In 2021, she was healthy and excited about starting a family with her partner. Nearly four years later, she is navigating life with a rare, aggressive illness, pursuing every treatment available while creating lasting memories for the daughter she once feared she might never meet. It began with a symptom that seemed more inconvenient than alarming, a sudden loss of mobility on an otherwise ordinary morning. Within days, the search for answers would reveal a condition so rare and aggressive that doctors were forced to measure her time in months, not years. https://www.instagram.com/lauradowntherabbithole/p/CvNa6URokk3/?mWidth=350&mHeight=655&dWidth=600&dHeight=968She was a young expectant mother whose days should have been filled with nursery plans and baby kicks, not scans and medical brie

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