Since I was diagnosed with COPD in July this year, I have been asking my Nurse and GP to be referred to Consultant. Several times I asked them and they kept saying that they only refer when they can no longer manage disease. I had spirometry in July with the Nurse at GP's and it came up 73%. Inhalers they gave me did no good and had 4 different ones - Qvar, Symbicort, Seretide. I was nervous going to see Consultant last week as had a heavy cold. It was at Southampton General Hospital which is a large teaching Hospital and seen top Consultant in Pulmonary Department. Firstly I spent 2 hours doing spirometry test in booth, only had pc with nurse before at GP's. Did 6 minute walk, loads of puffing and came up as 84% even with a cold. The guy explained that when you have spirometry at GP's it is always lower. Probably due to hospital having all the proper equipment. Had scan and chest x ray. I had 3 previous chest x rays which came back negative,. Finally saw Consultant and he was great. So patient and explained everything to me. He brought up readings on PC and said in his opinion I did not have COPD. He said... ' I dont go just by the 84% but the other readings on the test too ' and he says if he was shown this, then he would say................. person does not have COPD. Chris and my son where with me and we all sank into chair with relief. At very least.................... if I have COPD....................... it is very very mild. He is going along the route that I was diagnosed and been hyperventilating. Referring me to breathing Nurse and sleep apnea test. We came home and my son said................ at least you are in Hospital system now Mum. I have follow up with Consultant in March 2014. Have I been hyperventilating all this time? There was a lot of stress this year with illness with partner etc.
Seen Consultant: Since I was diagnosed... - Lung Conditions C...
Seen Consultant
What wonderful news. So pleased for you your family must be relieved. What a great christmas you'll be having.
Kim xxxxx
Thank you Fibberti. As a family, we did have a lot going on this year. I am going with believing the Consultant and NOT the Nurse at GP's. Spirometry, sitting in the booth felt more in depth
What a relief ! Those booths really are the best way to test for COPD in my opinion. Also the CT scan.
I'm going to see a consultant at my local hospital on the 19th I'm lucky my husbands company gives us health insurance and in return we give the tax man loads of money for the privilege however I have never been sent to the hospital and this all came about when I asked my GP if he would do a blood test for alpha 1 I'm sure mom had this.
I'm now level 4 COPD so think its time I saw a specialist I was diagnosed 10 years ago.
Hi Hypercat54, I have had numerous chest xrays over the last 5 years and all come back 'clear' wasnt until I had a cat scan that they diagnosed COPD, so try and have one of these as they show all xx
Hi hypercat
Have you thought about changing your gp. the way you have been treated is a total disgrace.
I am now waiting for my specialist appointment, My Spirometry in the doctors was the tube and usb in their PC which showed restrictive lung disease and I was 53% lung function I have night time gasping and problems breathing when flat. I recently found I had worked with asbestos for 10 years. I have waited over 18 months for my doctor to refer me!
Be Well
Good for you insisting on seeing a Consultant. Great news for Christmas! TAD xx
Thank you Tad xx
Fantastic news for you and your family Twinks. It's worrying about what the future affect of having this disease will have on my family that gets me down the most.
If I were you, I'd be partying like it's 1999 this Xmas. So lovely to read a positive story for a change. xx
This is great news Twinks, but I wonder how you have been diagnosed without seeing a consultant or having a cat scan. My doctor said he suspected COPD when I went to him in February but it was the consultant who eventually dignosed Bronchiectasis not COPDin April after tests and scan.So I wouldn't take GPs word for it they are not specialists.
If I were you I would party,party, party and we will all wish we could too.
Good news twinks - really pleased for you - nice to hear a good news story.
Love cx
Well you dont know what damage has been done Bev. They kept refusing to refer me to a Consultant and giving me different inhalers. 4 different ones in 5 months. I never got to see the same GP and as rarely gone to docs before July.......... they didnt know me. Finally they said I shouldnt have these symptoms at this early stage. They sent me for 3 chest x rays since July. I had one back in March when I had chest infection. I said to Chris, they think I am a paranoid crazy woman. They only took me seriously when Chris came to see GP with me. Then they said I may well be hyperventilating as Chris told them about his illnessess this year. Thats how I got Consultant referral. Consultant referring me to physio to work on my breathing and do sleep apnea test. I'm glad he is going to see me again in March. Email me if you want Bev xx
That's great news Twinks. Good luck to you and yours. You will have a lovely Xmas. Cheryl
twinks, it's so good to hear your good news for Christmas. Now relax as much as you can.
I was given a piece of advice on how to deal with hyperventilation. have a paper bag,NO plastic bag as these are dangerous! Breathe into the paper bag, in and out, until you feel freer. This is recommended by doctors for people who become anxious.
Will you have a pulmonary nurse? they are usually sweeter and down to earth more than doctors because they see people on a day to day basis and know how anxious a person can become.
The physiotherapist should be good to in showing this breathing technique to alleviate hyperventilation.
Do you do any exercise? At my gym, someone who is 81 years old just enrolled. but if you don't want to go to a gym, are you able to walk, do some Tai chi (great to relax) or yoga?
Best of progress and come to tell us about your progress. Cheers! Mike.
Please nag them to see a Consultant Bev. I'm not sure if COPD shows up in blood tests. Ask Nurse to explain it to you............ what test in her opinion showed up the COPD? My SOB hasnt gone and I guess I will have to work on that. Where it was great that my chest x rays came back clear each time............ I realise that it doesnt show everything. Ask to see your GP and not the Nurse Bev. Interestingly, the Consultant said to me that he feels the minute someone says they are a smoker or ex smoker with breathing problems - they are labelled with COPD. I do hope they sort it out for you as anxiety all adds to it as I now know. Please let me know how you get on Bev and if there is anything I can do to help xx
You're so right, I had more x-rays this year when I had a c/I, the doc said we know you have copd but when you come to us ill we have to check that it is that and not something else.
Oooo, I'm so cross with your GP s practice Bev.
NO, a normal xray doesn't show damage. You need a CT scan to show what is there.
Over the last few years I've lost count of the number of xrays I've had which came back 'clear'.
I was finally referred for a CT scan on 19th Dec 2012 after 4 months of chronic bronchitis and many different antibiotics that didn't work until finally Azithromycin over a further 2-3 months.
CT scan didn't happen for 6 months because cons refused. He was a rude dismissive pig so I refused to see him and saw a lovely young registrar. The first thing she said to me was 'looking at your history I'm wondering why you haven't had a CT scan, have you refused one'?
She organised it and after another couple of months I managed to see her again and she was brilliant in showing and explaining. She said she was very pleasantly surprised and had expected to see only holes (what ever that would mean). The damage was clear on both lungs but she said it was very good news and that I had a beautiful pair of lungs. I cannot tell you what a relief it was/is.
Its now my mission to stay as healthy as possible.
Others fag smoke, smelly candles and traffic fumes etc kill me so have to practice avoidance tactics but all in all things are going well.
My GP has doubled the Seretide to 500 2x daily for the winter and its brilliant.
Sorry to go on......... Just knowing i dont have bronchiectasis, emphasemia or aspergillosis has changed my life into no longer wasting it thinking up ways to end it and now look forward to the future.
I'm cash poor but was at the stage of trying to beg borrow or steal the money to get a private scan.
I know its your choice to smoke Bev but I hope you find the strength and courage to cut them down slowly to zero.
Can you change your GP? All the very best to you XxxX
Such brilliant news for you Twinks. I know just how you feel having had a similar experience and may not have copd. Still have moderate asthma but that's better controlled now.
Fantastic for you and your family