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COPD and the Coronavirus - recommendations, concerns, advice
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Courtney_J
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Courtney_J
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Last activity on 08/08/2022 at 11:09 AM
Joined in 2020
1,340 comments posted | 30 in the COPD Forum
6 of their responses were helpful to members
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@MJones99 Hello MJones99, thank you for your comment. I think many members are also worried about this. We just published an article on COPD and the coronavirus, I think you may find it helpful:
Everything you need to know about COPD and the Coronavirus
I hope it answers some of your questions!
Take care,
Courtney
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Courtney_J, Community Manager, Carenity US
MJones99
MJones99
Last activity on 02/09/2022 at 1:15 AM
Joined in 2020
I am really upset I tried to get unemployment but got denied and cant get thru to find out why. The only reason I am not working is because of my copd and this damn virus. Why cant people get help. Sorry to lay this all out but just very frustrating.
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Michelle Jones
Lillyw
Lillyw
Last activity on 05/01/2020 at 6:22 PM
Joined in 2020
@Courtney_J keep calling the police. That's what they are there for.
Lillyw
Lillyw
Last activity on 05/01/2020 at 6:22 PM
Joined in 2020
@Lillyw sorry wrong person.
Lillyw
Lillyw
Last activity on 05/01/2020 at 6:22 PM
Joined in 2020
@Lillyw I'm learning to do this posting thing. I have copd and scared of the virus. I live with someone who just doesn't care. I isolate to my bedroom most of the day and night. Going crazy.
Courtney_J
Community managerGood advisor
Courtney_J
Community manager
Last activity on 08/08/2022 at 11:09 AM
Joined in 2020
1,340 comments posted | 30 in the COPD Forum
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Hello everyone, it's been a few days since we've checked in on one another. How are you doing? Is the lockdown getting to you or are you managing to stay busy and positive?
@hmccu2224 @deborah72164 @Gingerghent @ConnieH @zoobiedo @Health2020 @dlmcmahill @shayes18
Take care,
Courtney
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Courtney_J, Community Manager, Carenity US
mrmiles
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mrmiles
Last activity on 05/05/2020 at 10:34 PM
Joined in 2018
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@Courtney_J I'm doing ok. I'm retired now so I haven't been at work like many people here. Staying positive and avoiding everyone and everything as much as possible! I wouldn't want any of us to catch it with our condition. I've heard it has lasting impact on the lungs, so with mine in such a rough shape already I don't know what it would do to me. But anyway, I've been staying safe at home and will still be doing that when the lockdown is lifted in my state until I feel like things are getting better. I've been working through my pile of sudokus and NYT crossword puzzles to pass the time. Stay safe everyone!
copd_healing
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copd_healing
Last activity on 07/03/2020 at 4:18 PM
Joined in 2018
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@Courtney_J I'm doing alright. I haven't been on here in a while and all that's going on has kind of brought me back. I'm supposed to go back to work next week but I'm trying to negociate with my team head to let me telework because of my condition. What is everyone doing about the end of the lockdown in your state? Are you going back to work or are you still working from home?
Courtney_J
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Courtney_J
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Last activity on 08/08/2022 at 11:09 AM
Joined in 2020
1,340 comments posted | 30 in the COPD Forum
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Hello everyone?
How are you today?
How are you managing your COPD now? Is it more complicated this time of year? Have you returned to a "normal life" after these few months of lockdown?
Feel free to share! We are all here to help each other!
Take care,
Courtney
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Courtney_J, Community Manager, Carenity US
LynninTx
LynninTx
Last activity on 08/10/2024 at 7:06 PM
Joined in 2020
Hi everyone. I have been social distancing. Doing a little walking and also Dr. started me on new meds. So far Ive been able to get off my oxygen during the day. I still sleep with it but I am feeling some better. Prayers for you all!!
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CarolSchmidt
@KathyA, please read what I wrote above on using oxygen. I am so, so, thrilled to have portable oxygen that gave me more of my life back. I was told in 2011 when I lived in San Miguel de Allende at 6,400 ft altitude that I needed to go on oxygen, but all I saw around town was one woman with the heavy metal canisters in a cart behind her, and that looked terrible. I moved back to near sea level and put off needing oxygen all day for another seven years, just a Bipap at night.
Finally I was huffing and having to stop every few feet even near sea level, but I still didn't want to be lugging a heavy canister behind me. I ran into an old friend who was always really active, ballroom dancing, hiking, fly fishing in rivers. And there she was with an Inogen in a backpack, doing everything she'd always done!
She showed me all about hers and the total package with machine, extra 8-hour battery, two battery chargers for house and car, carrying case, and extended warranty, was around $3,300!
Finally I saved enough for it and have loved it every minute since. I started on 2 for almost a year but had to go to 3 for every day. I switch to 4 liters a minute several times a day when I still get winded bad, and have gone up to 5 for stair climbing. I worry that I will need to go higher than 5 eventually, but I hope by then there will be sronger machines developed that go higher, though then the $500 batteries only last a few hours before needing recharging, instead of 6-8.
The portable ones now are breath-operated--you have to be breathing into the nose cannula for them to work. And my BiPap at night requires continuous flow, which the big oxygen machine Medicare covers provides, so I need both machines. Some day they may all be continuous flow and still portable.
There are cheaper, refurbished units available from the Inogen factory, too. After 1 1/2 years mine started sending strange messages and I called the factory and they sent a new one out the next day! I sent them the old one back no charge. So I am pleased with service, too.
Hope this helps you accept your machine. I am so, so happy I got mine and wish Medicare paid for everyone who needed one.(I understand in a few cases they will pay for one now, but not my particular Cigna Medicare Advantage plan.)
I bet when you go to your reunion you won't be the only one on oxygen! And everyone will be so old! The ones who are already dead and not there are the ones to think about--how many of them had COPD? Fourth leading cause of death in the US before Covid, so now we're fifth. Be glad for all the help you can get! I hope you have a wonderful reunion!
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cbholder3
@Thakera Yes, even on Medicare it was $400+ a month. My Pulmonologist arranged for me to get it with no copay from GSK, GlaxoSmithKline, you can look up their assistance program at https://www.gskforyou.com/ Hope it goes okay for you, I am just in the process fo renewing mine for next year.
GSKForYou | GSK Patient Assistance Program
Learn how our program can assist you if you need help paying for your GlaxoSmithKline prescription medicines and vaccines, whether you have coverage or not.
See the best comment
CarolSchmidt
@KathyA, please read what I wrote above on using oxygen. I am so, so, thrilled to have portable oxygen that gave me more of my life back. I was told in 2011 when I lived in San Miguel de Allende at 6,400 ft altitude that I needed to go on oxygen, but all I saw around town was one woman with the heavy metal canisters in a cart behind her, and that looked terrible. I moved back to near sea level and put off needing oxygen all day for another seven years, just a Bipap at night.
Finally I was huffing and having to stop every few feet even near sea level, but I still didn't want to be lugging a heavy canister behind me. I ran into an old friend who was always really active, ballroom dancing, hiking, fly fishing in rivers. And there she was with an Inogen in a backpack, doing everything she'd always done!
She showed me all about hers and the total package with machine, extra 8-hour battery, two battery chargers for house and car, carrying case, and extended warranty, was around $3,300!
Finally I saved enough for it and have loved it every minute since. I started on 2 for almost a year but had to go to 3 for every day. I switch to 4 liters a minute several times a day when I still get winded bad, and have gone up to 5 for stair climbing. I worry that I will need to go higher than 5 eventually, but I hope by then there will be sronger machines developed that go higher, though then the $500 batteries only last a few hours before needing recharging, instead of 6-8.
The portable ones now are breath-operated--you have to be breathing into the nose cannula for them to work. And my BiPap at night requires continuous flow, which the big oxygen machine Medicare covers provides, so I need both machines. Some day they may all be continuous flow and still portable.
There are cheaper, refurbished units available from the Inogen factory, too. After 1 1/2 years mine started sending strange messages and I called the factory and they sent a new one out the next day! I sent them the old one back no charge. So I am pleased with service, too.
Hope this helps you accept your machine. I am so, so happy I got mine and wish Medicare paid for everyone who needed one.(I understand in a few cases they will pay for one now, but not my particular Cigna Medicare Advantage plan.)
I bet when you go to your reunion you won't be the only one on oxygen! And everyone will be so old! The ones who are already dead and not there are the ones to think about--how many of them had COPD? Fourth leading cause of death in the US before Covid, so now we're fifth. Be glad for all the help you can get! I hope you have a wonderful reunion!
See the best comment
cbholder3
@Thakera Yes, even on Medicare it was $400+ a month. My Pulmonologist arranged for me to get it with no copay from GSK, GlaxoSmithKline, you can look up their assistance program at https://www.gskforyou.com/ Hope it goes okay for you, I am just in the process fo renewing mine for next year.
GSKForYou | GSK Patient Assistance Program
Learn how our program can assist you if you need help paying for your GlaxoSmithKline prescription medicines and vaccines, whether you have coverage or not.
See the best comment
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Courtney_J
Community managerGood advisor
Courtney_J
Community manager
Last activity on 08/08/2022 at 11:09 AM
Joined in 2020
1,340 comments posted | 30 in the COPD Forum
6 of their responses were helpful to members
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Hello everyone,
Patients with chronic respiratory diseases such as COPD are part of the population at risk of complications from Coronavirus infection. It's really important to follow recommendations and guidelines published by the CDC and other health organizations in order to best protect ourselves from infection.
Feel free to consult our two recent articles on the coronavirus and chronic illness for more information:
Coronavirus: What do you need to know?
Coronavirus and chronic illness
I've created this discussion so we can ask any questions or concerns about the current pandemic or just generally share our feelings about what is going on.
Have you consulted the recommendations? Who informed you first: you doctor, your pharmacist, a relative? Have you been taking any particular precautions? Have you been self-isolating? Do you have any advice for others?
Take care,
Courtney
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