This disease is so rare in children. I have a 7 year old daughter who was diagnosed in January 2008. She had a BMT is April and relapsed in July 2008. She was then infused again in July with Tcells and started GVHD in August. Overall this was a terrilble year for us but I am happy to say her engrafment is up to 99% and the GVHD is getting better. The runx1 gene that cause all this is gone also
![Stick Out Tongue](images/smilies/tongue.gif)
. I just want to know if anyone has a child who has beat this terrible diease?
![Confused](images/smilies/confused.gif)
All the stats on long term survival in children are not good.