Athena Merritt,  —

Sarcoidosis: A life of no Having sarcoidosis means I must say no to many things. That is why when Cinco de Mayo rolled around last week, I was sitting in while my friends did their part to keep Americans in the lead for tequila consumption. They tried to…

Sarcoidosis 101 Have you ever tried to explain sarcoidosis to someone? First, you have to phonetically walk them through the funny-sounding pronunciation. If you still have their attention after that, it’s usually gone by the time you hit the term “granuloma.” After being shellshocked by a sarcoidosis diagnosis,…

When I left my doctor’s office with a prescription for Restasis (cyclosporine) this month, I was hopeful I would be able to afford it under my insurance plan this year. But the nearly $500 upfront cost to fill it has put the medicine out of reach again. I’m hardly alone…

As a Marvel fan, this week’s long-awaited premiere of “Avengers: Endgame” has me thinking about the sarcoidosis community’s hidden superpowers. They aren’t flashy. We can’t fly. We can’t shoot webs from our wrists and swing through neighborhoods. And we can’t transform our bodies into a hulking green beast — though…

I was thrilled to find out the television network NBC will be airing a sarcoidosis PSA this month to raise awareness about the disease, which so many fail to recognize at the onset of symptoms. I did. Night sweats — which had me waking as drenched as if I…

The thing that attracted me to a career as a journalist — the unpredictability — is precisely what I despise most about living with a chronic illness. Over my nearly 17 years battling sarcoidosis, I’ve had good and bad days, and others that have fallen somewhere in between. I…