Everyone should be getting ready for the new enrollment periods for Medicare Advantage, Employer Benefit enrollment period, etc. Taking the time now to discuss with your healthcare team current therapy and anticipated changes to your therapy now so you can make sure you have the best insurance coverage for next year is important. Don't forget to consider out-of-pocket costs. Planning now can head off a lot of worries down the line.

Hi. I have procrastinated joining a group since I was diagnosed in 2018, but am so glad to have finally taken action. After a case of bronchitis and a visit to the ED because the coughing was so painful, a chest X-ray showed multiple rib fractures in various stages of healing. Things progressed from there to a MGUS dx, then on to MM, bone lesions on my femur and spine, up to having an internal fixator device placed in my left leg because of destruction to my femur. After surgery, I began treatment initially with Velcade and dexamethasone and later adding Revlimid with bisphosphonate therapy IV q 3 mos. Radiation on my spine helped with the pain and after 4 years of treatment, my MM blood panels remain stable. The journey up to this point has been a blessing as much as a burden. While spiritually and emotionally I have always been at peace; my physical state has been a challenge and some days, like today, I feel completely discouraged. Although I rejoice that this is as close to the unspoken state of "remission" as it gets; I am exhausted with the slightest activity, endure constant back pain, and am stifled by GI distress. While these side effects minimally affect my quality of life, all in all treatments have been tolerable. I did not experience vomiting or hair loss as typically shown on TV and the Velcade injections were not very uncomfortable. I guess I am just wondering if with a stable MM panel, should I continue to have this much fatigue? Although I have increased my exercise regimen, I can not go a day without a pretty long nap. I am off work now for the summer, but have serious concerns as to whether or not I will be able to return to work 40 hours a week because whenever I do, problems with my health begin to emerge. I appreciate your time and input and am praying for great outcomes for you all.

Hi, I'm new here, it's the first time I've written, I'm 51 years old and I was diagnosed 2 months ago in a preliminary way. My diagnosis is asymptomatic, I don't have bone lesions, my oncologist told me that I don't have anemia, however he prescribed me iron. He told me that since I did not have bone injuries, my pain was not associated with the diagnosis; however, I feel pain in the bones of my right arm, lower back, hips, and hands. My question is if there really shouldn't be pain as there are no injuries to the bones or is it possible that the disease causes pain for other reasons. Wishing everyone health!!!

I'm 51 years old and was just diagnosed with MM this week. I don't know much yet but, I know its advanced enough that my doctor recommended Chemotherapy right way and looking forward to Stem Cell treatment is likely within a few months. I really don't know very much yet. I have a 9yr daugher and a 8 month old daughter. I really want to be honest with my 9 year old. She is smart and can tell something is going on. I'm just not sure how much to tell her and how to go about it. I want to be honest and open but, I don't want to give her nightmares. Any advice from others who have been in a similar situation is appreciated.

Hi, Anybody out there who has experience with Johnsson & Johnsson's Talquetamab? As of 17th of july 2023 I entered the "MonumenTAL" study. A Phase III study in which a combination of drugs is being examined to see if Talquetamab is more effective when not administered on its own. I do suffer from serious side effects. Rash and an itchy skin all over my body, total loss of taste and significantly increased liver and gall blood values. Whether the treament has any impact on the disease I do not know. Oddly enough there have been no blood tests so far investigating the value of M-Proteïne and FLC. My iliac bone on the left side hurts tremendously. I can barely walk. Which is one of my favourite past times. I fear this bone ache has nothing to do with the "MonumenTAL" study. Please, do share your experience with Talquetamab. Whether it has been in a Phase 1, 2 or 3 study.

My husband was diagnosed in 2017and was told he is in remission about 9 months ago. Now come symptoms: extremely irritated stomach, loss of appetite, loss of sleep, weight loss, followed by trembling, some confusion, drooling. Got him some vitamins and appetite has improved but not much else. Is he in remission or not? Is this a new malady he must struggle with?

Hi all, I’ve had MM for 7 months numbers have been dropping but not fast enough, getting referred to more specific hospital U of M. My disease was diagnosed in between my 1st and 2nd back surgery. I’ve had a total of for surgeries to fix and repair 12 compression fractures and it did help the pain but I have 1 big problem still. I can’t get my body to adjust and allow my back to relax unless I set in a chair and concentrate with focused breathing. When I attempt to walk it just automatically tightens up, and I walk around with my shoulders shrugged up. I feel if somehow I can get my body to relax my back I would feel a lot better.

My husband is 58 and has had a stem cell transplant and just recently CAR-t with Carvykti. His stem cell only lasted 4 months before the cancer came back. The side effects from Car-t have been awful. His case is complex. Has anyone else had this with side effects? He was in ICU for CRS and now dealing with bad neurotoxicity. He had the severe headaches and now has numbing in his abdomen, back, feet and hands. Has anyone else had this? He is a month past the transplant.

Anyone on Isatuximab + VRD? Please share your experiences

Relatively newly published review article: Diagnostic and Treatment Strategies for AL Amyloidosis in an Era of Therapeutic Innovation https://ascopubs.org/doi/full/10.1200/OP.22.00396#