My finace has haemochromatosis, a genetic blood condition which means he has 200 times more iron in his blood than normal, he needs to be bled (have 500 mL of blood drained every 2 months) and he cant eat too many green vegetablles or red meat.
I found out that my sister and mother are also carriers of the gene, but dont have it full blown like my fiance.
I was tested, but do not have it.
But doctor was still concerned as to whether the baby may get it or be a carrier.
does anyone know more about this?
I dont think the baby can be tested for the disease, however wouldnt there be traces in my blood if my baby did have it.
Im not sure if it can be detected in young children, as my fiance didnt know he had it til he was 14 years old




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