I am 64, and was referred to a Consultant Neurologist 3 years ago to investigate damage to nerves in my feet. At that time I was able to walk unaided and very active. In the intervening period my symptoms have continued to worsen significantly and I now have to use a walking frame. I have had a number of diagnostic tests, but no treatment to date, and in June I was referred for a nerve biopsy for which I was devastated to learn that the waiting time was at least six months, which is totally unacceptable. We are led to believe that waiting times have shortened considerably and that patients have statutory 'rights' in this respect, but this has not been my experience and I feel I have been badly let down by the NHS - instead of being diagnosed within an acceptable timeframe, which would have halted the progression of my symptoms at an earlier stage, I have experienced interminable delays which are likely to leave me with a permanent disability. My NHS Trust claims to be unable to help to expedite this latest procedure. I am truly appalled!
I have been waiting 14 months, I have a nerve caught in my spine, the Primary Care Trust have taken me of the waiting list. Where does a pensioner get £1ooo pounds to go private, I am 75 payed into the National Health since I was 15yrs, in perfect health otherwise. Its an injection at Outpatients.
I tried to make an appointment at my Doctors today (Wood street Surgey in Mansfield) and the earliest appointment they could give me was 21st August - five weeks away. Disgusted
I thoroughly agree. Frequently I have had to wait at least four huors to see a doctor, even wit h strokes. Once after sitting freezing for hours ,my name still was not called. They only gave me a wheelchair when I collapsed. I have been in hospital over 20 times in the last ten years. I was really ill last wee. The oharmacist and the doctor both said I needed an ambulance, but I refused to go to hospital. They get everything wrong anyway.They are kindly but have poor memories!