Monday, January 28, 2013

Sometimes, All I Need is the Air That I Breathe



A few weeks ago, (the night of December 26, in fact), I had posted a status on Facebook that I was ensconced at the Courtyard Hotel in Farmington, wired up like an astronaut (or maybe a lab rat) for a sleep study. I haven’t said much about it since then and for anyone who cares, here’s the whole story.

Sometime in late November, Joy couldn’t sleep one night. She was awake in bed reading while I lay blissfully unaware, asleep and snoring. [Let me digress a moment and tell you that my father had one of the worst snoring problems you can imagine. How my mother put up with it I have no idea. It was so bad that it reached the degree of sounding like snoring you’d hear in a cartoon or Three Stooges movie. I’m not that bad but apparently I, too, snore.] Anyway, there I was, sleeping and snoring…until I stopped snoring. Joy noticed that not only was I not snoring, I wasn’t breathing. She started counting and when she got to twenty or so, she shook me and told me to roll on my side. [Another digression. Joy, prior to her weight loss surgery, had been diagnosed with Obstructive Sleep Apnea. In her case, she was in the passenger seat with her mother driving and she dozed off. Her mother, a retired nursing instructor, noticed that she was periodically stopping breathing. A sleep study or two later and she was diagnosed and had to sleep with a CPAP (Constant Positive Air Pressure) machine that forced her to keep breathing by keeping the air passage open while sleeping. She has not needed it since the day after her surgery. This is a long way towards saying that she knows a thing or two about sleep apnea.]

After that experience, she told me that I had to call our primary care physician. I called and left a message. I was home from work by the time he called. When I told him what had happened, he started asking about my observations. I told him that since I was sleeping, I had no observations but Joy could tell him what she had observed and I handed the phone to her. The first thing he said to her was, “Congratulations, you may have saved your husband’s life.” After they talked for a while, she handed the phone back to me and he said that he was going to order a sleep study for me ASAP.

ASAP turned into three weeks, not because the sleep lab was tardy. No, they called the day after and got me scheduled ASAP. But a bad cold that segued into a sinus infection and bronchitis forced me to postpone it. I scheduled it for December 26. Of course, that day, it chose to snow. Not a nice, fluffy, powdery, man is it cold out snow. No, it was a just under freezing point so it could snow but be heavy and sticky and messy snow. But there I was at the Courtyard where the sleep lab was located (and getting there was a real skid-fest). The technician (who came from a much farther distance than I did, was SO happy to see me. Everyone else scheduled that night had canceled.

So, after being wired up, I climbed into bed around 9:30, watched TV until I felt sleepy and turned off the light around 10:15. The technician woke me up (I later discovered around midnight) to tell me that I had stopped breathing and that she needed to put a CPAP on me. I slept the rest of the night with it. When the technician woke me up, she told me that I did have several episodes of sleep apnea. At one point my oxygen saturation had dropped to 75%. (A 6% drop is considered an “episode” so 25% is significant. Before I left she asked me if I wanted to take the CPAP mask I had used with me. I declined and said I was going to hope for the best.

January 1 we left for our cruise, returning January 13. While we were away I had gotten a call for me to make an appointment for the follow-up to get the results. I made the appointment, expecting the worst. It turns out it was NOT the worst. I only have moderate obstructive sleep apnea, not severe. It seems that at the worst, my oxygen saturation had dropped to 68%, dangerously low. That was what prompted the technician to put the CPAP on me. I had averaged over thirty “events” an hour. That means I had stopped breathing on an average of once every two minutes without the CPAP. Bottom line: Despite my optimism, I need to sleep with a CPAP.
I started looking around on the Internet about obstructive apnea and a lot of seemingly disconnected things started falling into place. First off, I wondered how I had developed it. I’m somewhat overweight 
but not obese. I found this list of risk factors:

·                   Being male
·                   Being overweight
·                   Being over age 40
·                   Having a large neck size (17 inches or greater in men and 16 inches or greater in women)
·                   Having large tonsils, a large tongue, or a small jaw bone
·                   Having a family history of sleep apnea
·                   Gastro-esophageal reflux, or GERD
·                    Nasal obstruction due to a deviated septum, allergies, or sinus problems

With the exception of the neck size, I had all the risk factors. It also seems that the reason I woke up most mornings with a headache can be traced to the apnea. They’re not sure what the connection is but seems undeniable. Apnea also leads to hypertension and high cholesterol. My blood pressure has been higher than I would expect and I am on cholesterol medication even though my diet is not horrible. The negative pressure created by not breathing can cause stomach reflux, something that has occurred a number of times in the past year. Another symptom is being constantly sleepy during the day. Any chance I got I would take a nap…or simply doze off.
Something that happened a number of times, although not in the last 25 years or so was that on several times, I would wake up and be paralyzed from the neck down. It would take several minutes for me to be able to move. I had concluded that the reason for this was that I had been sleeping in a certain way and that I must have pinched the nerves or spinal cord at the level of my neck. What I have, since, learned is that when we are in REM sleep, the brain shuts the body down so that we do not “act out” our dreams. There is a form of sleep disorder where REM sleep is interrupted and the sleeper awakens before the brain has restored motion to the body. Although this hasn’t happened recently, it placed me on the sleep disorder spectrum long before apnea.
What my doctor meant by telling Joy that she had saved my life is very simple. Obstructive sleep apnea has been linked with increased risk of stroke, heart attack and type-2 diabetes. The stress that lack of oxygen places on the heart weakens the heart. The increased risk of cholesterol leads to plaque build-up. Although a good diet and regular exercise are still necessary, addressing the apnea decreases the risk factors significantly.
I saw the sleep doctor on Monday. On Wednesday I got a call from the medical device provider and made an appointment for the following day. That morning, I went to get checked out on the CPAP. It’s actually rather small and comes in two pieces, the air pump and the humidifier. The mask they had selected for me is not so much a mask as a thick oxygen cannula. The plugs that actually blow air into my nostrils act as seals to prevent the air intake from leaking. [Yet another digression: The way a CPAP works is it provides a constant flow of oxygen (the constant positive pressure part). It forces the airway to remain open when you’re sleeping which prevents the throat from closing up and causing apnea. Therefore, a tight seal of the mask is crucial.] I sat with it on for about ten minutes and had no problem. So, off I went with my new device.
I found myself being fairly depressed and could not place a finger on what had occurred to make me depressed. We had just gotten home from a great vacation. In general I have been feeling good. After doing a bit more reading, I put it together. I was grieving. Life as I had known it had irrevocably changed. I will have to use a CPAP for the rest of my life. Every night for the remainder of my life, I will need the assistance of a mechanical device to be able to sleep properly and not starve my body of oxygen. Intellectually, I have accepted that reality. Emotionally, I am still struggling with it. But the success that I have had with it has been very encouraging. I don’t have headaches when I wake up. I sleep better and more restfully. Joy tells me that I am not as restless in terms of changing positions as I had been and don’t snore anymore. I’m not sleepy during the day and my general outlook on life has gotten better. Will the positive changes last? Only time will tell. I know I still need to get off my butt and get some exercise and I’m hoping that my endurance will have increased thanks to getting more and better sleep.

Unlike many people I have encountered on on-line CPAP forums, I have had no problem sleeping with the mask. Part of that may be that it is not really a mask. But that may only be part of it. I have never had a problem falling asleep. It’s almost a joke among family and friends that if I’m sitting in the same position for five minutes, I’m probably asleep. So the physical adjustment has been the least of my problems. And if I have to be tied to this thing the rest of my life, I guess it’s not that much of a price to pay for the benefits. So, sleep well, everybody, and if you’re NOT sleeping well, find out why.