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A Hampshire mother fundraises after her daughter, diagnosed with a rare genetic disorder, faces severe developmental delays and hundreds of seizures daily.
A Hampshire mother is fundraising to support her family after her six-year-old daughter Doris, born prematurely in 2019, was diagnosed with a rare genetic condition causing severe developmental delays and up to 500 seizures daily.
Despite a 2025 vagus nerve stimulator implant, Doris remains under palliative care, unable to sit, walk, talk, or smile.
Her mother, Alexandra Bufton, left her previous jobs to provide full-time care.
The family faces added strain after her husband, a self-employed builder, underwent urgent heart surgery.
They are relying on community support to cover medical and living expenses.
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Una madre de Hampshire recauda fondos después de que su hija, diagnosticada con un raro trastorno genético, enfrenta graves retrasos en el desarrollo y cientos de convulsiones diarias.