I would like to share this very inspirational post from Chris, who is living with MS. I relate to so much of what she writes as I live with dermatomyositis, an auto-immune where my muscles attack themselves. It includes a very motivating poem which is a wake-up call to us all xx Rowena
A new year is here and I feel very grateful to be alive. I am ‘walking’ hand in hand with January carrying optimism and hope, both vital for my well-being, and while I am not wishing away the days, I am very much looking forward to the springtime when I can once more greet the fresh air and spend precious time in its loving company.
I don’t make resolutions but I do take a look at certain aspects of my life and make a few adjustments here and there. MS obviously plays big role in this these days and I need to keep everything about it in perspective while firmly facing the truth of what it is.
Everyone with this condition lives with it on a very personal level and no two people are the same either symptom-wise or affected in the same way by the same symptoms others may…
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