r/multiplemyeloma is a subreddit with 8k members. The community frequently discusses treatment, multiple myeloma, diagnosis, mm, and myeloma, and they frequently recommend/review charities, and the most common flair used is ndmm (newly diagnosed), stem cell transplant, symptoms & side effects (pain, sleep, clots, eating, gi issues), rrmm (relapsed, refractory, disease progression, etc.), and living with mm.
This subreddit is for the discussion of the blood cancer Multiple Myeloma - myeloma related news, resources, stories, etc. associated with the disease. This forum is focused on post-diagnosis support and advice and does not allow pre-diagnosis posts.
Popular Topics in r/multiplemyeloma
#1
Treatment
55 posts
#2
Multiple Myeloma
40 posts
#3
Diagnosis
31 posts
#4
Mm
21 posts
#5
Myeloma
20 posts
#6
Symptoms
18 posts
#7
Stem Cell Transplant
17 posts
#8
Transplant
15 posts
#9
Diagnosed
14 posts
#10
Family
10 posts
Products Discussed in r/multiplemyeloma
Charities
2 reviews
#1
MMRF
5.0★ from 1 review
#2
Cancer Navigators
5.0★ from 1 review
Flair Used in r/multiplemyeloma
#1
NDMM (Newly Diagnosed)
: "One person's journey. A first year with MM."
30 posts
#2
Stem Cell Transplant
: "MRD Negative!"
23 posts
#3
Symptoms & Side Effects (Pain, Sleep, Clots, Eating, GI issues)
: "Emotional after remission"
11 posts
#4
RRMM (Relapsed, Refractory, Disease Progression, etc.)
: "Multiple Myeloma is like a bear in hibernation—eventually, it comes back out. After 6 years, my relapse is here."
8 posts
#5
Living with MM
: "Sharing Good News"
7 posts
#6
Discussions and Info (Misc MM, Articles, Tweets, etc.)
: "For adult children/family members of people with multiple myeloma: I would really like to hear about your experience and the things we don't usually say out loud"
6 posts
#7
MM+: PCL, AL, LCDD, EMD, Penias (low counts), etc.
: "At a loss"
5 posts
#8
Financial (Costs, Ins, Disability, etc.)
: "The brutal cost of Revlimid"
4 posts
#9
CAR T-Cell Class of Treatments (i.e. Abecma & Carvykti)
: "100 days post CAR-T"
2 posts
#10
Under 50-40-30
: "Just diagnosed with MM - Only 33. Anyone else?"
2 posts
Member Growth in r/multiplemyeloma
Yearly
+2k members(28.2%)
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Last updated: August 28, 2026