Breathing comes naturally until you are living with chronic lung disease. Unless we practiced meditation or relaxation techniques like yoga or Qi Gong, we have paid very little attention to [Read More]
News
PF Warriors Chooses Shelly Mathis
PF Warriors Chooses Shelly Mathis as its Executive Director Hope is what brought Bill Vick and Shelly Mathis together about eight years ago. Hope is what will ensure that their [Read More]
A Caregiver Wants you to Know
Being a caregiver for someone with interstitial lung disease is something you don’t understand unless you have lived it. The typical American caregiver is burdened with a role that most [Read More]
Newly Diagnosed with Pulmonary Fibrosis? Do These Things First
Learning that you have a rare lung disease is shocking, confusing, and just plain frightening. Often, people with pulmonary fibrosis see their primary care physician because they are concerned about [Read More]
Are You Prepared for a Disaster?
Wild fires. Floods. Tornados. Winter storms. Pandemic surges. There list of possible disasters can seem endless. It might seem unreasonable to say that you can prepare for the unexpected. When [Read More]
Talking to Family and Friends about Your Health
Talking to family and friends about your fibrotic lung disease can be frustrating. Pulmonary fibrosis and interstitial lung disease are rare and are not well-publicized, so many people have never [Read More]
Holiday Gift Ideas for People with Pulmonary Fibrosis
We’ve got ideas for thoughtful gifts for friends or family members who are living with a fibrotic lung disease. The importance of the gift is the consideration and love you [Read More]
5 Secrets from Patients Living with Pulmonary Fibrosis
I became a caregiver for my partner when she was diagnosed with non-specific interstitial pneumonia in 2014. She had a nagging cough which had persisted through November and December into [Read More]