I Worried It Was All In My Head — Until I Was Finally Diagnosed with Addison’s Disease
The diagnosis was there, waiting to be found, yet doctors saw me as a medical mystery
The diagnosis was there, waiting to be found, yet doctors saw me as a medical mystery
I’ve dedicated my life to raising awareness about hypertrophic cardiomyopathy — a life-threatening heart condition that runs in my family
I was dependent on the strongest narcotic pain meds until a pain management specialist really saw — and heard — me
We all need to understand that schizophrenia is a complicated diagnosis, but not a hopeless one
My artistry looks different with MS, but I’m determined to practice as long as I can
I read online that my multiple myeloma diagnosis was grim. The truth seems more hopeful.
Leí en el internet que un diagnóstico de mieloma múltiple era algo sombrío. La verdad parece más alentadora.
I’m glad I found out I had osteoporosis. You can’t treat it if you don’t know you have it.
Me alegro de que descubrí que tenía osteoporosis. No puedes tratar lo que no sabes que tienes.
Through genetic testing, I learned I had primary hyperoxaluria, or PH, a rare condition that caused my kidneys and liver to fail
Mediante pruebas genéticas, me enteré que tenía hiperoxaluria primaria o HP, un trastorno infrecuente que me causó insuficiencia renal
Finding the right care was hard work, but I finally found the support I needed