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Beta thalassemia intermedia

Blood Cancers & Disorders | Last Active: Mar 17 8:58am | Replies (10)

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@loribmt

Welcome to Connect, @palermo1. Thank you for sharing your son’s experience with receiving blood transfusions for his anemia and the need for chelation. While a life savers, the transfusions can leave the side effect of too much iron being stored in the body. Chelation is a means to remove the iron.
Beta thalassemia intermedia is an inherited condition. Do other members of your family have this as well? I’ve read that a bone marrow transplant can be a possibility of a long term treatment. How long has your son had his symptoms?

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Replies to "Welcome to Connect, @palermo1. Thank you for sharing your son’s experience with receiving blood transfusions for..."

Hi my son has been getting transfusions since age of 3 and started on chelator at the time it was deserol, which was sub q, at age 5, he is now 38, still getting transfusions every3 weeks and using jadenu, to get rid of extra iron, my husband and I are carriers of the thalassemia gene and didn't know about it when we had our son, but no one else in my family has the disease form of it, I hear there's gene therapy now but it takes a lot of time to recover my son is not wanting to to this at this time he may also be to old to have a good outcome.