Discussion Forums > Thalassemia Major

Daughter with thallassemia major

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Alia:
 hi every one,my daughter got thallassimia major.im living in a country where hardly anyone knows about this condition.The docters are not that familier with it eather,she is getting the best possble care but i love to here about other people who have this condition as i have very little understanding of this condition.my daughter is now 14 monthes old.   she started her first blood transfusion when she was six months old.i like to know about all diffrent ages of people who got this condiotion and how do they deal with it in everyday life,also how do they deal with the iron medecation they might be recieving.
Alia

Andy Battaglia:
Hi Alia and Welcome to our group,

What country are you in and which iron chelator is being recommended for your daughter?

Alia:
I live in newzealand im not sure what medication it is but she is going to started soon.thanks for your reply
alia

Christine Mary:
Welcome Alia!!!  :hithere

I'm fairly new at all of this, with my little one having Thal major as well.

Please know that whatever questions or concerns you might have, you've come to the right place to get the BEST advice!

 :flowers

Kathy11:
Hello Alia :wave :wave.

I hope that our forum help  in aleviating your worries regarding your daughters health problem,and provides support for you when in need I promise you, that is one of the best move you have made ,this is a fantastic site ,welcome and good luck.
Kathy

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