We’re in the process of reviewing our COPD patient passport ( passport.blf.org.uk/ ) and would like to talk to some people affected by COPD (including family and carers) to get their views on it.
We’d like to speak to both people who have used it and those who haven’t, either way, you can help. This would involve a half our phone call with our market research company at a time that suits you.
If you are interested, please could you send me a personal message on here (I wouldn’t want to ask anyone for their phone number on the public part of the forum) or send me an email at PatientVoice@blf.org.uk?
Without this input, we can’t guarantee the high standard of health information that you expect from us.
Thank you for reading and I hope to hear from some of you soon!