This really scares me, and also makes me thankful to God, i thank HIM that zainab was diagnosed at the right time, and we started to transfuse her,i know fighting with iron is very hard ,as you have to insert a needle in your kid's belly every night or at least three times a week (as in zainab's case right now, but i have done 5 nights a week also).but my point of view is that,if you are living in a country like mine,where there is a lack of awareness about thal, it's better not to have facial features like thal patients, coz i'd hate when people would look at my daughter as a goner,and would try to sympathize,so i am happy that when strangers or even relatives who doesn't know about her thal look at her, they can't doubt anything,her nose bridge is slightly flat but not prominent.
I wish you all luck and joy, and Manal and Dimple,plz tell Ahmed and Priya that i love them,and i hope our kids will meet sometime somehow.
ZAINI.