Sory all.. its been a while since my last visit here. im quite busy with working and lot of stuff to be done here and there. Busy at school, busy with children, etc.. Just to share, im nOw a member of thallasemia org in my state. we are going to have Thallasemia day for district level on this coming Sept, 17th. For that, im sooo very sory to those mail I've didn't reply.
Back to my first son's condition- Im regreted to say that the "MADULINA" is actually not working with him. he's nw getting his monthly transfusion. actually this MADULINA doesn't raised his HB at all but we've being fooled by the result of the clininc( the machine they use to checked the hb is not accurate). The result of my son's hb from this private clinic always indicate that his hb maintained to 10 and above but when looking at his physical condition, he's getting pallor each day. so we took him to the nearest govt hosp and the dr confirmed that my son hve to be transfused asap because his low hb-6.
Im so hurt to see both of my children laying in the very same bed at the very same ward.
MY APOLOGIZE TO ALL OF THE THAL PATIENTS AND FRIENDS FOR SPREADING FALSE HOPE OF THE MADULINA. I ALSO DIDN'T KNOW, MY INTENTION IS JUST TO SHARE AND HELP EACH OTHER. IM VERY SORRY.