Has anyone out there lost access to their liquid oxygen system? How did that loss affect your quality of life? We're looking for a few stories to add to a project that the American Lung Association and American Thoracic Society (among other groups) are driving to get the Medicare program to take another look at this kind of therapy.
If you're willing to share your story for the project, please let me know either here or at mhess@copdfoundation.org so that we can discuss further. Thank you!