Of the three well known chelating drugs, only deferiprone (L1, Ferrirpox, kelfer) is a small enough molecule to penetrate certain areas of the body and it also does a much better job accessing heart iron than the other chelators. These natural substance chelators can all get everywhere in your body. IP6 is already found in every cell in the body. Because they literally do penetrate all tissue, they can chelate where other chelators do little or nothing. This is making a big difference for those using these substances, even if they don't realize it.
I would actually like to see a controlled study of thalassemics who are given IP6 from birth, to see if there is any difference in pituitary scans. The antioxidant effect may be more important than its chelating effect in young children, as it is the oxidative stresses that are the most likely culprit in shrinkage of the pituitary, even in the presence of a low iron load. The pituitary gland eventually disappears in thals even when iron load has never been an apparent issue. When you look at what is caused by thalassemia itself and the unmatched globin chains created, the bad hemoglobin produced and the irregular red blood cells, there is much more than iron to combat. We should also be looking at fighting oxidation, oxygen depletion and nitric oxide depletion. If I was asked what I would give a newborn thal for supplements, the list would include vitamins D and E, IP6, some version of L-carnitine with alpha lipoic acid, folic acid and magnesium drops. Why not fight ALL of the problems of thal from day one, instead of waiting until iron is an issue before anything is done? Iron is only one of the battles. Oxidation will cause tremendous health issues if not confronted.