Has any one used or heard of infrared beds for the treatment of multiple myeloma?

Has anyone had experience with heart valve replacement and myeloma? Wondering how the type of valve used - artificial or cow or pig might affect future options for myeloma treatment. With the artificial valve lifelong anti coagulation with warfarin is required. Thanks.

Trying to understand what my life will look like living with multiple myeloma. I am in my 3rd cycle of the 4 drug treatment Dvrd. I have no stamina whatsoever. Dr. Said I should limit my what I lift to 30lbs. I'm planning to do the stem cell transplant in late December. What other adjustment should I plan for. Will I regain my stamina 6 months after SCT.? Will I always be restricted to 30lbs lifting? I just don't know what to expect and how to plan for what comes. Relapse in 4-5 years if I'm lucky. Thank you for your insights.

I am interested in contributing to knowledge/understanding re: how environmental factors contribute to multiple myeloma. Both of my neighbors have multiple myeloma. That's three multiple myeloma households in a row, including me. We live near East High School in Salt Lake City. Does anyone have any suggestions about who may find this useful for research? I intend to contact my water provider to check our water supply. I have also considered a neighborhood survey to see if there are other neighbors with MM or other blood cancers. Any other suggestions?

Hello, I underwent autologous stem cell transplant after achieving zero M-Spike and less than 5% of my bone marrow having Myeloma cells. Has anyone else undergone stem cell transplant while having a zero M-spike, or with very little Myeloma cells in their bone marrow (less than 5%)? If so, did this help you stay in remission longer, or how long was your remission? I presume the lower the disease is when going into transplant, the better the outcome, as opposed to getting a transplant when the disease is still looming high in the body. Thank you.

I have been diagnosed with MDS/MPN unspecified - I don’t see that as an option here under diagnosis. It is very confusing. Other than ferrous sulfate for anemia I’m in a watch and wait stage. So many questions.

Hello, I was wondering how common MRD- is at the 3-month mark of CAR-T? I had Carvykti on July 11 and am waiting on the results of my bone marrow biopsy. So far blood work looks good but I'm nervous about the biopsy results. If I don't achieve MRD-, is that bad? And does that mean it still may be achieved at some point? Thank you!

I am excited to have found this group.

Did you know that treatments for Multiple Myeloma (MM) and its early stages (MGUS and SMM) might affect our eyes? 👁️ Some patients experience conditions like cataracts or glaucoma, and we want to understand why. 🔍 Your insights can make a difference. 💬💡 Together, we can pave the way for better eye care 🧑‍⚕️👀 for MM patients! 🌟 Click here to take this quick survey.: https://healthtree.org/myeloma/curehub/private/research/wSBMWdUZegYLGW1XEFRc?utm_source=social+media&utm_medium=facebook&utm_campaign=eyehealth&utm_content=general

I’m 46 years old Italian woman and my myeloma was diagnosticated in 1997, 27 years ago , when I was just 18 years old. I had really a lot of Line theraphy and twice auto trasplantation. Now I have Dara + Poma + Dex, from about 2 years. I know I’m really luky but in this last year I feel my self too much tired for all day and all time, I have had stopped to work for this and I’ m very demoralized , every thing I have to do is very hard due to my fatigue and pain. Anyone can suggest me how to make my quality of life better ? Thanks ❤️

Good morning pray all are having a good day.

In response to the question about 1q gain. As always, every myeloma profile is different & every patient responds differently to treatment. I was diagnosed with aggressive myeloma 15 years ago (October 2009). It was considered so at least in part because of my FISH profile: 1q gain (4 copies). Since 2010 I have been through 5 lines of treatment, including 2 stem cell transplants (2010 & 2018) and most recently CAR-T therapy (2022). After every line I responded well, and my response to the CAR-T continues to this day. Note that I am 76, take 2 hours of physical exercise everyday, eat healthy, nutritious foods, stay positive whatever the circumstances, and I am optimistic about my survival prospects. These factors may be very important in my overall longevity despite the genetic profile & many lines of treatment. Good luck on your myeloma journeys.

CAR T therapy is a growing option for multiple myeloma patients and investigational CAR T treatments and targets are now in development. Investigational treatments using different targets could help patients who have relapsed after standard of care myeloma therapies including the newest BCMA-targeting immunotherapies.   The QUINTESSENTIAL Phase II clinical trial aims to test the impact of an investigational CAR T therapy called BMS-986393, which targets GPRC5D, in relapsed or refractory multiple myeloma patients.  This multi-center study is open in over 35 locations. Please click the link to learn more or to join the study: https://www.bmsclinicaltrials.com/us/en/clinical-trials/NCT06297226?cid=s_2839283 Funded by Bristol Myers Squibb

I have RRMM, IgG Kappa. I’m in the process for Car-T at Cleveland Clinic, having completed T-cell Harvest (for the second time due to low cell quality the first time around) three weeks ago. I’m waiting for the re-engineered cells with scheduled infusion date in early Nov. My bridge therapy is Selinexor/Dex/Darzalex, which is working pretty well to keep my Kappa protein in check. Lympho depletion is scheduled for a couple weeks out. I’m looking for someone who has gone through Car-T at CCL to share their experience with me, and provide any suggestions/guidance/perspective on what to expect from here on out and how to get through the next phases. The side effect possibilities look daunting. Thanks!

I have been diagnosed within the last 2 years and I am wondering if I am going to have to deal with the constant pain in my back. From what I have read it seems as though I will have the rest of my life with this condition. Is this true?