• This topic is empty.
Viewing 0 reply threads
  • Author
    Posts
    • #29891
      Christie Patient
      Moderator

      This is Latoya Hawkins’ story: After struggling with a chronic cough for years, Latoya was diagnosed with PF in 2019. She was prescribed oxygen, which made her disability more visible, but she says that her diagnosis liberated her! The long search for answers, and all the uncertainty were over. Finally having a name for her illness brought her peace of mind and allowed her to adjust her lifestyle.

      While her disease has led to some unpleasant lifestyle changes–like foregoing vacations–Latoya has found that she takes pride in maintaining her home independently. In fact, she says that accommodations spurred by the pandemic have helped her live more comfortably at home. Curbside pickup and delivery of necessities, along with a flexible work-from-home schedule are some of the ways things that help Latoya live independently with PF.

      I bet many of us in the rare disease community have enjoyed the benefits of our society working to accommodate more people at home!
      I hope that accommodations continue, and we care more for disabled and chronically ill folks even after the pandemic settles.

      Latoya also said that she enjoys connecting with others in the PF community in online support groups, since she hasn’t met anyone in real life that shares her diagnosis. Let’s continue the conversation and welcome Latoya to our forums! 🙂

Viewing 0 reply threads
  • You must be logged in to reply to this topic.

©2022 KLEO Template a premium and multipurpose theme from Seventh Queen

CONTACT US

We're not around right now. But you can send us an email and we'll get back to you, asap.

Sending

Log in with your credentials

or    

Forgot your details?

Create Account