Search results

They put a dye in near the end of my scan. So mine would have been with contrast. I'm really wondering now, what they actually saw on my scan

Thanks for your reply. I'm going to be talking to the neurologist this afternoon. I hoping I'll be able to think enough to ask questions. Maybe ask my Dr for the resulting letter as well, as it's always easier to understand when it's written up. I really don't know what to expect, but i'll soon...

Would be interested to know if anyone else had low pressure turn up on their MRI scan. Is it a common finding in folks with M.E. My brother (also has M.E.) has also had an MRi but that wasn't a finding of his.

My cousin had this too

Maybe it is the csf itself. Whenever I've had my blood pressure taken by doctors it's been normal. At home if I do it it's low normal usually 107/62 something like that.

Something I will ask the neurologist :):thumbup:

I would imagine that's what they mean

Mmm, they saying two types traumatic (head injury) which I don't fit and spontaneous (caused by hypertension) the opposite of my scan.

No;), when I did a search a couple of months ago, a lot of American sites came up about hypotension headaches and csf leaks. Will definitly read the st georges document. Thanks:hug:

Don't know, but I don't think those are recognised by the nhs/uk. Correct me if I'm wrong.

hi, had a MRI as in mid March I developed a severe migraine, vomiting on the first couple of days, unable to be upright for several weeks, developed double vision. I've had my eyes checked out, they felt there was a weakness in the muscle in my eyes and ordered an mri. The mri was mostly normal...

I would love to see the exercise folks in America put covid cases through a two day exercise test and see if they come out exactly the same as m.e. folks. Wonder if professor Garner's seen that piece of research? It's something he should be interested in.