What we do
We help organisations bring lived experience into strategy, research, policy, access and decision-making and turn insight into practical change.
Strategy & Patient Advocacy
We help organisations understand communities, build stronger relationships and develop strategies that reflect what matters to people affected by rare and complex conditions.
We can help with
- Patient advocacy and engagement strategy
- Community insight and needs assessment
- Stakeholder mapping and engagement
- Organisational and patient group strategy
- Partnership development and facilitation
- Bringing different perspectives together around complex challenges
We can help with
- Lived-experience-led research
- Co-production and PPIE
- Interviews, focus groups and surveys
- Peer researcher approaches
- Policy and programme evaluation
- Turning findings into clear recommendations and accessible outputs
Research & Policy Evaluation
We design and deliver research that puts lived experience at the centre and produces evidence that can be used in practice.
We can help with
- Patient involvement in HTA and access
- Access strategy and stakeholder engagement
- Evidence generation
- Patient organisation support and readiness
Workshops, tools and resources - Bringing patient, policy, clinical and industry perspectives together
Access & HTA
We support patient organisations and life sciences teams to understand and navigate access and HTA, ensuring patient and community perspectives are meaningfully represented.
We can help with
- Workshops and training programmes
- Practical toolkits and resources
- Coaching and mentoring
- Patient advocacy and engagement training
- Co-production and lived-experience training
- Support for organisations developing new capabilities
Training & Capacity Building
We create practical training and support that helps people and organisations build confidence, knowledge and skills
Let's work together
If you have a project, challenge or idea you’d like to discuss, we’d love to hear from you