Good news - we have got a room at the sick childrens trust house which means that this is our room now for the duration of our stay and we will not be moved again.
This is a charity and depends wholly on donations, but they do not charge parents a penny.
We intend to make a donation at the end of our stay, they do brilliant work for the families of children in GOSH although they are completely independent of the hospital.
Please take a look at the website http://www.sickchildrenstrust.org/ to see what they offer families of children in hospital.
skip to main |
skip to sidebar
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant
Oliver at 5 months
2 comments:
Oh the fighting spirit of a truely wonderful Mum - well done on getting a fabulous room! Glad to hear that Oliver is doing well, despite the bumps along the way. Look forward to hear more good news! Bee and Max x
Oh what a wonderful photograph of Oliver, can't wait to show Gigi when she gets home from school tonight,(wed 13.05.09). He looks quite cheerfull and totally gorgeous, I just want to scoop him up in my arms and kiss him! Sorry to hear of your crisis yesterday, however, its great to know you've still got that fighting spirit in you! Well done and keep up the good work. We miss you all terribly. Love to all, Tracey Richard Gigi Pips and Olivia xxxxx
Post a Comment