Terni Combats Parkinson’s with
Research & Community Support
In Terni, a province in central Italy, over 1,500 people grapple with the challenges of Parkinson’s disease. While waiting for a breakthrough cure, they find solace and support within a unique community. The “Associazione Parkinson Terni” tirelessly advocates for those impacted by the disease, driven by the ground-breaking research happening right on their doorstep.
Caterina, one of many individuals fueled by hope, emphasizes the importance of community. “Discovering Parkinson’s at sixty was a blow,” she admits, recalling the initial shock and struggles. “But with the support of my family and the assoication, I’ve learned to adapt and live a fulfilling life. We’re fortunate to have dedicated doctors and researchers working hard to find better treatments.”
The association, established five years ago by Professor Carlo Colosimo, a frontrunner in Parkinson’s research, collaborates with over 100 volunteers who help organize events to raise awareness and donations. The tireless efforts of the association are reflected in generous community support. National
Parkinson’s Day, held at the Bct literary café, brought together patients, researchers, and the community.
“Lifestyle changes are crucial in managing the disease,” explainsle professor, highlighting the importance of physical activity and maintaining a positive outlook. “At Santa Maria hospital, we are conducting two pivotal international studies.
One involves a monoclonal antibody, delivered intravenously. This “Padova study,” spanning nine Italian centers, shows promise in slowing disease progression.
The “Orchestra Study”, with five Italian centers, is simultaneously investigating the potential of a low molecular weight drug that can be taken orally.
“Both research avenues focus on blocking proteins that are transferred between brain cells. This approach is proving effective in patients diagnosed within two years of symptom onset,” explains Professor Colosimo.
Reassuringly, one of the studies has reached Phase III, placing ancient Italian town on the forefront of Parkinson’s research and highlighting the vital role played by the Heals follows a dynamic theme familiar to many – the quest for longevity. menopausal women hoping to optimize their health.
Roberto Palombi, the association’s new president, “We provide support and companionship.
Often, those affected by Parkinson’s lack sufficient support systems. We are determined
to be a constant source of support
for them and their families.”
Professor Adolfo Puxeddu, Professor emeritus of internal medicine at the university, highlighted the influence of lifestyle and environment on achieving a long and healthy life.
He emphasized the importance of healthy habits, citing Sardinian centenarians as prime examples.
Professor Colosimo affirmed, with hope in his voice, “We are making significant strides in understanding and treating Parkinson’s.”
recycling the Parkinson’s association volunteers gatherércoles.
How does the Associazione Parkinson Terni support individuals living with Parkinson’s disease and their families in the Terni community?
## Interview: Terni Stands Together Against Parkinson’s
**Interviewer:** Today, we’re talking about the incredible community spirit in Terni, Italy, where over 1,500 people live with Parkinson’s disease. Joining us is Caterina, a member of “Associazione Parkinson Terni”. Caterina, thank you for being here.
**Caterina:** Thank you for having me.
**Interviewer:** Can you tell us about the Association and the impact it has on people living with Parkinson’s in Terni?
**Caterina:** Absolutely. Being diagnosed with Parkinson’s at 60 was a difficult experience. The initial shock and confusion were incredibly tough to deal with. But finding the Associazione Parkinson Terni was a lifeline. They provide emotional support, practical advice, and a sense of community that’s been invaluable. We’re incredibly fortunate to have Professor Colosimo, a renowned Parkinson’s researcher, leading the Association. His dedication inspires us and gives us hope for the future.
**Interviewer:** What kind of events and initiatives does the Association organize?
**Caterina:** The Association does amazing work. They organize awareness campaigns and fundraising events, which bring the community together. National Parkinson’s Day is a big event for us, held at the Bct Literary Café. It’s a wonderful opportunity for patients, researchers, and the general public to connect, learn from each other, and show their support. Having over 100 volunteers dedicated to this cause shows the incredible strength of our community.
**Interviewer:**(Based on [1](https://www.mayoclinic.org/diseases-conditions/parkinsons-disease/symptoms-causes/syc-20376055)
What Parkinson’s symptoms are most challenging for you?
**Caterina**: One of the first symptoms I experienced was a tremor in my hand. Parkinson’s is a progressive disorder, so I know it will continue to present new challenges.
**Interviewer**: Is there anything particular you’d like to emphasize about living with Parkinson’s in Terni?
**Caterina**:
The message I want to share is one of hope and resilience. Living with Parkinson’s can be tough, but we are not alone. The support of the Association, our families, and our community makes a world of difference. We remain hopeful for a cure, but until then, we’re focused on living our lives to the fullest and supporting each other every step of the way.
**Interviewer**: Thank you, Caterina, for sharing your inspiring story.
