In this three part blog series, I have detailed my journey with Parkinson’s – both in terms of early diagnosis, and more recent treatment and support. My attempts to come to terms with and understand both the diagnosis and treatment led me to explore multiple avenues towards living well. I needed a multi-disciplinary approach, and … Continue reading Making Sense of my Parkinson’s: The European Centre for Parkinson’s
In my previous blog, I wrote about the impact of my Parkinson's diagnosis – and the information which would have been useful to receive at the outset. Making sense of Parkinson’s is a long journey however, and one which extends far past initial diagnosis to treatment and daily life. So what has life been like … Continue reading Making Sense of my Parkinson’s: Treatment and Support
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?