If things weren’t already frightening enough thanks to the pandemic, with the number of new cases climbing, and even more people dying, along comes a journal article that is rather disconcerting.
It is called Parkinsonism as a Third Wave of the COVID-19 Pandemic? I didn’t put the question mark at the end of the article title – this was placed there by the Melbourne-based authors. It is a question, a realistic and one that has to be faced and planned for.
Continue reading “Covid-19 and Parkinsonism”
The term brain fog is not an official medical term, but we all know what it means, and we have all experienced it. Serious and creative thinking is hard enough to do at the best of times, but when brain fog descends, it is even more difficult. Unfortunately brain foggery seems to happen more often as we get older which is even more frustrating…
Continue reading “Mental clarity vs brain fog”
I’ve had a few people ask me whether to stop medication for Parkinson’s disease when starting transcranial lights.
Continue reading “PD, medication and lights”
Just as Parkinson’s is an insidious disease that creeps up and takes things away, the effect on the life of partners is just the same – insidious and inexorable.
Photo by Nani Chavez on Unsplash
For everyone with Parkinson’s disease, Alzheimer’s disease or any other neurodegenerative disorder, there is almost always someone who walks alongside every step of the disease progression. It’s not the doc tor, or nurses or anyone from the local Parkinson’s disease association doing the twenty four hour shifts. It’s the partner.
Continue reading “Partners”
Exercise and photobiomodulation are both neuroprotective.
Yesterday I had a really long conversation with a physiotherapist who specialises in treating people with Parkinson’s disease. It was one of those enormously cheering conversations. Listening to someone who is extremely experienced, supremely competent and concerned for and about each patient is a delight. On top of that, to have the drive and energy to keep up with the medical literature and identify other ways to help patients is awe-inspiring.
One of the topics we discussed is the role of exercise in Parkinson’s disease. It seems that there are some who think that exercise has a minimal role in management of Parkinson’s. This is astonishing, given all the research that consistently shows that structured exercise makes a big difference.
Continue reading “Exercise and Light”
Mitochondria get a lot of airplay in this blog. (Here’s an early post.)
The mitochondrial experts of the world have been blown away by new research. It seems that our blood not only contains the various sorts of red and white cells, but it also contains nomadic mitochondria.
This is amazing! Here’s why.
Continue reading “Mitochondria in your blood”