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There's been many posts in the forum on the use of vibration therapies for PwP. People have posted on various non-invasive mechanisms such as physical movements, changing sounds, electrical and magnetic pulses, as well as the invasive DBS.
What these all have in common is that they add a stimulus to the CNS. In 2010, Imark3000 and Rick wrote about the use of entrainment to reduce tremor: http://neurotalk.psychcentral.com/sh...ht=entrainment See also Audio-visual entrainment, at Wikipedia: http://en.wikipedia.org/wiki/Audio%E...al_entrainment With the desire to reduce my tremor, I thought I'd try something in this area. My background is in computing, so it's easier for me to do something computer based. On the grounds that it's easier to program, I tried a different approach: creating the stimulus using strobe lighting only. I've written a program which generates many strobe lighting effects: - choice of frequency, color; - different left/right images, which can have a phase difference; - changes of frequency and colour with time and tremor. There are over 20 parameters that can be tweaked. Let me give the following warning: - flashing lights are dangerous for some people; - the images can make your tremors worse; - the images can make you sleepy. The program is online at: http://www.parkinsonsmeasurement.org/toolBox/strobe.htm I've set the parameters to give a taster session; running for 30 sec, the frequency starts at 6 Hz and decreases with time. My theory is that if the flashing starts close to the Parkinsonian frequency, 4-6Hz, the tremor links to the flashing and, as the flashing frequency is reduced, the tremor follows, decreasing with time. The reality is more complicated. The strobe effect on me is: - in the first few seconds my tremor gets worse; - after about 30 seconds of the strobe frequency slowly decreasing the tremor's amplitude starts to decrease; - after 3 minutes I may start to get sleepy, and the tremor gets less than it was at the start. I've not tested the program on any other PwP, so I don't know whether the effect on other PwPs is the same. I would like to have measured the effect, but I can't get any reliable results. I don't ask anyone to try the program. But, I would be grateful for any comments on the approach, especially the identification of any additional dangers. John
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Born 1955. Diagnosed PD 2005. Meds 2010-Nov 2016: Stalevo(75 mg) x 4, ropinirole xl 16 mg, rasagiline 1 mg Current meds: Stalevo(75 mg) x 5, ropinirole xl 8 mg, rasagiline 1 mg |
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"Thanks for this!" says: | Niggs (12-14-2016) |
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