COP, not COPD: I have had recurring... - Lung Conditions C...

Lung Conditions Community Forum

56,325 members66,956 posts

COP, not COPD

CKlein5852 profile image
11 Replies

I have had recurring upper respiratory infections and sinus infections for years, even decades. I rec’d a face full of mold spores, when cleaning a home humidifier that was attached to my furnace, when I was 58. Since then, every few months, after a typical course of antibiotics and Prednisone, I would be diagnosed with another bronchitis or even pneumonia.

Last Monday (two and a half days ago), I felt terrible. I had chills and wheezing. (I always cough.). I went to bed about 9:30 p.m.; and, about 12:30 a.m., my wife woke me up and said my wheezing had steadily worsened. We checked my blood oxygen level, which is normally 96 in the day and mid-80s at night.

My O2% was 84; but, it would not go up, which ch is not a good thing. I had severe respiratory issues. We went to the ER where I was diagnosed with Acute Pneumonia, and it was discovered I had Sepsis. Thankfully, it was at least a Level II Trauma Center (Baylor Scott White in Grapevine [North Dallas], Texas).

I was admitted, and they started IV antibiotics and steroids. A Pulmonologist was brought in to consult and, luckily, he is an Intensive Care Unit (ICU) doctor who also has a private practice. Once he took an extensive history of my complicated medical condition (I also have Chronic Atrial Fibrillation.), he said he sees a lot of COP among ICU patients; he thought I might have that, too.

Cryptogenic Organizing Pneumonia ( COP) is not a Pneumonia, it is an Auto Immune Disorder that presents like Pneumonia. Cultures were negative for bacteria, which is typical of COP, while almost any Pneumonia was a bacterial component. Rather than yet another round of antibiotics and a many day prescription for Prednisone, the treatment is 24 weeks (or longer) of Prednisone. There may be side effects, which can be treated.

I am from Kansas City, and my Internist, my asthma specialist, and my Pulmonologist there had settled on a diagnosis of Chronic Bronchitis (a form of COPD) with Asthma being secondary. No one took a sputum culture in five years of treatments! None of them were academics, and none of them practiced outside of their offices, such as in an ICU.

It is now Thursday, and I will probably go “home” (We were visiting our son’s 2-week-old baby.) today or tomorrow. COP is not Pneumonia, and it is not infectious.

Also, my mother had an AID, Sjogren’s Syndrome. IF you have a parent who has or had an AID, you have a greater propensity for an AID, although perhaps a different one. I hope this helps for people who may be struggling with finding a proper diagnosis.

Written by
CKlein5852 profile image
CKlein5852
To view profiles and participate in discussions please or .
Read more about...
11 Replies
CKlein5852 profile image
CKlein5852

I should have said I am 65 now. COP usually presents in one’s 50s or 60s.

sassy59 profile image
sassy59

Very interesting post so thank you for that CKlein. I wish you well. Xxxx

Robin77 profile image
Robin77

That's very interesting information. Thank you for sharing and hope you will be feeling better soon.

TwinklingStar profile image
TwinklingStar

Thank you for taking the trouble to educate us about this condition. I have never heard of COP before. The names of some of the conditions are quite confusing. I am so pleased you managed to get both conditions diagnosed - such a deadly combination!

I hope you are discharged by now and hope you are able to enjoy visiting your family.

Best wishes

from

Twinkling Star

CKlein5852 profile image
CKlein5852 in reply toTwinklingStar

I was discharged late yesterday afternoon. Now, I only have to take 100+ Prednisone tablets over the next months. However, that is so much better than what I had been experiencing! Thank you for your reply.

TwinklingStar profile image
TwinklingStar in reply toCKlein5852

Oh no! I had a terrible reaction to the Prednisolone drug. The problem was that I had been on it for over 4 weeks by the time I realised what it was doing to me and so it took months of careful reduction of the dose for me to be able to get off it. I think if I had NOT taken it at all I would not have survived though so probably a good thing that the severe side effects came as the levels built up in my body. It affected me physically as well as affecting my whole personality as well. The Consultant said the Prednisolone had caused me to suffer with secondary Cushing's Syndrome.

I hope you will be ok on it and will soon feel much better.

Best wishes

Twinkling Star

CKlein5852 profile image
CKlein5852 in reply toTwinklingStar

Hopefully, everyone is different. I have had Prednisone several times over the last few years. No problem so far; but I will have it a lot longer this time: at least 45 days. We’ll see.

TwinklingStar profile image
TwinklingStar in reply toCKlein5852

There are a lot of people on here who have to take it regularly and they don't seem to get the problems which I had so I hope you will also be fine. As you have had it before at least you know how you were last time. I hope you will soon be feeling much better.

CKlein5852 profile image
CKlein5852 in reply toTwinklingStar

So far, after 60mg Prednisone for two weeks and 40mg for two weeks, I am dropping to 30mg (today) for two weeks; then 20mg, 10mg, and 5mg at 2-week Intervals. I have slight “swelling” in my face, but it seems only noticeable to me. So far, so good.

Otherwise, I have been symptom free of the problems I had had! My diagnosis seems to be finally correct!

TwinklingStar profile image
TwinklingStar in reply toCKlein5852

I am pleased you have coped with the Prednisolone without anything drastic happening. So glad you are currently symptom free. It is often the delays in getting a diagnosis which causes the long term damage so it is always a relief that someone has got the diagnosis right for you.

Stay strong.

Love from Twinkling Star

ShebaAlfie profile image
ShebaAlfie

Hello, I have COP in 2008 and took Prednisone in a high dose tapering over 6 months and got the all clear. Then in 2014 it came back but when they tried Prednisone again I developed Diabetes so had to be put on Mycrphenolate which I am still on but not getting better but losing muscle and less active and more breathless. I have had 6 chest infections in 12 months which they give me a short dose of steroids for and antibiotics which seems to work for a little while and then the coughing and mucus comes back. I’m not feeling too bad at the moment but get scared when I go to work in my office where 30 people work. If you have any advice I’d like to hear from you. Thanks Sonia 57 years old

Not what you're looking for?

You may also like...

I have COP/BOOP

Well as I start this process, I find myself in unfamiliar territory. My name is Nadine Harder and I...
nharder profile image

any advice for copd?

hi i had bronchitis and pneumonia in october 2012, since then i have almost constant chest...
tuzzy99 profile image

Newly diagnosed with COP and NSIP

Newly diagnosed with Cryptogenic Organising Pneumonia (COP) and NSIP After 3 months in hospital 6...
SCM75 profile image

Hay fever turned to COPD. Can this happen?

Went to Dr's due to chest infection. Expected to be given antibiotics but Sent to hospital?...
pamsshed profile image

Normal FEV1 , Normal FVC , Reduced FEV1/FVC - but Dr insists its NOT COPD

FEV1/FVC reduced- but Pulmonologist insist it is not COPD . I am a 35 Year old male , who has never...
gopalansree profile image

Moderation team

See all
AsthmaandLung profile image
AsthmaandLungAdministrator
moderator_AandLUK profile image
moderator_AandLUKAdministrator
Claire_ALUK profile image
Claire_ALUKAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.