COPD360social MenuToggle Dropdown Community Activity Feed Questions and Answers COPD Digest / Blog Community Exchange How to Participate FAQ Video Tutorials How do I win points? How do I win badges? Community Guidelines Statement of Rights and Responsibilities
Need Some Guidance Return to previous page 11/25/2018 1550 Views 2 Answers Last Activity: 1 year ago, Stephanie Williams, RRT Tags: o2 Question: 0 Annie119 2 years ago I Care Report Comment Unlike I Care Report Comment Add an Answer Answers: Edit Remove Accept Unaccept Unlike I Care Report Comment Add an Answer Save Cancel Need Some Guidance Annie119 2 years ago Add an Answer Answers Answer View More Save Cancel Tags: Subscribe: Subscribe: Your question has been submitted and is awaiting moderation. It is low-quality It is spam It does not belong here Other (enter below) Thank you for reporting this content, moderators have been notified of your submission. Close Anonymous Unfriend Friend Requested Friend Load More Close Destination Page Area Group Destination Content Title Title Article Type Copy comments Good Morning I am a caregiver for my 74yr old mother. She has COPD and stage 3A lung cancer. The COPD is the bigger monster right now. She was receiving chemo and developed a bad cough. It was rather glazed over at the oncologists and they simply gave her cough medicine..it turned into pneumonia. She was hospitalized for two weeks then into a horrible rehab that should not even be in business. I checked her out after 2.5 weeks and she is at her appartment now with home healthcare beginning and in home rehab starting this week. Her big O2 concentrator at home is set on 3. Her resting O2 level is between 88 and 94. As soon as she gets up with her walker to do anything(very small apartment) her O2 will drop to the low 70’s and even 69 yesterday, heart rate about 105. Her O2 rebounds within 5 minutes of sitting. We cannot seem to get any education on how to manage. They just tell us if we raise her oxygen level it will hurt her body with COPD. I am so scared for her. I cry constantly. I visit her twice a day and tend to everything she needs. She has an appointment with her oncologist Monday and a pulmonologist on the 4th of December. She uses Breo once a day and albuterol as a rescue inhaler. She does have a nebulizer, but needs a new one so hasn’t used one since the hospital. Can anyone give me some guidance in the meantime or some positive words? Her dr immediately started talking about end of life and hospice and my mother isn’t there yet and it does more damage to our psyche than it helps. Thank you very much.
COPD360social posts are monitored by Vice President of Patient Experience and COPD360social Community Manager, Bill Clark, as well as staff Respiratory Therapists.
COPD360social MenuToggle Dropdown Community Activity Feed Questions and Answers COPD Digest / Blog Community Exchange How to Participate FAQ Video Tutorials How do I win points? How do I win badges? Community Guidelines Statement of Rights and Responsibilities
Join Us on COPD360social Join the Conversation Become a Member > Already a Member? Sign In to Participate >
Related Content Day 1-Follow-up 3 Low sats while lying down... but not asleep? Oxygen Saturation Levels - how much of a concern? Does anyone use an in line swivel on their O2 tubing? What causes SOB, yet O2 >94%? Have you Considered an O2 tube clip? Which is better, a POC or B size tanks? Oxygen settings while exercising Oximeter Want to learn more about O2? Looking for a POC? Are there concerns w/O2 and hand lotion? Fear of O2 dependency Any Tricks for Transitioning from BiPAP to O2 Canula? Home Hospice - Your Experience
Medical Advice It is not our intention to serve as a substitute for medical advice and any content posted should not be used for medical advice, diagnosis or treatment. While we encourage individuals to share their personal experiences with COPD, please consult a physician before making changes to your own COPD management plan.