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Empowering young adults and their families within rare disease communities
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Join date: Sep 4, 2023
Posts (3)

Feb 13, 2025 ∙ 6 min
Five minutes with...Linseigh Green
Linseigh Green about the lack of disability representation in the performing arts, the long-term outcomes of her condition, NEC.
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Jun 28, 2024 ∙ 4 min
Women in RARE: Next Gen: Linseigh Green
Welcome to Women in RARE: Next Gen. Here, we shine a spotlight on female rare disease advocates of the future. First featured in the...
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Sep 4, 2023 ∙ 8 min
I am not a defect or science—I am me
Linseigh discusses surviving necrotising enterocolitis, the abandonment of rare patients, and the pursuit of humanity in the midst of exploi
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Linseigh Green
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