Thank you for all the kind messages, Naomi has been for her biopsy, had her ct scan and has had her "wigglies" (lines for her chemo) put in. I have written a blog to keep my thoughts from getting stuck in my head and so I don't forget what i have been told over the next few months. If anyone would like to keep up with what has been going on the blog is at
www.jenmillard.blogspot.com
We are currently just waiting for the consultant to come and discuss the results of the biopsy and tell us what the official diagnosis is and what out treatment will be and how long for etc. its still very much a blur but we are getting through it as a family.
FormerMember
It's lovely that you are all together as a family and I wish you all the best in the world. Naomi is so brave and I'm sure that when the treatment starts she will be brave and strong. Children are so resiliant, in fact she will most probably be there for you as well. Hugs and kisses to you all and please keep up the blogs, they do help believe me. Annxxx
Just to say that if it is a Wilms tumour, they normally effect children under 5 and 9 times out of 10 they are completely curable so fingers crossed for you!
I know someone who,s daughter had this and they joined a group called Little Rays Of Sunshine, it is a childrens charity for children who have serious illness and they make dreams come true so to speak, ie if theres anything your little girly has always wanted to do they can make it happen for them-a bit like Jim,l Fi It lol! I know they have a website but if you google it you should find out more about it.
Iv just read all of your blog and my heart goes out to you, it really does, you are so brave and Naomi sounds a little star!
