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Do you have experience with Halo / Salt Therapy?
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restless98
restless98
Last activity on 07/21/2019 at 4:18 AM
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6 comments posted | 6 in the COPD Forum
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Hi there! I tried it in Colorado. I purchased a Himalayan salt lamp and that has worked well in allowing me to sleep without waking up every few hours coughing up mucus. I have read other places that there are man made salt caves; however I have not been able to get to any of those and speak to that. But the lamp has helped me sleep better and getting some needed rest.
As always, I would speak to your doctor if you are considering trying anything new.
cr90931!
cr90931!
Last activity on 06/15/2020 at 7:08 PM
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13 comments posted | 13 in the COPD Forum
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I did it here in Florida about 5 times. Overall, I feel like I had minimal positive effects in my ability to sleep and feel energized, but I still had a horrible cough and it was and still is hard for me to breath.
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I do not cough,mi problem is shortening of breath,usé ingelers ,oxigen can not do nothing outside without been conectes to oxigen .I have a salt lamp I will tray.
giggles
giggles
Last activity on 01/16/2022 at 9:54 PM
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7 comments posted | 2 in the COPD Forum
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hi.
what does everyone do for treatments for copd.?
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I'm on a Trilogy inhaler and I take a drug called Dalaresp that has done wonders for breaking up mucus and controlling cough.
Lee__R
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Lee__R
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Last activity on 04/03/2020 at 5:04 PM
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@Barbeesu what is the difference between the Trilogy Inhaler vs other inhalers? Do you feel this inhaler offers more benefits?
@Barbeesu @giggles and @Maria22
Have you ever tried salt therapy? Depending on your location, you can see if there are any places offering it close to you. You can visit this link to find a salt therapy (halo therapy) location in your state: https://www.vtsaltcaves.com/us-salt-caves
Some have found it to also be an effective option for relieving symptoms of COPD, resulting in easier breathing.
According to the Lung Institute: "Salt therapy proponents claim that salt cleanses the respiratory system and speeds up the elimination of toxins. Salt has the following properties: Antibacterial, Anti-inflammatory, Loosens excessive mucus and speeds up mucociliary transport, Removes pathogens (ie., airborne pollen), and Reduces IgE level (immune system oversensitivity).
Salt particles penetrate deep into the lungs to treat damaged tissue. Sometimes symptoms subside for up to 12 months following salt therapy."
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emphman
emphman
Last activity on 07/21/2019 at 4:33 AM
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15 comments posted | 11 in the COPD Forum
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@Barbeesu What did your pulmonologist say about the salt therapy? I wish there was a location near me, just to try it out... the science behind it makes sense.
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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
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
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brthfree
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brthfree
Last activity on 12/24/2023 at 10:47 PM
Joined in 2018
16 comments posted | 14 in the COPD Forum
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Hello,
Has anyone tried, or know of anyone who has tried, halo therapy (also known as salt therapy) for COPD? If so, any beneficial results?
Thank you.