Read Imogen's story of survival at www.imogendyson.co.uk - Imogen was born on 9th April 05 with a Congenital Diaphragmatic Hernia. Against the odds, Imogen defied the challenge set before her and to the amazement of many people is thankfully with us today. Imogen's site is aimed at parents diagnosed with CDH or other conditions causing uncertainty, with the hope of offering optimism and encouragement to others. We always welcome mail to lindseyandimogen@aol.com
Saturday, 17 February 2007
Date for Gastrostomy is a no go and holiday
Now then, got at date for the op after pestering for some time. Wouldn't you credit it, it's when we're away. We're a bit torn about cancelling the hol or postponing the op again. Unfortunately, we will opt to do the latter. We are going on a 5 day trip to Rainbow House at Hexham in Northumberland. This is a charity run retreat for parents and ill kids. Not that Immie is ill, but classed as high dependancy due to her oxy and feeding pump and they say we qualify. The people there look after parents while we look after Immie. They make your meals, washing and ironing etc. At short notice it's unlikely another couple could take our place hence our reason we are still going. Last time the hospital cancelled our appointment at the 11th hour and there's nowt to suggest they won't do it again. If anyone reads this, leave a post as we haven't had any yet apart from friends or family, (not that we aren't grateful). Be nice to know people are looking at the site. Th th th that's all folks... Baz
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