Jonathan Edwards
Senior Member (Voting Rights)
The point I have been trying to make is that 'Orthostatic Intolerance' simply means the symptom of not being able to tolerate staying standing up. Sasha was aware she had OI. If asked in a questionnaire 'do you find it difficult to tolerate staying standing up?' the answer would have been yes. People may not know that not being about to tolerate standing up is called OI but then a lot of people do not know that a black headed gull is called larus ridibundus. It makes no difference - they know it is a gull.
So 'OI' is like 'pain in the arm'. It is not an explanation of anything.
I am not suggesting that Dr Bateman is wrong but that her presentation is confusing - I think lots of the posts above indicate how confusing it is because they assume OI means more than it does.
I also think it is confusing to link brain fog and nausea to OI as if OI explained these. Brain fog and nausea are just other ways of describing symptoms. All these things may go together but if they do that is because of some cause, that we might call ME gives rise to them.
The reason I think this is important is that so many PWME seem to go away with the idea that we have explanations for symptoms, maybe relating to the autonomic nervous system. I am not at all sure that we have anything worked out. To me accounts of what the illness is actually like, like John Peters's interview or all the many comments on here are much more helpful scientifically than a lot of the stuff that gets presented a meetings supposedly making sense of it all.
It may not matter if people go away with confused ideas about explanations of their illness but I worry particularly that these confused explanations feed in to doctors thinking that people have unhelpful beliefs. And when that starts to get dangerous is when parents are thought to have unhelpful beliefs about their children's illnesses and children get taken into care because of it.
So 'OI' is like 'pain in the arm'. It is not an explanation of anything.
I am not suggesting that Dr Bateman is wrong but that her presentation is confusing - I think lots of the posts above indicate how confusing it is because they assume OI means more than it does.
I also think it is confusing to link brain fog and nausea to OI as if OI explained these. Brain fog and nausea are just other ways of describing symptoms. All these things may go together but if they do that is because of some cause, that we might call ME gives rise to them.
The reason I think this is important is that so many PWME seem to go away with the idea that we have explanations for symptoms, maybe relating to the autonomic nervous system. I am not at all sure that we have anything worked out. To me accounts of what the illness is actually like, like John Peters's interview or all the many comments on here are much more helpful scientifically than a lot of the stuff that gets presented a meetings supposedly making sense of it all.
It may not matter if people go away with confused ideas about explanations of their illness but I worry particularly that these confused explanations feed in to doctors thinking that people have unhelpful beliefs. And when that starts to get dangerous is when parents are thought to have unhelpful beliefs about their children's illnesses and children get taken into care because of it.