AdClub of Toronto’s Post

Do you or someone you know live with Parkinson's? I did and do. Parkinson Canada is conducting a survey to inform a socio-economic impact study. By participating, you can help to shape a more accurate picture of the challenges faced by people living with Parkinson's and care partners. Duration: The survey will take approximately 15-20 minutes to complete. It is open until January 23, 2024. Format: It is an online survey and can be accessed at this link: https://lnkd.in/gqbXXiWx? #parkinsonsdisease #parkinsonsawareness #parkinsons

Missed our webinar on the Citizens First 2023 survey results? Catch up with the recording!📺 Learn the latest insights on how citizens want to be engaged with their governments. #CitizenEngagement #SurveyResults #CitizensFirst2023 https://ow.ly/nRn750Q8n6e

Want to contribute to the #SocialValueSummit at UKREiiF? Please fill out the below survey to help inform the discussion. It takes about 5 minutes! https://lnkd.in/e4cn54dg 👍👍👍

📣Have your say: ARDC Stakeholder Survey closes 29 Sept Are you a member of the research community? Do you use ARDC services and resources? Tell us about your interactions with the ARDC and how you use our research infrastructure services. Your feedback will help improve the services we deliver to the Australian research community. Start the 5min survey now> https://ow.ly/XXKU50PJVty #NCRISimpact #eResearch #ARDCSurvey #research #survey

Do you have lived experience with burns injuries? Or caring for / treating someone with burns injury? This global research project wants to hear from you to determine what the research priorities should be going forward 👇 #burns #research

When leveraging the expertise, perspectives, and insights of People with Lived Experience (PWLE) in meaningful ways within health and human service systems, there are clear benefits for the agency, clients, and the person with lived experience. This research summary includes strategies for effectively integrating PWLE into the workforce, potential barriers and considerations, examples of promising state and county programs, and additional resources. Read more at https://lnkd.in/gKimsUwq

After much ado - out follow up survey is now available. Please share widely with those who might be interested in giving us their thoughts! We want to know what questions about burns care and treatment you want answered. We are a James Lind Alliance Priority Setting Partnership aiming to identify the top 10 global burns research priorities. We want to give a louder voice to patients, survivors of burns, their carers and burn health care professionals to make sure research focusses on what is most important to these key stakeholders. The top 10 priorities will shape the future of research, The survey should take less than 10 minutes to complete and will be available in seven languages (English, Spanish, French, Portuguese, Chinese (simplified), Chinese (traditional) and Vietnamese). The survey will ask you to select the ten questions about burns care that are most important to you. You can complete the survey here: https://lnkd.in/geGbAjC3 You can read more about our project on our website https://lnkd.in/gNKHeEBh and follow us on social media @burnspriorities, or email us at burnsresearch@bristol.ac.uk”  

Survey of People Affected by MS Launched to Understand the Importance of Being Actively Involved in Research: Eligible Individuals Are Highly Encouraged to Complete Survey. Surveys must be completed by 31 August. The survey is available in eight languages including: Arab, English, French, German, Italian, Polish, Spanish and Swedish. The International Progressive MS Alliance, in collaboration with MS organisations across the world, is conducting a global survey to find out how people affected by MS feel about being involved in research – including being an author of scientific publications. - Are you affected by multiple sclerosis (MS)? - Do you want people with MS to be credited for their input in research (science with patient input)? There is growing global consensus among scientists and clinicians regarding the importance of involving people affected by MS in research. By sharing your experience of living with MS, this ‘experiential’ form of knowledge can be integrated with scientific knowledge and lead to better research outcomes for everyone. If you are interested in taking part, please click the link below: https://lnkd.in/gFeinQAu Questions regarding the survey can be directed to multi-act@aism.it.

The Past, Present, and Future of the EM Workforce - what was predicted vs. the reality and implications for the future. Read more at https://ow.ly/c2wb50PMWmC

Your insights are invaluable to us.    We invite you to share your thoughts in our recent survey about how to improve #GISreports: https://lnkd.in/eudw8A9U