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Myeloma Stories

Carole L. – Dubois, PA

28 years ago I was told I had Myeloma. I could,not imagine what it was. I had never heard of it. In fact the Doctors were not sure about it either. I had a tumor eat through the 7th vertebrae in my neck. Again how could this happen. I never asked why I just said lets fix this.

Now 28 years later I can tell you that if you are a new Myeloma patient you are so lucky to have the many options I didn’t have. I have pioneered through all the chemo’s, radiation, and 3 transplants. It wasn’t always  easy, but in 28 years I have been able to watch science evolve with Myeloma now being recognized as a cancer that is growing.

What I can tell you is to be patient, have a Doctor that is knowledgeable in Myeloma, and never give up. If I can make it through 28 yrs. you can too.

God bless each and everyone, and give us strength.

– Carole

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Myeloma Stories

Marsha L. – Carlisle, PA

I was diagnosed (accidentally during routine blood tests- I had no symptoms) in 1997. It was a shock, and being a nurse, I feared I only had a few years to live! Instead, thanks to God, my physician, and my very supportive husband and family, I am alive and relatively healthy 17 years later!

I believe that one of the best things I did was to pick my initial physician very carefully! Then when he gave me the diagnosis, I asked “if it were your wife ,where would you go for a second opinion?” He did not bristle, or look disturbed or insulted (he worked in a prestigious medical center himself). I expected him to say one of the big med centers in Philadelphia or Johns Hopkins, in Baltimore. Instead he said, the Mayo Clinic or The University at Little Rock Arkansas!

My husband and I actually went to both within the first two years. Little Rock was the key. They started me on Thalidomide. My local doctor had not ever put a patient on it (it was brand new), but he was willing to try it. Within four months my IGg plummeted remarkably, and the rest is history.

I went into remission after about 3 years, and it lasted for about 8 years on just a maintenance dose of 50 mg. About 3 years ago I went out of remission, was put on higher doses of Thalomid, with some success. However, with lytic lesions appearing about 3 years ago, and not great results from the higher Thalomid doses, my doctor started me on Revlimid around January 1, 2014. After two months, my IGg plummeted over a 1,000″points”. I have relatively few side effects so far, so needless to say, I’m thrilled. I hope my story will inspire others who are newly diagnosed!

— Marsha L.

 

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Myeloma Stories

Carole L. – Dubois, PA

I look at my story as more of a journey because it was in 1987 that Multiple Myeloma came into my life. It is hard for to believe that 27 years ago MM became a way of life for me, but the key word in this sentence is life. What I want to pass on to those beginning their journey is that you are very lucky as you have so many options, and you can fight using these options. I have been able to see science move forward with new drugs, research, transplants, and education of MM.

I was blessed to be given these 27 years, and to see the progress being made. Thanks to 3 transplants, help from the new drugs, and brilliant Doctors I am able to continue to live my life without any regret. May God allow you the same.

— Carole L.