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A person with Beta Thalassemia Major is completely transfusion dependent from about 6-24 months of age requiring 2-4 units of blood every 15-30 days for survival apart from complex iron chelation to control the excess iron deposition due to the repeated blood transfusions and increased iron absorption caused by this ineffective red blood cell production

Eur J Biochem, 2000

Because evidence for cosmetic or wellness benefits is limited, we can't guarantee a specific result

Significant pathogenesis-related mechanisms are shared by, but not restricted to, Parkinsons disease (PD) and migraine headache

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The first couple of weeks begin at the lower end of that range, around 6 units, before stepping up to 8 units as the body adapts