Posts Tagged oxygen

New to Oxygen

April 11th, 2012 | Author: COPD Coach

Dear Coach,

My doctor has told me that I need to be on oxygen 24/7. I work full time because I have to.  I am 61 and single and live alone. I work for an international Flavor/Fragrance company in the Customer Service Department. How do you approach your boss, Human Resources, and your colleagues that you need to have oxygen all day?  I have no idea how or exactly what to do.

I have to find out the best oxygen unit that I can get and bring to work (it would have to last approx. 9 to 10 hours).

Any help or suggestions or experiences you can offer would be greatly appreciated.

New to Oxygen

Dear New to Oxygen,

From portableconcentratorz.com

The problems you are facing are like many an individual with COPD might face. As far as approaching your boss or the Human Resources department, I would have your doctor draft a letter explaining that you require full time supplemental oxygen, as well as specifying any other accommodations you might require, such as access to elevators, closer rest rooms, the size of your work space, or even in your case a “fragrance free” work environment. Presenting the letter will also explain to your employer the necessity that you might require occasional time off for medical appointments or illness related to your COPD. Actually, having to use oxygen will probably lessen the time off you require and allow you to be more productive, which is a definite plus for your employer! There are laws that protect your right to work and expect reasonable accommodations, laws which your HR Department is probably very familiar with. If any problems come up, don’t hesitate to contact an attorney.

As far as explaining to your colleagues, I think that no explanation is necessary. When they see you using supplemental oxygen they should  pretty much make the connection  after noticing that you were getting out of breath. Hopefully they are aware that you have COPD. Some may come up and ask you about using oxygen. Just be open and honest and tell them that your COPD has advanced to the point where your require it. Your mention of COPD and use of oxygen might well prove to be a “teachable moment” for many of your fellow workers who are at risk for COPD! In any case, why be concerned or embarrassed – remind them that we all require oxygen….you just need a little more of it!

Your last question is a little harder to answer without knowing more about your work environment. No portable oxygen concentrator is going to have the kind of battery life you specify. This is especially true with continuous flow concentrators. Much will depend on the type of concentrator (pulse or continuous) that your doctor orders. There are pulse units that have a duration of 5 hours up to 8 hours. As far and continuous flow models, because of the volume of oxygen they must produce, most models only will get a couple hours in continuous mode. In either case, you can purchase extra batteries, however you don’t want to get into a situation where you having to carry several extra batteries along with the unit.

If your work allows you to be stationary, a possible alternative might be to purchase a home concentrator to use in the office, and only use the portable unit when you need to move around or to get to and from work. Also in this scenario, if you are able to plug in your portable unit to AC power for a substantial part of the day, you might eliminate the need to carry a lot of extra batteries.

As I am writing this reply, I am struck by what a friend once told me. “People with COPD can do about anything that anyone else can, they just have to plan a little more, and do things a little differently.” I feel like your letter is a good example of this. I am quite sure that working with your oxygen supplier and your doctor (and maybe including your employer), you will find a solution that will continue to allow you to be a productive worker.

Please let us know how you are doing, and if we can be of any additional help.

The COPD Coach

Ask the Expert is aimed at providing information for individuals with COPD to take to your doctor, and is not in any way intended to be medical advice.

If you would like to submit a question to the Coaches Corner email us atcoachescorner@copdfoundation.org. We would love to hear your questions and comments. You can address your emails to any of the following: COPD Coach, Caregiver Coach, COPD Doctor or COPD RT.

Do nasal prays help curb respiratory infections?

February 1st, 2012 | Author: COPD Coach

Dear COPD Doctor,

My husband, 72, has COPD and gets a lung infection about once every 30-45 days.  He then does 5 days of Azithromycin and recovers within 4-5 days.  My question is, I read that some sinus nasal sprays are shown to reduce bacteria in the sinuses and respiratory tract. Have you heard any information about or against this?  My thought is that this might be worth trying as he is hooked to oxygen 24/7 and uses the water bottle so his nose does not dry out, which I would think adds to a problem of having bacteria or infection breathed into his lungs.

–Sinus Sprays and COPD

Dear Sinus Sprays,

First of all, thank you for your nice comments on our website and the Coaches Corner. We certainly appreciate hearing that the information we share is helpful!

To answer your question, there is no data I know of that would indicate that nasal spray would lower the frequency of your husband’s lung infections,  but it likely would do no harm and might well be worth a try. He might also talk with his doctors regarding using Zithromax on a regular basis, perhaps three times a week, as an immune modulator. This therapy has been effective in decreasing the frequency of exacerbations.

From: www.hillaryblakeley.net

If you have not already done so,  make sure your flu and pneumonia vaccines are up-to-date. It is also very important that he stay away from anyone exhibiting symptoms of cold and flu.

I hope this helps, and please keep in touch!

Best regards,

The COPD Doctor

Ask the Expert is aimed at providing information for individuals with COPD to take to your doctor, and is not in any way intended to be medical advice.

If you would like to submit a question to the Coaches Corner email us atcoachescorner@copdfoundation.org. We would love to hear your questions and comments. You can address your emails to any of the following: COPD Coach, Caregiver Coach, COPD Doctor or COPD RT.

TSA Cares – a new helpline for travelers!!

January 31st, 2012 | Author: Fabiana Talbot

(taken from bing.com)

Exciting news about support for special needs travelers!  According to an official statement released by the White House, The Transportation Security Administration (TSA) has launched “TSA Cares”, a new helpline number designed to assist travelers with disabilities and medical conditions. Travelers may call TSA Cares toll free at 1-855-787-2227 prior to traveling with questions about screening policies, procedures, and what to expect at the security checkpoint.

How It Works

  • When a passenger with a disability or medical condition calls TSA Cares, a representative will provide assistance, either with information about screening that is relevant to the passenger’s specific disability or medical condition, or the passenger may be referred to disability experts at TSA.
  • TSA recommends that passengers call approximately 72 hours ahead of travel so that TSA Cares has the opportunity to coordinate checkpoint support with a TSA Customer Service Manager located at the airport when necessary.
  • Every person and item must be screened before entering the secure area of an airport and the manner in which the screening is conducted will depend on the passenger’s abilities and any specific equipment brought to the security checkpoint.
  • All travelers may ask to speak to a TSA supervisor if questions about screening procedures arise while at the security checkpoint.
  • The hours of operation for the TSA Cares helpline are Monday through Friday 9 a.m. – 9 p.m. EST, excluding federal holidays. Travelers who are deaf or hard of hearing can use a relay service to contact TSA Cares or can e-mail TSA-ContactCenter@dhs.gov.

What a great resource for those traveling with O2!  What are your thoughts on this new program?

(taken from tsa.gov)

Overcoming Challenges

October 21st, 2011 | Author: Katelyn Harding

Sheila Favazza was diagnosed with COPD in 1986 at the age of 38. Read more…

Will Exercise Improve my Oxygen Saturation?

August 24th, 2011 | Author: Katelyn Harding

Dear COPD RT Coach,

I know it is important to have a regular exercise program to improve breathing Read more…

Discrimination in the New York Times?

August 8th, 2011 | Author: Fabiana Talbot

Though most of us would like to think we live in an age of acceptance and tolerance, Read more…

The Changing Seasons and COPD

May 13th, 2011 | Author: Katelyn Harding

This blog post was written by Joanna Murray. Read more…

Oxygen Needs

April 18th, 2011 | Author: Katelyn Harding

This blog post was written by Joanna Murray. Read more…

Protecting Your Access to At-Home Oxygen

April 13th, 2011 | Author: Jamie Lamson

Beginning in January of this year Medicare changed they way that they pay for certain categories of services Read more…

TSA Guidelines: Traveling with O2, Etc.

January 19th, 2011 | Author: Katelyn Harding

The Transportation Security Administration (TSA) Read more…