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This was my first albumin infusion for POTS — and it felt very different than any infusion I’ve had before. A private room, kind nurses, a warm blanket, no reaction, and a body that actually tolerated it. Those might sound like small things, but when you live with chronic illness, they’re everything. I’m learning that care doesn’t always look dramatic or obvious. Sometimes it looks like knitting in an infusion chair, watching something new, going home tired, and letting yourself rest without gui
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