We waited around Grandma's house all morning to find out if we had a bed in hospital, we packed our stuff and watched DVD's. At 12.30pm we finally found out that we could go in. Grandma and Grandpa took us down to help us unload our truck load of stuff.
Brody again had to have the nose test as he still has his runny nose. But his temperature is still normal. I think he must be getting something as he is not his normal self. The hospital has again put us in the isolation ward because of his running nose. As we dont want to effect any one else with what every Brody has. We made it to our room around 6.00pm. Brody had a rough day as he cried his little heart out because he didnt want to come and then when he had the nose test. He is getting so sick and tired of it all, which is also making it harder and harder for me to be strong.
Brody then watched some movies on the starlight machine and went fast asleep, until i had to wake him for eye drops and his medicines. The eye drops are to help his eyes as the chemo he is taking this time can effect his eyes. This job is hard to as he tried to be brave but i don't even know if it got in his eyes. They say to let him closes his eyes and once he opens them it goes in. But Brody hardly opened them and hated the feeling of it going onto his eye. We have to do this all the time, every 4 hours, while we are in here, not looking forward to this week.
Thank you to Chantelle's hubby for making me wonderful meals to eat, and her beautiful children for giving up their mummy to come and visit me, and the gorgeous lady Chantelle. Also big thank yous to Grace and the Autism Advisory and Support Service for wonderful sensory toys. Brody loved them, he really liked the fan with the lights. Thanks again xxxxxx
Wednesday, March 3, 2010
Subscribe to:
Posts (Atom)