I don’t know how you are but sometimes the obvious is not at all obvious to me. I use a CPAP machine faithfully and have for several years. Honestly, I do not sleep well at all without it. With that said, I never thought about what I would do if I didn’t have it available or if I lost it.
Recently I had a small stroke. My main concern was taking two baby aspirin and getting to the emergency room. I did grab my phone and charger (like any wise person would) and my insurance card but that was all. There was a flurry of activity in the ER; explaining my symptoms, inserting an IV, going for a CT scan and talking with a neurologist about taking the TPA clot busting shot. Before I knew it, they were transporting me by air ambulance to another hospital. There I had another CT scan, was taken to ICU and was pretty much out of it. Thoughts and words were there—just very slow.
My family got there only to be told that I needed silence and rest. Before they left they asked what I needed for the next day and I told them nothing yet. Here’s where the first obvious need wasn’t obvious to me. I didn’t have my CPAP. My family knows I need and rely on that machine but they didn’t think about it either. In fact, I didn’t think about it until almost midnight when it hit me that another reason why I was so restless and uncomfortable (besides nurses coming in to poke and prod) was that I wasn’t using my CPAP. In fact, my lovely CPAP was almost two hours away!
Fortunately, the hospital was able to get one for me to use. Unfortunately, it wasn’t MY machine or MY mask. It didn’t fit well and the humidifier was set too high. It made noises mine didn’t. The hose was too long and got tangled in my IV lines. Plus, I knew it would be one more expensive expense.
Even more recently, we took some time off to regroup and restore by taking a trip with our camper. I made sure to take my CPAP along and all was going great until a storm hit and we had to evacuate the camper. Again, I grabbed my phone and charger. Silly me. Once we were safe, I remembered my poor machine left behind in the camper, sure it would be blown away to Oz. It wasn’t and all was well except again the obvious was not obvious to me. Here are the obvious things I intend to do for the future:
The same moon shines over us all,
Ruby
The blog by Ruby was very informative. I've known for many years that I have Sleep Apnea. During one of my five hospital stays this year I was diagnosed with Sleep Apnea. I sleep against a wedge pillow to keep my head above my heart. I have a significant list of other life threatening medial issues that have taken priority for treatment. Other issues include Heart Failure and Stage IV Kidney disease.
While I was scheduled to receive a CPAP machine the vendor could not bring the machine when I was not working, and I'm concerned about infections arising form the use of these devices. Deductibles and Co-Pays for my five hospital stays are paid for by my part-time work. I've lost a significant number of hours due to hospitalization and recovery at home this year.
I've been trying to get my PCP to write a script for O2, but have not been successful. My oxygen saturation is typically in the upper 90's, but I oftentimes struggle to catch my breath during bending, light exertion or lying down due to fluid movement. I take strong diuretics that turn my body into a urine factory especially when I'm lying down. Due to the diuretics I have doubts as to what sleep benefit I would receive from the use of CPAP machine, and information provided in these blogs demonstrate a number of troublesome issues related to these devices.
If there are others who have Heart Failure or other significant heath issues who are benefiting from the use of a CPAP machine I would welcome their input.