{
  "id": 19503861,
  "title": "'Is this the best we can do?': B.C. mom of boy with muscular dystrophy calls for rare disease strategy",
  "url": "https://urgent.news/2026/11/11/is-this-the-best-we-can-do-b-c-mom-of-boy-with-muscular-dystrophy",
  "topic": "world",
  "section": "World",
  "published": "2026-11-11T13:00:03.000Z",
  "source": {
    "name": "Vancouver Sun",
    "slug": "vancouver-sun",
    "url": "https://vancouversun.com/news/bc-mom-of-boy-with-muscular-dystrophy-calls-for-rare-disease-strategy"
  },
  "original_language": "en",
  "account": null,
  "summary": "Kasha Mitton says kids with rare degenerative diseases shouldn't have to wait for drugs that have already been approved by Health Canada and other countries",
  "key_points": [],
  "editors_take": null,
  "illustration": null,
  "coverage": {
    "outlets": 1,
    "also_reported_by": []
  },
  "ai_generated": true,
  "disclaimer": "Summaries, key points and the editor’s take are written by software from other outlets’ reporting and may contain errors — always check the linked original."
}