After chatting with Tony yesterday , I got curious about how many people have kept
their numbers stable. Also for how long. Do you feel that you did anything to influence them being stable? ( If you didnt see Tonys post you should ck. It out. Hes very entertaining , as always )
Have a great day everyone
Rubyxx 😊 😊
Written by
rubyred777
To view profiles and participate in discussions please or .
The ability to reply to this post has been turned off.
Hi Ruby, i was dxd in 2000, i think FEV1 in 50s then; it went down for a few years, then i kept it at about 41 for about 4 years, then started intensity exercises suggested by a healer in the US (my version was climbing up and down stairs as quick as i could do it) then for another two years it was at 47%.
Now, since reflux has got worse (may be the cause, could be just a step down which can apparently happen) it's around 37-38% even though i do even more exercise, very annoying
I was dxd at a health fair in 2007 with a fev1 of 68. Then in 2008 I was 67, 20012- 74, 2013-69. Then I had an 12 mm cancer removed by wedge. ( march will be 2 yrs. On that) so my next test I dropped down to 62. Maybe because of the
wedge, don't know. So I'm waiting to get another test done. Plus I have to get a scan . Can't say I do alot of good things I am still doing office cleaning so I'm active. The one job I do go up and down the stairs three times. I keep an eye on my oxygen. My diffusion was 67% on my last test. I don't really get out of breath. Just have one inhaler. Qvar- I taKe one puff before I work.its a childs dosage actually.All in all I feel pretty good. Are you on oxygen?
Im glad you're feeling good Ruby, hope that continues and that the test and scan are ok :). Stairs are great exercise.
Yes, on ambulatory oxygen when I'm out walking (as opposed to strolling ), have to see about whether i can do without it in the summer - i use 2 lpm currently. Also use it for flying, and when i have exacerbations. Not really breathless at home, other than when ill. But I've always been breathless outside, even before needing oxygen, and even with medication since i have had severe asthma for a long time as well - Im kind of used to it now.
My consultant says that 5% either way (I assume he means either way from the last one) is not significant as it might be the machine. i never understand this, since i was stable for so long, then better for two years after adding in more exercise.
I think he's trying to make me feel better when the reading is worse which it has been the last two years. I might ask to have some new medication and see if things improve on that.
I was diagnosed with copd around 6 years ago with a lung function of 62%. The next one I had after being given proper meds was 73%. Last year it was 66%. Not doing anything differently. x
I am not really able to read my tests and come to a conclusion but I believe I have 39% diffusion capacity....I am not even sure I know what that means. Even after going to rehabilitation I know very little. I did find out that they do not use peak flow and I do not have a way of checking that. All I know is I have severe emphysema/copd and am on oxygen for exertion and supposed to have it for sleep but cannot afford it. I will have to wait until August and I asked for a sleep study any way. I do know that my oxygen drops easily on some days and not on others. When it drops below 88% I get all worried. I also learned that the purpose of the oxygen is in attempt to protect the heart . One thing at a time I will understand the things I need to understand...fev- 1 is a subject I am learning that different areas have different values so it is hard to compare with others, however the test gives a reference range. Well toodles for now.
I have the range and results yes the lab report says FEV-1 liters-reference 2.54 pre albuteroll-.88; % reference- 34 ; post albuterol-.94 % ; reference-37 % ; change - 10.
What all of that means is the after albuterol I had a 10% change. Rehab said it indicated a slight amount of asthma component to my illness.
The ability to reply to this post has been turned off.
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.