MS in 33
To feel my abilities slip away
To have more to do and say
Yet be unable to do even the
smallest of things
I know this is what my future brings
All stolen away
~Yeris~
I am working off two prompts. The OctPoWriMo prompt asks for a rhyming poem, and the Trifecta prompt asks for something that scares us (or a character of ours) in 33.
The loss of my abilities to MS does not scare me so much as it depresses me. I was diagnosed 12 years ago. I have periods of remission, which are like coming into the light from a dark cell. I know that these will become fewer and farther between as the disease progresses.
Ageing is scary.
ReplyDeleteThe sadness is self-evident in this poem. I too am losing a lot of those functions (for different reasons), so can empathise .
ReplyDeleteYou wrote of this tragedy well. I'm sorry you have to. X
ReplyDeletehttp://wp.me/p2Mm4H-bY
I have MS too. I'm sorry you have it. Mine is SP, so the disability is bad, but if yours still relapses, that is good. If you ever need to talk to someone who understands, feel free to stop by my blog. Nice entry, by the way. ;)
ReplyDeleteThank you all for commenting. I know Yeris will appreciate it. She doesn't participate as much as some of the other team members due to her limitations, but we <3 her!
ReplyDeleteI hope there will be a cure for MS someday. I hate seeing people sidelined by such diseases. I feel bad for always whining about my crappy knees when I know there are others who have challenges like this to endure.
God bless you smiles always !
ReplyDeleteI wish there was something to write to make the situation better but for some things there is no good side. I just hope you have more good days.
ReplyDeleteThis is so beautifully written. So heartfelt. I'm sorry your fear is real.
ReplyDeleteThat terrible anticipation hanging over...You captured it so well in your words.
ReplyDeleteThis is a horrible disease. I'm glad you wrote of your fear, but I'm sorry you know it. My best friend was diagnosed with MS nearly twenty years ago. Her mother also had MS and had a difficult life. I can't imagine coping with that kind of fear you describe. I hope you are able to keep your stress down and your body strong.
ReplyDeleteThank you all, on behalf of Yeris. She has support from her family and friends, and is in a good period right now so her symptoms are less bothersome. During those times, she keeps pretty busy doing things with her family. I admire her attitude greatly. I don't know that mine would be nearly as positive.
ReplyDeleteOh, jeez - one of the scariest things I can imagine. But oh so brave to write about it. Fabulous entry.
ReplyDeleteI'm sorry you're going through this and am hoping for a cure. Thanks for sharing it with us.
ReplyDeleteThank you trudgingthroughfog and Trifecta, on behalf of Yeris.
ReplyDeleteIt will be a wonderful day when there is a cure for this debilitating condition.
What a terrible disease to live with, but you have relayed that fear beautifully.
ReplyDeleteIt also works as a metaphor for the rest of us.
Kind thanks, Kymm, on behalf of Yeris. :-)
ReplyDeletesmiles for you..
ReplyDeleteThank you Payal, on behalf of Yeris.
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