coping with copd: I had COPD since 2006. It was... - COPD Friends

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coping with copd

Linlea profile image
10 Replies

I had COPD since 2006. It was very sever at that time and I was put on oxygen 24/7. I use a nebulizer and inhaler. I walk a little each day to keep the lung muscle strong. I am on 5 to 6 liters of Oxygen sitting and 7 to 8 moving around.. I can't handle heat or humidity well at all. And of course the winters in WY are so cold and I have to wear a mask in frigid temperatures and when the wind is blowing... I can't drive anymore and my travels are very limited.. I just take each day as a blessing and move forward. I do know without God in life I couldn't cope with it.

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Linlea profile image
Linlea
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10 Replies
Wi771am profile image
Wi771am

I use concentrator don't use oxy unless last resort,your body will get hooked on oxy

Linlea profile image
Linlea in reply toWi771am

I can't be without it. COPD to far gone. Can't breathe without.

Theresa-57 profile image
Theresa-57 in reply toWi771am

What is the difference in the two if I may ask?

glenda818 profile image
glenda818 in reply toTheresa-57

The concentrator supplies about 85% oxygen, so you are still breathing some room air. (Room air is only 15-20% oxygen.) when you use O2 tanks, they are giving out 100% oxygen, so your body gets spoiled to that increased good stuff.

Linlea profile image
Linlea in reply toWi771am

Your concentrator is oxygen just more convenient than tanks. I have a concentrator too..

lanesf profile image
lanesf

If I didn't have God I couldn't get by. God bless you

glenda818 profile image
glenda818 in reply tolanesf

Me, too, lanesf. Hope He's giving you a good day!

lanesf profile image
lanesf in reply toglenda818

My breathing was bad. I really shouldn't be on the reservation it was only bed open. I was able to get used jeans today. I have no idea why I didn't get $ from Bank before I left. Friday phone bill due and Mon June 20th I will be 54 thanks for your email

LORBIC profile image
LORBIC

If you aren't already you need to be under the care of pulmonary, they are the doctor's trained to treat this. Have you had a pulmonary function test done? For the heat and humidity I use fans but I know others have AC. I dislike it so much when cold weather comes and I have to turn on the heat. During the winter months my doctor has me on antibotics daily as I have almost constant flare ups. The antibotics help to make the flare ups less.

Linlea profile image
Linlea

Thank you . I have a couple of friends who sell the essential oils, I will check into them And yes I do the pursed lips breathing? I did pulmonary rehab for 18 weeks. I do the nebulizer 2 times a day with 2 meds in it. And have a long term dicus. My immune system is zero. If something is going around you can bet I'll get it. In March I had the croup and have been fighting infections ever since.

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