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Vitamin C for Thal?

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Andy Battaglia:
Thanks for finding the article, Sarah. I had no time all day to look for it and it's a big help.

For me, as one whose logic is perhaps too dominant, vitamin C has always created the biggest paradox of all in relation to thalassemia. I have always had a hard time accepting what is believed about vitamin C and thalassemics, but because of the observed danger in a relatively low dose of 800 mg daily, I have always gone along with the advice to limit the daily dosage of vitamin C in thal major and intermedia. But I have also been in fact, the one person recommending vitamin C to thal minors because of the obvious need created by oxidation. Thal majors test almost universally for severe vitamin C deficiency, yet they are instructed to avoid this extremely important antioxidant. I have often alluded to the idea that vitamin C and its use in thal should be much more thoroughly studied. This article only reinforces that belief. I cannot advise large doses of vitamin C to thals, which I find distressing since I generally take 6 grams daily myself, but as long as we don't know for sure, I suggest caution.

Interestingly, the FDA recently banned large intravenous doses of vitamin C for cancer patients, in spite of much testimony to its efficacy in treating cancer. Vitamin C is extremely cheap and no one is going to make a lot of money from a vitamin C solution to any disease or disorder. Because of that glaring fact, I feel that it may be difficult to get research moving in that direction under our current research for profit paradigm.

One thing that was startling in that article was that a patient was told he was dying from iron overload in 1990, when desferal was available. Stay vigilant with your doctors and make sure you don't know more about thal than they do.

Wildbill:
Thank you to Andy and all those who commented.  I appreciate this site for the information and support it provides.  It is difficult to find understandable information on theThalassemia / Hemaochromatosis combination.

In speaking with my physician, I am his only patient with iron-loading thal.  I'm on Exjade, which has been lowering ferratin from 2500 down to 650 within the last year, but it really wears me out.

I have been taking B-12, green tea extract, folic acid, vitamin D, but still feel very drained.   Hemoglobin stays around 7.7 to 8.5.

Thanks for all you do.  It is much appreciated.
Bill

Answers4N:
Hi Wildbill,

Do you know if it is the combination of Thalassemia minor and Hemaochromatosis that causes your hemoglobin to stay that low...? I thought that level was more closely related to intermedia.

I am curious because our son's hemoglobin is 8.3 with suspected Thal minor (at this point) and severe iron deficiency. Interestingly, I was just told recently that the Native American tribe that our son has heritage from has a very high incidence of sickle cell trait carriers. I tried to look that up and found that Native Americans do have a high rate compared with other ethnic heritages (with the exception of African Americans that had a higher rate), but I couldn't find a rate for his particular tribe. Now we are wondering if my husband might be a sickle cell trait carrier and that is combining with thal to create something with different effects.

I guess we wait patiently now for the genetic analysis....

Sarah :)

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