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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

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Doctors use Lenalidomide because it is highly effective at keeping myeloma
away. They know there is a small risk of it causing a second cancer later on, but they take that risk because the immediate danger of the myeloma is so high.

Nobody Fault: doctors were using the best global standards to save lives from first cancer. The fact that a second cancer developed is a tragic, known side effect of the treatment, but it was not done out of carelessness.

Faith and the Test

Thinking that Allah… read more

October 11 (edited)
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Multiple Myeloma Maintenance Therapy: 6 Facts Read Article...
A MyMyelomaTeam Member

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Yes, continuing the VRd regimen (Bortezomib, Lenalidomide, and Dexamethasone) for 40 months can cause an increased risk of a second cancer, primarily due to the lenalidomide component.

Going back to original concern about lenalidomide causing a second blood cancer (like MDS or AML) when those secondary conditions develop, the bone marrow struggles, causing overall blood work to decline. The fact with absolute numbers are stable and organ function is good means bone marrow is tolerating the VRd well.

Given ultra-high-risk genetics [t(4;14), del(17p), TP53], this degree of stability at 40 months is an excellent outcome. doctor will likely want to keep doing exactly what they are doing: monitoring these labs every few weeks to ensure the
stay stable

October 12
A MyMyelomaTeam Member

I'm a little tired, but made chicken noodle soup, walked 3100 steps so far, & getting ready to make steak & rice for dinner.

October 16
A MyMyelomaTeam Member

From what I understand, the secondary cancers that develop are predominantly bone marrow disorders- like Myelodysplastic Syndrome (MDS) and Leukemia. These cancers do not show up in your monthly blood draws for m-spike, light chains, and immunoglobulins, but do affect your standard blood cell count numbers. Secondary cancers cause your platelets, red and white blood cells numbers to drop as your body fails to produce healthy cells. Your doctors are monitoring all the results from your blood work and if they see a drop in your complete blood count (CBC) -red cells, white cells, and platelets, they then check your red cells for abnormalities. If they see abnormal cells, a bone biopsy is done to confirm the secondary cancer.

October 12
A MyMyelomaTeam Member

Mary 919, usually blood work is adequate to monitor myeloma. Unless you have non secretory myeloma that doesn't show up in blood work. Let you doctor know if you have new bone pain. Every center is different. I get a bone marrow biopsy yearly. This is my 9th year with myeloma. I'm getting a PET scan next month to see how things are.

October 12
A MyMyelomaTeam Member

Best wishes

October 11

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A MyMyelomaTeam Member asked a question 💭
New York, NY

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

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