Category: Pulmonary Fibrosis

patientMpower at Chest Annual Meeting

Friday, October 5th, 2018

thumb image

patientMpower are looking forward to attending the Chest Annual Meeting, which this year is being held in San Antonio from 6 – 10th October. We would like to invite you to come and meet with us at Chest to learn more about our specialist remote patient tracking platforms for Pulmonary Fibrosis and Lung Transplant and […]

Read More


Ndemic Creations Helps Spread Pulmonary Fibrosis Awareness

Wednesday, September 19th, 2018

thumb image

patientMpower and Ndemic Creations teamed up to promote awareness of pulmonary fibrosis during Pulmonary Fibrosis Awareness Month this September! Ndemic Creations is a leading, independent game studio founded by James Vaughan and is dedicated to making intelligent, sophisticated and ultra-high quality strategy games. Based in Bristol, UK, Ndemic achieved extreme success with its first game,  a […]

Read More


patientMpower at European Respiratory Society Congress

Saturday, September 15th, 2018

thumb image

patientMpower is looking forward to attending the European Respiratory Society (ERS) Congress, which this year is being held in Paris from 15 – 19th September. We invite you to meet with us at ERS to learn more about our specialist remote patient tracking platforms for pulmonary fibrosis and lung transplant and our Digital Biobank of […]

Read More


patientMpower PF awareness – Angela Perrillo from CHEST

Monday, September 10th, 2018

thumb image

For the latest in our video chats for Pulmonary Fibrosis awareness month, we’re joined by Angela Perillo from the American College of CHEST physicians. Angela talks through different educational activities which CHEST organizes to raise PF awareness, including next month’s annual CHEST meeting in San Antonio Texas.

Read More


Help Spread Awareness of Pulmonary Fibrosis during #PFMonth

Saturday, September 8th, 2018

thumb image

Buddy is ready to travel the world! Help him visit as many people, states, and countries as possible. First, take a photo with Buddy as you go about your day, visiting with family, at your pulmonary rehab session, or any other adventure you may be on. Second, share your photos with us on our social […]

Read More


patientMpower PF awareness – Video chat with Emmy award winner Mike Olsen

Thursday, September 6th, 2018

thumb image

September is a global month long campaign to help raise awareness of Pulmonary Fibrosis, aid timely diagnosis and help patients with pulmonary fibrosis to get the treatment and care that they need. This is our second Pulmonary Fibrosis chat of the month – & we’re delighted to be joined by Emmy award winner Mike Olsen. […]

Read More


patientMpower PF awareness month video chats – Michele Peters from Team Jeffery for PF

Saturday, September 1st, 2018

thumb image

September is a global month long campaign to help raise awareness of Pulmonary Fibrosis, aid timely diagnosis and help patients with pulmonary fibrosis to get the treatment and care that they need. At patientMpower we will be involved in lots of activities for Pulmonary Fibrosis month – This video is the first in our video […]

Read More


Endorsement by EU-IPFF

Wednesday, August 29th, 2018

thumb image

We are delighted that our app for IPF has been recently been endorsed by the EU-IPFF. The European Idiopathic Pulmonary Fibrosis and Related Disorders Federation (EU-IPFF) is a non-profit organization that brings together European national patient associations committed to defending their vision of equal access to treatment and care for all IPF patients. They aim […]

Read More


Air Quality & it’s impact on Idiopathic Pulmonary Fibrosis (IPF) patients

Thursday, July 12th, 2018

thumb image

We’re glad to see research from Johannson et al on impact of air pollution on Idiopathic Pulmonary Fibrosis (IPF) patients. Their research looked at home spirometry data and symptom diaries from 25 patients and used their residential address to estimate the weekly mean air pollution exposures from ozone (O3), nitrogen dioxide (NO2), and particulate matter […]

Read More


Top 3 Takeaways from CHEST Lung Health Experience

Tuesday, July 3rd, 2018

thumb image

This week I had the opportunity to attend the Lung Health Experience hosted by the American College of Chest Physicians (CHEST) in Chicago. This annual event helps spread awareness of asthma, COPD, lung cancer, pulmonary fibrosis and other lung health initiatives. There were many interactive components to the Lung Health Experience which we shared via […]

Read More


New patientMpower Function – Share Your Health Progress with Friends, Family and Caregivers!

Tuesday, June 19th, 2018

thumb image

We are pleased to announce the launch of the new caregiver, friends and family sharing tool for the patientMpower platform! Our goal at patientMpower is to EMPOWER you to have better outcomes by helping you manage your health. Sharing your progress with your loved ones, or others going through similar experiences, and having support from […]

Read More


patientMpower at the American Thoracic Society Conference 2018

Thursday, May 17th, 2018

thumb image

patientMpower will be exhibiting at ATS 2018 and we would like to invite you to come and visit us to learn more about our specialist remote patient tracking platforms for Pulmonary Fibrosis and Lung Transplant. Our mobile platforms for pulmonary fibrosis and lung transplant enable patients to track data relating to their pulmonary conditions remotely, […]

Read More


Watch a replay of our patient support web discussion

Tuesday, April 24th, 2018

thumb image

Missed our web discussion on Taking Control of Pulmonary Fibrosis? Click below to watch the replay of it in full. We had the pleasure of hosting: Jennifer Wescoe Founder, Executive Director Wescoe Foundation for Pulmonary Fibrosis. Matt Cullen European Patient Ambassador & Irish Lung Fibrosis Association (ILFA) Ambassador. Ron Flewett EU-IPFF member, Board of Pulmonary […]

Read More


Meet Carmen Who Uses patientMpower to Help Monitor Her Hermansky-Pudlak Syndrome

Monday, April 23rd, 2018

thumb image

“The fibrosis of Hermansky Pudlak, like any other pulmonary fibrosis, has no cure. All we can do for now is manage it. patentMpower helps me to do that.” – Carmen In honor of Hermansky-Pudlak Syndrome (HPS) Week we wanted to share the story of Carmen Camacho. Please read on below to learn more about HPS […]

Read More


Taking Control of Pulmonary Fibrosis: Join our Patient Support Web Discussion

Sunday, April 22nd, 2018

thumb image

Whether you have only been recently diagnosed with pulmonary fibrosis, or have been diagnosed for a while and are starting to experience new symptoms or have recently started new treatments, it can sometimes feel that pulmonary fibrosis is overwhelming. Getting support from others can be very helpful and so patientMpower will be hosting a web […]

Read More





Get Updates As They Happen

* indicates required

Download The App