Fan Mail: Aimee

I got fan mail again! And as I’ve said before, I LOVE mail. I love it so much that I put it up onto my site. (That’s a hint.)

Many thanks to Aimee for sharing her story. :D

Hi Clare! My name is Aimee! I’m 12 years old and obviously I’m and a type one diabetic! Some of my favorite things to do are rock climbing, acting, singing, playing my piano, and hanging out with my friends! I’m going to tell my story by months:

WHY AM I SO SKINNY (LATE MARCH):
Finally its Spring Break and I’m super excited to go to the Dominican Republic! We finally land and boy is it hot! We go to the villa and get settled in. Each night I have a huge bottle of water next to bed, since we can’t drink tap water there, I stumble out of my room and walk to the kitchen. I get the water and head back to my room. Meanwhile about 6 times a night I get up to go to the bathroom. Later during the trip we go to the beach I’m one of my favorite bikinis and when I get out of the changing room my sister’s friend says: “Aimee, how are you skinny, its like your anorexic! I know you really aren’t but…” I seem sort of offended by it, not because she was being mean but because I didn’t realize how skinny I was getting, and I didn’t want to be 
“anorexic skinny”. By the time I’m back in school it’s April.

TIRED (APRIL):
During gym and dance I’m extremely exhausted and feel like I can’t move anything after 5 minutes of exercising, but of course I can’t sit out because I don’t have an injury. Later in the month, our class takes a trip to the Guggenheim in NYC. While our tour guide is telling us about the museum, I start to drift off, almost fall asleep, and I can barely keep my eyes open. April 14, I go with my parents to see one of my favorite movies, Titanic. I drink probably 6 bottles of water during the movie and get up to use the bathroom, 6 or 7 times. At the end of the month my parents set up a doctor’s appointment for me in May.

THE TRUTH COMES OUT (MAY):
My parents know there’s something wrong with me. I go the doctor’s Friday after my mom picks me up from school. Walking up the flight of stairs to the parking lot, I feel like I might collapse I get into the car and take a load off; just sitting down makes me feel better. We get to the doctors and they weigh me and tell me to pee in a cup. I’m sitting in the room waiting for my mom to say something Doctor Juan comes in speaking in a hushed tone so I can just understand what he’s saying. “Her blood glucose reading is 378 and we aren’t positive but we are 99.9% sure that she has type one diabetes. I start to cry, I can’t get a grip on what’s happening, what is this? Is it some sort of disease? Am I going to die? Will I still grow up like a normal girl? Can I eat my favorite foods? I would soon learn the answers to these questions. Doctor Juan sends us to the Yale New Haven Hospital ER. I sit and talk to the nurse for 30 min. or so, and one of them puts me on two of my IV drips, then I am taken to the ICU where I will stay for the night. The nurses are extremely kind and make me smile even though I’m still a little upset. The next day we are educated about type one diabetes and everything else we needed to know. Later in the afternoon I am removed from the ICU and taken to a regular hospital room. I stay there until Sunday and I learn about counting carbs and watch Soul Surfer maybe 10 times. Late Sunday morning I leave the hospital and go home. I know it will take some adjusting for me but I’m ready to go back to school.

SCHOOL (MAY)
On my first day back my parents come in with me to talk to the school nurse, the head of my middle school, and my teachers about my condition. I have told only my friend about it so far and I am anxious but also scared to tell my other best friend. In gym later that day I am sitting out because my health care team wants me to get used to everything else I am doing before I start physical activity again. Another girl in my class named Lily is sitting out because of a sports injury. She asks why I’m sitting out so naturally I tell her the whole story. I feel like I might have overwhelmed her a bit but it felt good to tell someone else. On Wednesday I talk to my homeroom teacher about telling my homeroom and the rest of my grade. I decide to tell them both on Friday at different times. Friday morning my teacher and I gather my homeroom and I tell them everything not leaving a single detail out. I feel more comfortable about it now that more people know. In the afternoon we gather my whole grade and I tell them too, I feel like crying and when I look at their faces I notice some of them are crying too. Once I finish speaking everyone gets up and hugs me, I didn’t realize how loved I was until now.

I HATE THEM (SUMMER):
I have been doing shots for almost 4 months now and I hate them so much. They are the worst thing that’s ever happened to me. Sure they’re life saving, but I hate them. We have been trying to order my pump since July but the insurance company says we have to wait 6 months after the patient’s diagnosis that means I would have to wait until November but I really don’t want to do that. So together my diabetes team at Yale and my mom write letters to Aetna (insurance) on why I need the pump so desperately. And they agree! We order my pump Monday August 13th and it arrived just yesterday! (August 16) I got the One Touch Ping Pump by Animas: 
With the pump I get a meter remote the can tell my pump bolus and many other things. Unfortunately I have to wait to use it because the trainer needs to go to Yale and we need to be trained at Yale. But I still SUPER excited that its finally here and I can’t wait to use it!

I should go now because as I’m still on shots I have to eat my meals at a certain times and its BREAKFAST TIME!!! Yum my sister is making fried rice. I hope you enjoyed reading my letter and I hope to read some new blogs soon!

Best,
Aimee, Type 1 Diabetic, Injection User, Very Anxious to Use New Pump.

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Fan Mail: Leiren

Evidence

I sense a diabetic in the house. (Let’s pretend that it isn’t me.)

Moment of truth, guys. Do you find test strips all over your house? I know I do.

Diabetes test strip

The test strip didn’t quite make it into the trash can.

 

Diabetes test strip

Test strip on the stairs.

 

Diabetes test strip

Holy cow it is on the piano.

 

Diabetes test strip

In the garage? You’ve got to be kidding me.

 

Diabetes test strip

By the TV remote. This just gets weirder and weirder.

 

Diabetes test strip

I think our friend the test strip is browsing online for different blood types.

 

My family and I went to visit my grandfather in Delaware. And he was getting annoyed because he kept finding random test strips all over the house. So before we left my dad and I decided to hide them all over the house in deliberate locations.

Diabetes test strip

The toaster really confused him.

 

Diabetes test strip

I really would have liked to see his face.

 

Diabetes test strip

On the door handle.

 

Diabetes test strip

If you want to confuse your grandparents, this is how to do it.

Places not photographed include under the glass of his coffee table. I would pay to get a picture of when he discovered that one.

Where do you find your test strips? Comment to let me know!

Sincerely,

Claire Montgomery
Type 1 diabetic, Blood sugar tester, Prankster

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Insulin Pump Clips

broken insulin pump clip

Broken insulin pump clip.

Recently I’ve been investigating some handy ways to store your pump when you don’t have a clip. Mine broke. I was upset. What do you do with your pump when you don’t have pockets or a clip? (For some reason pockets that are actually usable doesn’t make sense with girl fashion. Don’t ask me why. I don’t know.)

The most obvious answer is to store it under your waistband. You think it would be strong and tight enough to hold the pump up. Or not.

Recently I’ve found that it’s best to store just under your underwear, but still in the waistband of your pants. For some reason that holds the pump up.

But you might not want to run or jump or really do any erratic movements while not having a clip. Or you might find yourself pump site-less. Not that it happened to me, which was pretty lucky.

Good luck!

Sincerely,

Claire Montgomery
Type 1 diabetic, diabetes blogger, pump clip-less

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Fan Mail: Leiren

As I’ve said in previous posts, I absolutely love it when my readers reach out to me. In this case it was via email, and I loved what Leiren said so much that I’ve decided to post it on my blog. Thanks Leiren!

Claire-

Hi! My name is Leiren (pronounced “leer,” like a creeper, and “in,” like walking through a door). I’m 16 years old and I live in Kentucky. I’m obsessed with musical theater and perform in community theater shows nearly constantly. As a triple threat (an actor/singer/dancer), my dream is to study all three in college and then hopefully one day make it to the Broadway stage. I’m a straight A student at a little school, I have an oversized (and insane!) Yorkie named PJ, I wish J.K. Rowling wrote my life, I love Star Wars and LOTR, my brother is my best friend in the whole wide world… You get the picture. I lead the life of a completely normal theater kid (I know, the words “normal” and “theater kid” should never be used together, but that’s my life! :D ).

That is, until three weeks ago.

I guess I should back up. In February, I had two really big auditions for projects that would happen over the summer. I kept my summer completely open, turning down camps, mission trips, vacation invitations from friends, and community theater auditions. I don’t want to sound cocky, but I’d never auditioned for something I hadn’t gotten before, so I kind of assumed I had a good shot at getting at least one of them. I was wrong. For the first time in my life, I nailed both auditions and didn’t get so much as a callback. I was devastated. Now, not only did I not have a big professional summer project to work on, I had turned down so many other opportunities and those deadlines were over. And so all I had to look forward to was a bleak summer of sitting behind a desk entering data; the only deadline I hadn’t missed was my summer job application! :/ “Something huge is coming for you this summer,” my mom told me. “That’s why nothing’s working out for you. I can feel it.”

Then came May. It was the end of the school year. I had finals, end of the year parties, teachers piling on tons of last minute homework, and, on top of that, I was the lead role in an extremely physically challenging show involving lots of tap dancing, singing my butt off, and moving furniture. I was exhausted, falling asleep in class every day, coming home and sleeping for my measly hour between school and rehearsal, collapsing in the car on the way home from rehearsal (not while driving, thankfully!), and just generally feeling very lackluster. Then there was the eating. I’ve always had a healthy appetite, especially for a petite girl of 4’10″), but I was getting hungrier all the time, so much so that near the end of May, people began to comment on how I was so lucky to be able to eat so much and still stay so thin. “You know, hollow leg!” I’d say, or, “Dancers need their energy.” I was laughing it off, but I began to worry that I was going to get fat. I couldn’t seem to control myself, though. I wasn’t gaining any weight, if anything the opposite, so I figured my body just really needed the extra food.

Well, you see where all this is going. For the next seven weeks, I began to feel worse and worse. I was waking up, eating as much as I could, drinking 6 glasses of water, grabbing food for my desk, going to work, practically crawling up the steps with my heart racing like I’d run a marathon, eating and drinking all day at work, coming home, passing out, waking up for dinner, stuffing my face, going back to bed, and doing it all over again. Through all of this I was having severe abdominal pain, sweet tastes in my mouth with a white film, leg cramps, blurry vision, frequent peeing, nausea, classic symptoms. Plus, I lost 14 pounds, which on a 110 pound girl is extremely noticeable. I was a (barely) walking skeleton.

Looking back, my mom and I don’t see how we didn’t realize what was happening, but honestly, the word diabetes never crossed my mind. The stomach pain was the most predominant, and I’d had mild stomach issues in the past, so we were so focused on treating that that we ignored the other symptoms that might’ve led us to a quicker correct diagnosis. The first doctor I saw put me on Prilosec and some other stomach medication. After several weeks of everything only worsening, my mom took me to a different doctor. She thought it was my gallbladder or maybe my thyroid, and she took blood to send off for a lab test, not to test my sugar specifically, but just to see what she could find. She scheduled a thyroid scan for two days later. I went and did the scan, came back home, and went to sleep. My mom came and woke me up an hour later. There was a hint of panic in her eyes. “Leiren,” she said, “we have to go to the hospital. Dr. Telle called.”

“Now?” I said groggily.

“Now. Your gallbladder function is a little low, but your blood tests came back and we have to go test your sugar.”

We went. I sat in the chair, they took my blood. “What’s a normal blood sugar?” I asked the lady taking my blood.

“Well,” she replied, “If you’ve had a really sugary lunch, it can be up to 140 or 160, but normal is around 120.”

“What was mine, Mom?”

It barely came out in a whisper: “400.”

The hospital told us to wait there until the results came back. About 20 minutes later, mom got a call from Dr. Telle. My sugar was 520.

We were rushed to Vanderbilt Children’s Hospital in Nashville, Tennessee. I was immediately admitted to the ER, placed on an insulin drip, and given one of those breathing tube looking things to monitor my CO2 levels, which were dangerously low. 12 hours and tons of needles later, my sugar was down to 128 and I was officially told that I was a Type 1 diabetic. I had been in Diabetic Ketoacidosis for about 6 weeks. Most people last two before they crash or go into a coma. The doctors kept saying it was a miracle I had stayed up for so long.

The last three weeks have been a whirlwind of education, carb counting, doctor’s appointments, and some really, really bad blood sugar readings. I feel so grateful to know what’s wrong with me( an that it is manageable) and also to be a part of the awesome diabetic community, but at the same time I realize that life as it once was will never be again. I can’t just go to the fridge and eat anymore, I have to watch for lows at rehearsal and dance class (and everywhere else), and I’m about to have to do shots and test my blood at school for the first time. I’m not complaining, but I know things are going to be very different.

My family is on vacation in Florida right now, and on the way here, I was looking up diabetes blogs online. The first thing that popped up was your post about wearing your pump on your boot. I don’t have a pump yet, but I clicked on it because it seemed so like something this fashionista would do! I spent the next three hours reading your posts, some to myself, and some aloud to my whole family. We were dying laughing at your story about your girl scout camp experience (you poor thing!!) and when you told your Tae Kwan Do teacher about having diabetes. I was “amen, sister!!” all through your post about Type 2 and Randy Jackson. I can’t tell you how many people have said things like, “Well, when you learn how to take care of yourself” (excuse me, I’m 100% positive that I’m a healthier eater than you are), or “When you cut back on the sugar,” (I’ve NEVER had much of a sweet tooth, and mashed potatoes or a biscuit have way more carbs than one Hershey’s kiss, thank you!), or, worst of all, “If you don’t quit sweets now, the insulin will stop working in about 10 or 15 years.” (Huh?? That stupidity doesn’t even deserve a response.) Everyone assumes that I have Type 2, and that drives me crazy! I’m a thin, healthy, active girl, and there is no way to reverse the fact that my pancreas simply DOESN’T PRODUCE insulin. I’m glad there’s someone else out there who understands this.

Your tips about school have been extremely helpful as well! I’m about to go to school with diabetes for the first time, and your advice has definitely put me at ease. I definitely see some Smarties in a pencil bag in my near future. :) I want to go to a diabetes camp this summer!! It sounds like a blast.

Well, I guess I’d better wrap things up or I’ll go on forever. Mom was right, something huge was coming for me this summer, and that’s why nothing was working out for me as far as plans went. Of course, I hoped it would be something fabulous like a record deal or a better audition opportunity, but this diagnosis could be one of the best things that’s ever happened to me. I’ve already met some amazing people and gotten the chance to educate some others on what Type 1 really is. I’ve come across your blog, which has given me hope that normalcy and an active life are extremely possible. God has placed me in the diabetic community for a reason, and I think great things will come from it.

Thanks for all the help and encouragement, and best of luck in all you do! I’ll be reading your posts and you’ll be in my prayers.

Your friend,

Leiren Jackson

Thanks again Leiren for sharing your story!

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My Closet is a Pharmacy

Literally.

So before I had the pump we used to shove all of my diabetes supplies in this one cabinet in the kitchen. And it didn’t really work out to well because it was just messy and cramped and unorganized and you couldn’t find anything. It came to the point where I was finding my supplies, and then shutting the door real fast so nothing would fall out. Basically what I would call a mess.

So a while ago I got tired of having all of my diabetes supplies fall out of the cabinet whenever I needed anything, and also I couldn’t fit anything else into the cabinet anymore. So I decided to move everything into my closet. And it turned out to be a really good idea.

Now everything is organized, and I have enough space. And I also get to freak my friends out whenever we look at clothes. And now my closet is no longer a closet, it’s a pharmacy. Which is awesome. Not many people get bragging rights over having a real pharmacy (well, real in my mind) in their CLOSET. Nope. So far I am the only person I know who calls the location of where they keep diabetes stuff a pharmacy. And that makes me awesome. To me at least.

So how do you store your diabetes things? Share your thoughts by commenting.

Sincerely,

Claire Montgomery
Type 1 Diabetic, Teenage Pharmacist

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Insulin Pump Fashion

A couple of days ago I wore a dress with some boots. And as I’m sure that my fellow female diabetic pumpers are aware of, even if you have shorts on underneath your dress, it’s pretty awkward to reach up your dress and take your insulin pump out. And then my problem is that I LOVE wearing dresses, and I would totally wear them every day if it weren’t for people saying, “Why are you wearing a dress?” whenever I DO wear a dress. It’s actually pretty annoying. “Because I felt like it.”

So this time I wore a dress with boots, and then I clipped my insulin pump onto my boots, so I could get my insulin pump without having to feel so awkward about it like I usually do.

So band was my first period, and people kept on bugging me out of genuine curiosity because they obviously didn’t have any idea what an insulin pump was, and I must say that I was enjoying the attention. After band I was checking the list to see who made it into Wind Ensemble (the highest band at my school) when a girl came up to me. Her name is Sam, and she told me that she really liked my Medtronic insulin pump, and that her’s was boring and black. It turns out that a flute who sits three feet away from me is a fellow type 1 diabetic. That pretty much made my day. We talked a little about going to diabetes camp, and then I had to leave to go to class.

So if you wear your insulin pump on your boot, you realize that people have a ton in common with you. That little thing made me happy for the rest of the day. :) And I still am happy.

Sincerely,

Claire Montgomery
Type 1 Diabetic, Diabetic blogger, Insulin pump fashion-ista.

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Smartie Spit

Get that picture into your mind: Smartie Spit. Now think of that spit going through a clarinet. Gross, huh. Don’t stop reading.

I play the clarinet. I’m in my high school’s symphonic band. It’s really fun, because I got first clarinet, and I just love love love music in general. It’s just so much fun. It’s really one of the best part of my days.

A couple of days ago I was low in band. Now that’s just awkward. I mean, try to imagine trying to inhale smarties during the rests (pauses while playing) and then forcing Smartie spit down your instrument. It’s really gross. And I’m not grossed out by many things, but this is just one of them.

And then in many cases your band teacher just gives you this look, that basically says, Why the heck are you eating and playing your instrument at the same time? Irresponsible student.

So you basically hope that you never get low during band.

Okay, and then you join the marching band. Which can technically be counted as exercise. Don’t get me wrong. Marching band is totally fun. Football games are the life. I mean, we’re all the “band geeks” so we really know nothing about football. So we just sit around and play little rifts and laugh and talk.

But throw the whole marching thing into the mix. We play at parades too. But how do you march in a contest in formation and get low in the middle of the song? It’s a puzzle, I tell you. A puzzle. My band teacher told me that I could just duck out when I needed to, and I’m not saying that I’m against the idea, but that it’s sort of awkward to playing our school’s fight song and then to duck out of the group when we’re all in formation.I will totally duck out if I need to, but it’s still weird. I still have a bag of Smarties in the pocket of my uniform. But I haven’t been low yet, which is a good thing.

Luckily, just now we’re only doing basketball games right now and no marching, so I wont have to worry about this until next school year, when we start marching again.

Well, adios for now!

Claire Montgomery
Type 1 diabetic, Diabetic blogger, Smartie spitter

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I Have Low Blood Sugars When I Ski

Who knew.

So after a couple of weekends of taking ski lessons at Copper Mountain I’ve deduced that I always end up in my 20s after my first run. And being 20 mg/dl is just scary. And my goal is not to have Ski Patrol come rescue me (even my mom says that they are hot). So what do you do? I hate being high, and I hate being low. But at this point in time I am guessing that I should send myself high in order not to go low. Any suggestions?

I already carry candy in my pocket: jelly beans and Smarties. The first time that I was low and skiing my dad freaked out so now whenever I go skiing my pockets are weighted down like I’m carrying a bowling ball or something. Which brings me to my next point.

For all you skiers, always bring something with you. That really should be common sense, but I just want to get out there so I can say that I’ve said it. I carry candy, my lunch, my tester, an extra lancet, and a shot with me. All in my pockets. But seriously, if you need something on the mountain, you wont be sorry that you had all of that stuff with you.

For example, one time during our ski lessons we skied down to the bottom of Resolution bowl on Copper Mountain. For those of you who don’t know, Resolution is the only lift were you aren’t at a base, or can’t ski down to a base. So if the mountain looses power, you’re stuck. And guess what? Just as we got to the bottom of Resolution, the whole entire mountain lost power! I know, right? CRAZY. And for some weird reason Copper decided that Resolution was going to use reserve power LAST. That’s right, LAST. So everyone else in the class was starving, but my brother and I had our lunches in our pocket, so we weren’t starving. I know that I wasn’t low, but what if I had been? That right there is a really good reason to have sugar with you right there.

So anyway. I’m asking for suggestions on what to do to stop being low on the mountain when I ski. Suggestions would be very helpful. Thanks!

Sincerely,

Claire Montgomery
Type 1 diabetic, Diabetic blogger, Diabetic skier

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Party in the Nurse’s Office!

Come all ye diabetics and lament about blood sugars…

…’Twill be fun. :

I love the nurse at my high school. She is so awesome and hip and cool. At my old middle school I didn’t really like the nurse, but here she’s awesome. So the other day I’d been having high blood sugars for pretty much the whole day so finally I just went down to the nurse so I could change my site because I figured it was a bad site. But when I got there I didn’t have any insulin so I had to call my dad so he could bring me insulin. I had all of the other supplies. Anyway. So I sat in the nurse’s office while I was waiting for my dad.

And then this kid named Noah came in. He was a diabetic and he was something like over 400 mg/dl. So we were sitting there and talking and lamenting about other nurses that we’ve had that we didn’t like and about insulin pumps and about medical IDs and about tattoos that serve as medical IDs (look them up). And we were talking about iPumps (don’t you think that would be totally wicked? It could count your carbs and test your blood sugar and be your pump AND be your phone, iPod, etc…). It was totally so much fun even though we were just so totally high. And being high is never fun except on that day it was because we could complain to each other and talk about things that nobody else would ever get. Just hanging out with diabetics is fun in general but it was even better this time because we were both high.

And then my dad came and he gave me my insulin and then he left and I gave myself a new site. Blah blah blah.

AND THEN a girl named Nicole came in and she just happened to be a diabetic and she just happened to be high. Join the club, sista. I swear, that’s the best time I’ve ever had in the nurse’s office, and I mean that quite literally. Three diabetics were high at the same time and lamenting about high blood sugars and were in the nurse’s office at the same time. IT WAS SO COOL!

So, a message to all you diabetics who are still in elementary, middle, or high school. Go to the nurse’s office when all the other diabetics in your school are high. It’s fun.

Adios for now!

Claire Montgomery
Type 1 diabetic, Diabetic blogger, Nurse’s office party thrower

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Skiing With Diabetes

So. I ski. I suppose it’s not that surprising, but I live in Colorado, so of course I ski. Stereotypical, huh? My grandfather rented out a house in Steamboat for winter vacation so all of my aunts, uncles, and grandparents (and my immediate family) came up to Steamboat to hang out and ski. Fun, right? But I’m sure that you’re all very surprised that skiing can get very complicated when mixed with diabetes (intense sarcasm). It’s like running for me. Really. I’ve had a crazy couple of days.

So you think I would go low, right? Well, I did, but I also went high. While I was there I skied for a total of two days, and on the first day I had some really low blood sugars. On the second day I had blood sugars that were in the 400 range. Not really perfect. And it makes it hard to find a pattern. And on the first day, when my blood sugar was low, I was in the 30′s. That’s the lowest I’ve ever been before, and it really scared me.

So I guess I am asking for advice, so please comment. :) I’m going skiing in a couple of weeks so I will be sure to try out some ideas.

Sincerely,

Claire Montgomery
Type 1 Diabetic, Diabetic skier, Powder shredder

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