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I had no new symptoms when I went in for my regular check up with my doctor. She ran a blood test and noticed an increase in my anemia. I had been on the edge, but now I was below the edge. She sent me to a hemotologist. I had no idea that she was checking for everything from anemia to leukemia or multiple myeloma. I was thinking "iron" pills. I had a bone biopsy that day and got the results about three weeks later at my next available appointment. It was a shock, and I was not ready for it. I was told that at this time it is rarely curable but treatable. No time frame of survival was given, and I was not able to ask any other questions as I had never heard of multiple myeloma. After three days of shock, I went on the web and gathered all the info I could and got my grown sons to help me look up more info. My whole family was in shock. I have been undergoing treatment for almost two years now, and I am tired, I have kidney problems, and I have one blood clot so far. So I am doing OK. I do go to a support group in San Diego, and it has been more then helpful.

My dad was 51 when his multiple myeloma was diagnosed in stage III. He had been very tired for quite some time. (One ignored hallmark of the disease manifested about three years previously. He had always donated blood but was refused at about 48 because his iron was low. No one advised him to immediately check into that. As a young and strong man, his iron should not have been that low ever) However, he was a firefighter getting ready for retirement, so, we all believed he would be much better after a few months in his dream home in Wisconsin. He became more and more exhausted. Finally, when he was sleeping close to round the clock, my aunt forced the issue that he go to the hospital immediately. (She was a nurse.) He was diagnosed within one day as his kidneys were shutting down. He lived beyond any expectation of the medical community (some good years). He worked hard to remodel his dream home, got to meet a few new grandchildren and died at 55. Moral: Low iron counts in an otherwise healthy younger male are never "normal." Extreme exhaustion in anyone is not always a sign of depression or fatigue. Multiple myeloma can strike any age or demographic; Dad didn't fit any of the stereotypes.

My multiple myeloma started with a headache that wouldn't go away. It became slightly more severe with time. After a few weeks, enough was enough. I went to a walk-in clinic and asked for treatment. The physician ordered an immediate CT of my head and neck area. The CT was negative, and I was referred to a neurologist. I was misdiagnosed initially, and it was six months before I had another CT (or MRI). That test showed a tumor had formed at the base of my skull and the top of my spinal column. By then, I was experiencing ringing in my ears, double-vision, fatigue and pain in my neck and upper back. The tumor was biopsied and determined to be a plasmacytoma. I was referred to an oncologist who tested my blood and bone marrow and diagnosed my multiple myeloma. I went through radiation therapy to destroy the tumor. Either the tumor or the treatment destroyed part of my C-1 and C-2 cervical vertebrae. After the tumor was found, the initial CT was re-examined and a “shadow” was noted where the tumor formed. I was treated with thalidomide and dexamethasone for several months. My M-protein level began to rise and eventually got to 1.7.

My father was diagnosed with multiple myeloma last October 2007. He had a very loose stool for a couple of days; later on he went to an urgent care facility. They told him it was a virus and to go home and take Imodium A-D. That was Saturday. Monday, he went to his primary care doctor. He checked him and said, “I think you have a virus too. But I want to do some blood tests before you go.” After receiving the blood tests, the doctor then sent him for X-rays. In just a couple of hours he was diagnosed with multiple myeloma, and now the fun begins!

My multiple myeloma was spotted very early through a blood test. The first real symptoms were excessive tiredness, noticeable tachycardia, and hyperventilation.

I found out that I had multiple myeloma (MM) when I was 39 years old. I was always tried and just could not get enough energy to do much of anything. When I fell and could not walk for more than a month is when my family found out something was wrong. During this time, I almost lost my life because my kidney was shutting down, and I still could not walk. My husband then took me to another hospital where they found out that I had MM. We have been dealing with this for seven years, and we just found out that I am out of remission. I have to find a new treatment to go with now after already going through one bone marrow transplant, 17 treatments of radiation, a blood transfusion, and chemo. Now we have to go through this all over again.