|
Just Between Us -
"To" COPD'ers ....with Love and Understanding...... Prior to publishing this web site, I asked a few folks living with COPD to write and say something directly to you. These are individuals whom I have met these past few years on line and for whom I have tremendous respect. They have helped me, by their knowledge of the disease, sharing of same, and more than anything, their friendship and understanding... I PROUDLY introduce them (NOTE to the reader. COPDer's refer to their lung function capacity by their FEV1 number)
From John O To You
"I have lived with COPD for 27 years."
As a child I was never what you'd call in great health. I was
underweight, had asthma and allergies (which no one really knew how to
treat back then) and was just generally sick a lot more than the average
kid. My parents were both heavy drinkers and smokers, two habits I was
all too happy to get into when I reached my teens. I was smoking more than
two packs a day, often lighting one from another, until, at 36, I was
inspired by my brother, who had quit, to follow his example. And did, cold
turkey, before the gum and patches and other aids had made their
appearance.
Even quitting at that relatively young age (this was in 1974) it
wasn't soon enough. Added to what I think some day will turn out to be
genetic markers for COPD I was already having symptoms of sob, which I
routinely rationalized and denied (didn't everyone in their late 30s get
out of breath climbing stairs, or playing sports?) Six years later, in
1980, I had some chest tightness and went to a doctor. He (he was about
80) took an x-ray and told me that other than "a little emphysema" I was
fine, not to worry.
I was shocked. What did he mean, "a little emphysema"? And not to
worry about it. I didn't get much sleep that night, and the next morning
started calling around for a second opinion. The next doc was a
pulmonologist (the first guy hadn't been) and correctly told me I had COPD,
explained what it was, told me it was incurable but manageable, and
prescribed an Alupent inhaler, an early version of albuterol. Said to
check back with him. I kept this doctor for the next 22 years. Meanwhile
my breathing got seriously worse, and to this day I don't know why. But
after trying Atrovent, Vanceril, theophylline, and finally the dreaded
prednisone, by the end of the year I was in the hospital, with the usual
IVs antibiotics and steroids. Maybe it was pneumonia--I don't really
remember. Thing was, I was really bummed out. At 43, even after doing the
right thing by quitting smoking, it seemed like my life was just about
over.
But here's the amazing thing: for the next 15 years, except for
the occasional head cold, I was never sick. And though I had an
exacerbation,
treated at home with antis and pred, in 1995, after that, until 2002, I
was mostly OK, and lived an active life, traveling, working and enjoying a
variety of activities. COPD didn't keep my wife and I from traveling, to
most of the US and all the Canadian provinces, in the late 90's.
But then I got sick in that
same year (2002), and went to the hospital, and
again, twice, in 2003, and again in 2004 and 2006, all hospital stays, as
well as numerous exacerbations in between. As recently as the summer of
2001, I was hiking in the Canadian Rockies with just a pocketful of
inhalers. SOB (shortness of breath)? Sure, but manageable. And now
this--O2 around the clock, pred (prednisone) most of the time, I even had
Levaquin break my Achilles tendon in '03, and couldn't really walk for
weeks.
By that time I was in my mid-60s--how to explain this radical
decline? I came to the conclusion that I was thoughtlessly exposing myself
to germs and that as I got sicker my immunity to the diseases that the
germs carried got whittled down--a vicious circle. Example: my wife and I
volunteered in the public school system, putting on programs during the
school year, many of them in the wintertime.
I'll put it in the words of a nurse I had: "You were around
hundreds of small children. In a public school. In the winter....
Hello!!!" This is just the worst of many examples. After getting junked up
for months in the early part of 2006, ending in yet another trip to the
hospital, I decided to simply avoid many situations involving any real
numbers of people. That meant giving up the gym and working out at home;
going to movies and other events at non peak times. Same with shopping. But
here's another important thing: no doctor gave me any of these tips. I
got them from other COPDers on online forums. Sharing experiences with
others who have been through the same things I have has helped me deal
with the disease immensely.
Today? It's been 15 months since I've been in the hospital or had an
exacerbation, and almost a year since I've had any prednisone. I feel
better than at any time since '03 or so, and just turned 70. I
live an active life,
taking my LOX portable whenever I go out. I publish a newsletter in my
neighborhood and am learning to play the piano. The forums have showed me
by the examples of many of their members that
life is not over because of COPD, even
if you're getting older. Keeping
active with a daily exercise program will go a long way to
creating a positive attitude; and the attitude, in turn, keeps me part of
the larger world around me. I try not to dwell on the fact that I have
COPD, but I don't forget it either, and the adjustments one needs to make
with it, and that I've had to make through trial and error for the last 27
years.
You CAN do this too. But; you've got to want it. I hope you will.
John O.
With Love From WendyCO.... "When I first found out I had COPD my FEV1 was 34%, now it's 20%.It’s been almost 10 years ago that I was diagnosed with this disease COPD. I never had heard the word before and sure didn’t have a clue what it meant other than the fact I thought I might as well curl up into a ball and die. It took me a while to believe deep down that this was not a death sentence, that I could live a “good” life…and I do…..maybe not as active as I once was but I am still around to enjoy my kids and grandkids, and the seasons, and the holidays, and the sunsets, and the sunrises and the birds flying and the chatter of friends, and the sound of rushing water while hiking.....and all the things I may have done before but now a little slower……I could have listed so many things but hopefully you get the idea….Life goes on and so do you. I work a little harder at exercise than before and it truly can take my breath away LOL, but it also gives me the strength to breath easier…. If I could only give one piece of advice it would be to learn all you can and listen to what everyone with the disease has to say…sort through it and find what works or you and throw out the rest of it…. And while on this journey of life, don’t forget to live! From LindaMT My story: You can still have
a very good quality of life.
|
|