My perforated bowel - a result of undiagnosed Diverticulitis
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On the morning of 17th July 2007 I was particularly happy. Summer Term had just ended so I had 6 weeks of holiday from my Teaching Assistant job ahead, my husband was coming back from a 3 week research visit to Australia on Friday and my first grandchild was due in August. Life seemed very good – I was listening to Women’s Hour, and my 16 year old son was asleep as usual upstairs. I felt a need to rush to the downstairs toilet and whilst sitting there fell forward with agonising and unexpected pain. I recall trying to shout my son’s name but being able to do so only weakly. After what seemed like hours, he arrived sleepily at the toilet door and asked what was wrong. I replied ‘this is the worst pain since childbirth’ (already acknowledged in my family as the gold standard for pain after two 3 day labours!) and he said’ better ring an ambulance then’……I recall a paramedic trying to open the toilet door to get to me, and then…….
I awoke 8 days later in Intensive Care.
So this part of my story is what everyone told me later. I was admitted to A&E and there were several hours of uncertainty as to what was occurring. Fortunately an experienced Consultant passed by and noticed how ill I was and took over the case, sending me for an X-ray which revealed air in the abdomen which meant a perforated organ, probably a bowel. He arranged for emergency surgery as the contents of the bowel would be leaking into the body effectively poisoning my system. My son called his best friend’s mother (and my friend) who came to the hospital and spoke with the consultant who said that my husband should be called as there was an 80% and rising chance that I would die in the next few hours. She made the call to my husband in Sydney and then passed the phone to the doctor who explained that I was to go into emergency surgery for a perforated bowel, would probably not survive and he needed to return at once. My husband immediately left for the airport where Singapore Airlines got him onto the next available flight to the UK with 32+ hours of travel ahead not knowing what he would find on arrival. As my son was only 16, they also called my brother as someone could be needed to make life and death decisions and my friend was asked if my husband would trust her to make those decisions in the meantime. The operation took place in the middle of night and lasted several hours – nearly a foot of bowel was removed and a stoma created to allow the bowel to heal. There had been a lot of bowel content dispersed over the body and severe sepsis had set in and after the surgery I was taken to ICU ventilated and sedated and not expected to survive.
My elder son was also called back from Sri Lanka where he was volunteering in a children’s home – he was called by his elder brother, my husband’s oldest son, who also arranged for a car to meet my husband at Heathrow and called him in Singapore to update him on the situation. It would be his story to describe his feelings but it doesn’t take much imagination to realise what a nightmare journey that must have been.
He arrived back very early Wednesday morning and the taxi driver rushed him to Leicester from Heathrow and to see me in ICU – the usual frightening scenario with lots of tubes, machines breathing for me, feeding me through tubes and monitoring all my vital signs.
Over the next few days his life had the nightmarish quality you would expect – hours at my bedside and then going home to deal with phone calls from family and friends and feeding the children, doing the washing and trying to keep some sort of normality in the home, whilst being told that the staff were concerned that I had not come round and each day like that was increasingly worrying.
I meanwhile was in a horror movie in my head where I was being held prisoner in the desert in the Middle East and then taken to an institution where I was to have my organs harvested whilst I was still alive. (I later learned that such hallucinations are normal and a result of both the drugs given and the general sedation experience).
When I awoke I saw my husband hovering at the end of the bed like a hologram and assumed it was some new Skype phone development where he could send me his picture whilst telephoning from Australia. He was unable to convince me that he was actually in the UK or that I had had emergency surgery and a colostomy. I assumed that the staff were lying to him too (paranoia is also a key feature of a stay in ICU).
Eventually I was transferred to a general ward where I spent 5 weeks recovering, and was discharged with a colostomy and a massive 11” long open wound – my abdomen had burst open after the surgery because of the systemic infection I had. Naively my husband and I thought that the wound would close in a few months and I would regain my strength and become one of those people where others said “Isn’t she marvellous, she’s had a colostomy but you’d never know”.
In fact the wound was still open when I returned to the hospital 11 months later to have to colostomy reversed - it never healed. This second surgery resulted in an ileostomy which was also reversed 6 months later, and another 12 months later I had my fourth surgery in December 2009 to repair the large incisional hernia the other operations left me with. I adapted well to having a colostomy, being in a wheelchair for a period, and to every aspect of my life being medicalised. I found the support of organisations like the Colostomy Association invaluable but was increasingly irritated by the stories of how so-and-so had climbed Everest with a stoma, or travelled round China or the Amazon basin. I’d never wanted to do those things before I was ill and I certainly don’t now. I found the incessant cultural clamour to be a ‘brave’ patient, to bear quietly and stoically my misfortunes, and to keep quiet about them as the months went by and family and friends were ready to move on and I wasn’t, particularly difficult.
I can only thank all the NHS staff who took care of me so well in those three years.
It is now over three years later and I am writing my story down because I couldn’t find out anything about perforated bowel when it happened to me, and I want someone to read this knowing that they are not the only person it happens to, and you can return to health afterwards. I would also recommend the website ICUsteps which is very helpful to people who’ve been in Intensive Care.
12 likes, 126 replies
kim58939 barbs55
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lorey67968 barbs55
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barbs55 lorey67968
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You are so right to encourage people to go to the hospital with serious stomach pains as perorated bowel/appendix are serious life-threatening conditions.
birminghamcityfan barbs55
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As you will recall my emergency was April 2013 ,reversal (eventually) April 2014 ...and spending 3 weeks in hospital due to "ilius" .Now i am backwards and forwards to my GP (as i had been discharged by the consultant ) as i have developed a large incisional hernia ,The GPs seem (well are ) unprepared to refer me ,at what point did you get the repair ,and was it successful ?
Still 8 months on from the reversal and having left the hospital with an open wound and a Vac dressing ,it still hasnt completely healed ,i have now got a wound infection ..Is it just me that feels let down by the NHS aftercare ?
The other hard part i have to look at is 18 months of being laid up ,is trying to lose the 3 stone ive put on by lack of exercise ,should i go for hernia repair if its offered ?
barbs55 birminghamcityfan
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After I got through the original surgeries, I began to walk half-an-hour every day just a circular route in the streets near my house. I did that even when the hernia was quite large (I tried various hernia belts and so on but found Sloggi pants the most comfortable support.) I've carried on doing that ever since, and when the ileostomy was reversed I started gentle swimming too which I did with the hernia. I'm still a little 'fat' but I am quite fit and healthy. I think it helps to try and fit in some simple walking into your day, at the beginning I could only walk with a stick to one lampost, then to the second lampost and so on until I could do half-an-hour with a stick, and then I weaned myself off the stick (we're talking months here, it's slow and steady progress you want).
I can't recommend the laparascopic hernia repair too highly, it is fantastic....and no open wound to heal after.
I think you need more information about why the GP doesn't want to refer you yet? maybe they are waiting for the open wound to heal first? sometimes we do have to be patient and it is very hard. My own experience is that another incision to repair the hernia didn't work, so I would go for the laparascopic repair with the mesh.
I think it would be reasonable to ask for a referral to the Hernia clinic to discuss your options, just so you don't feel so stuck, even if they say they won't do it for 6 months or a year, there is always a long waiting list (because it's not regarded as a crucial operation) so you want to at least get in the system and on the waiting list as soon as possible. It's possible they won't operate until you lose some wight anyway, but at least that would be a target to motivate you to do a little walking or whatever?
I did tell my GP that the hernia stopped me exercising as much I would like (because you get that dragging down pain after a while of walking) and that I felt quite depressed by it all, so you could try that. You really need the medical explanation of why they are not referring you yet, and whether they will in future, so you have some hope.
Good luck with it all, hope your wound closes soon.
I think they would perhaps try to repair the hernia and reclose the wound in one operation, so that would be worth going for.
barbs55
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em38 barbs55
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thankyou in advance Em :-)
DebRava barbs55
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Saturday night when I visited my father, he was looking the worst he had ever looked. When I asked for more pain medication for him they decided to do blood tests and take him for the CT scan he was meant to have 3 days earlier. The head nurse decided to call a surgeon up to the ward from casualty to assess my dad. She seemed to know immediately what was going on with this poor man. Emergency surgery was ordered for 7.30pm that night. My mum and 2 sisters were present when the doctor told us it was a very serious situation.
Surgery took approximately 5 hrs with dad making it through. The surgeon very happy with how everything went. THIS WAS ONLY THE BEGINNING of his very long journey. He spent 2wks in ICU receiving expert care. He was then transferred to 4 different wards within a week because none of the nursing staff were experienced in his treatment and care plan.
It has now been 6 weeks since his operation. He has a stoma which is being drain every 2 hrs. He is being feed with 2 separate feed lines as well as fluids and antibiotics. What is being drain from the stoma is being put through a sieve and put back through another line to keep his large bowel etc healthy and active. This procedure is apparently very unusual. So far the surgeon is very happy with his progress.
Unfortunately he will be hospitalised for up to 6 months!! My strong body and minded father is slowly being broken down day by day. He doesn't have the strength to shower and toilet himself. Everything that comes out of his body is measured and recorded. He has no self preservation left. He is definitely not giving in although he is a mere shadow of himself. He is now allowed to have fluids.....soups custard ice cream every day. He doesn't have a lot of strength to feed himself.
My mother is a rock although skating pretty close to the edge. Two parents very independent and extremely close. It is very hard for the family to see them both go through this. As much as I try to help out I feel I'm doing the wrong thing. We all have turns at visiting because he is often too tired to have visitors. I would like to help with taking him in soup or something.....he has only just wanted to have the tv and a paper today. He is extremely upset about having to stay hospitalised for so long. I believe that it is only the start of a very long road to recovery. Reading some stories of loss I think my dad has been extremely lucky.
Any ideas or suggestions would be greatly appreciated.
Many thanks
vic_07103 DebRava
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vic_07103 barbs55
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birminghamcityfan vic_07103
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barbs55 vic_07103
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alex36014 barbs55
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gutless2toad barbs55
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I found myself on life support and medical coma for 15 days, ICU for 21 Days, because of c-diff from a rupture, that was treated with round the clock antibiotics. Total removal of my colon and large intestine, Stoma and Illiostomy bag. Open incision from breast bone to pubic bone.Total hospital stay 65 days. Not expected to live, I feel fortunate that I beat the odds. But now I seem to cry all the time I don't even know why. Thank you for sharing your story.
barbs55 gutless2toad
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I have now healed both physically, and mentally, but I too still have days when I want to cry about it. That's normal I think!
vic_07103 gutless2toad
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