Parkinson's Way

Parkinson's Way ​At Parkinson's Way, we are dedicated to supporting, uplifting, and connecting the Parkinson’s community.

​Parkinson’s Way is ​a dedicated hub for supporting, uplifting, and connecting our community. Whether you are living with Parkinson’s or caring for a loved one, we provide the latest research, practical symptom management tips, and inspiring stories of resilience. Together, we navigate the journey with strength, unity, and a shared path forward.

04/05/2026

Resilience is Not a Performance

May is Mental Health Awareness Month, and it’s time to talk about the part of Parkinson’s that doesn’t always show up in a physical exam: the emotional toll.
We often talk about "staying positive," but living with a chronic condition is exhausting. It is okay to acknowledge that today is difficult. Mental health isn't about pretending everything is fine; it’s about having the tools to handle it when things aren't.
The Invisible Symptoms
Parkinson’s is more than a motor disorder. Anxiety, depression, and apathy are clinical symptoms of the disease, just like a tremor or bradykinesia. They are caused by the same chemical changes in the brain, and they deserve the same level of medical attention.
Taking Action This Month:
• Acknowledge the Weight: If you are feeling overwhelmed, it isn't a "lack of willpower." It’s biology.
• Speak Up: Mention your mood to your neurologist. Mental health care is a vital part of your treatment plan.
• Connect: Isolation feeds depression. Reach out to one person today—even if it’s just a text.
Your value isn't measured by your productivity or your "bravery." It’s okay to just be.

23/04/2026

St George’s Day

Today is St George’s Day, and across England people will raise a flag, raise a glass, and think about what it means to be brave.
The legend is a simple one. A knight faces a dragon. He does not run. He does not pretend the dragon is not there. He stands his ground and fights, not because he is fearless, but because something greater than fear drives him forward.
For anyone living with Parkinson’s, that story is not a fairy tale. It is Tuesday morning.
Every day, people with Parkinson’s face a dragon of their own. It is invisible to most of the world, but those who carry it know its weight. The tremor that arrives uninvited. The stiffness that turns a simple task into a negotiation. The fatigue that lands without warning and does not ask permission to stay. The slow, relentless nature of a condition that does not pause for weekends or holidays or the days when you just need a break.
And yet people get up. They make the tea, they take the medication, they go for the walk even when every step feels like a small argument with their own body. They show up for the people they love, and they carry the dragon with them rather than letting it carry them.
That is a kind of courage St George would recognise.
There is something else worth saying on a day like this. St George did not fight alone. In most versions of the story there is a community around him, people who had been living in fear, who had been quietly enduring, waiting for something to change. His act of courage gave others permission to believe that the dragon could be faced.
That is what the Parkinson’s community does for itself, every day. The person who speaks openly about their diagnosis, so that someone newly diagnosed feels less alone. The carer who shares what the hard days really look like, so that another carer knows they are not failing. The advocate who keeps pushing for better services, better research, better understanding, even when progress feels painfully slow.
These are not small things. These are acts of courage, repeated quietly, in living rooms and hospital waiting areas and community halls and online spaces all over the country.
St George’s Day is a day for England, yes, but the values it points to belong to everyone. Courage is not the absence of fear. It is the decision to keep moving despite it. And in the Parkinson’s community, that decision is made every single morning by thousands of people who deserve to be seen and celebrated.
So today, if you are living with Parkinson’s, or loving someone who is, or walking alongside the community in any way, know this. You are not a bystander in someone else’s story. You are the knight. You are already fighting.
The dragon is real. And so are you.

Written for Parkinsons Way. St George’s Day, 23 April 2026.

22/04/2026

Something new has arrived at Parkinson’s Way, and we think you are going to find it really useful.
We have just launched two new features on the website to help you stay informed and supported.
Parkinson’s News brings you the latest news and developments from the Parkinson’s world, all in one place, updated regularly. No more searching around for what matters. Find it on our front page at www.parkinsonsway.co.uk
The Parkinson’s Way Support Assistant is there for you any time you need it. Whether you have a question about Parkinson’s, need some guidance, or just want to find the right information quickly, our Assistant is ready to help. Visit it directly at www.parkinsonsway.co.uk/Support-Assistant.html
Both services are free, available worldwide, and designed with the Parkinson’s community in mind.
Go and take a look and let us know what you think in the comments. Your feedback helps us make Parkinson’s Way better for everyone.

April is Parkinson’s Awareness Month, and this week we were reminded why raising that awareness matters.Tom Dumont, guit...
20/04/2026

April is Parkinson’s Awareness Month, and this week we were reminded why raising that awareness matters.
Tom Dumont, guitarist with No Doubt, has just shared publicly that he is living with early-onset Parkinson’s. His words were honest and brave. He said it is a struggle every day, but that he can still play, still create, still be himself. That takes courage to say out loud.
Stories like Tom’s matter. Every time someone in the public eye speaks openly about Parkinson’s, it makes it a little easier for the rest of us to do the same.
Here at Parkinson’s Way, that is exactly what we are here for. A community where no one has to carry this alone.
If you are new here, welcome. Shaky Radio streams Parkinson’s podcast content 24 hours a day, Monday to Friday, with music at the weekends. Come and listen any time at www.shakyradio.co.uk
And this month especially, if you know someone living with Parkinson’s, share this group with them. They might just need it.

We share real stories, expert advice, and practical insights through engaging podcasts created by and for people affected by Parkinson’s.

🆕 Exciting News from Parkinsons Way!We are delighted to introduce our brand new Support Assistant, available right now o...
18/04/2026

🆕 Exciting News from Parkinsons Way!
We are delighted to introduce our brand new Support Assistant, available right now on the Parkinsons Way website.
Whether you have just received a Parkinson’s diagnosis, are caring for a loved one, or simply have a question at any time of the day or night, our Support Assistant is here for you. It offers warm, knowledgeable, and patient responses on everything from symptoms and medication to support services available right here in Scotland.
And the best part? It is completely free to use, with no sign-up needed. Just visit the website and start asking.
👉 Try it now at https://www.parkinsonsway.co.uk/Support-Assistant.html
Please share this post with anyone in your circle who might benefit. Together we can make sure no one in the Parkinson’s community faces their questions alone.
⚕️ Please note: the assistant provides general information only and is not a substitute for advice from your GP or specialist.

Living with Parkinson’s can feel like navigating a maze without a map. Whether you are newly diagnosed, a long-term warrior, or caring for a loved one, our Parkinsons Way Support Assistant is here for you 24/7. Managed by our community for our community, this AI-powered companion is trained to pro...

18/04/2026
14/04/2026

🌟 PARKINSON’S NEWS ROUNDUP | April 2026 🌟
It’s Parkinson’s Awareness Month, and there is a lot happening across the Parkinson’s community right now. Here’s what’s been making headlines.

🎸 A Famous Face Speaks Out
Tom Dumont, guitarist for No Doubt, has publicly shared his early-onset Parkinson’s diagnosis ahead of the band’s Las Vegas residency. He says symptoms began years ago, and while it’s been a daily struggle, the good news is that he can still play guitar. He credited others who have spoken openly about their own health for inspiring him to come forward. The more voices, the less stigma. Thank you, Tom.

💉 A New Treatment Changing Lives
Rebecca King Crews, wife of actor Terry Crews, has revealed she has been living with Parkinson’s for over a decade. She recently underwent a focused ultrasound procedure and says her tremors on one side are gone and her balance has improved significantly. She is now able to write her name and dates with her right hand for the first time in around three years. Inspiring news.

🔬 A Possible Environmental Trigger Discovered
Scientists at Northwestern Medicine have found that a usually harmless virus called Human Pegivirus (HPgV) was present in the brains of Parkinson’s patients but not in people without the condition. This suggests it could be an environmental factor that interacts with the body in ways not previously understood. Exciting early-stage research that could change how we understand the causes of Parkinson’s.

🧪 Fat Metabolism and Brain Cell Damage
Researchers at Nanyang Technological University in Singapore have identified a fat-producing enzyme in brain cells that may amplify the harmful effects of alpha-synuclein, the protein that accumulates in the brains of people with Parkinson’s. Reducing the activity of this enzyme led to less brain cell damage in lab tests. Another promising new avenue for future treatments.

💊 The Research Pipeline is Busy
The Michael J. Fox Foundation awarded $101 million at the end of 2025 and into early 2026 to advance research into better Parkinson’s treatments. Multiple clinical trials are currently underway exploring disease-modifying therapies, and results are expected throughout 2026.

💙 A Reminder
April is National Parkinson’s Awareness Month. Advanced treatments today are helping people with Parkinson’s stay active and independent for longer. With the right team and the right plan, people with Parkinson’s can have independent, high-functioning lives, according to neurologists working in the field.
There is so much hope in the headlines this month. Share this post to help spread awareness and let people know they are not alone on this journey.

💙 Parkinsons Way Community Voice |

27/03/2026

Headline: Your favorite companion is now just a voice command away! 🎙️✨

We are thrilled to announce that Shaky Radio is officially available on Amazon Alexa!

Living with Parkinson’s can be a daily challenge, but staying connected to your community shouldn't be. Whether you’re in the kitchen, the garden, or just relaxing, you can now listen to our music, news, and support sessions entirely hands-free.

How to listen:

Say: "Alexa, enable Shaky Radio" (the first time only).

Then just say: "Alexa, play Shaky Radio."

Spread the word and let’s get the community listening! 🎧💙

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