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Old 07-11-2017, 07:58 AM
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PamelaJune PamelaJune is offline
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Join Date: Dec 2013
Location: Where my heart is
Posts: 1,140
10 yr Member
PamelaJune PamelaJune is offline
Senior Member
PamelaJune's Avatar
 
Join Date: Dec 2013
Location: Where my heart is
Posts: 1,140
10 yr Member
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This is nothing to do with alcohol and addition recovery, but I imagine it something many will have faced. I'm reliably informed, and in fact it's something they are working hard on here in my home town at the moment. There is a moment in time when an addict says I need help. If they were looking for that moment in this dialogue below than I'm afraid to say they've failed badly before they've even commenced. I've recorded it, because I truly do intend to do something with it. I'm now 6 days post this event, I'm still hospitalised within a private facility and they've just had to do some nuclear imaging as they fear there is seriously wrong with a 1/2 pedicle screw that's been left behind in my spine since 1994.

Here the story in its whole glory; I apologise upfront if I offend anyone. Please note, my own mother trained at this facility 68 years ago in 1949, my sister began her training there in 1971 and was the last intake of combined hands on patient/ combined with lecturing. Prior to her training it was all hands on learning;

1. Paramedics called to home, I was collapsed on the bed in the garage and couldn't move, I was sobbing hysterically and in severe pain. DB and my colleagues who took me home from work insisted on calling an ambulance.
2. On examination I told the paramedics I'd had three falls in the last 12 months twice caused by big dogs, one I had severe abrasions and broken / dislocated middle left knuckle / finger which I put back in myself, the remainder falls I slipped on a wet floor in laundry or over the dog on the wooden floor
3. I told paramedics I've been moving heavy furniture due to house refurb in last month.
4. I told paramedics I'd moved heavy limestone bricks to create a garden bed 2 weeks ago
5. Thursday the queen size mattress and frame fell back against the wall from the middle of the room taking me with it and me landing heavily against it but no actual fall as such. I had to move and straighten up a very heavy base and mattress and re-site them from middle of room to closer to wall to prevent another fall. They were very heavy to move on my own.
6. I told them I suddenly developed a struggle to control my bladder & will wet myself if I don't go as soon as I have the urge. This is a new sensation. Post having had epidurals earlier this year, these will be well worn off by now. I explained on Thursday morning on arising from bed in the early hours I had wet myself involuntarily.
7. The paramedics tried to insert a canula for pain control but couldn't get a vein, they gave me instead the green pipe thing to suck/ inhale.
8. Arrived at ED, paramedics handed over all the detail I had told them and suggested I get something for my pain quite quickly as they were unable to control it in the ambulance.
9. Paramedics also told the nurses I needed to go to the toilet & I was worried about incontinence.
10. So from the moment I arrived I spoke to the nurses & told them I needed to go to the toilet as when I get the urge I'll wet my pants if I don't go. I explained this is new, I've had it previously after epidurals but I've had none since early April. I went to the toilet 3 times while in ED. I told the nurses I wet my self getting out of bed early Thursday morning the day before
11. I told the nurses my right leg kept buckling when I was walking, I said it won't hold me up
12. I said I have temgesic and oxynorm at home, it's not controlling the pain, this is not my normal chronic pain it's something new and it's acute. I've had to come to hospital for help because I can't control this at home with the medication I have and I feel there is something really wrong.
13. The nurse was very compassionate she said she'd get the doctor as she believed I would need a canula so I could get IV pain relief. She also said I'd have to have an X-ray to see what was going on.
14. The ED doctor arrived, she told me (repeatedly) ED aim is to control and minimise patients pain so they can go home. I asked her outright, are you suggesting I should go home. She said well you have plenty of drugs there so why not.
15. The ED doctor reported on the discharge letter 5mg oxynorm given in ED I said had provided relief. I queried this and told the administrator - The nurse asked me if it had and I said no it hadn't. It's definitely not true, it provided no relief at all. I would have said if it did.
16. The ED doctor was angry when I said I can't take Voltarin, I explain it causes terrible high solar plexus / stomach pain & I get enough pain with all my bowel obstructions so I've been told Not ever to take ant inflammatory drugs.
17. ED doctor said well you can have Celebrex, I said no, I'm not allowed that either; she got angrier still & rolled her eyes when I said I'm not allowed Celebrex, both my father and I were told not to take it. I think it had something to do with the heart but I can't remember it was so long ago. I didn't say it as a tablet I'm allergic to as I'm not, it's in the same category of anti inflammatory tablets, I've just been told not to take them but I'm not allergic as such.
18. I said I'm allergic to omnypon it makes me swell, turn pink and itch, maxalon makes me lactate (another eye roll) tramadol makes me projectile vomit and elastoplast itches and when removed leaves a mark that looks like an angry burn.
19. I asked if I was going to have an X-ray the ED doctor said no there is no need to and she doesn't think I have a fracture, it's just my chronic pain condition and I need to see my specialist not attend ED.
20. The ED doctor walked away and minutes later a man came to take me for X-ray, I think it was arranged by the previous ED doctor or nurse before she went on handover.
21. I had the scans, I got told I have a 6mm spondylolisthesis on L5, it also looked like the 1/2 pedicle screw left behind may have moved some, no doubt both of them causing the pain.
22. I returned to the ward and the ED doctor arrived, she angrily discussed oxynorm and she said she would only give me a short supply, when I said I don't have enough at home, like only 3 left, she said she couldn't give me anymore, I said that's ok I understand, she reappeared with a discharge letter which said discharged with IR oxynorm & IR buprenorphine script. I queried this discharge letter with one of the nurses because the ED doctor had come to me and said here is a script for short supply 10 tablets buprenorphine & I'm to take 1or 2 every 4 hours. I showed the nurse the discharge letter and said this needs to be corrected if I need the oxynorm my doctors won't give it to me as it says here you have given me a script and you haven't, they will think I'm a liar & won't give me a script for oxynorm.
23. ED doctor then told me abruptly there is no obvious fracture so I can go home, the purpose of ED is to treat & minimise pain. She has said this 4 times. It was obvious I was exasperating her. I was discharged in as much, if not more pain than when I arrived. The nurse looking after me was due to go on his break he said he will tell the ED doctor I need a wheel chair to get out, it's too far for me to walk when I couldn't even walk to the toilet without collapsing or crying.
24. So the time came for me to leave, I asked a nurse to help me dress as I couldn't do it myself, I asked where was the wheelchair the other nurse said he'd get for me. I was told ED doctor said I don't need one and I'm to walk and move as much as possible. I was discharged in severe pain and agony down a narrow corridor where it looked like they had all their ER stock stuff. I was made to walk to the waiting room over 100 yards unaided without a stick or wheelchair, hanging onto the wall with every step and just a young thin nurse holding my arm. We came through to the waiting area & I was told to sit & wait for my husband in the hard grey chairs by the sliding entry door. I was just left there sobbing not even an offer of tissues.
25. The nurse who had accompanied me then went over to the triage nurse and loudly told the triage nurse to leave me alone, I'm there waiting for my husband. I felt that was unnecessary unless she was implying just ignore me. (Which the triage nurse then did despite me crying).
26. DB arrived and was shocked to find me in the lobby, he had to virtually carry me to the car. Triage ignored us and no offer of help.
27. I feel as if I was labelled a chronic pain patient with a history of medical interventions and I was attention seeking and at most more or perhaps better drugs. I was shocked when the the ED doctor rolled her eyes in exasperation when I said I can't take Celebrex.
28. The nurses all thought I should have a canula put in for pain relief, so did the paramedics but the paramedics tried and couldn't get a vein. The ED doctor didn't think I needed it at all, she offered me Panamax and on discharge told me to take Panamax every 6 hours and the the nurse who walked me out told me to walk as much as I could sitting or standing still wasn't doing me any favours.

Just as an extra point to note, I was collapsed sobbing on my bed at my home unable to move when the ambulance was called. There were 3 people who witnessed that along with the two paramedics.

I feel my whole experience in ED at RPH was humiliating, being made to walk out as I did sobbing for over 100yards trying desperately to hang on to the wall with every step, my hair all over the place, tears and snot running down my face & then just left there completely on my own in the cold draft of the opening sliding doors. I genuinely believe I was being made to feel like I was there just for drug seeking as a chronic pain patient. As a 56 year old, I have never ever been treated so appallingly.

The ED doctor told me to see my pain Mgt specialist or my doctor on Monday. It is highly unlikely I will get into either at such short notice. She would have to have been aware if that, I genuinely believe she just wanted me out if there.

The pain remains as severe with no abatement. The Right leg is still collapsing on me when I go to the toilet which is every hour and my mother has phoned my husband to discuss taking me to a private hospital where I won't be treated in such an appalling manner. Is this how we treat people less fortunate?

Saturday morning I spoke the my mum by messenger, she said she will be there within 20 minutes, she and DB have taken me to a private hospital I've been her now for 5 days and it seems the nuclear testing they did this afternoon has shown there is a significant problem.

I hope I get some printable results I can fax the the head OF RPH with attention the ED doctors name. I don't care how tired she was or is. I'm a human being, if made the mistake of thinking of me as some sad old sad grey old hag she is in for a rude shock. Sad old Gry hag I may be. But I've got a brain and I've got the support of a big business benind me. Happy days are coming to you lovey, happy days indeed. If only I didn't feel so bad, I do believe I'd manage to crack a smile. I do hope I get the chance to take a photo of her face as she realises her lack of compassion and discrimination has come home to roost...


Admin, I do hope I'm allowed to post this, please feel free to remove it's it's to inflammatory, it highlights the injustice so many of us face, but I understand if it's too confronting.
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I can still remember what life was like before pain became my life long companion
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