This is a tragedy for sure - I'm just perplexed that the parents seem to have allowed this to become, in my view, a sideshow with them in the starring roles.
I'd have thought this would be a private matter for most families in these awful circumstances.
I agree - why on earth would you opt for all this publicity.
I can understand in cases where perhaps publicity might mean donations that may help send the child to a private clinic for treatment. But that doesn't seem to be the case here.
It's actually sounding more and more implausible. If she isn't terminally ill then presumably the medical team could be in all sorts of trouble for this. I dunno, I smell a rat.
If it's all genuine then it's just bizarre.
I haven't found any evidence to suggest that CMT as a disease is ever terminal. And actually if you get into the details it isn't clear that the medical staff in this case are claiming it to be.
The focus seems to be on invasive intervention that might be necessary were she to develop pneumonia and be unable (due to her condition) to clear fluid from her lungs. The issue seems to be whether this life saving intervention should be provided in the future if she needs it. And to balance that against the quality (and quantity of life) if she lives rather than dies.
Now there doesn't actually seem to be an issue on quantity of life, the medical opinion seems clear that patients even with extreme CMT have a life expectancy the same as, or barely shorter than, those without the condition.
There is clearly an issue on quality of life - if an intervention is highly invasive, painful and distressing but merely perpetuates a life that has very little quality, and perhaps only briefly then quite reasonably that intervention may be seen to be 'futile' and not recommended. Do not resuscitate notices being obvious examples.
But here is the tricky thing in this case. Imagine the parents had chosen not to allow intervention last time and she had dies (and she presumably would have done), the child would have lost more than a year of life with parents, friends, family etc which (from what I gather) has been pretty good (as far as it can be in her circumstances). There seems to be a clear view that currently she is 'living life to the full' as much as her condition allows. So image in another years time she gets an infection and develops pneumonia requiring naso-tracheal suctioning - which is pretty awful - what to do. With this she might have another 2 years before needing this again, and so on. Who is to know how either the parents, or even the child, will feel about that when the time comes, and in retrospect whether they'd feel this was the right thing to do or the wrong thing. I'm not getting any feeling that the parents feel they should have let her die last time.
This seems to be the heart of the issue (which is sensationalised and brought across inaccurately by the popular press).
But the bottom line is that although this should be considered and discussed, a decision should only be taken at the time it is needed. The parents and the child might feel very different is she needs intervention at the age of 7 than they do now when she is 5.