After three years of living with the diagnosis of Parkinson’s Disease, I have begun to formulate some thoughts and suggestions for improving current Parkinson’s services. These suggestions are based on my personal experience as both a doctor and patient, and fit into five main categories: presenting symptoms, specialist referral, secondary care consultation, medical research, and … Continue reading How can current Parkinson’s Services be improved?
Is the recent NHS homeopathy ban a good idea?
In short, I believe it is not. The NHS needs to understand the value of the placebo response and its effectiveness in relieving symptoms. Having said this, I firmly believe that homeopathy should not be offered as a treatment for established disease or to create an immune response when given instead of vaccination. It does … Continue reading Is the recent NHS homeopathy ban a good idea?
How do we more fully see the whole person behind the clinical diagnosis of Parkinson’s disease?
As a patient I have witnessed the need to bring together a fragmented team to create personalised medicine. My experience of hospital and GP contacts: Long waits! Seeing a consultant neurologist privately – after waiting over 16 weeks for an NHS appointment. August 2017: Brief neurological assessment; blunt ‘you have Parkinson’s Disease’. Medication only offered … Continue reading How do we more fully see the whole person behind the clinical diagnosis of Parkinson’s disease?