I commit myself to communicate with other patients and patient organisations
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I pledge to engage with members of the public in a meaningful way in order to co-create truly co-produced materials and information including our RDS website
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I'll contact patients and take the time to listen to their experience, opinions and contribution
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We will keep clear lines of communication during the guideline development process, and follow up after important meetings
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Listen
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I commit to listening to patients when setting up training courses for staff
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I will attend one patient group/association meeting in the diseases I work for
Travaux en coursI will proactively share my proposals for patient relevant projects (support programs, information piece) with at least 1 patient organisations
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It is essential that we do not just listen to patients but that we hear them and we act on what they tell us. Small changes can make big differences
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