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Dad may have been incorrectly diagnosed with IPF but thanks to BLF we are now on the road to getting more precise diagnosis.

xeus profile image
xeus
8 Replies

My dad was diagnosed with Idiopathic Pulmonary Fibrosis earlier this year after having a CT scan carried out. We just went to the hospital that our GP referred us to and for the past 10 months have just taken their diagnosis as being correct and obviously very concerning.

In our last visit to the hospital 2 weeks ago I was getting concerned that the doctors did not seem to be that confident in answering our questions about the state of my dad's condition and how bad it was so we decided to contact the BLF for further information.

The first thing they said was to watch a new webinar that had been produced by a specialist in IPF and that they would follow up with us after watching it. Well that webinar was fantastic. It was really informative and took us through the condition thoroughly, how it would be diagnosed and what possible treatments might work and what was in a trial state.

It made us realise that the hospital that my father was being seen at did not truly understand this condition and that we needed to get second opinion.

Last night we went to see a specialist at the Royal Brompton who, after looking at the CT scan is not convinced that IPF is present in my dad's lung and is going to carry out some further tests (which were never offered and talked about at the current hospital).

The relief we all had after that appointment was immense. We still need to wait for the new tests but the outlook seems like IPF may well be incorrect and there may be another diagnosis which may not be as serious.

This whole episode just makes us realise how little is really known by doctors about some lung conditions but what puzzles us is why our initial doctors did not advise us to see an IPF specialist if they themselves could not be that confident of the diagnosis.

That webinar about IPF is really useful and I hope that anyone who is diagnosed with IPF is pointed in the direction of this webinar so they too can judge whether or not they are getting the right diagnosis. It would probably help if all Respiratory consultants all saw it as well before they make such worrying judgements about someone's health.

Thankyou to the BLF for pointing us in the right direction.

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xeus
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8 Replies

What great news xeus! Fingers crossed that there will be a better outlook for you and your family now! P :)

Lynne1955 profile image
Lynne1955

What an informative post and hopefully, good news for your Dad.

It just shows the really good work done by the BLF.

Lynne x

Well done BLF! So pleased for you and your dad. x

Athar profile image
Athar

Hi Xeus

What a great post! So nice to see that our webinars can make a difference. I have now added the recording to our IPF page on the site here

blf.org.uk/Conditions/Detai...

and if anyone hasn't had a chance to watch it yet then here it is

youtube.com/watch?v=EMvoGAv...

We're planning our next webinar topics now. Has anyone got any suggestions? We'd love to hear from you.

Thanks for giving us this great feedback - I'll make sure Vicky sees your comments. If anyone else would like to speak to Vicky or any of the other Helpline nurses after seeing the webinair, please call the Helpline - 03000 030 555.

Thanks again

Mark

kimmy59 profile image
kimmy59

Fantastic news everything crossed for you.

Kim xxx

cofdrop-UK profile image
cofdrop-UK

Hi Xeus

Good news. Glad you changed docs and went to the Brompton - hope they get your Dad dx soon and on an effective treatment regime.

Love C xxx

xeus profile image
xeus

All,

Thankyou for all your kind words.

My question to the BLF: Are there any awareness programs in place to try and educate the rest of the medical profession and other patients diagnosed with lung conditions with these kind of webinars especially for conditions which are very under represented throughout the NHS like IPF.

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