Facebook-f Twitter Instagram Podcast Youtube Tiktok Linkedin-in Pinterest Envelope Share
CLICK HERE TO SHARE YOUR STORY!
  • About
    • Meet Our Contributors
    • Meet Our Partners
    • Meet the Patient Worthy Team
    • Collaborative Content On Patient Worthy
  • Diseases
  • Share Your Story
    • Patient Worthy Content Submission Guidelines
    • Patient Worthy Writing Prompts
    • Submit Your Story
    • Patient Stories
  • Resources
    • Library
    • Events
    • Patient Worthy FAQs
  • Podcast
  • Contact
Menu
  • About
    • Meet Our Contributors
    • Meet Our Partners
    • Meet the Patient Worthy Team
    • Collaborative Content On Patient Worthy
  • Diseases
  • Share Your Story
    • Patient Worthy Content Submission Guidelines
    • Patient Worthy Writing Prompts
    • Submit Your Story
    • Patient Stories
  • Resources
    • Library
    • Events
    • Patient Worthy FAQs
  • Podcast
  • Contact
  • Join PW

Idiopathic Pulmonary Fibrosis

  1. Home>
  2. Idiopathic Pulmonary Fibrosis>
  3. Page 6
You Gotta See This Innovative New Research for IPF
Source: pixabay.com

You Gotta See This Innovative New Research for IPF

  • Post author:PW Blogger
  • Post published:December 12, 2016
  • Post category:Idiopathic Pulmonary Fibrosis/IPF/Rare Disease

Movies, television shows, and books can create a vision of a world with endless possibilities. The future can be portrayed in ways that we would find impossible in the present…

Continue Reading You Gotta See This Innovative New Research for IPF
What Do You Know About Diet and IPF?
Source: Pexels.com

What Do You Know About Diet and IPF?

  • Post author:EmpatheticBadass
  • Post published:December 7, 2016
  • Post category:Idiopathic Pulmonary Fibrosis/IPF/Rare Disease

When your body has to work extra hard to breathe because of lung issues such as idiopathic pulmonary fibrosis (IPF), help it out by “eating healthy.” Digesting big, heavy meals…

Continue Reading What Do You Know About Diet and IPF?
The 2016 Presidential Campaign: An IPF Love Story
Source: pixabay.com

The 2016 Presidential Campaign: An IPF Love Story

  • Post author:Kiki Jones
  • Post published:November 3, 2016
  • Post category:Idiopathic Pulmonary Fibrosis/IPF/Rare Disease

2016 has been a very bizarre, upsetting year. As an American, I can’t wait until I can bury most everything about 2016 in the back corner of the history books.…

Continue Reading The 2016 Presidential Campaign: An IPF Love Story
IPF: Here’s How to Empower Patients Who’ve Given Up Hope
Pixabay

IPF: Here’s How to Empower Patients Who’ve Given Up Hope

  • Post author:Alisha Stone
  • Post published:September 30, 2016
  • Post category:IPF/Rare Disease

“You’ve come a long way, baby!” was a hugely popular phrase back in the late 1960s that I grew up with and still refer to often. I often say it…

Continue Reading IPF: Here’s How to Empower Patients Who’ve Given Up Hope
Would You Believe Something This Simple Can Change the World?
Source: www.pixabay.com

Would You Believe Something This Simple Can Change the World?

  • Post author:Lady Kehveen Abernathy
  • Post published:August 16, 2016
  • Post category:IPF/Rare Disease

"From belonging to an healthiest elite organisation to being hit by a rare disease is a leap which is not easy to accept." What is it about stories? Why do…

Continue Reading Would You Believe Something This Simple Can Change the World?
How to Get New (and Better) IPF Drugs in 3 Easy Steps
Pixabay

How to Get New (and Better) IPF Drugs in 3 Easy Steps

  • Post author:James Ernest Cassady
  • Post published:August 1, 2016
  • Post category:IPF/Timely

Last November, Janet Woodcock - the Director for the FDA's Center for Drug Evaluation and Research - gave the keynote address at the Pulmonary Fibrosis Foundation's summit in Washington, D.C.…

Continue Reading How to Get New (and Better) IPF Drugs in 3 Easy Steps
On The Outside Looking In On One Woman’s Life With IPF
Source: https://pixabay.com/en/window-broke-glass-wall-dirty-1861888/

On The Outside Looking In On One Woman’s Life With IPF

  • Post author:Lady Kehveen Abernathy
  • Post published:July 29, 2016
  • Post category:IPF/Rare Disease

"You'll be fine. You're just depressed." How many times have you heard a doctor tell you that—when you KNOW something is seriously wrong? Marilyn heard the exact same thing. "I ain't…

Continue Reading On The Outside Looking In On One Woman’s Life With IPF
This Man Doesn’t Need a Sexy Headline to Inspire Hope

This Man Doesn’t Need a Sexy Headline to Inspire Hope

  • Post author:Lady Kehveen Abernathy
  • Post published:July 22, 2016
  • Post category:IPF/Rare Disease

When diagnosed with idiopathic pulmonary fibrosis (IPF), physical activity is pretty much out of the cards. Or is it? With IPF, heavy scarring in the lungs hardens the tissue and makes…

Continue Reading This Man Doesn’t Need a Sexy Headline to Inspire Hope
Pulmonary Fibrosis Foundation Care Center Network Adds 19 New Sites
[Source: Pixabay]

Pulmonary Fibrosis Foundation Care Center Network Adds 19 New Sites

  • Post author:Farrah Fontaine
  • Post published:June 30, 2016
  • Post category:IPF/Rare Disease

One of the difficulties facing the IPF community has been a lack of knowledge and awareness about the disease among many doctors and even specialists. An aggressive disease, idiopathic pulmonary…

Continue Reading Pulmonary Fibrosis Foundation Care Center Network Adds 19 New Sites
What Do You Know About Your Rights As An IPF Patient?
Source: www.giphy.com

What Do You Know About Your Rights As An IPF Patient?

  • Post author:James Ernest Cassady
  • Post published:June 22, 2016
  • Post category:IPF/Rare Disease

In 2013, the British Lung Foundation (BLF) released a Patient Charter for people living with IPF, or idiopathic pulmonary fibrosis. In it, they outline the five basic rights of people with…

Continue Reading What Do You Know About Your Rights As An IPF Patient?
Millions Find Hope From a Celebrity IPF Survivor

Millions Find Hope From a Celebrity IPF Survivor

  • Post author:PW Blogger
  • Post published:June 15, 2016
  • Post category:IPF

The world was his audience, and everyone was watching. It was time to say "I have Idiopathic Pulmonary Fibrosis" If you are like most ordinary people, you are likely not familiar…

Continue Reading Millions Find Hope From a Celebrity IPF Survivor
  • Go to the previous page
  • 1
  • …
  • 3
  • 4
  • 5
  • 6
Finding Light Through Story-The Power of Ambassadorship in the Endometrial Cancer Community
*cancer that cannot be removed with surgery or has spread to other parts of the body. GEJ= gastroesophageal junction (where the esophagus joins the stomach)
CLICK HERE TO SHARE YOUR STORY!
We believe rare disease patients are people, not a diagnosis. Through education, awareness and some humor, we help patients, caregivers and support persons by providing relevant and often inspirational news and stories.
Our goals are to share stories, cultivate strong community, provide the latest medical findings, connect people and pioneer production of patient worthy information. Help us attain these goals by telling us a little bit about yourself!

Let’s Work Together!

Partner With Us
Submit a Story

Keep Up to Date

Subscribe to Our Newsletter
Check Out Rare Events
Get Inspired By Our Memes

Learn More

About Us
Rare Diseases and Conditions
Terms of Use
Privacy Notice
Privacy Policy for CA Residents
EU/UK Privacy Notice
Data Privacy Framework: Consumer Privacy Policy
Consumer Health Data Privacy Policy
Cookie Notice

Facebook-f Twitter Instagram Podcast Youtube Tiktok Linkedin-in Pinterest Envelope

© Copyright 2024 Patient Worthy

Sign Up With a Patient Worthy Account and Share Your Rare Story

- OR -

Sign Up For Our Patient Panel

Make a difference, share your experiences and get paid. Opt-in and join Patient Worthy's panel for paid opportunities such as surveys, market research, patient advisory panels and more.

More Info

We're Happy You're Here!

What best describes you when it comes to rare disease? (check all that apply)

What rare disease(s)/conditions are most important to you?

Visit Home Page or

Thank you for signing up for a Patient Worthy Account!

Have a rare disease story to share? Let us know

Share Story

- OR -

Sign Up For Our Patient Panel

Make a difference, share your experiences and get paid. Opt-in and join Patient Worthy's panel for paid opportunities such as surveys, market research, patient advisory panels and more.

More Info