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  • Writer: Erin Spineto
    Erin Spineto
  • 2 min read

Three? Three at a time? Really? Three? Didn’t they learned in Kindergarten like the rest of us that’s it is the polite thing to take turns.

I could even have handle two of them at a time, but three? Why couldn’t it be that when the bronchitis wants a turn the diabetes politely says, “Oh, Bronny, you haven’t had a turn in a while, and I’m getting sick of this rain. Why don’t I take a little vacation to the Bahamas and you can have your turn with Erin.”

That way, when I have to take the steroids to return my lungs to the working condition, my blood sugars would remain stable instead of them climbing so high and being so unreasonably determined to remain that way. And when I have to stop exercising because my lungs no longer work it won’t cause my body to be resistant to the very insulin I need to stay alive.

And when my thyroid wants to join in on the party he would say kindly to Bronny and the diabetes in some haughty British accent, “Bronny, Tess, would you two mind considerably if I were to take a go with her. I have learned much from watching the both of you in your differing assaults on her health and would love the opportunity to try my hand.”

They both would acquiesce and be off. And while they are doing such a good job being so polite, possibly they could post a sign on the door that would elegantly deny access to my family from any other sort of illness that was hoping to take up residence.

As if its not hard enough to deal with a “very bad case” (said tongue firmly planted in cheek) of Diabetes, bronchitis so bad that to blow the propeller on my son’s remote control helicopter almost causes me to pass out, and a thyroid that has decided no longer to listen to its regulatory inputs and instead produce copious amounts of hormone whenever it feels the desire, I have a daughter with a stomach ache so bad to keep her out of school for a couple of days and a husband who has come down with a chest shaking cough only days before his biggest triathlon of the year.

So maybe I should bring that exasperated cry up to Five? Five at a time? Really? Five?

  • Writer: Erin Spineto
    Erin Spineto
  • 2 min read

The details of this illness and how it has been shaping my life for the last two years are long and dull, so I won't bother with a list of all the ways it sucks to be me right now, except to mention that it is a very weird place to be when none of your emotions are actually tied into reality.

My thyroid's got my limbic system all screwed up so that feelings come drifting through me with no stimulus and no connection to what is really going on outside, and they are getting more and more unreasonable. (The docs say this thing can actually make you clinically insane).

I was driving up to Orange County the other day and it was finally quiet in the car for a moment and I'm looking out the window, round about Camp Pendelton, and I notice two red cars. They start to form this momentary attachement in my mind. A few seconds later I start noticing a couple other red cars, so now there are five.

And they are shifting their location relative to one another, nothing major, not even a lane change, just that the one in the front is slowing a bit and the fourth one has closed in on the bumper of the third. I notice that they are all a slightly different shade of red and this frustrates me and taunts me.

I cannot really call them all red because this one is slightly mauve and that one is a little more orange and the other one is a little shinier. For a minute or two, I am exasperated by these cars, until I notice a building sign that is also another shade of red which further complicates things.

But the spell is quickly broken by the helicopter taking off from the field to my left and a whole other stream of thoughts jump into my head. I spend my whole day like this, one random thought interrupting another, none of them having anything to do with one another.

Usually I like spending the whole day in my head, slowly meandering through analysis of my younger self and what I said when I went out last week and how I like flowers, but now my thoughts are so quick and jolting that they are almost painful to experience and none of them can be described as fun or enjoyable or even pleasant. Mostly they are depressing and guilty and panicked and anxious.

I miss my old relaxed, mellow self. I cant wait to meet her again and to be able to follow a train of thought for more than fifteen seconds at a time before it speeds away taking with it any sense of peace or tranquility.

  • Writer: Erin Spineto
    Erin Spineto
  • 5 min read

When you fist get diagnosed with Diabetes the doctors give you a brief education on the disease. I had mine while wasting time locked in a hospital for the weekend. The nurse would wheel in a TV with a VCR hooked up to it (this was in 1996) and play some outdated video very similar to the types you would see in drivers ed in high school.

They would show you the basics and try to scare the crap out of you by telling you about all of the complications that can happen if you don't take good care of yourself (think, red asphalt for diabetes). They show you how to shoot up, sorry, to inject insulin and how to test the amount of sugar in your blood.

But the education is brief and shallow. They don't mention the social implications of a disease that involves such a social passtime, eating. They don't mention the fear of not waking up that comes when your go to sleep the night after your blood sugars have dropped so low you had to call 911 on yourself because you knew it was very likely you would pass out in the next few minutes with no one in the house to help. And they don't mention a million other things that you learn along the way.

After fourteen years with the disease, I thought I had pretty much experienced all of the cautionary tales and knew how to keep myself safe. Last week, however, I found there was a new lesson to learn. I have been dealing with a new, temporary, chronic disease, Mulitnodular Toxic Goiter, which in essence speeds up all of the processes in your body. It is like being on speed 24 hours a day.

It sounds like a great condition to have because you could get so much done and have massive amounts of energy. The problem is that your body actually needs rest. It needs sleep and down-time and relaxation. My body no longer gets this.

I thrash around at night and never get any deep sleep. I am forever in that light phase of sleep where you dream, the most useless level of sleep. And so I am tired. I am tired every day at every moment.

I have started playing around with ways to get some sleep. I have tried a nice drink before bed, but with my hyperexcited state it doesn't do a thing. I have tried meditation before bed, staying up extra late, and turning down the lights 30 minutes before bed. I have recently even tried Tylenol PM. The tylenol my doctor has recommended to reduce the swelling in my thyroid and the P.M. sounded good to me so I took 2, the recommended dose.

And, oh what a sleep I had. After about nine months of not really sleeping it was welcomed as much as a sweet summer rain. The problem came when my blood sugars dropped in the middle of the night.

Plummeting blood sugars in the middle of the night are not a rare occurrence for me, although they can be a scary one. It is a bit disconcerting to be awakened, shaking and sweaty, and somewhat disoriented. I feel my way into the kitchen through the darkened house, trying not to bump into too many walls so as not to wake my sleeping family. I stumble to the fridge and pull out the milk, make my way to the cupboard to get the chocolate milk mix and hopefully remember a cup before I pour a gallon of milk on the counter.

I have done this enough times that it is pretty much on auto-pilot. But this night was different. With those sleeping pills on board, I was barely able to function. I felt low, but the thought that I needed to do something about it didn't occur. I simply felt low and knew that was bad.

After about 30 minutes of laying in bed like this, I thought I should do something about it, but the only thing I could think was to stand up. Once I was up, I was lost. Bathroom? No. TV? No. Kitchen? Maybe, let's go see.

Once in the kitchen the overwhelming need to eat started. So I looked around and could not figure out where to find food. I just stood there staring at a closed cupboard, a sink, the skylight, fridge door, 3 inch square white tile with grey blue grout that had at one point in time been white, but, after years of use had been tinged with the food and spilled drinks.

Maybe I should buy something to clean that, I'm sure someone has come up with a new caustic cleaner that will turn the gout back to white, but will poison all of the food we will put on the counter for years to come until we each have 4 arms and 6 legs and can walk on the walls.

Maybe I should just use some Simple Green, but I can't find it at Costco anymore, or anywhere for that matter. Maybe they went out of business, but when I am up at my parent splace I still see their factory building standing with their name still on it. Oh crap, food. Try the cupboard door. Almonds, spaghetti noodles, chocolate milk mix. Hmmmm. Fridge, Left over pizza, ketchup, pickles, milk. We're getting somewhere now. Milk plus chocolate milk mix makes something, I just know it. Cup. Spoon. Pour milk. Spoon up mix.

I watch my hand try to scoop up the mix which it does just fine. The problem comes when my shaking hand tries to transfer the mix from the canister to the cup of milk. Half of it ends up on the counter.

So I go for another 5 scoops just to make sure I get enough in the cup.

Mix. Drink.

Ignore the incredible mess I have just made on the counter, one for which I know I will be mercilessly teased by my husband, Tony, in the morning, but all I can think of now is BED. I stumble back and pass out. When the morning comes, I am refreshed from the first good night of sleep in months, but I know it will be quite some time before I risk that again. The chances of a diabetic dying in her sleep are always there.

We try to reduce our odds by being in good control in the day and by training ourselves to be sensitive to the body sensations of being low so we can wake ourselves up. I have even become aware of the types of dreams I usually have when I am low (typically food based) and have trained myself to wake up.

But taking sleeping pills, although effective for sleep, really increase our odds of not catching a low and reaping the consequences. The body cannot live on too little sugar in the blood. It will simply stop living.

For me, I choose to be tired. Life is much better than sleep. The old saying, "I'll sleep when I'm dead" has new meaning for me lately, one in whihc I do not want to learn firsthand.

ABOUT THE AUTHOR

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Erin Spineto is an author, adventurer, and advocate for type 1 diabetes. Read more-->

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Disclaimer: This site is not intended to replace, change, or modify anything your doctor tells you. Consult with your doctor before implementing any changes to your diabetes management routine.

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