What an irritating misinterpretation we have here.
Let's use an analogy, referring to my own personal life. I had a close female relative who developed her first eating disorder (bulimia) aged 14. She 'recovered' from bulimia, in that she managed to stop her binge-purge cycles, but she did that by switching to pure calorie-restriction, i.e. she developed anorexia, with a surface layer of orthorexia.
The late teens are a pivotal time for bone development in female adolescents, which is inextricably linked to the menstrual cycle. Her malnutrition led to menstrual disruptions, which led to osteoporosis. Within approximately 30 years of first developing bulimia, she was diagnosed with advanced osteoporosis. She only lived another decade, and that decade was filled with suffering, because the repeated fractures could not heal fully. Each time, she lost mobility in the affected limb, and this led to other complications. The over-stretched NHS could not meet her needs.
My ringside seat as an unwilling witness to the lifelong ramifications of eating disorders has shown me exactly how awful they are. I want less people in the world to develop eating disorders. This does not mean that I am glad my loved one is dead. It certainly does not mean I wish death upon young women like her today.
It means that I want those young women to lead lives that are not devastated by the physical effects of one of the most dangerous mental illnesses we have, as would anyone capable of empathy with an emotional IQ above 51. Happily, most people on this thread meet that criterion.
Seriously, shouldn't a sane world have a huge problem with it when teenagers starve themselves into disability and death? Are we supposed to say "her body, her choice" about it, in case someone assumes our only problem with teenagers with anorexia is that they're not dead yet?