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Devon Mother With Rare Pain Disorder Raises Funds for Italian Therapy as NHS Apologises

Despite new medication trials, she remains in constant daily pain with no breakthrough treatment announced.

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Overview

  • Ms Bradford’s erythromelalgia was not diagnosed until February 2025 after her initial symptoms were dismissed as pregnancy-related.
  • Her relentless burning pain has stripped away her mobility, independence and ability to care for her one-year-old son.
  • Torbay and South Devon NHS Foundation Trust formally apologised for her care and is reviewing the case to identify improvements.
  • She has raised more than £2,000 via GoFundMe to travel to Italy for scrambler therapy after standard NHS pain management provided limited relief.
  • Despite new medication trials, no breakthrough treatment has been announced, highlighting the challenges of managing rare chronic pain under current NHS protocols.