thank you so much auntie claire for setting this page up for me.
we all love you loads liam!!!! xxxx
The T shirts and Badges are lovely well done Rose xxx
I have just submitted a comment form Blog and it has vanished into thin air ?? :<( hoping it has found its way into Claires email box -
In nov 2001 our baby boy was born, liam matthew rice weighing 10pound 2 ounces beautiful with jet black hair.It was a very long labour day's infact, liam was eventually born by emergency c section due to his size and his heart rate was dropping. The first time i held him i felt something was wrong he wasnt breathing properly, i was assured lot's of times by the nurse's that he had been checked and was fine,but call it mother's instint i dont know why i could settle on that, i keeped asking for another doctor, eventually to shut me up another doctor came and whisked liam straight to intensive care. I cried seeing liam with tube's everywhere, i was slightly reasured by liam's size he filled to incubator from top to bottom side to side, all the other babies looked so fragile. When i asked the nurse if liam would survive she said it was 50/50 but against the odd's liam got better. I know liam has the same stength and determination now as back then with family and freind's supporting us and a little bit of angel power there will hopefully be a cure soon.
very happy to join this charity and link it into my 30th birthday on 10th of august where we will raise more money at the railway tavern fishponds
that is very kind thank you so much xxxxx
thanks hunnie. ive got some collection tins. do you still want 1? xx
thank you for donating for me im realy happy
baby boy we will do any thing to make you happy! tell me what you want more than any thing else in the world? xx
to marry maici and have babies
I Love You So Much Baby Boy xoxoxoxoxo
i would like to thank everyone who has shown so much kindness and support you dont know how much it means to us .Together we can make good things happen , make dreams come true,and give my beautifull son every chance and opertunity to fight against this horrible condition. FIGHTERS FIGHT AND WE ARE FIGHTERS Liams words not mine, thankyou once again we think you are amazing.
did you here about the 10 k run
my mum did the 10 k run
You guys are an amazing family and deserve every little bit of help we can offer! Liam, you are an inspiration and we'll do all we can to raise awareness for you!!! Xxx
I really like this article.I undeniably will undoubtedly revisit.I wish to apprentice while you amend your website.This article is very interesting.
Encouraged each other and learn from each other,I find it is really useful for me.I will be coming back to your blog for more soon.Thanks for your sharing!
How frustrating and annoying, that after six months waiting to see the neuro doctor that told us liam has F.A. he knew less than us on the condition. In feb when we were told, the information was to much to take in, don't know y I thought he had the answers. Liam's rate of progression should be so slow that we wouldn't notice a change in him yet but we do, I have found out that the repeat in his dna reveals the answer of how fast the progression is the longer the chain will no break the faster the progression. At the start of r F.A journey I was shown liam's repeat by the genetics doctor which from memory was long no breaks, I need to see this again because at the time I had no knowledge, but now they won't let me. Also we have been given a perscription That every chemist we have taken it to can not make up for us, it looks like the medication might have to come from a different country, but as r lovely doc is sunning himself on his hols we just have to wait for three weeks. I will get the answers and any medication liam needs I'm never going to give up.
book of ra kostenlsoe spielen auf games onlne flash