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
gemma39613 barbs55
Posted
Glad everything worked out for you my mum age 49 wasn't so lucky after 3 years of tummy aches MRI scans that said everything was fine her bowel perforated on 3rd December 2015 the machines were breathing for her and she had the opp to give her a bag she did wake up and fighter for 6 long weeks but the bag did not take and everything she ate she sicked back up as her tummy wasn't working it had completely packed up so she was null by mouth for 5 weeks without even a drop of water and her stomoke was so swollen it broke 2 of her ribs my best friend my everything passed away on the 7th Jan 2016 and i miss her more than anything witnessing everything she went threw and the pain she was in is undescribable there was just nothing i could do to help my mother i am so glad your opp went well you are so lucky x
vic_07103 gemma39613
Posted
Gemma, I am so so very sorry for the loss of your sweet mum under these most tragic circumstances. She was young and my heart ?? breaks for you Gemma! You have come to the right forum. My bowel also perforated, and on the same day I broke my neck, my (crushed 15 vertebrae) back, 14 ribs & received 180 staples in my head. God wants me here but wanted your sweet mum.
barbs55 gemma39613
Posted
gemma39613 vic_07103
Posted
Chrissie1952 barbs55
Posted
Hi there, I've read your very helpful post and thank you for your open honesty, forgetting all about embarrassment & telling your story like it is!
It's over 8 years since you shared your horrific experience and I can't thank you enough.
I've suffered with bowel difficulties & bladder problems. The latter eventually resulted in an all singing & dancing supra pubic catheter which has caused immeasurable problems. I'm now allergic to most antibiotics, have extreme constipation leading to a double dose of laxatives, then stuck on the toilet for hours. Really affects any quality to life & affects daily living. I have primary progressive multiple sclerosis, getting worse each year.
Ah well, that's off my chest & I realise I need to be more assertive & not be fobbed off.
If anyone reads this, please respond with any helpful suggestions. 😕
gemma39613 Chrissie1952
Posted
Really sorry to hear tour going through all of that 😭 have you had a camera to check for any sort of blockages? My mother had bad constipation which caused the most terrible stomoke aches that I wouldn't wish on anyone and really do hope the doctors find out what is causing it for you xx
anne16851 Chrissie1952
Posted
wow .....so many stories like mine ....i had the exact illness as barbs and shortly after that i was diagnoised with primary progressive MS ....i too am allergic to all most all antibiotics ....this is a great forum to speak with people who have shared the same illnesses ..,,,hope you are feeling a bit better ...
anne16851 barbs55
Posted
omg ....your story is exactly my story .....i had my colostomy for 1 year ....my last surgery was to rebuild my abdominal wall from all the hernias .....that was in 2002.....they used a large amount of surgical mesh for the repair ....now in 2019 the mesh has collapsed and there is fluid in my abdomen ....my surgeon wont operate or even remove the fluid with a needle because hes afraid I'll become septic....8 years ago i was diagnoised with MS ....It's always something ...,i hope you are doing well
barbs55 anne16851
Posted
It is good to hear other people with similar stories because you can feel very isolated and alone with this condition. So sorry you were then diagnosed with MS - life can seem terribly unfair (I felt that a perforated bowel was enough for a lifetime and then I had to have my gallbladder removed and I was so cross that something else had happened to me). That is worrying that the mesh has collapsed - do they know why that has happened? I can understand that the surgeon might be reluctant to intervene because of the risk of sepsis, but are they offering you any other treatment? I am glad you have found this group.
anne16851 barbs55
Posted
thank you....yes i am happy to have found this group .....they do not know what caused it .....the mesh may have been defective ......there are many cases of defective mesh and many lawsuits ....i had some issues right after the surgery ....i had a seroma (fluid buildup).....i also started having severe attacks of vomiting ......i would feel perfectly fine and then would start vomiting....up to 70 times in one hour .....i would have to be hospitalized for dehydration ....this started about 2 years after the hernia repair with the mesh .....no one associated it with the mesh and they ran every test in the book( they thought it was my gallbladder ) but it was not ...but low and behold since the mesh collapsed not a single vomiting attack ....thats one good thing .....the plan for now is watchful waiting ..as they feel the risk of the surgery at this point is riskier than the consequences of the collapsed mesh ...... the fluid may be come infected on its own .....then they would be forced to go in and correct it .....the mesh may be attached to organs which is really a messy situation .....thank you for sharing your story and listening to mine
barbs55 anne16851
Posted
What a rough time you have had. I hope that watchful waiting will work out for you as none of us wants any more surgery. Sending you best wishes
anne16851 barbs55
Posted
thanks ...yes i think we've all had enough surgery to last a life time ....,wishing you good health