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
Making Sense of my Parkinson’s: Diagnosis
The first in a three part blog series: The shock of the Parkinson's diagnosis came in August 2017. It was ultimately made by consultant neurologist Mr. William Gibb, privately in Southampton. My symptoms finally made sense to me. Muscle stiffness was preceded by unexplained symptoms of sleep disturbance with vivid dreams (5 years); shoulder stiffness … Continue reading Making Sense of my Parkinson’s: Diagnosis
How can current Parkinson’s Services be improved?
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?
Being Human: PNI and the links between stress and dis-ease
I am currently re-reading a book called When the Body Says No - The Cost of Hidden Stress by Gabor Maté. Descriptions of many medical stories are detailed where serious ill-health is a consequence of sustained stress. Our book Reclaim Health also details symptoms resulting from chronic stress that are often misinterpreted as due to … Continue reading Being Human: PNI and the links between stress and dis-ease