Since myasthenia gravis and spoonie life is not something that others without your disease, no matter how sympathetic they may be, can ever really understand, I compiled some of the most relatable (and some funny) memes about myasthenia gravis and chronic illness from Instagram and the internet. When you’re having one of no one can relate kind of days, look these over and know you’re not alone. 18 Memes About Myasthenia Gravis and Chronic Illness Memes About Myasthenia Gravis a[...]
For those of you that are new to IWWB, Pass the Mic is a way to give other spoonie warriors a platform to share their chronic illness journeys with each other. Sharing helps us feel a little less alone in our battles. Wanna be featured? All you have to do click here. This month's PTM warrior is Jasmine. She is a fellow Snowflake spoonie. Let's see how her journey with Myasthenia Gravis has been. So what's your name and where are you from? Jasmine J from Chesapeake, VA How[...]
One of the questions I’ve been asked is what it’s like living with myasthenia gravis (MG). I often tell people the symptoms of MG that I experience but I rarely share the impact that living with myasthenia gravis has on my daily life. Don’t get me wrong, I do a lot of the same things I did before my diagnosis. However, it’s more taxing on my body. It requires more time and more effort. How does myasthenia gravis affect daily life? MG differs a lot from person to person in t[...]
One of the things that we learn about myasthenia gravis (MG) is that it's not considered terminal like cancer. However, when you have MG there's the possibility of going into myasthenia gravis crisis which is life-threatening if not treated quickly and properly. Life with myasthenia gravis (MG) is very up and down. One minute I'm fine and the next I'm not. Things can easily go from bad to worse and before you know it, you're in the middle of a myasthenia gravis crisis. The Differen[...]
I’ve experienced most if not every myasthenia gravis symptom there is. But I’ll never forget the beginning, my first myasthenia gravis symptom that told me “something is wrong, Sis”. Today I’d like to talk about my first myasthenia gravis symptom. My First Symptom My first myasthenia gravis symptom was actually two - ptosis (double vision) and diplopia (droopy lid). However, I noticed the ptosis first because it was making everything blurry. I’ve always been told I h[...]
Today we have a guest post by Anne-Marie D'Acry-Sharpe from Pathways. Chronic pain is defined as pain which lasts longer than 3 to 6 months, and which “persists past normal healing time and hence lacks the acute warning function of physiological nociception". There is a wide range of chronic pain conditions, all with varying symptoms. Even within one individual diagnosis, symptoms can vary from person to person and over time. While the pain itself is certainly a core symptom of[...]