← Return to Smoldering Myeloma: Coping with the emotional toll and acceptance

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Thank you for sharing this. When I was diagnosed with MGUS in June 2023 with Monoclonal protein 1.6 g/dl IgG lambda, i was told not to worry it only progresses 1% per year. By January 2024 it was 1.8 g/dl, January 2025 it was 2.2 g/dl and they ordered a bone marrow biopsy in April which presented 20-30% plasma cells, monoclonal protein and a free light chain ratio of less than 0.1 with lambda restriction. I am now in Smoldering Myeloma phase with 2 high risk markers. I had a PET/CT scan which showed some areas in both femurs and ordered a pelvic MRI September 15 which showed a 13 mm focal enhancement in my pubic bone and suggested retesting to see if it went away or increased. I am still waiting for results of the retest from two weeks ago.

At first I was full of anxiety and fear and remembered that I can choose to Forget Everything And Run or Face Everything And Rise. I chose to spend time with the people I love, do things I love to do and started limiting time and energy on things I can’t control…accepting that whatever will be- will be. I will cross that bridge when it arrives. As a “doer “ by nature, watching and waiting does not come easy to me. I want to obliterate the monoclonal cells in my blood and be free from it forever….but, I am told this will never go away and I am just hoping for the opportunity to stop it from progressing.

I send you strength of spirit as you navigate this journey. May this mantra give you comfort…

In this moment, I am safe.
My body is strong and holding me.
I do not need every answer right now — only enough light for the next step.
I am surrounded by love, even when I walk this part of the road quietly.
I trust the strength within me that has already carried me this far.

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Replies to "Thank you for sharing this. When I was diagnosed with MGUS in June 2023 with Monoclonal..."

@donna195 I am also SMM newly diagnosed in June. My next lab draws are Dec 22 with a phone conversation New Year’s Eve with the hematologist/oncologist. Hoping for the best for as long as possible.

@donna195
thanks for the good wishes. I never experience MGUS, just Smoldering. I have hand and foot numbness. Had it for years. Neurologist was the one who actually started the process. Abnormal nerve study. Blood work. And there you go. M proteins, Lambda, well it was a shock. Numbness to pre-cancer. I went to Rochester to start one of their clinical trials. 1q21.3 and 15% plasma cells in bone marrow was the only alert. All other blood work was on the low end. So Mayo criteria determined that its low probability. My story continues, so does everyone else. A collision course to destinies we can not control, but live with day in and day out.