Lockie - awoken by me taking his photo as he lay dozing in his bed in the Children's Ward following admission for a partial bowel obstruction. Good timing [well sort of] as this all took place during the second week of the school holidays - less to cancel and work around as we juggled being there in the hospital with Lockie, and being at home for Bella.
Needless to say, Fraz and I only glimpsed each other briefly, in passing, during this time but we both pulled together when it counted and got through it. Lockie was in for 5 days [one of us stayed in each night beside him], and when he was 'going' again he bounced back quickly and we were out of there as fast as possible ;) During his stay he had a nasogastric tube fitted, and IV fluids to keep him going - nil by mouth for 4 days! The medical staff still can't decide the true cause of this problem so they gave us a BIG bottle of Lactulose to keep him going regularly and minimise blockages in the future - sorry if this grosses you out, reader!! All part of the fun of being the parent of a child with cf... Lockie was out in time for the new term of school and several days later it's all a distant memory. One good thing to come of it is that I intend to become a Volunteer to man the Ronald McDonald Family Room at the hospital - a wonderful peaceful haven for parents and family members of sick kids in the wards, where they can go for coffee and food, a shower, a nap, or a rest in a quiet atmosphere, away from the bleeping and constant noise of the wards.
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1 comment:
wow.... the things you (and lockie of course!) go through... i think you are amazing anna! xxx ps i wanna see a photo of that BIG bottle of lactulose...
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