Just checking to see if anybody has the same side-effect rhythm that I do with the Fast-Pro. I get the shot the last Thursday of the month. Thursday I feel fine. Friday I feel okay. By Friday evening I feel a little funky. Saturday morning I feel like a can of busted biscuits, headache, fatigue. Sunday the same. By Monday I am back to my normal self. (as normal as anyone on chemo can be). Does anyone else have this delayed reaction.

A new Phase 2 clinical trial, DOMMINO-1, is now recruiting people living with advanced multiple myeloma who have already received several prior treatments. This study is evaluating inobrodib in combination with pomalidomide and dexamethasone to better understand how this approach may work for patients whose disease has become more difficult to treat. Learn more about participation and see if this study could be an option for you: https://clinicaltrials.gov/study/NCT07096778 clinical@cellcentric.com +44 1799 531130

I am 4 months into my CAR-T cell transplant experience and have lost my sense of taste. Has anyone else had this happen? How long does it last?

Today’s the day – UTAHGIVES is here 💙 It’s a 24-hour celebration of generosity across Utah, and we’re coming together to support blood cancer patients and families. Our goal is to rally as many unique donors as possible and show the strength of this amazing community—no matter where you’re joining from. At HealthTree, we’re working every day to accelerate research, provide trusted tools, and connect patients with the support they need. And we truly can’t do it without you. If you’re able, we’d love your support today. Give here: https://www.utahgives.org/organization/Crowdcare-Foundation And if donating isn’t possible, sharing this with others makes a huge difference too 💙 #UtahGives #GiveWhereYouLive #GiveTogetherGrowTogether

I'm on maintenance therapy with lenalidomide and isatuximab, 1 year after asct. There is possibility of switching from isatuximab biweekly to monthly. Any of you have done that? Is it as effective? How long you have been on monthly?

Hi everyone! Fatigue is something many people living with MPNs (ET, PV, MF) experience, but it can show up differently for each person and is still not fully understood. HealthTree is partnering with MPN specialist John Mascarenhas, MD, to better understand how fatigue affects daily life, emotional well-being, and how people cope. 🕒 The survey takes about 15–25 minutes and includes questions about fatigue patterns, triggers, and real-life impact. Your experience can truly make a difference in helping researchers improve care and quality of life for MPN patients. 👉 Learn more here:https://healthtree.org/myeloproliferative-neoplasm/curehub/private/research/TIWa4HkKxF3OI183UGmV?utm_source=&utm_medium=meta&utm_campaign=socialmediaorganic&utm_content=general

Hi everyone! Fatigue is something many people living with MPNs (ET, PV, MF) experience, but it can show up differently for each person and is still not fully understood. HealthTree is partnering with MPN specialist John Mascarenhas, MD, to better understand how fatigue affects daily life, emotional well-being, and how people cope. 🕒 The survey takes about 15–25 minutes and includes questions about fatigue patterns, triggers, and real-life impact. Your experience can truly make a difference in helping researchers improve care and quality of life for MPN patients. 👉 Learn more here:https://healthtree.org/myeloproliferative-neoplasm/curehub/private/research/TIWa4HkKxF3OI183UGmV?utm_source=&utm_medium=meta&utm_campaign=socialmediaorganic&utm_content=general

Hi everyone! Fatigue is something many people living with MPNs (ET, PV, MF) experience, but it can show up differently for each person and is still not fully understood. HealthTree is partnering with MPN specialist John Mascarenhas, MD, to better understand how fatigue affects daily life, emotional well-being, and how people cope. 🕒 The survey takes about 15–25 minutes and includes questions about fatigue patterns, triggers, and real-life impact. Your experience can truly make a difference in helping researchers improve care and quality of life for MPN patients. 👉 Learn more here:https://healthtree.org/myeloproliferative-neoplasm/curehub/private/research/TIWa4HkKxF3OI183UGmV?utm_source=&utm_medium=meta&utm_campaign=socialmediaorganic&utm_content=general

$10,000 available through Patient Advocate Foundation: https://copays.org/funds/multiple-myeloma/ Household Income Requirements: 500% or less of Federal Poverty Guideline (FPG) (adjusted for Cost of Living Index (COLI) and number in household) Insurance Requirements: Medicare, Medicaid, or Military Benefits Residency Requirements: Must reside and receive treatment in the United States. Also $8000 from Health Well Foundation for Medicare patients: https://www.healthwellfoundation.org/fund/multiple-myeloma-medicare-access/ Household Income Requirements: 500% or less of Federal Poverty Guideline (FPG) (adjusted for Cost of Living Index (COLI) and number in household) Insurance Requirements: Medicare Federal Poverty Guidelines for 2026 Annual Income Persons in Family 500% 1 $79,800.00 2 $108,200.00 3 $136,600.00 4 $165,000.00 5 $193,400.00 6 $221,800.00 7 $250,200.00 8 $278,600.00