Hello Lovelies!!!!
Well, I do not know if I am thal minor or not or what the heck is up with me, just that my daughter is a minor and I have been told there is something wrong with the iron in my blood. My uncle recently had bloodwork and his iron was too high and he donated blood and felt better.
I had the feeling that I should donate blood. Just so you know, I have no money and no access to medical care, so I guess and I do whatever I can that is free!
I did a bit of research and discovered that according to the CDC, there are over one million Americans of European descent that have a gene mutation that causes iron overload which leads to hemochromatosis. An internet description on the womenshealth site stated that this is serious and chronic and that the build up of iron can damage organs like the heart and liver. The testing is supposed to be a fasting blood test of both the transferrin saturation and the serum ferritin. Many of the symptoms listed are things that I deal with and disease states that have killed family members.
So, is this related to thalassemia or is it another mutation entirely?
I did go and donate blood. All I can tell you is my observations. I immediately felt less pain in my neck and shoulders. I have this baggy area underneath my eyes that I feel looks dreadful and it seems to have lessened a bit. I also feel that it is a little easier to breath.
As you are all the experts in this area, I thought I would ask you about all of this and your personal experience with symptoms as they relate to elevated iron levels.
I love you all!!!!
Linda