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Our Engagement Network unites all kinds of people, groups and organisations, from all over Europe, to shape the future of how Parkinson's is managed, treated and maybe, one day, cured.

Who the network is for

It's for anyone who wants to be actively engaged in helping themselves, or others, improve life with Parkinson's. You may be a person with Parkinson's interested to hear about physical activities or new cutting edge research in which to take part, or perhaps you are a healthcare professional who needs to know of new education opportunities so you can better help Parkinson's patients. You could be an organisation developing a promising new medication or appliance to help manage the condition, and learning from the Parkinson's community will improve it. Either way, you all have one thing in common: helping people with Parkinson's live their best life.  Parkinson's Europe wants to join the dots by introducing you to each other, and to the information and opportunities that will help you achieve this.

Network members – Individuals who have an interest in actively changing the Parkinson’s landscape

Network stakeholders – Organisations or groups who would like to share ‘doing’ opportunities with the Parkinson’s community

How does it work

You sign up to become a network member and tell us exactly what opportunities you are interested in hearing about. As soon as one of those opportunities becomes available we will email you. And then you take the next step if you want to take part. It's as simple as that. The more you get involved with, the more impact you will have on the world of Parkinson’s.

What kind of opportunities are available

If you are are a person with Parkinson’s, a partner, carer provider or relative, you will:

  • be the first to be offered the opportunity to be part of education sessions or webinars to increase your understanding about Parkinson’s;

  • take part in new research trials, putting you in touch with experts in the field of Parkinsons;

  • bring your voice forward as part of lobbying governments and decision makers to hear how you want change;

  • donate your opinions and experiences to help professionals in the world of medicine, care and research to understand more about the effects of Parkinson's, enabling them to improve products, treatment and services;

  • learn about activities you can be part of across Europe, in your country or linked to your local or regional Parkinson’s organisation.

Yes please - sign me up

If you are a medical or healthcare professional, you will be able to:

  • keep abreast of the latest Europe-wide research activities so you can signpost you patients to them;

  • offer your own expertise and insight to enrich research and development into Parkinsons;

  • take advantage of education opportunities to enhance your professional development in the field of Parkinson's;

  • be part of workshops that need your voice to make sure that changes being made in the Parkinson’s clinical world represent you;

  • get involved with advocacy initiatives to improve the Parkinson’s picture in Europe.

Yes please - sign me up

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