Up to 8 adult individuals with lived experience, as a patient of, or as a carer or parent of someone with, atopic dermatitis (eczema) who would be willing to review patient-facing documents online and give feedback on how clearly the information has been written and presented.

Participants will take part in one workshop, which is expected to last for approximately 2 hours and 30 mins with breaks, either online or in-person in West London. During the workshop, we will ask participants to:
• Share their views on an intervention that will help improve patients to take oral capecitabine treatment as recommended
• Participants will either help us narrow down intervention options from a shortlist or develop the chosen intervention in more detail

The Fatherhood Project CIC operates a permanent community hub in Luton, delivering trauma-informed mentoring and emotional regulation for 60+ young men (14–25) facing school exclusion or violence. Backed by deep community trust and robust data tracking, we want to partner with a university or NHS Trust to co-produce evidence-based research. We offer unparalleled fieldwork access and lived-experience insights to co-apply for joint health, social care, or community engagement funding.

Have you, or someone you care for, experienced a stroke over one year ago.

Researchers would like to hear from local people who have experienced a stroke, or carers of someone who has experienced a stroke over one year ago. We are interested in speaking with people who have noticed any changes or ongoing effects affecting the use of their arm, hand, shoulder, or upper body following a stroke.

People living with spine conditions and those who undergo spine surgery can experience pain, changes in independence, and emotional challenges such as anxiety, worry or low mood. While research has explored clinical outcomes, less is known about how people personally experience the surgical journey. This study aims to understand patients’ psychological and emotional experiences from before to after spine surgery through a one-to-one online interview, helping to inform more holistic patient care.

We’re developing research for people with asthma who still feel breathless despite medication, often linked to reduced muscular control of breathing. A new physiotherapy treatment has been created and will be compared with NHS treatment.
We invite you to a 1 hour online focus group to share feedback on the study, help improve recruitment, and identify barriers to participation. Camera and active discussion required.
Please see attachment for further details and the link to express an interest.

Expression of interest to refine a physiotherapy based intervention for asthma patients – Fill out form

I am seeking volunteers with lived experience to review findings from qualitative interviews and help assess their relevance, interpretation, and practical application. This will be a small online focus group discussion lasting 60–90 minutes, with a maximum of two sessions. Participants will help shape actionable recommendations for dissemination and implementation. No payment is offered. A community of practice has also been consulted to inform the work. Feedback will be shared.

We are looking for pregnant women, or mothers with children under 1 to join a friendly Patient and Public Involvement (PPI) discussion group. We welcome people from all backgrounds, experiences and circumstances. You do not need any specialist knowledge – we are just interested in your views and experiences.

Taking part involves joining an online focus group lasting 2 hours at 11am on Thursday 2nd July. Share your views in a supportive and friendly group setting.

Researchers from the University of Stirling are conducting a survey to understand the impact of socio-economic factors on the recovery of health and wellbeing for cancer survivors following primary cancer treatment. This is an online survey which will take around 15 minutes to complete.

Adults living in Scotland who have completed cancer treatment are eligible. These findings will provide an insight into the impact of deprivation on the health and wellbeing outcomes of cancer survivors.

My PhD is investigating how parents understand and respond to their children\'s symptoms when they are unwell. We are looking for parents and guardians based in England, with at least one child aged 0-11, to join our Public & Community Involvement & Engagement (PCIEP) group. The group will attend quarterly meetings, and provide feedback on documents and material. More information and to apply: https://forms.cloud.microsoft/e/sSr8zYAk5Q