Back to square one?
I feel like I am back to step one, after nine months of pushing through. Fighting every side effect. Fighting every symptom. I’m tired now.
Patients share their experiences living with dermatomyositis, one of a group of rare autoimmune diseases, the idiopathic inflammatory myopathies.
I feel like I am back to step one, after nine months of pushing through. Fighting every side effect. Fighting every symptom. I’m tired now.
My husband honors his vow; in sickness and health. But for me, when will I no longer grieve the person I once was? The girl...
I admit that I’m very very tired. It’s been a long 6 years of steadily worsening symptoms, especially pain and weakness, and lung involvement again...
Somehow, when you are sick, there is that feeling of dread that comes with being single that just makes you feel like this is it....
I don’t want dermatomyositis to define me or take over my life, but sometimes I’m vulnerable and not the strongest version of myself.
This image represents my determination, stubbornness, and desperation for something normal and happy in my #MyositisLife.
People keep telling me how resilient I am, but really, I'm just too stubborn. Too stubborn to take no for an answer. Too stubborn to...
What I learned in those years is that this disease is not just pain, weakness, and fatigue, this is about mental toughness.
I am not a vampire. However, at the direction of my dermatologist, I am living a “full vampiric life.”
How creative outlets such as art and writing have helped me cope with difficult things such as Dermatomyositis.
We are going to be here for a while. So, make yourself comfortable. Dig out those blankets for the sofa. Stock up (but don’t hoard)...
It could have all gone horribly wrong, but it didn’t. And yes, a lot of that is luck. But a lot of it is also...
I must learn to accept that I cannot rush my body. It needs rest. I cannot change this. I can change my attitude to this...