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The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.message sent
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Burden of Proof: The Privilege of My Visible Disability
When I enter a room, my disability is always one step ahead of me. My powered wheelchair gives me nowhere to hide from the palpable intrigue hanging in the air, and I have perfected a sweet smile in response to the eyes that inevitably drift my way as I pass by. I tell myself it must be my cute outfit, but the reality is that having a highly visible disability defines my interpersonal life and is a lens through which I interact with the world around me.
I exist at the intersection of society’s deeply embedded stereotypes about disability, my own internalized ableism and my identity aside from my diagnosis of Spinal Muscular Atrophy (SMA) — but the visibility of my disability means that the latter is forever framed by my four wheels.
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