What a thoroughly unpleasant post! I hope it's not representative of his other 3000+.
I was unable to respond immediately as I've been in the toilet cleaning my wife up for the third or fourth time today. It's probably just as well that I've had the opportunity to reflect. One course would be to ignore him, as he has announced his departure from the thread. But other people may be following the discussion.
It might have been for the best if the simple and true answer to this question, which was given very early on, had marked the end of the thread. However, we had the long post from owly which seemed to me to be a mix of suggestions for which there is evidence, some which were less well-evidenced, and some which seemed the kind of thing you'd 'learn' from a YouTube video, as one of them turned out to be.
I gave some examples of ideas which were, at best, unproven. We discussed aluminium then I asked about the evidence that electromagnetism caused clotting. This, for some reason, seemed to upset JPG1.
However, we did eventually get the reference to the YouTube video from owly.
For the record, I 'use' TP (a normal usage of the word, BTW, that he chooses to make an issue of) both to get support and advice myself (and it's very helpful at a practiical level) and to discuss questions and ideas which might be helpful to me as a carer and possibly to others.
It worries me, particularly when people first find the forums, that some users quickly rush in with statements that are unproven or untrue. They sometimes write with an unwarranted certainty and this in itself might mislead people who are new to the conditions we are concerned with so I sometimes ask people to provide their evidence or I suggest a qualification.
It's simply not good enough to say that anything that anyone wants to say about the nature of the diseases or the way to treatment, based on their own experience or not, should automatically go unchallenged which is what JPG1 appears to be saying.
Some of the things posted on here can cause unnecessary alarm and anxiety and I when I see them I sometimes point this out. I'll continue to do so. As I've said before, carers have enough legitimate anxieties.