hi everyone,
my daughter was diagnosed with thal intermedia: compound heterozygous for HPFH 3 / codon 15 β0-thalassemia mutation
there isn't much information available on quality of life for patients with this condition as there aren't many patients with this condition. however, we learned at the appointment that she is iron deficient. upon talking to Eileen from the thalassemia foundation, i learned that's it is uncommon for thal patients to develop iron deficiency. currently she has been prescribed iron drops 2ml everyday. please share your wealth of knowledge on this topic. we plan to visit pediatric hematologists in India when we go sometime end of year. if you also know of any pediatric hematologists in the state of Gujarat, India please let me know as well.
please see attachment for lab results.