Hi there! While I'm pleased to make your acquaintance forgive me if I don't feel overjoyed at having done so through an MS forum. Let's face it, none us wants our points of assimilation being a disease. But, alas here I am and there you are so, "Hello!" .
I'm a 48 year old female. I had ON in 2013. I refused an MRI at the time and chalked it up to stress. I've had odd incidents here and there since but nothing huge. Then 2020 came. As if 2020 weren't history book worthy enough, my body started to seriously fight against me. I have tremors, heavy legs and arms and my memory started failing me. I waited 88 days for an MRI (thanks, Ontario sick-care system ). It's back and, yep, there are lesions. I see the doc on Wednesday to be referred out to neuro. Lovely, this is exactly how I pictured my later years. Well, it is what it is.
That's my story. It's not my legacy because, dammit, I won't let MS be my legacy, but it's my story. Thanks for reading!
I'm a 48 year old female. I had ON in 2013. I refused an MRI at the time and chalked it up to stress. I've had odd incidents here and there since but nothing huge. Then 2020 came. As if 2020 weren't history book worthy enough, my body started to seriously fight against me. I have tremors, heavy legs and arms and my memory started failing me. I waited 88 days for an MRI (thanks, Ontario sick-care system ). It's back and, yep, there are lesions. I see the doc on Wednesday to be referred out to neuro. Lovely, this is exactly how I pictured my later years. Well, it is what it is.
That's my story. It's not my legacy because, dammit, I won't let MS be my legacy, but it's my story. Thanks for reading!
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