In December 2022, at 49 years old, I began experiencing symptoms that led to my diagnosis of early-onset Parkinson’s disease.
Since then, I’ve often felt frustrated by how hard it is to find clear, easy-to-understand information. It’s not that information isn’t available, but navigating it can be overwhelming—and it often feels like there isn’t enough time for doctors to really explain things in a way that makes sense.
Another challenge I’ve encountered is the medical community’s cautious approach. At times, it seems overly focused on limitations—and honestly, that can be discouraging.
That’s why I created this space: to gather and share the most up-to-date, cutting-edge information that could truly make a difference. This website is, in a way, my personal organizer—public by design. And there’s Dopa VOX, where I post random thoughts—and so can you.
My mission here is simple: to provide unbiased, evidence-based information. I don’t promote or sell any products, supplements, or services, and I have absolutely no commercial interests influencing my content.
"Currently, stem cell research for Parkinson’s disease remains with therapies being tested in the brains of monkeys." - My neurologist, 10 April 2025 - (with a hint of pity for my lack of knowledge, and my hope being misplaced.)
Me, after spending 5 minutes on the Internet:
May 08, 2024: "Parkinson’s patient moves freely again after world-first implant of lab-grown cells into his brain" - Euro News Article Here
Ask your neurologist and let me know their response, I'll paste it below.