Brian Walker Parkinsons and Stem Cells Journey

Brian Walker Parkinsons and Stem Cells Journey This page shares my journey with Parkinsons and how stem cell therapy restored my hope and quality of life. In those early days, it was hard to find hope.

My goal is to raise awareness, inspire others, and explore the potential of stem cell therapy to the community Brian Walker: A Journey of Resilience, Renewal, and Advocacy

Three years ago, my life took a detour I never saw coming. I was diagnosed with Parkinson’s Disease—a condition that would challenge not only my body but also my spirit. At first, it began subtly, with a gentle tremor in my right hand. I brushed it off as a minor nuisance, unaware of the storm that lay ahead. Over time, the tremors spread to my left hand and jaw. My movements slowed, my posture stooped, and I felt as though I was ageing decades in mere months. Parkinson’s was relentless, taking more from me than I was prepared to give. It wasn’t just the physical symptoms; the disease seeped into the unnoticed corners of my life. I struggled with nightmares so vivid they shook me awake, chronic constipation I couldn’t explain, and an emotional weight I didn’t fully understand. It wasn’t until a conversation with a specialist that I realised these were all part of the same battle. Treatment options seemed limited, and I wasn’t sure what path to take. That’s when my wife, Jo, became my guiding light. Her determination and belief in finding a better way led us to explore stem cell therapy—a treatment I was initially hesitant about due to its lack of regulation and mixed reviews. But Jo’s persistence paid off when she found a credible company in Japan specialising in stem cell therapy for Parkinson’s. The decision to pursue treatment was one of the hardest—and best—choices I’ve ever made. It started with a trip to Korea for a cell harvest, followed by my first stem cell session in Japan. What happened next was nothing short of transformative. After the initial treatment, I began to feel like myself again. My mood lifted, and for the first time in years, I realised how deeply depression had taken hold of me. My thoughts were sharper, my posture straighter, and my mobility more fluid. Friends and family saw it too, commenting on how I seemed revitalised, as if the clock had turned back 15 years. Every subsequent treatment brought more improvements. Nightmares and constipation vanished, my tremors eased, and I began walking with confidence again. My neurologist, who had been monitoring my progress, confirmed the changes weren’t just in my head—they were real and measurable. As my journey unfolded, I realised something profound: Parkinson’s may have altered my path, but it also gave me a purpose. The therapy didn’t just restore my life; it gave me a story worth sharing. That’s why I created the Brian Walker Parkinson’s and Stem Cells Journey page—not just to document my experiences but to inspire and empower others facing similar battles. This advocacy is about more than just my story; it’s about raising awareness, sharing hope, and encouraging others to explore new possibilities. Today, I feel stronger than ever—not just physically, but mentally and emotionally. While Parkinson’s hasn’t completely disappeared, it no longer defines me. Instead, I’ve chosen to define it by sharing my journey, breaking stigmas, and fostering a community of resilience and hope. This is my story—a testament to the power of determination, the support of loved ones, and the life-changing potential of innovative treatment. Together, we can rewrite the narrative of Parkinson’s Disease, one step at a time.

22/08/2025

🌿 𝐔𝐩𝐝𝐚𝐭𝐞 𝐀𝐟𝐭𝐞𝐫 𝐌𝐲 𝟗𝐭𝐡 𝐓𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭 𝐨𝐧 𝟐𝐧𝐝 𝐀𝐮𝐠𝐮𝐬𝐭 𝟐𝟎𝟐𝟓 🌿

I may not see a huge difference compared to my last session, but the important thing is—things are not getting worse. As I haven’t got much to report, here are some general observations:

1️⃣ I can still put on my trousers without holding on to anything.
2️⃣ The tremors in my hands are more noticeable when I’m stressed.
3️⃣ My neurologist, who has been monitoring me closely, said that before treatment I was already at advanced stage 2 (moderate to severe). Now, he says I’ve gone back to stage 1.
4️⃣ My hair keeps growing fast - so yes, I’m spending more on haircuts 😂
5️⃣ Before treatment, I was declining quickly, partly due to loss of appetite. Since the start of the treatment, I’ve pushed myself to eat - and now I don’t have to force myself anymore, because I eat almost everything I see. I believe this has contributed to my progress.

As time passes, it’s easy to forget how tough things once were because you’ve grown used to the progress you’re experiencing now. Sometimes it’s worth looking back - just to see how far you’ve come in this Parkinson’s journey.

11/06/2025

𝐅𝐑𝐄𝐐𝐔𝐄𝐍𝐓𝐋𝐘 𝐀𝐒𝐊𝐄𝐃 𝐐𝐔𝐄𝐒𝐓𝐈𝐎𝐍𝐒 (𝐅𝐀𝐐𝐬)

𝟏. 𝐃𝐨 𝐈 𝐭𝐚𝐤𝐞 𝐚𝐧𝐲 𝐦𝐞𝐝𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬?
A: I was once prescribed medication by a neurosurgeon in the Philippines when I was exploring the option of laser brain surgery. But after he explained the procedure—involving drilling holes into my skull to lock everything in place, followed by being strapped into a CT scanner for three hours—I figured the process might kill me before Parkinson’s ever could! I did go through with the CT scan, though, just to check if my skull was thick enough to survive the drilling... which felt more like prepping for a sci-fi experiment than a medical procedure.
So, to answer the question: no, I never actually took any Parkinson’s medication—before or after the stem cell treatment.

𝟐. 𝐖𝐡𝐚𝐭 𝐦𝐚𝐝𝐞 𝐲𝐨𝐮 𝐝𝐞𝐜𝐢𝐝𝐞 𝐭𝐨 𝐭𝐚𝐤𝐞 𝐭𝐡𝐞 𝐬𝐭𝐞𝐦 𝐜𝐞𝐥𝐥 𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭?
A: It was mostly thanks to my wife, Jo—she was absolutely determined that I should try stem cell treatment. It was becoming more common at the time, but I was skeptical. A lot of the people promoting it seemed more interested in selling whatever stem cells they had on hand, rather than finding the right fit for me.
But Jo was persistent (as she usually is!), and then we came across an article from South Korea about a specific stem cell therapy that targeted both Alzheimer’s and Parkinson’s. After reading it, we contacted the company directly and eventually decided to visit them.
It was a bit nerve-racking—we didn’t speak the language and didn’t know a single soul in the country—but we took the leap anyway.

𝟑. 𝐇𝐨𝐰 𝐝𝐢𝐝 𝐲𝐨𝐮 𝐝𝐞𝐜𝐢𝐝𝐞 𝐰𝐡𝐢𝐜𝐡 𝐬𝐭𝐞𝐦 𝐜𝐞𝐥𝐥 𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭 𝐭𝐨 𝐠𝐞𝐭 𝐰𝐢𝐭𝐡 𝐬𝐨 𝐦𝐚𝐧𝐲 𝐨𝐩𝐭𝐢𝐨𝐧𝐬 𝐚𝐯𝐚𝐢𝐥𝐚𝐛𝐥𝐞?
A: One of the main reasons I chose this particular treatment was because they used my own stem cells—harvested directly from me—instead of ones from a third party. That made me feel much more comfortable and confident in the process.

𝟒. 𝐖𝐡𝐚𝐭 𝐢𝐬 𝐲𝐨𝐮𝐫 𝐟𝐢𝐫𝐬𝐭-𝐡𝐚𝐧𝐝 𝐞𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞 𝐰𝐢𝐭𝐡 𝐬𝐭𝐞𝐦 𝐜𝐞𝐥𝐥 𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭?
A: I’ve added the dates on which I had the injections, and I’d be happy to answer anything you're curious about. The clinic I’ve been visiting has been a bit difficult to get information from—likely due to the language barrier—but their care and treatment have been superb.

𝟓. 𝐖𝐡𝐚𝐭 𝐢𝐬 𝐲𝐨𝐮𝐫 𝐩𝐨𝐬𝐭-𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭 𝐞𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞 𝐰𝐢𝐭𝐡 𝐬𝐭𝐞𝐦 𝐜𝐞𝐥𝐥 𝐭𝐡𝐞𝐫𝐚𝐩𝐲?
A: I’ve updated all the dates when I received my injections. If you have any specific questions, I’d be more than happy to answer them.

𝟔. 𝐇𝐨𝐰 𝐬𝐨𝐨𝐧 𝐚𝐟𝐭𝐞𝐫 𝐲𝐨𝐮𝐫 𝐢𝐧𝐟𝐮𝐬𝐢𝐨𝐧𝐬/𝐬𝐩𝐢𝐧𝐚𝐥 𝐢𝐧𝐣𝐞𝐜𝐭𝐢𝐨𝐧𝐬 𝐝𝐢𝐝 𝐲𝐨𝐮 𝐛𝐞𝐠𝐢𝐧 𝐧𝐨𝐭𝐢𝐜𝐢𝐧𝐠 𝐢𝐦𝐩𝐫𝐨𝐯𝐞𝐦𝐞𝐧𝐭𝐬, 𝐚𝐧𝐝 𝐡𝐨𝐰 𝐥𝐚𝐬𝐭𝐢𝐧𝐠 𝐡𝐚𝐯𝐞 𝐭𝐡𝐨𝐬𝐞 𝐛𝐞𝐧𝐞𝐟𝐢𝐭𝐬 𝐛𝐞𝐞𝐧?
A: Some improvements were noticeable quite early on, though it’s hard to say with certainty whether they were directly related to Parkinson’s. Communication at the start was limited, and the treatment felt like a significant gamble—you simply don’t know what the outcome will be.
My neurosurgeon, who initially advised me not to go ahead with the treatment, continued to monitor my progress. After my second injection, he noted that my facial muscles had improved and my posture had changed dramatically.
Now, more than a year after my first injection, I saw him again—and he admitted that while he was once a skeptic, he’s now a firm believer. Personally, aside from the tremors—which have significantly reduced and are sometimes entirely absent—I feel like my mind, posture, and overall condition have improved so much that I no longer feel like I have Parkinson’s.

𝟕. 𝐇𝐚𝐯𝐞 𝐲𝐨𝐮 𝐞𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞𝐝 𝐚𝐧𝐲 𝐬𝐢𝐠𝐧𝐢𝐟𝐢𝐜𝐚𝐧𝐭 𝐬𝐢𝐝𝐞 𝐞𝐟𝐟𝐞𝐜𝐭𝐬?
A: The only issue for me has been my personal fear of needles. The spinal injections can be uncomfortable, and I occasionally experienced a mild fever the night after treatment. However, as the rounds continued, these minor side effects became less noticeable.

𝟖. 𝐇𝐨𝐰 𝐦𝐚𝐧𝐲 𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭 𝐜𝐲𝐜𝐥𝐞𝐬 𝐡𝐚𝐯𝐞 𝐲𝐨𝐮 𝐮𝐧𝐝𝐞𝐫𝐠𝐨𝐧𝐞 𝐢𝐧 𝐭𝐨𝐭𝐚𝐥?
A: I’ve just completed my 8th injection so far.

𝟗. 𝐖𝐡𝐨 𝐢𝐬 𝐭𝐡𝐞 𝐛𝐞𝐬𝐭 𝐩𝐨𝐢𝐧𝐭 𝐨𝐟 𝐜𝐨𝐧𝐭𝐚𝐜𝐭 𝐟𝐨𝐫 𝐬𝐨𝐦𝐞𝐨𝐧𝐞 𝐢𝐧𝐭𝐞𝐫𝐞𝐬𝐭𝐞𝐝 𝐢𝐧 𝐛𝐞𝐢𝐧𝐠 𝐞𝐯𝐚𝐥𝐮𝐚𝐭𝐞𝐝?
A: In my experience, the clinic doesn’t conduct formal evaluations. Instead, you’ll need to provide a letter from your doctor outlining your current condition. This letter must confirm a diagnosis of either Parkinson’s or Alzheimer’s.

𝟏𝟎. 𝐁𝐞𝐟𝐨𝐫𝐞 𝐲𝐨𝐮 𝐬𝐭𝐚𝐫𝐭𝐞𝐝 𝐭𝐡𝐞 𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭, 𝐰𝐡𝐚𝐭 𝐬𝐭𝐚𝐠𝐞 𝐨𝐟 𝐏𝐚𝐫𝐤𝐢𝐧𝐬𝐨𝐧’𝐬 𝐰𝐞𝐫𝐞 𝐲𝐨𝐮 𝐢𝐧?
A: I was at Stage 2 moderate to severe Parkinsons

𝟏𝟏. 𝐇𝐨𝐰 𝐦𝐮𝐜𝐡 𝐝𝐢𝐝 𝐢𝐭 𝐜𝐨𝐬𝐭?
A: Unfortunately, the procedure is quite expensive. Harvesting the stem cells once and undergoing five intravenous treatments and five spinal treatments costs around $100,000. This amount includes the cultivation of the stem cells and the treatments at the clinic.

11/06/2025

"𝐇𝐨𝐰 𝐦𝐚𝐧𝐲 𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭 𝐬𝐞𝐬𝐬𝐢𝐨𝐧𝐬 𝐨𝐟 𝐬𝐭𝐞𝐦 𝐜𝐞𝐥𝐥 𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭 𝐝𝐢𝐝 𝐲𝐨𝐮 𝐮𝐧𝐝𝐞𝐫𝐰𝐞𝐧𝐭?"

It took approximately six weeks after harvesting for the stem cells to be prepared for my first round of injections, which was done in South Korea. The injections themselves were administered in Japan over two days per session: a spinal injection on the first day, which takes around 10–15 minutes (followed by about 2 hours of lying flat without raising any part of the body), and an intravenous injection on the second day, which takes approximately three hours (or vise versa).

Injection Dates:

18/07/2024 – First session

22/08/2024 – Second session

26/09/2024 – Third session

30/10/2024 – Fourth session

05/12/2024 – Fifth session

05/02/2025 – Sixth session

02/04/2025 – Seventh session

29/05/2025 – Eighth session

If you have any questions about my treatment or the results, feel free to send me a direct message. Will be more than happy to share my experience!

10/06/2025

𝐇𝐨𝐰 𝐒𝐭𝐞𝐦 𝐂𝐞𝐥𝐥 𝐓𝐡𝐞𝐫𝐚𝐩𝐲 𝐆𝐚𝐯𝐞 𝐌𝐞 𝐁𝐚𝐜𝐤 𝐌𝐲 𝐋𝐢𝐟𝐞

Three years ago, my world changed forever. I was diagnosed with Parkinson’s Disease—a condition that would challenge not only my body but also my sense of identity. It began with a subtle tremor in my right hand. I dismissed it at first, not realising that it was just the beginning of a long, exhausting battle. As time went on, the tremors spread to my left hand and jaw, my movements slowed, and even my posture began to stoop. It felt like I was ageing decades in a matter of months.

Parkinson’s took a toll not just physically, but emotionally. Nightmares, chronic constipation, and a heaviness in my spirit became constant companions. I later learnt that these too were symptoms of the disease. At the time, hope felt distant. Traditional treatments offered only limited relief, and I wasn’t sure where to turn.

That’s when my wife, Jo, became the cornerstone of a new chapter in my life. Unwilling to accept the status quo, she began researching alternative treatments. Her relentless determination led us to something that would transform everything: 𝐬𝐭𝐞𝐦 𝐜𝐞𝐥𝐥 𝐭𝐡𝐞𝐫𝐚𝐩𝐲.

At first, I was sceptical. Stem cell therapy had a mixed reputation, often associated with unregulated clinics and unproven claims. But Jo found a reputable company in Japan that was pioneering stem cell treatments for Parkinson’s. Despite my doubts, we took a leap of faith. It began with a trip to Korea for a cell harvest, followed by the first treatment session in Japan.

What happened next was nothing short of miraculous.

After just the initial therapy, the changes were undeniable. My depression began to lift—something I hadn’t even fully realised I was battling. My thoughts became clearer, my posture straighter, and I moved with a confidence I hadn’t felt in years. Friends and family noticed it too, saying I looked and sounded like the old Brian again—like someone had turned back the clock 15 years.

Each session brought even more progress. The tremors began to ease. My nightmares and digestive issues disappeared. I walked without hesitation, and for the first time in a long time, I felt in control of my body again. My neurologist confirmed what we already knew: the improvements weren’t just in my head—they were real, measurable, and life-changing.

Stem cell therapy didn’t just treat my symptoms—it gave me back my life.

This experience reshaped my purpose. I created the Brian Walker Parkinson’s and Stem Cells Journey page to document my recovery and, more importantly, to inspire others who might feel lost in their own battles. My advocacy is no longer about managing disease; it’s about exploring new possibilities, spreading hope, and challenging what we think we know about Parkinson’s treatment.

Today, while Parkinson’s is still a part of my life, it no longer controls it. Thanks to stem cell therapy—and the unwavering love and support of my wife—I’ve found a renewed sense of strength, clarity, and purpose.

This is more than my story. It’s a message to others: there is always hope, and sometimes it lies in places you’ve never thought to look. With innovation, courage, and community, we can redefine what’s possible—𝒐𝒏𝒆 𝒔𝒕𝒆𝒎 𝒄𝒆𝒍𝒍 𝒂𝒕 𝒂 𝒕𝒊𝒎𝒆.

𝑩𝒓𝒊𝒂𝒏 𝑾𝒂𝒍𝒌𝒆𝒓

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