Hi vanessalee thank you for your reply.
Oooh, I am so pleased to hear that you have gone from severe to moderate so quickly. Wow FEV1 score has risen 11 points and in just 3months too. Must be great to know that all that you are doing to help yourself is paying off!!!!
I do try to keep as active as possible, having a family and a home to run, being on the committee at our church I do keep busy but I do tend to get tired more quickly lately, may possibly have something to do with weather not being very wonderful and being stuck in for most of the winter.
Nurse said I’ve remained exactly the same since my last spirometry test in 2008. Until Thursday I didn’t know much at all other than I have had COPD for a few years and have to have this test annually.
I only found that out by being nosy a year or two ago on a visit to see Doctor about a waterworks problem. When she was testing my water sample I peeped at screen and saw COPD. I then asked are those my medical notes? I wasn’t aware I had COPD! The doctor was a locum and looked surprised I had not been told. She said yes, that diagnoses was made when I went to the hospital for a load of lung function tests that was back in 2005, was told routine test to make sure I’m still on the right medication will be notified if doctor wanted to see me. I remember I have had two of these and each time had to have chest x-rays & suck and blow into a lot of machines. Oh my, after each visit my chest was shocking for a few weeks after.
This visit is the first time that I’ve been called back for results! Might be because surgery has moved to a brand new health centre and the Sister is a new one.
I have to go back to see Sister in July she said we will discuss Pulmonary Rehabilitation. I am in the meantime to have some physiotherapy and to take more light exercise such as walking. My dog will be pleased to get out more, hate walking alone unless I’m just popping to local shop, I take him with me, when he stops to sniff or pee I can catch my breath.
You say spirometry test conducted during an exacerbation can give a poorer score. My chest was quite clear when I had the test. I have gone downhill since having the test, plus, the recent hot stuffy weather hasn’t helped.
I am on the following Medications for about two years now. FLUTICASONE+SALMETEROL dry pdr inh 250/50microgrms, two puffs twice a day, UNIPHYLLIN CONTINUS tablets, 1 every 12hrs. SPIRIVA 18 MICROGRAM caps for inhalation .One cap daily. ACCOLATE 20MG TABLETS. 1 every 12hrs PREDNISOLONE TABLETS 5MG (For Exacerbations of COPD) Plus of course, the good old faithful VENTOLIN INHALER.
Thank you very much for your advice, I will have a good look around internet plus it mentions 1 or two books in the booklet Sister gave me on Thursday. Might even take a longer walk and pay our local library a visit.
I think I may even make another appointment with my GP quite soon and have a good talk. Well discuss as much as we can in the 10mins that is allocated for each patient, might even ask receptionist if it is possible for me to have a longer appointment.
Good luck with your battle with this horrid disease.
Jen
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