"Still operating in the dark ages - but what choice..."
About: The Royal Victoria Infirmary The Royal Victoria Infirmary Newcastle Upon Tyne NE1 4LP
Posted by Anonymous
Let me explain. As a patient, choice is supposed to be important, but, in terms of neurosurgery we only have one department in the region; a 'centre of excellence'. Although I don't think I have many general concerns over the competency of the surgical skills the teams at the RVI demonstrate, I have grave concerns that some consultants work purely to what they perceive the scans to show, rather than what the patient actually tells them. The wait for appointments post-referral and the actual in-hospital out-patient wait are both unacceptably high. Once I had to wait four months for an appointment and then four hours to see a doctor once in the department. All this, for a consultation that barely took 2 (two!) minutes and could easily have been sorted out months previously via telephone. I had been led to believe that neurosurgery had 'put its house in order' when compared to the general air of arrogance and lack of empathy shown by surgeons in the past. I have yet to experience this.
Some flesh on the bones... Unfortunately I 'slipped a couple of discs' in my neck in May 2011 and, unfortunately, I am medically qualified as a doctor although do not currently engage in clinical work. I suffered really bad arm pain and had some numbness and a slight weakness in one arm. I had the appropriate initial medical management and was referred urgently to neurosurgery on presentation of the power deficit, whereupon I had an MRI which showed (amongst other things) two slipped discs in my neck. My limited understanding of neurosurgery told me that really, in order to obtain the best longterm result (especially in relation to the numbness and power issues) was to operate quickly. I was, eventually, listed for an operation - single-level ACDF (with no discussion or explanation as to why the higher level was left alone, despite (what had been shown to me to be a prolapse on MRI) some seven months later. (To be absolutely fair, I did have a nerve root injection that produced a good result for a limited length of time but the result had been 'misfiled' and mysteriously not found until I actually managed to get a response from my surgeon.) After the op, all was well, in fact, brilliant for six weeks. But that's where the goodness ceases. Since this time (over a year now) I have higher level symptoms bilaterally in both hands, arms, shoulders and my neck. I have numbness, am dropping and smashing things regularly, have twitching fingers and stonking headaches all of which have produced the reply, "Well the scan doesn't look too bad" from my consultant!!! And I'm a knowledgeable person - a member of the profession - how are they treating those who do not have this knowledge? I am now at my wits end taking analgesics four times a day, every day and crying in pain if I miss them (I even set an alarm!) and a whacking dose of a longer-acting medication. I've had another root injection - which was great! For two days!!! And then a review in four months! Aaaaarrrrgggghhhhh!