8 December 2011

Thursday 1.05 pm

We're back again - different room with a nice big window. Surprisingly nothing's changed since we were last here.

Michael's going to have a 3 day course of steroids intravenously - 500mg each day. To give you an indication of what a huge dose that is - when Michael's Crohn's was at it's worst, the highest dosage would have been no more than 60mg. Obviously loads of bloods tests each day as well to check levels of everything.

Didn't have time to blog yesterday but was going to tell you how life was with Michael at home. Not much point now - back to hospital mode. Hoping by Sunday he'll be back at home and I resume 'life at home'.

Not looking forward to telling the kids later - I always get the tough jobs :(


Justine

read my blog:www.the-transplant-wife.blogspot.com

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