Monday 10 August 2009

Sorry for delay

Sorry for the delay in posting its been non stop with the kids being on holiday from school. Alan is much the same from the last post,still struggling with medicine and the having to take them.Emma our psychologist came out to the house and went through how Alan's body works and why he needs to take tablets, he seemed to enjoy listening to her and we came up with the idea of making a reward chart for him when he takes his medicine so my hubby has been busy making one, a army one, hopefully it will be finished today, i will post a pic next time i update, it is looking really smart, lets hope it works.

The kids are back to school on Monday and I'm hoping things get better for Alan, the school nurse was out yesterday going over his medical form so i made her aware of how Alan is feeling about things so she was going to a meeting with the headmaster so he is in the know of whats going on.We are also waiting on a swab result coming back,Alan's been suffering with a bug for the last 2 weeks, he had a course if antibiotics so we will see if its clear although I'm not hopeful he is still coughing really badly, I'm hoping we will find out today.

3 comments:

  1. Hi Julie, I am Marcy from LovinLane.... Lane is 5, and diagnosed with CF at age four... I just wanted to introduce myself... I look forward to reading your blog and getting to know your family... Hugs Marcy

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  2. Hi Julie,

    Just received Alan's handmade tiger card. Could you please tell him that I'm chuffed with it and it's sitting on my T.V.
    I've got to go into hospital tomorrow and he has really cheered me up.
    Thank you

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  3. Hi,
    I hope everything is going ok with you all and that the start of the school term went ok.
    Love Jessica x

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