My experience being diagnosed with multiple myeloma
Patient Jawanna describes her experience of recieving a diagnosis and treatment for multiple myeloma.
Transcript
I want to say between four and five times I went to the hospital before I actually was able to get help that I needed.
[MUSIC PLAYING]
I was diagnosed with multiple myeloma in February of 2020. I faced many barriers trying to find treatment.
The first hurdle was me just being diagnosed and getting an answer to what was going on. The two biggest factors for me not being taken seriously,
I believe, is my age and my race. I was in my 30s. A lot of times doctors will not test
for certain diseases or certain conditions because they might feel like I'm too young to have that particular condition or disease.
And just race, because I've seen how a lot of times African American people are not served as well as their counterparts
in the medical field. I've heard stories with my sister and with my friends.
It was one thing to go through pain physically, but it also-- it takes a big mental toll on you when you don't know
what's going on with you and you cannot get the answer that you need. [AUDIO LOGO]
multiple myeloma
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