"Just a migraine"
Posted , 6 users are following.
That is how the neurologist at the local A&E diagnosed me with and prescribed Imagrin and 3 days in a darkened room! This was despite the fact that both myself and my GP (who had phoned the neurologist department and spoken to a neurologist who said they would see me straight away if I went up to A&E) that this was nothing like any migraine I had ever suffered and I have suffered since 3 years of age (I'm now 50), anyway to cut a long story short I followed his advice and on the 5th day of suffering (I sat up A&E for nearly 6 Hours) I went back to my GP and was re-refered back to the neurologist who originally said they would see me and had sent their colleague, she organised an eye test as I still had what they described as an Aura, I past the eye test although it was obvious that some of my sight was restricted and I responded slower to the light! Anyway the neurologist said that she was also convinced it was just a lingering migraine, but if my vision had not come back by the Friday (8 day mark) she would arrange an MRI scan, she phoned me to check first and then made the arrangements for my scan which took place on the 2 week mark, then I had to wait a further 2 weeks for the results....well the results came in last Friday and it turns out I had a stroke of the left visual cortex which has taken a patch the size of a 10p piece! So the neurologist who gave me the bad news on Friday was the first one I saw at A&E, he prescribed me a life long drug to reduce my platelets and informed me that I will be having loads more tests including tests on my heart. Anyway when I got home my husband read the patient information leaflet and to his horror found out that the drugs the neurologist had prescribed could NOT be taken by some one with peanut allergy (I'm allergic to all nuts and this is stated all over my notes and something I always mention when a Dr is prescribing any medication) so I phoned the hospital on Saturday morning and was told not to take them and they would get back to me on Monday (which is today) to let me know about my new drugs and sorting out my perscription (I live 14 miles away from the hospital, but they think it is just next door!) well it is now nearly 5 in the afternoon and all I'm getting when I phone them is engaged, to say I'm getting stressed out is just a little bit of an understatement as I'm now 32 days since my stroke and only received treatment a stroke victim is not supposed to have!!!! I feel like a ticking time bomb! As any one else had such shoddy treatment because the dr's believed it was"just a migraine"
0 likes, 16 replies
fraggles Helen03706
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Helen03706 fraggles
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fraggles Helen03706
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Helen03706 fraggles
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fraggles Helen03706
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Helen03706 fraggles
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Scouser65 Helen03706
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samuels Helen03706
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Yes I have been treated like that on my second suspected TIA, I have never suffered from migraines or headaches for that matter until I was put onto GTN for Prinzmetal Angina, You get a thumping headache when you have it for the first week or 2 but it passes or with the aid of Panadol. Because it was a suspected TIA by Emergency doctors for the second time a Neurologist came down and saw me, he made the decision that it was just a migraine and sent me on my way even after explaining that I have never suffered from migraines, his responce to that was " you can develop migraines at any age" ....I suppose this could be true... but in my case I don't think it was, I've had 2 more episodes in the last 2 years, I just don't bother going to emergency anymore for suspected TIA's, If I'm drooling or having trouble talking or go funny on the left side I just go and lie down until it passes, usually gone after 15-30 minutes, my very first TIA lasted not quite an hour, close but not quite.
Helen03706 samuels
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mike93015 Helen03706
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Over the next 48 hours I developed total nerve pain, tingling, numbness on my right side below the chest down to the foot. I complained to GP that i may have had a stroke, he practically laughed my opinion off saying I was too young (45 at the time) and didnt smoke. When I first saw a Neurologist some 3 or 4 months later I had an MRI Scan and he said it was clear and discharged me after also checking my spine. I have had the same symptoms ever since together with slight sppech problems and balance problems. I finally got a second referral to a Neurologist at the same hospital, straight away he thought it was a stroke, used the same MRI scan originally said to be clear and diagnosed the stroke. 18 months of no treatment, now with what appears to be lifetime nerve damage, and medication to prevent another. It had recently been reported that there has been a massive increase in the number of strokes suffered by our age bracket, I think they should report it to their own hospital staff. If there is a possibility of Migraine with a worse case Scenario of stroke, the MRI Scan should be carried out immediately. The very best of look with everything Helen, I know exactly hopw your feel regarding the ticking timb bomb, I have felt that way for 2 years, try not to worry but the best advice I can give you is to perservere with the Docs and dont let them fob you off x
Helen03706 mike93015
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mike93015 Helen03706
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pauline59158 Helen03706
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I displayed signs following a day out, my family noticed my speech was garbled and sought advice. Fortunately my son is a Paramedic and advised my husband to get me top hospital straight away.
Within minutes of arriving at A&E I was seen by a Dr. Another 2 hours with a CT scan I was diagnosed. At this time my Memory had gone and my face dropped. Obviously I don't remember any of this. I spent 3 weeks the Stroke Unit, my treatment was excellent. I'm on warfarin and have blood tests every few weeks. This should be universal, in my opinion.
3 years on, I have had several TIA's and still have memory issues.
I still live in dread of having another stroke and suffer with depression. I'm not sure that will ever go.
I wish you all a speedy resolution to all your issues, but would support your drive to make the hospitals accountable.
Pauline
fraggles pauline59158
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Winnie143 Helen03706
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I had an SAH/Stroke, but a few months before this I went to a new Optician who said I had a wonky disc, I never knew what he was on about and gave my letter to the Doc who never knew either !! I often wonder if a good Optician can see things in your eyes. I wish you all good luck and Stress is bad for us all, so either sing a happy song or smile xx asier said than done also but it helps xx
Winnie143
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