After I was diagnosed with Parkinson's Disease (PD) in 2013 my life became increasingly constrained, both psychologically and physically. While I occasionally justified an "off" day using my age, unfit state or hypertension, this was not realistic. So, in February 2020, I contacted the neurologist who featured in a December 2019 Carte Blanche documentary mentioned in my last post. The earliest appointment at the Durban Neurolaser Clinic was mid-June 2020.
I was told by the receptionist that an initial assessment by the neurologist would be followed by a series of roughly one-hour laser therapy sessions. However, as the Coronavirus lockdown period resulted in his many patients not being able to travel to KwaZulu-Natal, I was able to secure an earlier assessment followed by the initial phase of therapy. (His busy schedule indicated public interest in the approach.) The neurologist explained that I would need to complete a series of ten carefully spaced treatments and then take a months' break.
What I noted from that first assessment interview was that it would be up to me, as the patient, to do the pre- and post-treatment assessments. These comprised physical tests of gait (walking) and fine motor skills (finger and hand actions) using videoclips. I decided to add writing, typing and hand dominance. As a practitioner researcher - this was described in an earlier post - his "subjective" evidence approach suited me: I would have to evaluate what was happening to me.
As a result of our being in stage 4 of the lockdown period during my therapy, the Durban Neurolaser Clinic sent me a permit to travel and as their rooms are at a hospital, I felt relatively safe going there. I was instructed to wear a mask and to bring gloves. There were stringent precautions at the hospital entrance before entry with two staff recording each patient's details, body temperatures and sanitising before allowing entry. Every one of the members of staff inside the clinic wore full personal protective equipment (PPE), consisting of a white onesie, white booties, white masks and white goggles. "Area 51" often crossed my mind and made me smile.
For the first week of therapy, besides working out gender, I had no idea of who was assisting me as they all looked singularly similar except for their height. This was a tad confusing as I was making notes after each therapy session regarding what exactly occurred, who did what and how. All I was aware of was four voices, accompanying accents and their varied approaches to initiating therapy. For obvious reasons, I had opted not to wear my hearing aid, which made things doubly difficult.
The primary pad contained a combination of super luminous red and low level Infrared diodes combined into a single diode. This pad was placed on various parts of my cranium, base of the skull and once on my stomach. During each day's treatment, the pad was used in three different areas for about 12 minutes each, depending on the programme. That was followed by about 10 minutes of the two hand-held lasers (manipulated by "Area 51" staff) meticulously tracing patterns around the front, top and back of my skull.
The total treatment time for PD - thrice with the pad and twice with the red and the black probes - depending on the programme, was just under an hour per day for ten days. The recommendation was for the first five therapies on consecutive days and the remaining five on alternating days.
From what I have read, the function of the diodes is for light energy to penetrate the skull through the radiation so it may be absorbed by cells' membranes. The resulting complex reactions are physiological in nature. Seeing that the blood vessels are dilated during treatment I always felt warm during therapy. In the 10th post, I cited an excerpt from an article regarding scepticism in the field of photobiomodulation (PBM) that, hopefully, piqued your curiosity. I will not attempt to further fine-tune what occurs. If you're interested, then do use Google or Safari or Duckduckgo or other search engines, dear reader.
Next time I'll share what I feel like after the first couple of weeks of PBM for PD.
