So the idea behind this second test was to try out a mask and see if the CPAP helps. With the obstructive apnea they're usually able to use the continuous air pressure to keep the airway open. They just have to find a level of pressure that works, program a machine, and you're good to go. She said that the central is where it gets tricky. Until they try it out, there's no telling what kind of help the mask will be. I did learn that there are actually three different kinds of masks. The CPAP is the continuous positive air pressure. I don't remember what the other two are called, but one of them has two different levels of pressure. One for when you're inhaling and a lower pressure when you're exhaling. The third kind is super smart (which to me says super expensive) and can actually tell what type of apnea you're having then adjust itself to do whatever you need right then. Who knew?
She couldn't tell me much in the morning since the doctor still has to review the test, but she said she thought I did better on the mask and that my apnea was tricky. She had to do a lot of adjusting and just when she thought I was at a good level I would apnea again. I have a couple of weeks before I can expect that test to be at my doctor's so until then, there's no telling what the plan will be.
Now for the experience. Ugh. They put a ton of things hooked up to wires all over your head and on your chest and back and face and legs. They use this horrible gluey goop in your hair that does not come off unless you put your head under super hot water for like 20 minutes. But that's not the worst part. The first test they had what looked like an oxygen nasal tube up the nose AND a little wire thing up the nose. So I felt like I couldn't breathe the whole time. This go round they put on the mask that had "pillows" that plug into your nose to push the air up into it. If you open your mouth the air comes right on out. It's the strangest sensation and I had a hard time talking when she asked me a question. Then throughout the night they would adjust my levels of air pressure. When I would stop breathing it would fill my mouth with air and I'd wake up spitting out air. It's hard to describe. I also had a hard time breathing out when she turned it up higher so I felt almost like I was suffocating on too much air. Again, hard to describe, really strange, and hard to envision getting used to it enough to actually sleep every night.
| Pre-mask Jeff said I look like a robot and I'm inclined to agree |
I definitely didn't wake up rested. In fact, I went home, got the goop out of my hair and went back to sleep for another 5 hours or so. I really hope this is the last time I have to do this. I can't see how this gives all that accurate of a reading considering I can't sleep the whole night. But modern medicine has come a long way and it must be accurate enough.
Despite the testing, I've still been trying to do those tips to help with the fatigue. The one I've done the worst on is the waking up the same time every day. I definitely need to work on that. I have done a little more exercising though. I started doing a little 20 minute yoga video every couple of days. Do You Yoga has a 30 day challenge on You Tube and I've loved it so far. It's enough to get me stretching but not so intense that I want to die. Just great for beginners. I've also tried to ride a bike or a horse or something a couple of times a week. My next goal is to take a short jog with my dog. Hey that rhymes! She's doing well running beside the bike with Jeff so I think she'll do well jogging. In fact, earlier this week Jeff took one of the horses out so I tagged along with the dog and ran around the park a little with her. She did well so I'm hopeful this will make me want to exercise a little more. I figure the exercise is good on a couple of levels. Not only should it help a little with my energy level but it will also get my heart in better shape to deal with the apnea. It's just my own theory but it makes sense to me.
I've also been working on doing a little bit of housework every day. I've tried not to get too crazy when I feel good so I don't hit the wall of sleepy too hard, but to still get something accomplished whether I feel good or bad. I have a long way to go to get my place looking like a human being lives there but I feel a lot better about myself when I do even just that little bit. I've also been going on a 15 minute walk during my lunch break once a week or so. It's quite refreshing for the mind and gets the blood flowing.
I haven't really noticed a change in my energy level yet but I know I need to take the small victories and not expect too much too fast. To be continued...




