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Playlist: Autologous Stem Cell Transplant (ASCT)

Hi, I am not a patient, however, my dad was diagnosed with M M in March. He is in his final week of his quad treatment, and for the most part has done very well. However, he has been experiencing migraines for the last two weeks. They are progressively getting more frequent and are debilitating. His local oncologist prescribed him Sumatriptan which helps for a little while, but they come back. He also scheduled him to have an MRI this week. Has anyone experienced this with the quad treatment? Does anybody have any recommendations for something else that can be prescribed to him? He does not meet with his specialist at city of Hope until July 8 and his local oncologist is on vacation for a week. His primary care doctor will not prescribe him anything because of his treatment. Thank you in advance!

How long will I be immunocompromised? How can I prevent infection after transplant?

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JohnEustace

Multiple Myeloma Discussion • June 28, 2025

Myeloma Minutes Podcast: New Schedule

Playlist: Autologous Stem Cell Transplant (ASCT)

Those of us awaiting a new episode of themyelomaminutes.podbean.com I have news! Jam and Sally have decided to publish every other week. So 14 should be with us next Thursday. hnPlease look out for it and tell others Jo

Thumbnail for How long is the average stay for an ASCT? How will the doctor know when I am able to return home or no longer come for daily clinic visits?

How long is the average stay for an ASCT? How will the doctor know when I am able to return home or no longer come for daily clinic visits?

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Question: Does No M-Protein Mean Remission?

Belantamab Mafodotin Updates & How to Manage Eye Side Effects | Evangelos Terpos, MD, PhD | #EHA2025

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Gebharka

Multiple Myeloma Discussion • June 28, 2025

I was diagnosed with MM in 2018 stage 4. I started chemo and velcade. Didn't get Stem Cell because soon after I was diagnosed Covid started. So after a year and a half I was reduced to only Remicade (pill form) now I am told I am in remission because there are M-protien showing in my blood work ( also must add this is my 3rd doctor in this practice, due to alot of the doctors leaving this practice. I am starting to not feel comfortable anymore. So is it true that if there are no M-protien that you are in remission?

New Insights into High-Risk Amyloidosis Staging | Jahanzaib Khwaja, MD, FRCPath | #EHA2025

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Increasing Dara on Maintenance: Any Success?

Revolutionizing Myeloma Care: AI Matches Patients to Trials | Jorge Hurtado Martinez, MD | EHA 2025

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redRhinoceros

Multiple Myeloma Discussion • June 27, 2025

I've been on daratumumab maintenace for 2 years after reaching CR. I receive dara every 8 weeks and just recently had a bone marrow biopsy which showed no plasma cells in the marrow but my clonal cells have increased from 800 to 5,000 per million. I will be asking my oncologist to increase dara to every 4 weeks. Has anyone had a similar experience of increasing dara during the maintenance phase and seeing improved results? The other option will be to add on pomalyst but I'm hoping to stick with dara only for a while.

Belantamab Mafodotin in the Real World: Promising Myeloma Data | Fredrik Schjesvold, MD, PhD | #EHA2025

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CONCEPT Trial | Isa-KRd : New Hope for High-Risk Myeloma Patients | Lisa Leypoldt, MD | #EHA2025

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Advancing Myeloma Care: Immunotherapy Trials Now Underway at Sylvester Center

Jun 26, 2025

04:00PM - 05:00PM EDT

Tips for Managing Anemia with MDS?

HealthTree Nurse Advisory Board

ADVANCE Trial | Dara‑KRd in NDMM yields ~ 60% MRD‑Negativity| Ola Landgren, MD, PhD- #EHA25 #myeloma

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Lindak

Multiple Myeloma Discussion • June 26, 2025

08:30AM - 09:30AM EDT In the city timezone

Hi. I was recently diagnosed with MDS with Anemia. My doctor is monitoring my hemoglobin and will start injections with hormones if it drops below a certain level. I want to learn all I can do I can be prepared if necessary. I read that MDS typically is found in patients 60 years of age or older. But I had a second cousin who died from this when she was 26. There is a lot of cancer on my Mom's side of the family. I want to know what I can do for the anemia. If anyone has any suggestions please reach out to me. I plan on attending the session at UCF on Saturday. Linda

Spend An Hour With Matthew Pianko, MD

Jun 26, 2025

Weber’s Boutique Hotel - Ann Arbor, Michigan

Bone Biopsy for Slow Recovery After SCT?

IRAKLIA Trial: On-Body Subcutaneous Isatuximab Delivery in Myeloma | Muhamed Baljevic, MD | #EHA2025

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FDA Approves Simpler Way to Take Zanubrutinib (Brukinsa)

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Molly

Multiple Myeloma Discussion • June 26, 2025

Hi My doctor wants me to have a bone biopsy as my hemoglobin levels are still struggling to come back up after my SCT back in September 24. He thinks the bone marrow may have been damaged. Has anyone else has this issue? Thank you!

Seeking Recommendations for Top CLL Specialists

HDP‑101: Promising Anti‑BCMA ADC with Novel Payload for Myeloma | Shambavi Richard, MD | EHA 2025

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Donnabaxter

Chronic Lymphocytic Leukemia Discussion • June 25, 2025

Does anyone have a strong recommendation for the best CLL doctor and hospital in the nation? Thank you!

Understanding Your CLL Lab Tests

Jun 25, 2025

04:00PM - 05:00PM EDT

Coping with Blood Cancer Uncertainty: Practical Tools to Manage Stress and Anxiety

Jun 25, 2025

12:30PM - 01:30PM EDT

Experiencing New Symptoms After Stopping Revlimid?

TamaraMac

Multiple Myeloma Discussion • June 25, 2025