Slow SMM with carnivore diet, plant based has too much sugar and carbs, spikes blood sugar type 2 diabetes

Want info on slow progression SMM Sloan Kettering plant based diet

💛 Soothing foods can help when treatment side effects make eating harder. Soft, easy-to-digest options like soups, smoothies, gentle fruits, and well-cooked vegetables may feel more tolerable during nausea, low appetite, or digestive discomfort. Always listen to your body and speak with your doctor before making changes. 🎉 Join the fun. Download Nutrition tips. 👉 https://healthtree.org/myeloma/community/january-nutrition-guide

anyone have an issue with being nauseous and belching for over 10 days

Hi, I had a SCT September 24 and since had clear bone marrow biopsy June 24, clear scans in November 25 and clear bloods in Jan 26. I have started to have a sore leg and just wondering has anyone else had clear results and still had myeloma active. I a bit paranoid! Thank you

Hi everyone, first time here in this link. I was diagnosed with Multiple myeloma in Dec 2024 and have been in treatment since then. I first started with the 4 drug treatment in February 2025 (daratumumab (Darzalex), bortezomib (Velcade), lenalidomide (Revlimid), and dexamethasone (Dara-VRd). Everything was working good and i did not have any side effects, but in april we had to take velcade off due to a rash. Then i did my stem cell harvesting but did not do my transplant as my numbers went from 45 percent cancer cells to 1 percent. I then continued with the maintenance of dara and dexmathasone, revlimid. we did a biopsy and pet scan in december of 2025, my pet scan came back great with no active cancer, but my biopsy came back that my numbers went back to 10 percent. We are starting a new treatment next week of carfilzomib and pomalidome. Dr is telling me that i should really think about doing the stem cell transplant as we already have the good cells stored. i want to hear from everyone here, what are your thoughts and experiences about the stem cell transplant and is it worth it as i am 62 years old at the moment. please let mek now your thoughts and experiences of your stem cell transplant. Thank you !

Hello friends Anyone receiving Zometa infusions and how often do you get it . I’ve read different articles , I get it every month but recently read it should be given every 3 months . Thanks , Linda

t(11;14) : 28% cells Monosomy 13 : 30% 1q gain : 5% cells MYC translocation t(8;?) : 15% cells 17p deletion (TP53) : No 1p deletion : No Hyperdiploidy : No This report is in Standard risk. Intermediate risk or high risk ?