Copied and pasted from another thread Hopefully this will help posters like User understand the situation.
Venusflytwat Sun 02-Jul-17 08:26:52
I tried to post this into Charlie's Army but the moderators didn't approve it, so I'm posting it here instead. The lack of understanding makes me sad but to deliberately block it makes me angry.
"I have spent a long time wondering whether to post this. I think it will probably be deleted but I beg you to read it before it is.
The MRI scans were presented in court. If you read the court judgement they are clearly referred to in there, I have posted the link to the judgement further down.
I can understand how the MRI reads if you haven't been trained in medicine or imaging at all, and where this misunderstanding comes from. In the instance of brain damage, MRIs look for damage like tumours, or blood clots, or haemorrhages. This is not the sort of brain damage Charlie has. Charlie's brain FUNCTION is damaged at a cellular level. The cells cannot produce the energy to function, because they do not have enough mitochondria. They have no energy and so they cannot function. You would not see this on an MRI. You WOULD see this on other studies such as EEGs. These have been repeatedly done on Charlie and show extensive encephalopathy- this means extensive damage and dysfunction to the function of his brain. Again, I repeat: you would not see this on an MRI.
Please take the time to read the actual court judgement. I have provided the link here, it is all in there. The MRIs you want to wave WERE seen by the court, they are referred to in there. They were not suppressed. Please also take note of how many different hospitals were asked by the court for their advice, both in the UK and abroad. They ALL agree with GOSH's assessment of Charlie's condition. This decision was not informed by GOSH alone.
Charlie's illness is a terrible, cruel tragedy. But clinging to false internet rumours doesn't help him or his poor parents now. Please take a few moments to read the full facts for yourself before taking action based on things which are simply not true, however well intentioned.
I pray nothing but peace and love and light for Charlie and his family tonight and in the coming days."
www.bailii.org/ew/cases/EWHC/Fam/2017/972.html
Notes:
Dr. B confirmed that, whilst Charlie is not brain dead, he is persistently encephalopathic. In other words, there are no usual signs of normal brain activities such as responsiveness, interaction or crying. Dr. B confirmed that this is supported by repeated electrical tests in the form of EEGs.
Dr. B explained in his oral evidence that, even before Charlie began to suffer from seizures on 15th December 2016, the clinical consensus was that his quality of life was so poor that he should not be subject to long term ventilation, resulting in the advice of the Ethics Committee in November 2016 not to offer Charlie a tracheostomy. Dr. B said that, since that time, Charlie has suffered significant deterioration in brain function evidenced by the development of persistent seizures. The court has also been provided with a letter from Dr. E, Consultant and Senior Lecturer in Paediatric Neurology at the Newcastle Upon Tyne NHS Foundation Trust. Dr. E specialises in rare mitochondrial disorders and is regarded as a world expert in the subject. He referred, in particular, to the fact that Charlie has developed an epileptic encephalopathy, which has been detailed on several EEGs, some of which have been prolonged recordings capturing a wealth of neurophysiological data on Charlie whilst awake and asleep as well as during seizures. Dr. E said this:
- "Indeed, the most recent EEG performed on 10th January 2017 was very similar to that recorded in December 2016 and which was indicative of a severe epileptic encephalopathy with frequent sub-clinical seizure activity. Subsequent to Charlie's initial cranial MRI scan performed on 7th October 2016, he has had two further scans on 19th October and 6th January 2017. The most recent of these does not show any major pathology, but does reveal some subtle increased signal in the subcortical white matter of the occipital lobes. This would be a typical finding in patients with mitochondrial DNA depletion syndrome."