Microvascular Decompression
Posted , 35 users are following.
Hi im new to this forum. I am due to get the microvascular decompression operation in a few months to cure my trigeminal neuralgia. I am wondering if anyone has had this op because i would like to know a bit about recovery etc... I know about the operation itself as i have researched it and even watched the operation online but i would like to know about after the op. Thank you
4 likes, 68 replies
cfb
Posted
part was the effect of the general anaesthetic (vomiting) later that night. I felt no pain or discomfort - no need for paracetamol even. I was discharged after 48hours and told to report to my GPs' surgery to have the 27
staples removed after a week. As well as staples over the cut there were 4 on the top of my head which had been screwed to the operating table to keep me motionless. I was td mnot to wash my hair for 3/4 days and than to use a mild shampoo eg Simple.The actual scar is about 5cm long and is now covered by hair. If
you watched the american film on YouTube you know what's in store!. There is also an
old TV series made in 2006 called Brain Doctors about the pioneering work of the Bristol Frenchay hospital.
I hope this may be of some use.
Good Luck I'm sure you won't regret it.
barbara4711 cfb
Posted
It has been over a year since your operation... Are you still happy and totally pain free?
cfb barbara4711
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jbbell cfb
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Trengove1
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Thank you
I hope surgery goes well for you
YKL
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Neilupandown
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I had TN for 5 years steadily getting worse and worse untill i couldnt function with the pain and drugs.
I had my MVD in july 2011 and all went well initially.
But due to some complications i contracted meningitus. 4 lumbar punctures and 2 weeks in hospital later i was fine no symptoms no TN and off the tablets.
Now nearly two years later i have started to have the occasional "Shock and pain" this time on the same side but in my front teeth and top lip. I am so so worried, dont know how i will cope if it develops into what it was two years ago, off to the Docs. tomorrow to see my options.
cfb
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the front of the face are affected.
I had my MVD operation in June 2011 at Frenchay hospital, Bristol and touching wood and crossing
everything I haven't had any pain since then. The operation was 100% successful. I am so grateful to
everyone who made it possible.
In passing I would like to add that the side effects of the medication (Tegritol first & then Trileptal) that I took
for 3 years before the operation, have finally disappeared. My memory is back to what it used to be (!) and I
no longer fall over.
dgb1952
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Sf17 dgb1952
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alicot Loopylee
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dgb1952 Loopylee
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Since the op, my wife gets occasional 'twinges' which I put down to the nerve, which is a huge bundle of fibres, destressing itself from the days it was being pushed out of shape by the blood vessels. (3 in my wifes case).
Go here for a nice story
http://neurotalk.psychcentral.com/thread2052.html
Yet another example of the mess the Welsh NHS is in.
mommaphipps Loopylee
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marielouise1966 mommaphipps
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Loopylee marielouise1966
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marielouise1966 Loopylee
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