Any suggestions for consultants in th... - PCD Family Suppor...

PCD Family Support Group (UK)

610 members301 posts

Any suggestions for consultants in the North West?

Thehappyhammer profile image
8 Replies

Hi, I'm in my 50's and live in Manchester. I was diagnosed with PCD about 25 years ago. I also have bronchiectasis and situs inversus. I was referred to the Brompton when we lived in London but I haven't been under anyone since we moved up North 20 years ago. I'm getting a bit fed up with my coughing and glue ear which is affecting my work. Can anyone recommend a consultant that I can ask my GP to refer me to?

Thanks

Written by
Thehappyhammer profile image
Thehappyhammer
To view profiles and participate in discussions please or .
Read more about...
8 Replies
TerryBun profile image
TerryBunAdministrator

Hello

It definitely sounds like you should get yourself checked out.

If you don't fancy the trip back down to the Royal Brompton, it seems the two places nearest to Manchester would be Dr. Peckham at Leeds or Dr Range at Leicester.

In the meantime some extra physio will never go amiss when you are coughing a lot more. Good luck.

Terry

Thehappyhammer profile image
Thehappyhammer in reply to TerryBun

Thanks very much Terry - much appreciated. By the way, I was prescribed co-amoxiclav tablets for my ear infection last week and it seems to have had a dramatic impact on my coughing - I'm barely coughing at all for the first time in, well ..ever! Have you heard of similar impacts from other PCD-ers? Are many adult PCD-ers on full-time antibiotics? I appreciate you are not a medical expert but i wonder if you had a general idea. Thanks again

TerryBun profile image
TerryBunAdministrator in reply to Thehappyhammer

Brilliant news about the coughing, although I sometimes find if I stop coughing significantly it's because of plugging and so extra physio helps with that. Getting the ears sorted may have helped a bit though, especially if the ears and nose were draining a lot more previously...that's my guess, as I'm not medical expert either, but whatever works for you then great.

I know of quite a few of the adults with PCD who are on prophylactic antibiotics (Azithromycin), taking them three times a week. I have been on Azithromycin for quite a number of years myself.

Hope you get to see a PCD specialist soon.

Terry

Thehappyhammer profile image
Thehappyhammer in reply to TerryBun

Thanks again terry

PCDalisonj profile image
PCDalisonj

University of south Manchester ( Wythenshawe ) has a large and excellent lung centre.

Thehappyhammer profile image
Thehappyhammer in reply to PCDalisonj

Thanks for that Alison. I have heard of it and I live v close to it but I had heard that it perhaps wasn't the best for PCD. Maybe I'm doing them a disservice.

PCDalisonj profile image
PCDalisonj in reply to Thehappyhammer

In my experience prof woodcock is very helpful

Thehappyhammer profile image
Thehappyhammer in reply to PCDalisonj

That's very helpful - thanks again. I'll take your advice and ask to be referred to him. Fingers crossed!

You may also like...

Adults with PCD & hearing issues

Does anyone here (adults) with PCD have trouble with their ears? I had grommets when I was much...

Anyone experience with ear tubes / grommets?

wonder if we should try ear tubes / grommets. So has anyone experiences with ear tubes? And has...

Athritic pain and PCD

wanted to know if anyone knew if there was a link between PCD and arthritis? My consultant never...

Recurring Ear Infections with Ear Tubes

diagnosed with PCD (By genetic testing) and also has situs inversus. She has had many ear...

Hello, I’m new here my Name is nicola

times a week as I have had 5 chest infections last year and twice ended up in hospital stay. The...