The Shut down has effecttively ended. The Affordable Care Act Subsidies will expire at the end of the year

I have MGUS. How do I find my M Spike number. I am new to this community.

🚨Breaking Myeloma News The FDA has approved Darzalex Faspro (daratumumab + hyaluronidase) as the first treatment for adults with high-risk smoldering multiple myeloma. This approval marks a major step toward earlier intervention and better outcomes. 🧬 Learn more: https://healthtree.org/myeloma/community/articles/25-daratumumab-darzalex-faspro-hrsmm?utm_source=social_media&utm_medium=meta&utm_campaign=socialmediaorganic&utm_content=general #WeCareWeCure #Myeloma #FDANews #BloodCancerResearch

Im on Talvey and seem to have lost my sense of taste. Has anyone experienced this before and how long would it last for?

💜 This November, let’s fill our community with gratitude! 💬 Share in the comments 1–3 words that express your love, admiration, or thanks for the caregivers who inspire you, whether it’s a family member, friend, or someone who has cared for you during your journey. Let’s fill this space with kindness, encouragement, and appreciation Thank you for your words!

💜 This November, let’s fill our community with gratitude! 💬 Share in the comments 1–3 words that express your love, admiration, or thanks for the caregivers who inspire you, whether it’s a family member, friend, or someone who has cared for you during your journey. Let’s fill this space with kindness, encouragement, and appreciation Thank you for your words!

I am in complete remission from IgA Kappa NDMM with a 1q gain scheduled to start 10mg Revlamid daily and monthly Dara Fastpro with Dex as a premed at 130 days post ASCT. Is it typical to start maintenance so soon?

My husband had his ASCT on Aug 28th 2025. After 4weeks his bone pain started in his arms. His pain is more only at night. The doctor suggested for a radiation consult and they said it’s not necessary now. Any one has this experience and why radiation? We have an appointment with his oncologist later this month. Should we ask for a PET scan and is bone marrow biopsy required?

Telehealth has practically completely gone away unless you are in a rural area. Accessibility has expired. The gov't shutdown has exacerbated the issue.

What is the best method to reduce swelling in my ankle?

Has anyone has had teeth implant while on multiple myeloma? I’m interesting about inthe healing process of teeth implant. I wanted to have one, but I’m kind of scared just in case it doesn’t heal properly. Any one ?????

That’s a wrap on the 2025 HealthTree Challenge: Hike + Wellness Fundraiser for All Blood Cancers! 🏔️ This incredible team of 20 participants pushed themselves physically and mentally, raising vital funds to fuel blood cancer research. Huge thanks to our 2025 Challengers and their amazing supporters for believing in HealthTree’s mission. Inspired to continue making an impact? Meet our Challengers and support them in reaching their goals! https://give.healthtree.org/event/healthtree-challenge-hike-and-wellness/e663485?c_src=socialmedia Together We Care. Together We Cure.

Encountering severe body hives with my 1st Rx after my ASCT in MAR. Lenalidomide 25mg was part of my induction therapy (KRd) and I had some minor rashes, but now at 10mg, I just cannot tolerate the hives. I can't take it for any longer than 7 days and I have to stop, use steriods, then try again. I have been trying this since the end of AUG. Anyone else experience this? If so, did a reduced dose ot 5mg or 2.5mg help? Thanks in advance.

I am 64 years old, diagnosed with MM last August. I was in a medical trial but ended up in the "control" group receiving a ASCT in June. My latest bone marrow aspiration is in....I am MRD Negative (1:100,000)! I am happy beyond belief. We always hope for these results, but don't believe that it can really happen! Well, it does! Happy to share my experiences with anyone. I am posting this both to share this great news and also to advertise that ASCT really does work. It's doesn't work for everyone and not as well for everyone, but it is still the Gold Standard of Treatment for Newly Diagnosed MM patience - I am a living example! Moshe Lichtenstein mlichtenstein.mbl@gmail.com