Nobody Believed My Pain Was Real Until Endometriosis Landed Me in a Coma
For six years, I lived alone in agony, dismissed by doctor after doctor
For six years, I lived alone in agony, dismissed by doctor after doctor
For a long time, I thought I was the only one who had an intense fear of socializing. Now, I use my art to help raise awareness about social anxiety disorder and other mental health conditions.
My stroke at birth affected the left side of my body. Now, I’m helping raise awareness about cerebral palsy and living with limitations online.
After doctors dismissed my test results — twice — I’ve learned the importance of advocating for your health
To survive months alone in the hospital during Covid, I turned to my faith — and my phone
Para sobrevivir meses sola en el hospital durante la pandemia de covid, recurrí a mi fe y a mi teléfono
I found my way to the truest, happiest version of myself through mindfulness and radical self-acceptance
My skin itched, swelled and left me hopeless until my chronic spontaneous urticaria was finally treated successfully
Mi piel me picaba, estaba inflamada y yo había perdido la esperanza hasta que finalmente trataron mi urticaria crónica espontánea con éxito
Catching lung cancer in an early stage is lucky and rare, so why do we screen only when it’s too late?
Detectar el cáncer pulmonar en una etapa temprana es algo fortuito e infrecuente, entonces, ¿por qué hacemos pruebas de detección solo cuando es demasiado tarde?
PMDD is not just PMS. It’s a mood disorder — and not enough people are aware it exists.
Living on a reservation means limited access to nutrition and medical care. Self-empowerment and education are crucial
My diagnosis at 31 inspired me to start Mom on the Spectrum — an online platform to help other autistic adults
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