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Multiple Myeloma is a cancer..but im not sure if it has a cure...? |
My dad has Multiple Myeloma - His doctor says there is a 100% cure...but in pamphlets and others it says it has a temporary cure - stem cell transplants and bone marrow transplants...did anyone you know ever have it? what happened? oh yea...and the doctor im talking about is from the Mayo Clinic in Rochester, Minnesota (which is a pretty good place) so idk...and the pamphlets are also from Mayo..so im sooo confused I'm not sure there's a 100% cure for anything. I would suggest that you do some of your own research, educate yourself about the different treatments, and then ask the doctor again. Maybe this was just a miscommunication of some kind. Check out the sources below to get started. Usually it's treated with chemo, and hopefully a bone marrow transplant. It can be cured. According to the American Cancer Society, 33% of patients with multiple myeloma survive at least 5 years from the time of diagnosis. Younger people tend to survive longer than older people with this diagnosis. Oncologist don't like using the word cure because cure implies it will not return. Remission is the better word. There is nothing that is 100%. Even in the best type of cancers that is "curable", such as testicular cancer or Hodgkin lymphoma, cure rates maybe up to 90+% but not absolute. Hi, My dad has multiple myeloma, he is at the V.A. in Dallas ,Tx. The Dr. say no cure. It is treatable . It can only be managed. New drugs are coming every day. There is a center in Arkansas, that does research and treats. He is 65 and I am not hoping for much, just that he does not suffer. |
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Average survival depends on the stage of the disease, which is determined by various lab values (see the first source below for more details). As for the patient you mention, it is very difficult ... I am very very sorry for your loss ,My father in law died from the same 'Multiple Myeloma' 7 years ago.what you have been told is absolutely correct it is a very rare form of cancer about... Hi, yopur question go posted twice; see your other question for some information or read my email, thanks, jewells 34 months and still here ...Hi, Amyloids is a rare side effect "malady" of MM; I know that Mayo Clinic is doing some work on this. For more specific information I would call the IMF hot line: staffed by tr... M proteins refer to an elevation in a particular immunoglobulin (the antibodies that our white cells make to fight infections and what-not). Most of the time this elevation is termed polyclonal in... My wife get's irritated when I answer these. She says that you are lazy and you should research it yourself since it's part of your nursing program. Don't start taking shortcuts, it&... Hi, I'm so sorry to hear of your mom's diagnosis. My dad had this and they told him right away. They also told him that it isn't curable but it IS treatable. I would make sure she... Hi, Stage II doesn't say much with MM. It depends on the age of the person, the M Spike level, how they are responidng to treatment, damage MM did before diagnosis and a lot of other... |
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