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Showing posts with label stoma. Show all posts
Showing posts with label stoma. Show all posts

Sunday, 12 April 2015

Harriet's Stoma Reversal Operation - The Worst Case Scenario.

Being a cup half full kind of person I genuinely thought that Harriet's reversal operation would go something like this: 

Go to hospital.

Have operation.

Baby fixed.

Come home.

What an idiot...

Apologies for dragging this out but I would like to think that any other parent in the same situation would want to know all the details - I know that I would. 

When we went down to recovery to collect Harriet she looked so pale lying there. I had to laugh as she was on her side and the nurse that had been sitting with her said she had tried several times to lie her on her back but she just kept forcing herself back over. In the end she had given up and just let her! Unbelievable. We got her back up to the ward and she seemed comfortable as she was hooked up to a morphine machine. She was asleep most of the time but spent the night crying out in pain every ten to fifteen minutes. Thankfully she didn't need any extra oxygen and all of her observations looked good. She remained nil by mouth, which in the beginning was easy as she was heavily sedated from the intravenous pain relief. 

Saturday passed without incident and despite still looking a little puffy and pale everything seemed to be good. Being a weekend, none of our usual doctors were around and later that night Harriet's temperature spiked. The nurse sent for the resident HSO who immediately suspected an infection of some sort and wanted to take bloods for analysis. When he tried to find a vein she barely flinched which he later said was when alarm bells rang. The surgeon who had assisted in her surgery appeared (straight from theatre still in scrubs at one in the morning!) and he began to discuss possible causes of infection, one being that her bowel was leaking at the join and that Harriet would have to return to theatre immediately. Needless to say I was distraught. This was not part of the plan. 

Firstly they would try antibiotics overnight to see if that reduced her temperature. The wound site looked so inflamed and angry, and she was so pale and listless. The doctors were clearly very concerned and there was absolutely nothing I could do to help. I just sat by her bedside the whole night praying she would pick up and thankfully she did. By morning her colour had returned a little and the wound looked better. Throughout that Sunday she started to slowly wake up, her morphine was reduced, she played with some toys and things seemed to be looking up. Harriet continued this way all through Monday and some of Tuesday but all the while we were still waiting for that elusive first dirty nappy. As nothing was happening, her tummy was starting to become very distended and by the time the CF team came mid-morning on Tuesday they were visibly concerned at just how swollen she had become. The surgeons on the other hand assured us that this was all normal and we just had to be patient. The CF team wanted a routine chest X-ray so we headed down there at lunch time. On our way out the radiographer ran out after us and asked us to come back. The consultant down there had spotted something and said that Harriet needed an abdominal X-ray immediately.

By this stage Harriet's tummy was so big that all of her internal organs were getting squashed and breathing was becoming very difficult for her. We returned to our room to hear the outcome of the X-rays, not really expecting much if anything at all. The surgeon returned and from looking at the X-ray broke the news that he had now changed his mind and felt that the best way forward at this point was going to theatre again. Now. This was all beginning to feel like a nightmare. What on earth had been seen that had caused such a dramatic U-turn in events? 

We were given a few different scenarios ranging from okay to horrific - always what you want to hear - and we faced the walk down to theatre again. The only saving grace here was that it all happened so fast. Basically, we were facing what we had been told only that morning would be a worst case scenario. During our wait while she was in theatre I really struggled to think positive as I would normally. I discussed it with Chris and said I was sick of always concentrating on the good and focussing on a positive outcome because every time I have been left floored and totally unprepared for what we have been left to deal with. Maybe I should at least allow myself to consider the worst case scenarios instead of dismissing them so readily.  To this end I then convinced myself she would return from theatre with her stoma again and that she would have it for life. Probably a bit over the top looking back but at the time I was certainly not in control of my emotions! 

Finally the surgeon came back and told us that the cause of her distension was her cystic fibrosis and he had now treated the problem. He had to go in again to rule out all possibilities and the blockage she had suffered again was down to CF. If this was to happen in the future they have ways to unblock without resorting to surgery. As if all this wasn't enough they had inserted a long line into her chest by making an incision in her neck. It looked horrendous but meant they could give her nutrients (TPN) and take blood without having to continuously use her as a pin cushion which was obviously never pleasant. 

We were now back to square one in terms of recovery and the next day was spent with Harriet mostly sleeping off two anaesthetics and boatloads of morphine. Then, finally, two days post-op we got there - the first ever dirty nappy! What a relief after everything that had gone on. And I am pleased to say, like any other baby, she's not stopped since! In terms of her weight, she gained over two kilos in fluid and literally looked like some had inflated her! Again, after a few days and a lot of wet nappies, this subsided. Throughout all of this Harriet had no problems or issues chest-wise which was another bonus. 

Spending a holiday weekend in hospital was not fun but there were a few perks. We got to meet some of the Newcastle Falcons rugby team who came in dishing out lots of chocolate and Easter eggs. The hospital had that many donated eggs I was getting them on a daily basis (goodbye old clothes) and the staff on our ward were all so lovely which made things so much more bearable. 

On Easter Sunday we got our first laugh and smile out of her for over a week. She had come back to us and gradually became the happy little baby we were used to. Her milk was reintroduced, in very small volumes at first, and again I faced something that I hadn't expected. She was now ravenous! I had next to no sleep for two nights as she was given tiny amounts of milk every three hours. It did get better as the volumes went up but it was very hard in the beginning. Once she got close to her usual milk volumes I began to wear everyone down and eventually they let us go home mere days after her second surgery! Not bad all things considered. 

It is amazing to see the stages of recovery happening before your eyes and despite things not going quite to plan we got there eventually. I really hope this helps parents facing similar circumstances. I would definitely have liked to have been a little prepared for what might have happened but hindsight is a wonderful thing. It's done, we got through it and so will many others. 


Comment below if you have any questions or get in touch via my social media profiles Facebook or Twitter. Please do not hesitate if you want to discuss anything mentioned in this blog post. 

Sunday, 8 March 2015

Harriet's Five Month Update

Three Weeks
I have decided to follow up last week’s post with another detailed Harriet one simply because I hope(!) people will want to know how she is doing today. As I have previously mentioned, they won’t all be about her and cystic fibrosis – I promise!  A LOT has happened in the last five months so I will attempt the short version and condense it as best I can into one post. 

The weeks following our discharge from hospital were a whirlwind to say the very least. Every day we had a different health care professional come out to our house. Harriet has a nurse, dietician, physiotherapist and social worker so alongside your usual midwife, GP and health visitor checks we were inundated. We had to become fast friends with our local chemist as the list of medication we need on a weekly basis is mind-boggling. We were also facing the challenge of learning to care for her stoma. I couldn’t even bring myself to do it at first, and if her bag showed signs of coming away or leaking and Chris wasn’t around I would become totally overwhelmed with panic. Chris did all the bag changes for a long time - he’s an amazing dad. Though these days I could actually brag that I do the best ones! I could do one in my sleep really and, to be honest, I probably have!

One Month
Health-wise, Harriet was fine until she was seven weeks old and developed a cough. As we don’t have a clue what we are dealing with, Chris ended up in A&E with her in the middle of the night. She was checked out with no major worries but after a few days there was little improvement. Fortunately she had a routine check-up at the CF clinic and, unfortunately, it was a chest infection. She was rushed off for an X-ray on her lungs and, upsettingly, we were told to hold her down in case she fussed or cried. Of course she didn’t. She dealt with it in her usual laid-back manner; a few smiles, gurgles and giggles for the radiographer which lessened the tension and made their job much easier. Thankfully some extra antibiotics were prescribed and we avoided a hospital admission. It is completely normal for Harriet to catch coughs and colds like any other child. If Nancy had a sniffle at that age we wouldn’t really think much of it but now any sign of a cough can be worrisome as an untreated infection can cause irreparable lung damage. 


Two Months
When she was poorly she naturally lost some weight, and it was at this point that the dietician introduced a different supplementary feed for her - a high calorie milk to consume four times a day. I was breast-feeding but had been able to give Harriet a bottle which was a huge achievement as I could never do this with Nancy. I had racked up that many hours on the breast pump during our initial stint in hospital that I actually came away with a huge sack full of the stuff, and had to clear out my freezer to store it all. Chris jokes that I must have been a wet nurse in a past life!



Morning Medicines
Everything was now focussed on Harriet putting on the pounds. At five months she is 13lb and on the 25th centile. It doesn’t sound much but when you factor in having major surgery then being poorly she has actually done really well to catch up this much. Her weight has continued to go up steadily; so much so, in fact, that in January the surgeons were so pleased with her progress that they gave the go-ahead for her stoma reversal. We had hoped it would have been over and done with by now but the hospital waiting lists dictate when it will be. Harriet has had the pre-op procedure, probably not the most pleasant of things to endure but it didn't bother her in the slightest. Like any other mother I am dreading it but it will be the end of that chapter and we can just focus on her CF treatments.


Three Months
Sometimes it feels like we are at the hospital on a weekly basis. I feel for Nancy as she often has to come with us, and does so well to sit for so long without complaint. Chris uses holidays for hospital time which makes me sad. Chris and I have only been out together once for our wedding anniversary, and even then we were five minutes’ drive from home and were gone for two hours at most! It may sound ridiculous but until she has her stoma reversed we can’t really leave her for long with anyone. Of course we could show them how to care for her but as her operation could literally be next week there’s very little point.




Four Months
Nothing will ever be the same again but I know we can deal with it as best we can as a family. On the flip side we have the most beautiful, happy and contented baby. I used to joke throughout my second pregnancy that this was going to be my ‘good’ one and for once I was right. And by that I mean well behaved! We can now look back and laugh at the completely crazy time we had with Nancy and have come to the conclusion that she just really did not like being a baby!
In terms of development, Harriet is now starting to grab and hold toys, trying to sit herself up and has really found her voice. The one thing I can’t get over is just how smiley she is. She is always so happy and just an absolute joy to have.


Five Months
I plan to do monthly updates for her and hopefully the six month one will involve good news about her operation.


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