Hi Everyone!
I'm April and I have recently been diagnosed as thal trait. So was my husband. Glad to have found this forum, as I feel kind of lost in the thal world. We only found out that there is such a thing as Thalassemia when our son died last Dec. 23, '09 at 8.5 months, when I had an emergency c-section having accidentally found out that there was no more amniotic fluid in my womb. We had a partial biopsy done and it was discovered that among other things, his heart, liver, spleen and lungs were affected.
Well...I will be reading around this forum as there seems to be so much information. Actually, I've been reading up in the forum for a few days now, but I often suffer from information overload! Also, it's a bit confusing to differentiate Thal alpha and beta advice, so I think I have to read a bit more. Hope you guys won't mind, but I'm surely going to ask ALOT of questions later on.
Take care, everyone, and pleased to meet you all.
April