An Introduction to Navigating the PF Journey

Welcome to our new recurring webinar – ‘An Introduction to Navigating the PF Journey’ – where a panel of experts will talk you through the basics of pulmonary fibrosis.

Have you or a loved one recently been told that you have pulmonary fibrosis (PF)?

Do you want to:

  • understand more about what to expect with PF?
  • find out more about how Action for Pulmonary Fibrosis (APF) can support you and your loved ones on your PF journey?
  • have your questions answered by our team of experts?

If so, this is the webinar for you!

When is it?

Our new recurring webinar, ‘An Introduction to Navigating the PF Journey’ is an educational session that repeats on the first Wednesday of every month*, from 3-4pm. We’ll run the same webinar every month, so you only need to sign up to one session.

Who is it for?

It’s designed for people who have been told they (or a loved one) have PF in the last 6 months and will be a basic introduction to pulmonary fibrosis and the support available from APF. However, registration is open to anyone affected by PF who is interested in coming along to learn more.

What will I get from it?

Our expert panel of healthcare professionals and individuals with lived experience of PF will be talking about:

  • The basics of pulmonary fibrosis, including what it is, and the main signs and symptoms.
  • Coming to terms with your diagnosis and things you can do to make this easier.
  • Tips on how to tell people about your diagnosis.
  • The support available from Action for Pulmonary Fibrosis for you and your loved ones throughout your PF journey.

You’ll also have the opportunity to get your questions answered.

Helpful information

This session will not be recorded and there are limited places available to ensure that we can answer everyone’s questions, so if you can’t join us live this month, you can have a look at our list of upcoming sessions (below) and register for a different session.

If the time doesn’t work for you, but you are interested in receiving the information in the session, please get in touch and we’ll be happy to help.

Our speakers offer general information during this session. We cannot respond to personal medical questions or give medical advice, so please bear this in mind when submitting questions.

Upcoming Sessions: 

This session repeats on the first Wednesday of every month, 3-4pm: 

  • Wednesday 2nd July, 3.00 - 4.00pm, register here.
  • Wednesday 6th August, 3.00 - 4.00pm, register here.
  • Wednesday 3rd September, 3.00 - 4.00pm, register here.

*Please note that there may be circumstances where we need to cancel a scheduled session. We will always endeavour to avoid this as far as possible, but in the event that cancellation is necessary, everyone who has registered will be notified via email.

Information provided by Action for Pulmonary Fibrosis (APF) is not a substitute for professional medical advice. It’s intended as general information only. APF is not responsible for any errors or omissions or for any loss or damage suffered by users resulting from the information published on actionpf.org.

Further information for carers:

Your essential caring guide (PDF)
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