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[quote=Anonymous][quote=Anonymous][quote=Anonymous][quote=Anonymous][quote=Anonymous]The doctor is the one who suggested and gave ketamine to Maya, not Beata. They saw her dramatically improve with freedom of pain. So Beata wanted to continue with the treatment that seemed to have helped her daughter. I dont see how that’s abuse from Beata.[/quote]

Bc you can find a doctor anywhere to say anything. Let’s say you go to a doctor who tells you your chemo needing child can instead eat a raw food diet and get sunlight daily. Can you shrug and say it’s on the doctor bc I trusted what he said?[/quote]

It's not that clear, as there aren't that many doctors who specialize in CRPS. In addition, the approach to CRPS has shifted since the events in the documentary to an approach that focuses on therapy and physical therapy and not medications. [b]The documentary does not offer a clear timeline, but it does reflect that the family tried other things, including lower doses of ketamine, before going to Mexico for treatment. [/b][/quote]
The timeline seemed pretty clear to me?? Maya started presenting with pain in July 2015 and they flew to Mexico for the ketamine coma in November 2015. IDK, that seems like a pretty short amount of time to decide to fly your kid to Mexico for a treatment that isn't legal in the US...
[/quote]
Yeah. Per court docs symptoms start in July 2015, Ketamine coma 2.5 months later, ketamine protocol from then until October 16th when she was admitted, released to her father in January 2017, completed PT and was walking around and resuming all normal activities by August 2017.[/quote]

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