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Thumbnail for Impact of Hospital Readmission on Quality of Life in AML | Ayobami Olafimihan, MD | #ASH24
Playlist: ASH 2024

Impact of Hospital Readmission on Quality of Life in AML | Ayobami Olafimihan, MD | #ASH24

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Thumbnail for Good Responses to Phase 2 CLIA + Ven Therapy for Acute Myeloid Leukemia | Tapan Kadia, MD | #ASH24
Playlist: ASH 2024

Good Responses to Phase 2 CLIA + Ven Therapy for Acute Myeloid Leukemia | Tapan Kadia, MD | #ASH24

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Thumbnail for Menin Inhibitor Study Results: Ziftomenib for Newly Diagnosed AML Patients | Amer Zeidan, MBBS | #ASH24
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Menin Inhibitor Study Results: Ziftomenib for Newly Diagnosed AML Patients | Amer Zeidan, MBBS | #ASH24

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Thumbnail for VEN + IVO + AZA Combination Therapy in IDH1-Mutated AML, MDS & MPNs | Jennifer Marvin Peek, MD | #ASH24
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VEN + IVO + AZA Combination Therapy in IDH1-Mutated AML, MDS & MPNs | Jennifer Marvin Peek, MD | #ASH24

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Thumbnail for CAR-T Cell Therapy for Transformed Follicular Lymphoma | Matthew Cortese, MD | #ASH24
Playlist: ASH 2024

CAR-T Cell Therapy for Transformed Follicular Lymphoma | Matthew Cortese, MD | #ASH24

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Lindsay
Multiple Myeloma Discussion • January 4, 2025
Relieving Pain From Stomach Injections?
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Hello everyone, My fiance has been getting the chemo injections in his stomach and they are very painful. I was wondering if there was anything that helps relieve the pain?
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MAD78
Multiple Myeloma Discussion • January 3, 2025
Managing Talquetamab Skin & Taste Issues?
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Dear all happy new year!! My name is Marzia and I’ m italian Myeloma patient from 27 years, now I’m 46 years old. II’ve started talquetamab, just twice infusion but already I have a lot of side effedt: my hand and face Skin is all peel off and I totally loose taste, Can you give me some suggestion to contain this side effect? Thanks you all Marzia
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DIahanna • Admin
Multiple Myeloma Discussion • January 3, 2025
Managing Drug Costs: New Part D $2k Cap
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Hello Everyone, January 1st was the start of the $2000.00 max out of pocket for prescriptions that are covered as formulary in your Part D drug plan...
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NKP64
Multiple Myeloma Discussion • January 2, 2025
Managing Bone Pain With Stable MM?
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Hi all First of all, Happy New Year to everyone in the community! Thank you for the much-needed support and positivity here—it's been truly amazing. I hope 2025 brings great things to all of us. I have a query: Even when multiple myeloma (MM) is stable with a low SPEP, can bone pain still be an issue? Should this be considered normal, and is taking paracetamol advisable in such cases? What are the other solutions?
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Chenke
Multiple Myeloma Discussion • December 31, 2024
Low-Level MRD in Remission - Anyone Else?
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Happy New Year to all of you! My doctor has told me I am still in remission but instead of my MRD being 0, it shows 6 cells out of a million this time. Although it’s still considered remission it really scares me. Does anyone else have a similar experience? Also- I am one year out from having a stem cell transplant.
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joewheeldon
Multiple Myeloma Discussion • December 31, 2024
Allo Transplant: Quality of Life & Family Tips?
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Hello, I was diagnosed with MM in 2017. After a variety of treatments, including back-to-back Auto Transplants in 2018/19, I will be doing an Allo Transplant in March 2025. Given my Auto experience and general understanding of the transplant process, I would appreciate hearing about 'quality-of-life' tools that were important for you and your family. For example, in my Auto transplant, I really appreciated having multiple people stay with me, as it showed how many people were supporting me on the cancer journey (even while it was difficult for my spouse, as she struggled with feelings of guilt for not being able to be there the whole time). Thank you in advance for your thoughts and experiences. Sincerely, Joe Wheeldon
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thegurns
Multiple Myeloma Discussion • December 31, 2024
Experience With CAR T-Cell Therapy?
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Researchers are finding new ways to fight multiple myeloma, including a new treatment called CAR T-cell therapy. It's still experimental, but you may get a chance to join a clinical trial if your other treatments aren't working. CAR T-cell therapy works differently from other cancer treatments. Does anyone have experience with this ? Thank, Keith
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Carol
Multiple Myeloma Discussion • December 31, 2024
Shingles Without a Rash From Treatment?
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Hello Everyone, I have completed 2 cycles of quad therapy with Dexa, Revlimid, Velcade and Dara. I had issues with extreme bloating. Then the left side of abdomen, back and side became numb. I’m on antiviral medicine. My hematologist/oncologist didn’t have an answer so I saw a neurologist who said I was getting shingles but there was no rash. Apparently the anti viral was keeping it at bay and looks like internal shingles and they treated me increasing the anti viral. It’s been over 2 weeks and still numb with sensitive skin. I am 54 and only had 2 cycles 21 days and this occurred. Now it’s holding up my treatment. Has any else gotten this from treatment for multiple myeloma? Does anyone have insights referencing shingles during treatment? Thank to very much.
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peachRabbit
Multiple Myeloma Discussion • December 31, 2024
Sharing a Positive Revlimid Experience
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Revlimid is the best medication I’ve used to date. It gave me long remissions for years. (I was diagnosed in 2013.) The side effects were manageable. Good luck!
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Rross7
Multiple Myeloma Discussion • December 30, 2024
Choosing Maintenance Over ASCT? Anyone Else?
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Had a bone marrow biopsy. Looks like I am MRD- and in Remission. I am scheduled for ASCT the end of January. Waiting to hear from the Doctor, and hoping to go on Maintenance instead. Has anyone chosen to do this instead of ASCT?
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jelvove
Multiple Myeloma Discussion • December 30, 2024
Considering Kepivance Pre-SCT: Any Experiences?
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Kepivance Can anyone tell me if they've had Kepivance (Palifermin) prior to an autogolous stem cell transplant (SCT)? https://www.drugs.com/kepivance.html https://www.drugs.com/pro/kepivance.html I ask because it's being suggested I take it because I've previously experienced radiation and there's a concern that when I receive my Melphalan dose before my SCT, it would be better to take the Kepivance to stave off the potential impact of mucositis and re-radiation that can be a side effect from Melphalan. Interestingly, there are two places where I can receive a SCT in my area and one recommends I take it and the other doesn't. If I do take it, I'll do so for 3 days straight starting a week before my SCT then again for 3 days straight some time after my SCT. From Google AI: Should I Take Kepivance? Based on the provided search results, Kepivance (palifermin) is a medication indicated to decrease the incidence and duration of severe oral mucositis in patients with hematologic malignancies receiving myelotoxic therapy in the setting of autologous hematopoietic stem cell support. It is not indicated for patients with non-hematologic malignancies. Before deciding whether to take Kepivance, consider the following: Your diagnosis: Kepivance is only recommended for patients with hematologic malignancies (blood cancers) undergoing autologous hematopoietic stem cell transplantation. If you have a different type of cancer, Kepivance may not be suitable for you. Your treatment plan: Kepivance is used as supportive care for preparative regimens predicted to result in ≥ WHO Grade 3 mucositis in the majority of patients. If your treatment plan does not involve myelotoxic chemotherapy and autologous stem cell transplantation, Kepivance may not be necessary. Potential side effects: Kepivance may cause common adverse reactions such as rash, fever, elevated serum amylase, pruritus, erythema, and edema. It may also interact with heparin and increase systemic exposure. Breastfeeding and fertility: Kepivance is not recommended for breastfeeding women, as it may harm the breastfed child. Additionally, animal studies suggest it may impair fertility in both males and females, although the reversibility of this effect is unknown. Alternative options: If you are considering Kepivance, discuss alternative treatments and their potential benefits and risks with your healthcare provider. Based on these factors, you should consult with your healthcare provider to determine whether Kepivance is appropriate for your specific situation. They will help you weigh the potential benefits against the risks and consider alternative options.