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Being a patient, family member or caregiver is hard enough. Finding the information that you need doesn’t need to be hard. Here is a list of some of the things I wished I had when I was diagnosed.

What is Multiple Myeloma?

https://themmrf.org/multiple-myeloma

https://healthtree.org/myeloma/university/modules/z9489RAmujCcdQ3TqAGE

What is a Stem Cell Transplant

[https://www.cancer.org/cancer/managing-cancer/treatment-types/stem-cell-transplant.html

What is CAR-T

https://www.cancer.gov/about-cancer/treatment/research/car-t-cells

Support Groups

https://www.myeloma.org/support-groups

Financial Help

https://www.myeloma.org/online-resources/financial-assistance

https://themmrf.org/support/financial-assistance-and-transportation/