Hear from our PPI partners
The insights, ideas and lived experiences that people and patients bring can help shape research that matters to them and strengthen the impact research can have within local and national communities. We welcome anyone with an interest in research. This section is featuring case studies, statements/ testimonials from existing PPI partners.
"Testimonial"
“I joined my local area Renal PPI group to 'give something back' after decades of being cared for by so many incredible healthcare professionals. I believe that medical care and research can only be truly effective if the 'voice of the patient' is listened to and real life experiences are taken into account. By being part of a PPI group, I feel that I can play a (small) part in helping to ensure that research is relevant to the real-life challenges that patients face in their everyday lives. The whole experience has been incredibly rewarding - not just the opportunity to help shape future research but also the privilege of meeting so many wonderful people along the way.”What does it mean being PPI member
People can choose to get involved as much or as little as they wish. This might include hearing about current research projects, sharing views on research ideas, or contributing perspectives based on lived experience. Group activities may take place online, through meetings, or via workshops, and participants can choose whether to attend in person or join remotely.
More information about becoming a member is available in this video featuring Dr Tracey Ibbotson who leads several PPI groups and is responsible for coordinating PPI activities across the School of Health and Wellbeing, ensuring that the voices of people and patients are meaningfully embedded in research.
MVLS Public and Patient Involvement Steering Group
The MVLS Public and Patient Involvement Steering Group includes patients, carers and members of the public from a wide range of backgrounds and experiences. The group is based in Glasgow but is happy to include members from across Scotland. Members of the steering committee review research related documents such as funding proposals, lay summaries, PPI plans, consent forms, patient information leaflets, public engagement plans, recruitment strategies. This group meets five times a year (currently via ZOOM) but can review via email.
Contact details: MVLS-PPIE@glasgow.ac.uk