- Messages
- 4
- Location
- Staffordshire
Has any one experienced pins and needles in their brain?
I have just been reading on Dr Myhills site (with one eye to try to help my double vision!!) and it says that in ME blood flow to the brain is affected.
I said 1 so many times to the Drs....on the day that was the start of my demise (this time round) my brain went cold and then I had pins and needles in my brain, I told them have had intermittent circular 'patches' or areas in my brain that have felt like pins and needles for years, but they came and went so I ignored them.
To me - the common sense explanation for that was clearly - blood flow to my brain had stopped - thats why you get pins and needles durrr - but no one listened to me.
They also kept twisting my words and wrote in my notes, pins and needles on scalp...I kept saying NO, not on my head...in my brain!!
When I went to the consultant he said my MRI was fine - he could see there was an area where blood used to flow, but doesn't any more, but is was on an extra part of my brain that I don't need so not to worry about it....
this was the same guy, when I told him how much my legs hurt, and that I had double vision...he said ahhh, don't worry about it....this was annoying yes, but third in line to the dr who hurt me on purpose to see if I was faking paralysis, and the dr who said I was being either hysterical or abused at home.....
Really interested to know if anyone else has had this pins and needles experience xxxx
I have just been reading on Dr Myhills site (with one eye to try to help my double vision!!) and it says that in ME blood flow to the brain is affected.
I said 1 so many times to the Drs....on the day that was the start of my demise (this time round) my brain went cold and then I had pins and needles in my brain, I told them have had intermittent circular 'patches' or areas in my brain that have felt like pins and needles for years, but they came and went so I ignored them.
To me - the common sense explanation for that was clearly - blood flow to my brain had stopped - thats why you get pins and needles durrr - but no one listened to me.
They also kept twisting my words and wrote in my notes, pins and needles on scalp...I kept saying NO, not on my head...in my brain!!
When I went to the consultant he said my MRI was fine - he could see there was an area where blood used to flow, but doesn't any more, but is was on an extra part of my brain that I don't need so not to worry about it....
this was the same guy, when I told him how much my legs hurt, and that I had double vision...he said ahhh, don't worry about it....this was annoying yes, but third in line to the dr who hurt me on purpose to see if I was faking paralysis, and the dr who said I was being either hysterical or abused at home.....
Really interested to know if anyone else has had this pins and needles experience xxxx