Last One

Hi,  alls fine here and we’re just killing time waiting to come home.  I’ve done most of the packing, the train tickets are bought and i just need to do the last minute things tomorrow night. 

Tomorrow is Grace’s last injection and is only an i.v. which takes about half an hour.  I’ve then sneaked in an extra o.t. session tomorrow afternoon.  Our train leaves for Beijing at 9.30am  and we’re meeting up with Michael and spending the night there before the flight home Saturday.

Apologies if you thought Grace trying to crawl was something new, she’s been doing it for a while but is nowhere near yet.  She just looked funny stuck to the floor so mentioned it.

This will be the last post till we get home and settled.  Thankyou all for your support.

Leanne & Grace

8 Responses to “Last One”

  1. Orla says:

    Hi Leanne and Grace,

    Have a great trip home and have a lovely reunion with Daddy and Rose.

    Best wishes
    Orla xxx

  2. Siobhan says:

    todays word ‘facetious’

    Hi,

    HOME TIME! Have a safe journey home. Looking forward to coming up to visit when ye get back.

    Love,
    Siobhan (a.k.a. Fatty Boom Boom!)

  3. mum says:

    Hiya

    Just wanted to wish you both a very safe and pleasant journey home and Enjoy Beijing for the short time you are there.

    See you Saturday night.

    lots of love and big hugs to Grace

    Mum, Ged and Rose xxx

  4. Cerys says:

    Hi leanne and Grace glad to hear your both doing ok and everythings gone well. Great news that it’s back off home, you sound like you are ready for it, you both deserve a well earned rest. I missed not seeing Grace 1st day bck at school. Can’t wait to catch up with her for a good old gossip we know how she likes her gossip! Have a safe journey. Leanne make sure you put your feet up when you get home you have done a fab job, and I hope you get your full meal to yourself allthough you might have Rose aswell wanting to share your dinner
    Take care, big hugs for Grace
    Cerysxxx

  5. Lianne says:

    HI to you both!!
    So pleased you are on your way home, it will be fantastic to see you soon.
    I laughed like a drain when I read how much Grace has been eating, hilarious!!
    It was our first day with all the children at school today and it went really well, if exhausting! I was helping out in Foundation and was amazed at how well the children just came in and got on with it, brilliant!
    I saw Jojo, Alex and Millie during break time when we were being blown about by the wind! They all looked fab and I think they have settled fine. I can’t wait to see Grace, her lovely smile and giggle will cheer us all up!!

    Take care and have a peaceful journey HOME, bet you can’t wait!
    You are amazing Leanne for everything you do! Lianne xx

  6. Tracy says:

    Wow, that’s gone so quick! Can’t believe you’re nearly finished there! A bet you’re looking forward to a proper cuppa, proper fish and chips, proper beer etc!!!!

    Hope the flight’s not too horrendous for you and see you soon

    take care
    tracy
    x

  7. Muhammad Younus says:

    Hi Leanne and Grace,

    My name is Younus and I have 9 years son with CP condition. I have heard alot for STEM CELL theraphy, referred many neuro doctors to check about this treatment. All of them are not very familiar with this type of treatment or they don’t want to give any adivice.

    I am writing to you, as you have gone through with this treatment, how do you find it and do you realy get some benefit out of it.

    He as only motor control issue, hence can’t balance his body lack of coordinating movement of body. Can speak, ready, count, understand maths science. Doctors recommend him to admit in normal school, but school refused to accepts due to his condition.

    Please help me in arriving some conclusion for my son, should I go for this treatment or not.

    Thanks and waiting for your response.

    Regards
    Younus
    Poor father

  8. CP Social says:

    Dear Grace

    There is a new CP website http://www.CerebralPalsySocial.org and I suspect you will probably want to know about it. It’s for people who cope with cerebral palsy directly or indirectly, on a daily basis.

    So what can I say about it. It pays to have a look because you’ll see we’ve taken our first steps and now want to increase membership to make it more useful for all who use it.

    You are invited to open a blog, use the bookmark function, start polling, open a group or join an existing group, connect your Twitter or FriendFeed to your profile, and the options are growing all the time. Most of all, you can stay in touch with your friends and make new ones!

    So, stay well and stay in touch.

    The CerebralPalsySocial.org team

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