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
dmheil
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rosie43616 dmheil
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birminghamcityfan
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I will say this expect the tiredness to continue for some time ,what everyone here had was major .
barbs55
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Love this! - it's really the only thing to hang on to during the long recovery process. The feeling of everything sort of 'falling over' when you lay on your side is very familiar.....I don't think I managed to lie on my side for months. (much later on I was diagnosed with an abdominal hernia which seems to be a common 'side-effect' of large abdominal incisions)
On recovery times, one of my surgeons says it takes a month to recover for every hour you were under anaesthetic so if yours was 4 hours that is 4 months, and that's just the recovery from having had any operation!
Also recovery isn't linear, it's very much two steps forward, one step back, so expect it to be up and down and you won't be so disaapointed on the 'bad days' . Pace yourself, especially with work, and expect to betired after any exertion, and need lots of rest time.
You are doing fantastically well at the moment, and well done to your surgeons for avoiding the colostomy. Perforated bowel has to be seen like a burst appendix - accept that it just happens and there is probably nothing you or the doctors could have done to prevent it. My surgeon told me that having removed a good 12" of bowel where the diverticula normally are, means that there is nowhere left for it to happen again, so no need to worry about that!
Sending you best wishes for your recovery process.
dmheil
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As I read what some of you went through I realize my situation could have been so very much worse. Barbs....you are amazing. No other way to phrase it. My complaints are minor compared to what you experienced. Last night for whatever reason I just couldn't sleep in any position so I came downstairs to the chair where I managed a few hours. that entire feeling of "everything falling over" was keeping me awake so I just slept a few hours in the chair. I am pleased to know this is not an unusual feeling. Just knowing others have experienced this is a comfort to me and it lets me know on top of everything else I'm not loosing my mind as well. I have already discovered that the recovery process is going to be slow. For everything I try to do, even small things, I need to rest afterwards. But, I'm here and that could very easily have been a different result.
barbs55
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dmheil
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lana17
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lana17
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barbs55
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I can only tell you about my experience. I recognise the muscle weakness after ICU. I was only in ICU 8 days and it took me months to get over, it is a 'one day at a time' situation but you do get better very slowly. Each surgery (like the reversal) tends to knock you back a bit but generally it is all slow progress in the right direction. I can say that my reversal was completely successful, I have one fully formed Bowel Movement every morning (although I don't get much warning it's coming so I need to be around a toilet!) but apart from that after some initial soreness and being all over the place it DID settle down with a week or so. I'm aware that not everyone is so lucky but the reversal is still easier to manage than the stoma was for most people. The operation is very simple compared with the previous one and you're more prepared as it's not an emergency.
Wishing you all the best with it, and enjoy your baby as much as you can.
jlaw4005
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I can only say if someone is diagnosed with diverticular disease - listen to your Dr. and eat correctly!!!
barbs55
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jlaw4005
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I wonder if these two incidents of rupture mean I have very thin intestinal walls? I'll have to ask my surgeon at my next appointment.
birminghamcityfan
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barbs55
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emergencies. Have you got a new date for the operation? And the stress is so exhausting itself with all the missing sleep too. They will be careful to ensure it doesn't happen again to you - the staff don't like doing it to patients either.
I actually began to meditate after I was referred to a therapist for mindfulness training during my recovery and referral for PTSD and that really helps me now. I would not have believed it before I did the training though, as I was always very cynical about this sort of thing but it has really helped me to deal with anxious thoughts. I use a programme that's free to start off called Headspace if you want to give it a go.
Really hope you get a new date really quickly and relax a bit in the waiting time.