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<b>Introduction:</b> Palliative care can help people at varying stages of pulmonary hypertension (PH), but previous research has highlighted barriers to early access to this type of care. <b>Objectives:</b> This study aimed to discover what people affected by PH understand about palliative care and how many access it. <b>Methods:</b> The study used an online survey to gather information, promoted via the PHA UK social media channels, website, and via an e-newsletter to PHA UK members. It was open to anyone with a diagnosis of PH and their partners / family members too. <b>Results:</b> 97 responses were received. Of these, 82% had PH and 18% had a loved one with PH. The results showed there are misconceptions about palliative care which may be preventing some people to access this support. 55% wrongly think palliative care is only for those at the end of their lives and 17% think palliative care is only for the person with the diagnosis. Only 12% said they have had palliative care discussed with them by their medical team. Those discussions were with a mixture of GPs, consultants and nurses. Just 9% have accessed palliative care, with 6% of that number accessing it more than a year ago. 99% of respondents said if the PHA UK produced information and resources about palliative care and its role in supporting people with PH they would find this useful or very useful. <b>Conclusions:</b> Lack of understanding of palliative care could be preventing some people affected by PH from accessing this type of support, and there is a clear need for information in this field.