sometimes we just need to allow people to die.  Not play God and attempt miracles. We all have to die sometime. We all, as individuals and the NHS just need to learn to let them. 

The NHS cannot put a sticking plaster on the whole of society. As an ambulance crew friend once told me: if you just need a plaster, you don’t need us. 

If you’ve enjoyed this blog come find me on Facebook https://www.facebook.com/themadnessthatismylife/ or follow me on Twitter @101madness

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Elephant in the room.

02 Monday Feb 2015

Posted by themadnessthatismylife in Emotions, Friends, Relationships, Uncategorized

≈ 2 Comments

Tags

death, dignity, dying, family, illness, love

Death is nothing at all… That’s a line from a popular choice of readings at many of the  funeral services that I have attended. The thing is,  death is a big thing. It’s that elephant in the room, the thing we all know is coming, and yet we try our best not to acknowledge.  We ignore it,  we try not to even speak it’s name, we say someone has passed on gone to meet their maker, become an angel. Very rarely do we say someone is dead, it’s euphemisms all the way.

The thing is, we need to deal with Death. We need to accept it,  after all,  as a friend of mine says, good health is just the slowest possible way to die!  It’s an unfortunate truth. No matter how much we don’t like it, it is one thing we can guarantee. 

I have recently been faced with Death and the dying fairly frequently.  I’ve been working on the ambulances and have seen a lot of ill people. Most of these are old people,  people who have lived full and varied lives,  and are proud, strong and fascinating human beings.  All too many of them have been reduced to the remnants of the people that they once were. Some may be unsteady on their feet,  and so have fallen and injured themselves, or just don’t have the strength to get up. Others may just be weak with age or exhausted from breathing or heart conditions,  many have dementia. 

But it’s not all elderly people who die. My 7 year old son came home today with news of a school friend who died at the weekend. Younger people die too, no matter how much we want to ignore it. And it’s heart wrenching and horribly sad,  and doesn’t bear thinking about,  but think about it we should. 

In my mind, death shouldn’t be taboo. It should be a subject that we talk about, without dread, we plan so many things in our lives, but very few people plan for their deaths. We leave this most important part of life to our family and friends,  people who, with the best will in the world are the least likely to be in the frame of mind to make rational, life or death decisions. 

My Nana was probably the person who I have been closest to that has died. I loved my Nana fiercely,  and she loved us all fiercely back. None of us would ever want her to be in pain or distressed.  She was very ill,  she had been fairly I’ll for a long time. She had COPD and was on oxygen constantly, but she was still firing on all cylinders and bossy as hell!

Then one day, she got a chest infection,  and was admitted to hospital. Despite treatment, she didn’t improve.  The Dr’s wanted to withdraw treatment and in that moment,  I would have done anything to save her. Even in the poor health that she was in, I wasn’t ready to let her die. It wasn’t about her. I was selfishly thinking of myself, i didn’t think that my Nana was suffering and would hate to be like this. I just felt that I could not let her go. Luckily I was able to cry it out,  talk to my friends and family and ultimately, it wasn’t up to me to let her go. Probably a good job,  as I don’t think I would have had the strength. I’d want them to keep her alive, not for her but for me. My Nana slipped away quietly in her sleep early one morning soon after.

The funny thing is that after she died I felt relief. Not that she was dead,  but that she was gone without suffering:  she never lost her mind to dementia, or her independence. She died after a short illness and was peaceful. It took my mum and aunt a lot to allow them to withdraw treatment but ultimately it was the right thing to do. Nana would have hated to be a burden and if she had survived she wouldn’t have had the life she was used to.

And that’s why it is important that we face that elephant in the room, that we talk about death and dying, and give our loved ones an idea of what we want or don’t want to be done to keep us alive. It’s not fair to leave a grieving loved one to make decisions on your life or death completely in the dark. It’s not fair on them,  and it’s certainly not fair on you. As humans we are ultimately selfish.  We don’t like pain,  and the pain of losing someone we think we can’t live without is too much. Some people can’t put that aside and think of the other person.  And that says nothing about them,  and more about being human.

So we should all make our feelings clear. Talk about them,  write them down.  Be unequivocal.  Speak about death, and life,  and the conditions in which we would choose death over life. How much should we be prepared to let Dr’s intervene to prolong our life?  If we lose our ability to choose the best for us,  who do we trust to choose it instead. What do we want done with our bodies when we die, are we leaving them to medical science?  Being buried, cremated?  How do we feel about organ donation?  All of us,  none of us, or only some parts? All of these things are important, they mean that we know what will happen to us, and it takes the guilt and pain and decision making away from a loved one who is in an impossible situation. 

So I’ll start it now: if I get dementia,  or have a stroke or any other condition that means I have no mental capacity and no hope for recovery,  I would like treatment to be withdrawn.  I would like my family with me and I’d like to die. If I am able to,  I would like any of my organs to be donated. I don’t mind if I’m buried or cremated but I’d like a grave that people can visit if they want to. And most of all,  I want my family to know that it is my choice and not theirs. There is no guilt,  it’s what I would want.

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