NetGalley review
I was young when Sally Roberts was enduring legal battles over informed consent for her son, Neon, and so I only had a vague memory of hearing about it on the news when I went into this book. Having just lost a loved one to their treatment for AML, cancer is no stranger to me, nor are the conventional treatments given to cancer patients, but it was still chilling to see the ignorance, arrogance, and biases Sally experienced from professionals at the hospitals where Neon received his care. This book deals with Sally's relationship with her ex-husband, her hardship when she had become single once more, her fear at Neon's diagnosis, and her search for a better treatment - what would later become the gold standard in cancer care for children in the UK, but at the time was regarded as quackery. Unfortunately the ordeal this family went through is not unique to them. The same overstepping of the medical establishment happens today, the same ignorance of nutrition, toxicity, and better wellness, the same disregard for a patient's (and in a child's case, a parent's) informed consent. There are good doctors out there who are just as much held captive by a broken medical system as we patients are. Cancer isn't the only area of medicine where this happens. I can only hope that Sally's story - and the many, many stories like hers - bring awareness to this issue so that we can finally see lasting change.

