Welcome! Did you know that May 12th was MECFS International Awareness Day? With that in mind, during the month of May, I’m joining in on Instagram with other chronically ill people on the below pictured spoonie challenges, posting once daily as able, to spread awareness on a variety of MECFS topics. In order to try …
Continue reading ME/CFS (Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome) Awareness Week 3
Welcome! Did you know that May 12th was MECFS International Awareness Day? With that in mind, during the month of May, I’m joining in on Instagram with other chronically ill people on the below pictured spoonie challenges, posting once daily as able, to spread awareness on a variety of MECFS topics. In order to try …
Continue reading ME/CFS (Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome) Awareness Week 2💙
You know that pesky saying – the grass is always greener? Don’t you hate it when you have to admit you've fallen prey to that belief? 😊 Folks, I’ve been wishing for telehealth appointments since my son was little. Sitting on the ‘sick’ side of the pediatrician’s office with other children open-mouth coughing was never …
Continue reading Telehealth Appointments and First-World Problems
Thank you for stopping in today! Can you believe tomorrow is April? Obviously lots going on out there in the world right now, actually, if I'm to be honest, it's all feels like too much. I find myself vacillating between taking it all in, and hiding from it all, often in the same hour of …
This is a full on rant about my last two day with health insurance. It's more of a diary entry so I just thought I better add this disclaimer in case you were popping in for something uplifting. 🌸 Where to begin… A little back story. At the end of last year, I decided …
