I don't have kidneys.
Does anyone here have both Multiple Myeloma and Kidney Disease? My husband has Stage 3, high risk MM and Stage4/5 kidney disease. The myeloma has damaged his kidneys. Does anyone else deal with both of these?
I have asked this before but now it has been 15 months since the SCT and things are not getting better with fatigue, concentration, insomnia and back pain. I am only 53 but since I was diagnosed 3 years ago and I have not woken up and said boy I feel good. My confusion and concentration seem to be getting worse. My numbers from the blood tests are good but this seems crazy. They tell me “well each cancer patient is different” I went down to 24 hours a week and no help at all. Any thoughts?
I am Iswandi 61 years old from Indonesia .. I was diagnosed with MM in July 2019 .. dialysis 16 times and was given velcade dexa and revlimid (6 cycles) and declared remission. I am still actively working and playing tennis 2 times a week. Do I need to do a transplant ..
What does your specialist say? Transplant is still a good option for patients with high risk disease. Do your homework. The Healthtree Foundation and the International Myeloma Foundation have… read more
My mum is with the following levels:
Kappa chain: 50.36 mg/L
Lambda chain: 22.59 mg/L
Kappa/Lambda rate: 2.23, it should be between 0.52 and 2.42
She is with daratumumab treatment (one dosis each one or two months, depending on doctor's decision.).
After a bone marrow biopsy, she got 0.0024% of clonal plasma cell cyIgL Kappa CD38+d (crowded) CD56* CD19- CD45- CD138+ Beta2micro+ CD117- CD81- This result is equal than the last bone marrow biopsy (0.0025% one year and a half ago).
She is doing… read more
I’m worried it’s something else, my small town doctor goes so fast. Heading to MD Anderson next week for a 2nd opinion. 😟