I am a wife, mother & keen photographer with an obsession for Scrap booking. My motto is live life to the max and don't regret too much!
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So today was the final visit at the RSV clinic. No jabs today, just a follow up clinic. I met pamela outside, the researcher from Sheffield University who is doing research into continuaty of care after special needs children have left hospital. This was our 2nd meeting. Ironically she is interested in waiting times and although we normally wait no longer than say 10 mins today we waited about 45 mins as Coreys consultant was delayed in surgery! I had to sign more consent forms which is a real pain as they had been changed and then Dr P saw him. He was pleased with how he is doing and although he is majorly grumpy with a constant runny nose he wasn't worried. After i explained about the decline in eating and some vomitting at night time he agreed that we should give the Omeprazole a try again, it won't do him any harm certainly, so we are back on the meds. I was really suprised as we left to receive a lovely gift from the Reseacrh nurse for Corey. It was a little house with different shaped animals that slotted in the roof, it really was a lovely touch and i must remember to send them a Thankyou card. I only thought after leaving the clinic that this will be the last time i see Sue and Moira, the research nurses, so it was a sad moment too really. So afterwards we went to the University where i had a meeting with Pamela and we talked about my experiences. Corey fell asleep which gave us some good time to chat and amazingly he slept for well over an hour which i unheard of. Anyway we had a good meeting and then off home we went. It's been quite a good day, one where you feel you have achieved alot, but now i'm exhausted!
Name: Cath Home: Sheffield, United Kingdom About Me: A baby will make love stronger, days shorter, nights longer, bankroll smaller, home happier, clothes shabbier, the past forgotten, and the future worth living for. See my complete profile
