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What has helped you ask for MG accommodations at work or school?
Asking for accommodations can feel intimidating, especially when your symptoms fluctuate or you worry about being judged. But accommodations aren’t favors — they’re tools that help you function safely and sustainably.
For me, the hardest part was naming what I needed without minimizing it. Once I did, conversations became easier. Clear examples helped, like: “By the afternoon, my voice fades and my breathing gets harder,” or “Heat makes my symptoms worse, so I need a cooler workspace.”
What accommodations have helped you?
And what made those conversations easier — or harder?
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