01/08/2025
I have been really enjoying speaking at these Navigating PF sessions. A life limiting diagnosis comes with a whole raft of grief and loss, both for the person and their loved ones. During these sessions I talk about coming to terms with a diagnosis like pulmonary fibrosis, sharing simple changes you can make to help manage your mental wellbeing and adapt to any new challenges you may face.
The next session is on Wednesday 6th August, 3-4pm and it's open to anyone affected by pulmonary fibrosis.
If you have been impacted by a life limiting illness and are looking for support, please don't hesitate to reach out.
Have you or a loved one recently been told you have pulmonary fibrosis (PF)? You are not alone, and we are here to help.💜
📅Join us for our upcoming recurring webinar, An Introduction to Navigating the PF Journey, on Wednesday 6 August, from 3-4pm.
This month we'll be joined by Kate Osborne, an ILD nurse specialist from Guys and St Thomas', Chris McIndoe a grief specialist, and Sarah Webster, who is living with PF.
Topics include:
- What pulmonary fibrosis is
- Coming to terms with a diagnosis
- How to talk to friends and family about it
We’ll also introduce the range of support that we offer at Action for Pulmonary Fibrosis, and you’ll have the chance to ask your own questions in a live Q&A with our expert panel.
The webinar is a recurring series and will repeat on the first Wednesday of every month between 3-4pm, so if you can't make this one, you can always join a future session.
Find out more and sign up here:
https://ow.ly/AO5C50WxmYZ