Living with Parkinson's can be challenging, but nobody should have to face it alone. Through Parkinson's Pals, Parkie Farts, PD Secrets, and my public speaking work, I'm building a positive community where people affected by Parkinson's can connect, share experiences, find support, and sometimes have a laugh along the way.
Whether you're living with Parkinson's, supporting someone who is, struggling with the hidden challenges of the condition, or simply looking for hope and understanding, you'll find a warm welcome here.
No miracle cures. No judgement. Just honest conversations, lived experience, peer support, and a determination to help people live well despite Parkinson's.
Together, we'll talk, laugh, learn, support one another, and prove that Parkinson's may affect how we move—but it doesn't get to decide how we live.
Parkinson's Pals
Free online peer-support group for people living with Parkinson's and those who care for them. We meet every Monday evening from 19:00 to 21:00 GMT, creating a welcoming space where people can connect, share experiences, support each other, and, whenever possible, have a laugh together. This isn't therapy. This isn't a lecture. And we're certainly not claiming to have all the answers. What we do offer is something equally valuable: People who genuinely understand.
Join Us!
Contact us to receive your link invitation and join our growing community.
What Can You Expect?
- Friendly and informal conversations
- Support from people who "get it"
- Space to share challenges and successes
- Laughter, encouragement, and friendship
- A safe, confidential, judgement-free environment
- Support for both people living with Parkinson's and their carers
Whether you've recently been diagnosed or have been living with Parkinson's for many years, or are supporting a loved one through their journey, you'll find a warm welcome waiting for you.
No Cures Offered. Just Understanding.
Living with Parkinson's can sometimes feel overwhelming, isolating, or simply exhausting. At Parkinson's Pals, we believe nobody should have to go through that alone. Sometimes the greatest support comes from hearing: "I understand." Because when people who share similar experiences come together, something powerful happens. Friendships form. Confidence grows. Hope returns. And the journey becomes a little easier to carry.
Parkie Farts
Comedy show raising awareness about Parkinson's disease. Check out social media for the next venue!
Yes, the name is cheeky... and that's exactly the point. Let's address the elephant in the room. "Parkie Farts?" Really? Absolutely. For anyone unfamiliar with Parkinson's, the title might raise an eyebrow. For many of us living with the condition, however, it perfectly captures those moments that Parkinson's throws at us when we're least expecting them. The wobble. The stumble. The dropped cup of tea. The frozen feet. The shirt wearing more of your lunch than you do. The moment you walk confidently into a room and immediately forget why you're there. You know the ones. Those little Parkinson's moments that can leave us feeling frustrated, embarrassed, or defeated. I call them Parkie Farts. Not because Parkinson's is funny. But because sometimes, laughing at what Parkinson's throws at us is far more powerful than letting it laugh at us.
More Than Just a Laugh
Parkie Farts isn't about making fun of Parkinson's. It's about refusing to let Parkinson's have the last word. When I was diagnosed, I quickly realised that Parkinson's affects much more than movement. It can affect confidence, relationships, identity, independence, and mental wellbeing. What I've learned along the way is that humour can be one of the most powerful tools we have. It helps us talk about difficult subjects. It helps us connect with others. It helps reduce feelings of fear and isolation. Most importantly, it reminds us that we are still the same people we were before Parkinson's came crashing into our lives.
Because We Are More Than Our Conditions
One of the biggest challenges of any long-term condition is figuring out who you are now. The old version of you may have changed. Some things may have been lost. Some plans may have been rewritten. But your story isn't over. Far from it. Parkie Farts is about finding a new way forward—one that's built on resilience, friendship, understanding, honesty, and the occasional belly laugh. Because living with Parkinson's isn't just about surviving. It's about continuing to live. Continuing to connect. Continuing to laugh. Continuing to be yourself.
A Community Built on Real Life
Here you'll find:
- Honest conversations about Parkinson's and mental health
- Humour, where humour helps
- Support when life gets tough
- The occasional Parkie Fart moment that deserves to be shared with the world.
No judgement. No miracle cures. No pretending everything is okay when it isn't. Just people supporting people.
PD secrets
PD Secrets is a safe and supportive space dedicated to the challenges of impulsive behaviour linked to Parkinsons medications.
Some people living with Parkinson's can experience changes in behaviour linked to their medication. These changes can affect impulse control, judgement, and decision-making, sometimes leading to behaviours that feel completely out of character.
This can include:
- Problem gambling
- Excessive spending
- Risk-taking behaviours
- Secretive behaviours
- Compulsive hobbies or activities
- Difficulties controlling impulses
These experiences might have serious consequences for finances, relationships, confidence, and mental wellbeing. People affected by Parkinson's might carry these burdens and feel unable to discuss them with family, friends, or even healthcare professionals.
The Hidden Impact
One of the most powerful stories highlighting this issue is explored in the BBC Radio 4 podcast series Shadow World: Impulsive, which shares the experiences of people whose lives were profoundly affected by impulse-control problems linked to Parkinson's treatment. For some individuals, what started as a harmless interest gradually became something they felt unable to control. For others, the consequences affected their families, finances, careers, and mental health. The common theme throughout these stories is not weakness. It is vulnerability. And vulnerability deserves support, not judgement.
If This Is Happening To You
Maybe you've started gambling more than you intended. Maybe you've hidden spending from loved ones. Maybe you've found yourself behaving in ways that simply don't feel like "you." Maybe you're carrying a secret that feels too heavy to share. If so, please don't suffer alone. The first and most important step is speaking to your clinical team, Parkinson's nurse, GP, or specialist as medication may need reviewing. But alongside professional support, sometimes you also need someone who understands the emotional impact. Someone who won't judge, but who will simply listen.
Reach Out
If you are affected by side effects of Parkinson's medications which manifest as impulsive behaviour, and you feel you have no one to talk to, reach out. PD Secrets aims to change that by encouraging open conversations, reducing stigma, and helping people find support when they need it most. Because the things we keep secret are often the very things that need understanding the most.
What we can offer is:
- A listening ear
- Understanding and compassion
- Total confidentiality
- No judgement
- Support in helping you find the right help
Important: If you believe your medication may be affecting your behaviour or impulse control, please speak to your Parkinson's specialist, Parkinson's nurse, or GP as soon as possible. Do not stop taking prescribed medication without professional medical advice.
Public Speaking
Inspiring Conversations. Real Stories. Lasting Impact.
I am available to speak at conferences, support groups, NHS events, disability networks, community organisations, and wellbeing events on the subjects I know best through both professional experience and personal lived experience.
My speaking topics include:
- Living with Parkinson's Disease
- Parkinson's and Mental Health
- Men's Mental Health
- Disability, Inclusion and Belonging
- Building Resilience Through Adversity
- The Power of Humour in Long-Term Conditions
- Peer Support and Community Building
With over 30 years of leadership experience, eight years supporting men's mental health, and my own journey with Parkinson's, I bring a unique combination of professional insight, personal honesty, and humour. My talks are engaging, relatable, and thought-provoking, helping audiences better understand the realities of living with long-term conditions while leaving them feeling informed, inspired, and hopeful.
If you're looking for a speaker who combines lived experience, practical wisdom, authenticity, and the occasional laugh, I'd love to hear from you.
About
Hi, I'm Declan Moore founder of Declan's Parkinson's. Welcome, and thank you for taking the time to visit my website. If you're here because Parkinson's has become part of your life—whether you're living with the condition yourself or supporting someone who is—then you've come to the right place. Like many people, I never imagined that Parkinson's would become part of my story. Yet here I am, learning every day how to navigate the challenges it brings whilst refusing to let it define who I am. For over 30 years, I worked in health and safety, helping organisations protect people and manage risk. Alongside my professional career, I spent eight years as a lead facilitator for a men's mental health group, supporting thousands of men through some of the toughest periods of their lives. What I didn't know then was that those experiences would one day become invaluable in helping me manage my own journey with Parkinson's.
My Journey
I have been diagnosed with Parkinson's in 2020. Living with Parkinson's is not always easy. Some days I feel strong, capable, and ready to take on the world. Other days, Parkinson's has other ideas. I've learned that Parkinson's doesn't just affect movement—it can affect confidence, relationships, identity, and mental wellbeing. The physical symptoms are often visible, but the emotional battles can be just as challenging. Over time, I've discovered that whilst Parkinson's can take away certain abilities, it cannot take away hope, purpose, humour, or the ability to help others. I created DeclansParkinsons because I believe no one should have to face Parkinson's alone.
What I bring
There are plenty of websites that focus on symptoms, treatments, and medical information. Those things are important. But what about the everyday reality? The frustrations. The funny moments. The fears. The victories. The questions that only someone living with Parkinson's truly understands. This website is about the human side of Parkinson's. It's about supporting one another, sharing experiences, protecting our mental health, and learning how to live well despite the challenges.
I don't claim to have all the answers.
I don't offer miracle cures.
What I do offer is:
- Lived experience of Parkinson's.
- Over 30 years of leadership in people-focused roles.
- 8 years supporting men's mental health and wellbeing.
- A belief that connection, friendship, and shared understanding can make a huge difference.
- A healthy sense of humour when Parkinson's decides to throw one of its infamous curveballs.
Most importantly, I offer a listening ear and a commitment to helping others feel less alone.