It’s been an extremely challenging year for people with and impacted by Pulmonary Fibrosis.

It’s been a year since Covid-19 was declared a pandemic by the World Health Organization in March 2020. The pandemic has impacted everyone this year, but our community has been disproportionately affected. This time has been particularly difficult for people fighting lung diseases like Pulmonary Fibrosis (PF), since they are at a higher risk for developing serious illness from Covid-19. 

We’ve responded by continuing our commitment to fighting PF right now!

As always, we have dedicated the past year to our mission: using research, interactive learning, and self-monitoring to educate the public about all treatments, including natural, supplemental, and alternative therapies for treating chronic PF. Especially with PF emerging as a serious complication of Covid-19, it’s become even more important to increase awareness about this rare disease and all its treatments. 

Our Director, Dr. Neha Shah, has been conducting research on potential ways to combat Covid-19 and reduce post-Covid fatigue. The results were recently published and are very promising. This interview explains how a natural treatment that is used to help people with PF is now also being used to help people with Covid-19 recover more quickly. 

Our staff have also been offering virtual support groups on the 2nd Tuesday of every month at 3:30pm PST / 6:30pm EST. People with PF and people impacted by PF (such as caregivers or relatives) have been helping each other heal from all the grief, fear, and uncertainty. The community’s compassion, knowledge, and advocacy has been increasingly visible daily in our Facebook group, which grew to include over 200 active members! 

Our resources for online learning expanded too, with lots of new blog posts addressing key concerns about PF and Covid-19. Here is our recent article on the vaccines for Covid-19, and here are some ideas to help you through social distancing and quarantines. 

Together, we’ll continue to fight PF now!

We are so grateful to everyone who has helped us fight PF and brought hope to those struggling with the impacts of Covid-19. Here are a few things you can do to help this next year be easier for people with or impacted by PF: 

  1. Share the news about our research
  2. Join our online community
  3. Attend our virtual support groups on Zoom. You can register here
  4. Talk to your doctor about the vaccine for Covid-19

Related Post

8 Tips for Leading an Active Lifestyle with Pulmonary Fibrosis
Adult Exercise Sport Activity

Just because you suffer from pulmonary fibrosis — a condition that causes damaged and scarred lung tissue — doesn’t mean Read more

How to Support a Friend with Pulmonary Fibrosis
Two girls hug on the sidewalk

Being diagnosed with pulmonary fibrosis can be a scary and isolating experience, and the same is true of those who Read more

Coronavirus and Pulmonary Fibrosis: What You Need to Know
listening to lungs with stethoscope

Given the recent spreading of the novel COVID-19 strain of the Coronavirus, it is important to be aware of the Read more

15 Hobbies for People with Chronic Illness During Times of Social Distancing and Quarantine

As a result of COVID-19, many communities have been ordered to social distance and stay home. For patients with chronic Read more

Leave a comment

PulmonaryFibrosisNow.org
  • Newsletter Signup