We are delighted that our solution for ILD has been named by Pulmonary Fibrosis News as one of the top seven apps for chronic disease management.
Our ILD platform was designed in consultation with ILD patients and patient organisations across Ireland, the UK and the US. At patientMpower we put equal focus on designing solutions that meet the needs of patients as well as the needs of their clinicians. So as well as enabling healthcare professionals to monitor and provide remote care to their patients, we build in features that can also help people better manage their own conditions. In clinical trials 93% of ILD patients reported that using the patientMpower app had a positive impact on their well-being and daily life.
Our work with patient organisations has also taught us a lot about the importance of peer support for people and caregivers affected by ILD. Referring patients to a support group can be really valuable in helping them live well with their condition. We have been delighted to partner with national organisations including ILFA in Ireland, Action for Pulmonary Fibrosis and the Pulmonary Fibrosis Trust in the UK, and the US headquartered PF Warriors. And there’s lots more local patient support groups which you can find out about here.
For first hand reports on how patientMpower helps people better manage their pulmonary fibrosis see the video stories from Matt and Ron. For more details on how we might be able to help you monitor and support your ILD patients get in touch.