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A MyMyelomaTeam Member asked a question 💭
want to share a little update about my journey. Recently I went for a CT scan of my lungs, and today the doctor explained the results to me. They found some changes in my left lung compared to before. There are areas where the lung lining looks thicker, and a small mass in the lower part of the left lung has grown a bit since my last scan. Because of these changes, the doctors want to do another test called a bronchoscopy, where they use a small camera to look inside the airways and take samples to understand it better. Hearing all this was not easy for me. It made me emotional because it feels like one thing after another. But at the same time, I am thankful that I am already under medical care and the doctors are taking steps to find out exactly what

I don’t know what to explain to my friends or relatives about the MM Cancer, they didn’t know about it.
When you say it lymphoma or leukemia they know it’s something to do with blood cancer and if you said Multiple Myeloma and they said what is that???
Did any of the MM team have the same problem or talking about MM that they did not know!!!!
So to all MM warriors do not stop fighting and fighting the disease to the end.
Hope you felling better and Never Give Up.May your prayers be answered 🙏🤲

April 9, 2025
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Reactions
A MyMyelomaTeam Member

Hi MAD I had never heard of mm before even the doctor was not sure as we only have about 5000 cases a year in the UK they kept thinking I had prostate cancer and no one in my family had heard of it and so you Google it and that can be scary as a lot of information is outdated or wrong I'm still fighting good luck to you in your journey.

April 9, 2025
A MyMyelomaTeam Member

I just say it’s bone marrow cancer.

April 11, 2025
A MyMyelomaTeam Member

We had not heard of it before Andy got his diagnosis. The first oncologist he saw, freaked him out. She said he had stage 3 and it’s very serious. He nearly passed out. Thankfully, he has come a long way, but people don’t really understand MM. It is complex and everyone is so different.

April 9, 2025
A MyMyelomaTeam Member

I was told by my transplant doctor, nine years ago, that they really didn't know the cause of MM. They suspected (and still do, I suppose) what are called VOC's -- volatile organic compounds. One example of these is solvents used in oil based paints. I was self-employed as a carpenter/painter/remodeler at the time. He didn't want me to paint at all anymore. But he compromised and told me to use only latex paints. They contain VOC's, but much less.
Petroleum products like gasoline and diesel are VOC's. As is charcoal lighter fluid.
Various bug and weed killers contain them also. They are strongly suspected causes of MM. But unless things have changed, researchers are not sure what the cause is. I don't think they believe it's hereditary.

April 10, 2025
A MyMyelomaTeam Member

I just tell them either google or look it up on you tube that seems to work the best because it’s hard to explain.

April 9, 2025

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