Category: patientMpower users

Help Spread Awareness of Pulmonary Fibrosis during #PFMonth

Saturday, September 8th, 2018

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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 […]

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

Thursday, September 6th, 2018

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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. […]

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

Tuesday, June 19th, 2018

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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 […]

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Watch a replay of our patient support web discussion

Tuesday, April 24th, 2018

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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 […]

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

Monday, April 23rd, 2018

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“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 […]

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

Sunday, April 22nd, 2018

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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 […]

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Meet Kevin who uses patientMpower after his lung transplant due to IPF

Monday, April 9th, 2018

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My name is Kevin Seals. I am 60 years old and live in Bone Gap, IL. I was diagnosed in October of 2012 with Idiopathic Pulmonary Fibrosis (IPF). I first noticed I had constant fatigue, chills, and leg cramps. I was unable to improve my jogging even after working out for six months. On April […]

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Meet patientMpower user Seán O’Muircheartaigh

Wednesday, March 28th, 2018

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Hi, my name is Seán O’Muircheartaigh, I’m 73 and located in Galway, Ireland. I was a patient in Galway Regional Hospital with an undiagnosed illness about five years ago. A computed tomography (CT) scan identified by my doctor showed suspicious darkening at the base of my lung. I was transferred to another hospital where they […]

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eHealth Ireland Interview with Eamonn Costello and Colin Edwards

Sunday, March 25th, 2018

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Tell us about patientMpower in brief: patientMpower is a digital healthcare company providing technology solutions for patients across a range of therapy areas including pulmonary fibrosis (IPF), renal dialysis and renal transplant. Our aim is to empower better outcomes by facilitating patients to better manage their care. Our mobile platform enables patients to track their […]

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Meet patientMpower user & Emmy award winner, Mike Olsen!

Monday, March 5th, 2018

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Hi, my name is Mike Olsen and I’m from Louisville Kentucky. I am an idiopathic pulmonary fibrosis (IPF) warrior patient. I started having trouble after an ice storm in December 2012. I kept also having allergy problems and when I kept being treated time and time again for sinus infections my allergy doctor sent me […]

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Meet patientMpower user Glenda Rouland

Monday, February 19th, 2018

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Hello! My name is Glenda Rouland, I’m from Birmingham, Alabama and I’m 65 years old. I was diagnosed with idiopathic pulmonary fibrosis (IPF) in October of 2015 after I went to see my Doctor because of feeling short of breath. I heard about the patientMpower app on a Facebook support group. I read where I […]

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Meet patientMpower user Ron Flewett

Monday, February 12th, 2018

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My name is Ron Flewett I am 57 and live with my wife Maxine near Lincoln in the UK. It all started with a cough and feeling out of breath when walking up a flight of stairs or slight incline. I visited my local GP several times, and the x-rays kept coming back clear. He […]

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Meet patientMpower user Beth Hunley

Monday, February 5th, 2018

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Hello! My name is Beth Hunley and I am 56 years old. I live in Portland, Indiana. I was diagnosed with idiopathic pulmonary fibrosis (IPF) by a lung biopsy in April of 2014. I am currently on the lung transplant list as of March 2017. My first symptoms of PF were shortness of breath, chest […]

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Meet patientMpower user Curt Thompson

Saturday, January 27th, 2018

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Hi, my name is Curt Thompson of Richland, Mississippi and I’m 71 years old. I was diagnosed with idiopathic pulmonary fibrosis (IPF) in August of 2015. My wife, her identical twin sister and one of their cousins (a 62 year old male) have all passed from IPF. During the spring of 2015 I had a […]

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Meet Nicola Cassidy from The Irish Lung Fibrosis Association (ILFA)

Monday, January 22nd, 2018

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Hello! My name is Nicola and I am a Director of the Irish Lung Fibrosis Association (ILFA), the national patient organisation for patients and carers affected by lung fibrosis in Ireland. My mother, Denise, was diagnosed with idiopathic pulmonary fibrosis (IPF) at 56 years of age and I was her caregiver when her health deteriorated. […]

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