Editor’s Choice: How Dystonia Feels, POTS and Sugar, and More!
Welcome to this week's Editor's Choice Patient Worthians! This week, we want to spread some info on what it feels like to actually live with rare disease. Not just about…
Welcome to this week's Editor's Choice Patient Worthians! This week, we want to spread some info on what it feels like to actually live with rare disease. Not just about…
Happy Friday Patient Worthians! Just because Cystic Fibrosis and Lyme Disease Awareness Month is over, doesn't mean we won't stop fighting the good fight for spreading awareness about these diseases! We…
While I truly believe that people are well-intentioned, their opinions and comments often miss the mark when it comes to what we experience living with dystonia, or any other chronic…
Living with a chronic health condition that dramatically alters one’s life can be very confusing, scary, and lonely. I lived in this mental misery for years when I developed dystonia,…
Happy Easter Weekend Patient Worthians! And if you don't celebrate it, Passover is only a month away. If you don't celebrate either one, then why not celebrate life?! This week we…
In the summer of 2001, my neck muscles began to involuntarily contract, causing my head to pull to the right. I had no idea what was wrong. My doctors were…
Patient Worthy Library Want more Patient Worthy content? Then check out our library! Here, you can find motivational and relatable writings by our own Patient Worthy Contributors. Are you in…
Meet our Patient Worthy Contributors Ms. Stephanie ErnstTAPS Nerd and FounderA self-confessed TAPS Nerd,her passion is to deliver information about TAPS that is up to date and easy to understand. Stichting…