I am well aware of the reality of MS and the unknown risks, dangers, symptoms, and limitations it comes with. I research, I hope, I struggle, I try to do everything in my power to stay informed and as ‘ahead’ of this disease as I can. The reality and the weight of this disease keeps my feet firmly planted to the ground. Almost literally as well.
But I am also a dreamer. My head is high in the clouds. I envision myself climbing mountains, crossing prairies, hiking through fields and forests. Dancing till the wee hours, and singing at the top of my lungs.
And when my legs pull me down, when I fall to the ground, when I run out of breath, I simply look to the skies. I search for rainbows, feel the rain on my skin, I imagine myself as a bird flying through the clouds, reaching the highest summits. I watch the sunsets, I see hope and possibilities in my children’s eyes. I lie in the grass to feel levelled, I look up to feel far, I drive with the windows down to feel the wind in my hair. I write to feel grounded but I paint to be free.
I may be standing still, feet planted. But it is not where my head is at.
I am not where I am

That photo says it all. A photo is worth a million words. I might not be sick, but we are all sick in our own ways.
You should paint that photo. It’s extremely meaningful. I’m going through hell right now, but reading the last two post and viewing that photo made me realize that it’s not hell but reality and grounded.
Thank you for sharing it!
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Sometimes I feel like if I were to switch bodies with someone, I would hit the ceiling…and they would crumble to the floor.
But I’ve been realizing lately that many feel that way.
I don’t think I could paint feet. Maybe happy feet, but not the ones from my picture. Not my feet
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Lol. I just thought it was a cool photo worth a thousand words.
Most of us wish we were grounded, well atleast I wish I was grounded. I feel like ever step I take, it gets harder as I grow older.
I’d give you my body for a day or two! Wish I could
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