Girls and Pumps: Fashion

I recently received a letter from a girl named Sam who had a pump wearing tip for girls.

Hi! I’m a diabetic too! I read your post about wearing your insulin pump on your boot while you wear a dress, and I have a tip. It’s sort of strange and not to everyone’s liking, but I love it! I wear my pumpinsulin_pump in my shirt on an everyday basis. If I’m wearing a sports bra I just stick my pump in it. I rarely feel it there! Also, you can buy thigh bands for when you wear dresses that have pump pockets. These are ways that don’t make wearing a dress uncomfortable, and that also make it less “awkward” when taking your pump out. Take care!!

I’ve heard putting your pump on your bra, but I’ve never tried it. I guess that’s something I’m going to have to go do.

However, I’ve never heard of thigh bands, and that would be awesome to try out. I’ve always worn shorts under my dresses, and I have mastered the “how to take your pump off under your dress without anyone noticing” technique. It’s really handy.

Thanks for the tip, Sam!


Claire Montgomery

Related Posts:

Fan Mail: Amanda
Fan Mail: Lily
Fan Mail: Sophie
Fan Mail: Aimee
Fan Mail: Leiren

Fan Mail: Amanda

Thanks for sending me mail! I love it. 🙂

Hi Claire! It’s Amanda from school :).  Although I could just tell you this in person on Tuesday, I figured that I know you love fan mail, so I may as well send you a message 😀

I came across your blog from the link you put on Facebook, and although I don’t have diabetes, I clicked on it anyways and read several of your posts. I know we sort of know each other through school, but I’m glad I got to see this side of you through your blog. You are such a strong and inspirational girl and I think it’s wonderful how you’re not afraid to talk about diabetes both on this blog and in everyday life.

I’ll be the first to admit that I tend to exaggerate bad things that happen to me and make them seem like my life is so terrible. I have a bad hip that sometimes causes me a lot of pain. I have seasonal affective disorder and am in therapy for it. And a lot of times I convince myself that living like this is so awful. “I hate having to miss dance class because my hip is hurting” or “what will my roommates in college say when I have to do half an hour of light therapy each morning?” get me down easily. Hearing about what you deal with and how you keep a positive attitude helps remind me that I need to keep my mind off the little things and focus on what makes my life good. Really, dealing with things like a hurting hip or SAD isn’t nearly like dealing with diabetes, and I need to remember that more often.

So the bottom line: you are such an inspiration and I am blessed to know you 🙂

Thanks so much, Amanda, for taking the time to write me a note. It really means a lot to me.

Like me on Facebook!
Follow me on Twitter!

Fan Mail: Lily

I like fan mail. So I just have to share.

Hi Claire. My name is Lily, and I have read ALL your posts. First I thought it would be horrible to have a pump because it would be uncomfortable but because that you said its really good, I suddenly want one!!! Thank you for helping me like the pump with your awesome and funny posts!!

Writing this blog seems worthwhile to me when I am able to reach out to people and help them with their own journey with diabetes.

Related Posts:

Fan Mail: Sophie
Fan Mail: Leiren
Fan Mail: Aimee

Diabetes Supplies in Mexico

I received a comment on one of my previous posts that reads:

Hi. I have a question. I see you have lived in Mexico. I am having horrible issues finding pump supplies here you have any ideas?

So I thought I would answer the question. images

When I lived in Mexico, I knew that I was only going to be there for ten months, so I brought all of the pump supplies that I was going to need with me. To do that, I had to go to my doctor and get a special prescription that said I could order more pump supplies then I usually needed.

I don’t know if that helps, because my circumstances were different then people who live in Mexico all year round.

Hope that helps!


Claire Montgomery

Related Posts:

I Live in Mexico
Give Me The Candy!

Fan Mail: Sophie

I’ve said before that I really like it when people email me. This email is a little different because it comes from someone who isn’t a diabetic. But personally, it makes the email so much cooler. It’s actually nice to have people trying to learn about diabetes, instead on just assuming something and then taking their assumptions as gospel. Props to Sophie!

Hey, Claire!

I was just reading your blog and think it’s so cool that you are sharing with others what it is like to have diabetes. I love how you write from such an honest, relatable point of view.

I don’t have diabetes, and I can’t completely sympathize, but I realize the hardship of it, and how other people are so uneducated about the topic.

It’s really amazing how honest your point of view, and I think your stories and advice will help hundreds of thousands of kids. You are an inspiration to not only people with diabetes, but also people without diabetes. Your blog has opened my eyes to diabetes and all the experiences that come along with it…

You are an inspiration! Hope to talk to you soon. 🙂

-Sophie 🙂

Sophie, you are awesome, and thanks for emailing me!

Related Posts:

Fan Mail: Leiren
Fan Mail: Aimee

New Find! Teenage Diabetes Blog




Have I mentioned that I LOVE fan mail? You guys are probably thinking by now that it’s only been about a hundred times. Well a couple of weeks ago another person emailed me, and I thought that I would share.

Hi Claire! I’m Sam and I have been a type 1 diabetic for 2 years now. I’m 16 years old and a junior in high school. I absolutely love your blog!! You are amazing and I can relate to pretty much everything that you post. You are so inspiring! I have a blog through blogspot. It’s called Just Your Average Teenage Type 1 Diabetic. I was just wondering if you would consider checking it out and letting me know what you think and possibly give me some advice to what people like/dislike on here. Thanks so much!!

the link to it is

<3 Sam

So what did I do? Naturally I checked out her blog. Which is pretty cool. And I thought that since the diabetic community has been so helpful with giving me support by reading my blog, we could repay Samantha the favor by checking out her blog.


Claire Montgomery
Type 1 Diabetic, Blog Supporter, Awesome

Related Posts:

Fan Mail: Leiren
Fan Mail: Aimee


A couple of weeks ago, I got an email from a guy who runs a diabetes website based in Iran. Which is totally cool. He asked me if I would be willing to do an interview with them. And I couldn’t say no, so I answered a few questions. How many chances like that do people usually get? So of course I went for it. I now have the link, and also the interview, which I will post below.

Check out the link! It looks so cool to see my answers translated into Arabic!

1-Dear Claire, first of all, please introduce yourself (i.e. the date of your birth, the year that you found out you have diabetes, where you live, and what you are doing etc).

My name is Claire Montgomery and I am fifteen years old. I was born on December 17, 1996. I was diagnosed with diabetes when I was ten years old on March 6, 2007. I live in Denver, Colorado in the United States of America.

2-How do you find out that you have diabetes?

I was taking ski lessons and I threw up in the parking lot. My parents thought I had a stomache bug so my dad stayed with me while I slept at the place where we were staying. That night we went ice skating and I remember feeling really miserable because I had no energy to skate but I really wanted to. The next day I started to breathe really hard so I didn’t help with clean up at all but rather felt really bad. On the way home in the car I started to have mini hallucinations so we stopped along the way at a town and everyone got candy sticks. That was when my parents called the doctor. My dad dropped my brother and sister off with my mom at home and then we immediately left for the doctor. When I finally got into an examining room the doctor took one look at me and sent me to pee in a cup. Apparently she had guessed what I had at first glance. It was confirmed that I had diabetes and the doctor told me that I had to go to the emergency room immediately. I was a textbook case soo all of the other doctors in the office came in to look at me so they could see what diabetes looked like. The doctor called ahead to Children’s Hospital in Denver and my dad drove me there. Once I got there they took me in immediately and hooked me up to an IV. I spent the night in the Intensive Care Unit and was released from the hospital the next day. I spent the next two days in training with my parents.

3-What was your image about diabetes when you knew the first time about your diabetes and what was your feeling in that time?

At first I was really a little bit stunned and hadn’t really gotten what had happened. It had been a really busy couple of days and there wasn’t any time to think about what had happened. However once I actually had time to understand what had happened I cried.

4-How did you accept this fact and become a friend with your diabetes?

In all honesty, I am not really sure of how to answer this question. I don’t think that I have ever become friends with my diabetes. But have learned to live with it. It is a part of me, and no matter how much I complain, it will not just magically disappear.

5-What is your highest and lowest blood sugar experience till now, and what you did in these situations?

My lowest blood sugar yet has been was 39 mg/dL. I can’t really remember what happened because it happened so long ago, but I assume that I drank A LOT of juice, and waited and tested again. Actually, I have never been unconscious because of a low. The only experience I’ve had where I wasn’t able to concentrate or function was when I was at the beach with my family when we were on vacation. Everyone except my mom was in the ocean. I was probably 80 mg/dL, but I must’ve been going down really fast because I had no idea what was going on. Mom kept on giving me juice, but I kept on wandering down to the water (even though I couldn’t walk straight). Finally Mom made me sit down and drink. It turned out fine. My highest blood sugar was around 500 mg/dL. This was also a long time ago, so again I can’t really remember but I know that it was right before bed, and it was also back when I was still taking injections. My mom gave me a shot, and then I went to bed. I do remember feeling miserable though.

6-How much your diabetes affect your personal life, your family life, your education and your happiness, at the beginning and now.

My parents and I have actually had huge arguments about this. I would prefer not to tell my friends about diabetes and make it not a big deal, though my parents wanted to tell everyone on the face of the earth (or so it seemed). We still haven’t figured out a balance. I have gotten bad grades on tests and such because of high blood sugars, but other then that diabetes hasn’t really been a big deal concerning my education. Naturally the school nurse and I are best friends. My happiness? Well. There are times where I hate diabetes, and I can’t say that I necessary love it. But it just is, and I exist with it. It has become a part of my life, so I can’t really say that it affects my happiness. It’s only when I’m high that it affects my happiness, because I feel really bad.

7-If you are a member of association for diabetic patients, what is your activity in that association and what kind of activity that association do for his members?

I am not really involved in an association for diabetic patients. I mostly do outreach stuff, like my blog ( and go to events that are hosted by associations. For example I have gone to diabetes camps that the American Diabetes Association puts on, and I also have gone to fundraisers and other things for the Juvenile Diabetes Research Foundation.

8-You are living in U.S. and you are enjoy living in a developed country. I would like to know how such a country like U.S. helps people with type 1 diabetes.

Well. In the USA we have programs like support groups and things like that. There is also the American Diabetes Association, and they try to spread the word about diabetes and to help people with diabetes by giving information. There aren’t that many doctors offices that are purely dedicated to just diabetes, however. Many people go to their regular physician. I am lucky because I live in Colorado, home of one of the two best diabetes facilities in the country. It is called the Barbara Davis Center. When you are first diagnosed, many people reach out to you. I think almost every diabetic in America that is about my age has a bear named Rufus. Rufus is a bear that the JDRF donates to new diabetics. It has patches on its body for places where you can give yourself injections or get your fingers poked. There are also many outreach groups like blogs and websites that are focused on diabetes.

9-You said in your personal website that you are using insulin pump. How much of its expense is covered by the insurance.

I am honestly not sure how much, but about two thirds of the expense for the insulin pump was covered by insurance.

10- How many percentage of diabetics that you know are using insulin pump?

Well, I am not really sure, but according to Google there is more then 30 percent of diabetics using an insulin pump.

11-Diabetic people that do not use insulin pump, what kind of insulin do they use?

In the United States, there are two kinds of fast acting insulin: Novolog and Humalog. People on either pumps or injections can use either of these insulins. There are two other types of insulin that only people on injections use. The first is called NPH. This is an intermediate acting insulin which is given at breakfast so a shot doesn’t need to be taken at lunch. It starts working about five hours after it’s been injected. NPH is also optional because you can just as easily take a lunch injection. The last kind of insulin that people who take injections use is called Lantus. Lantus lasts about twenty four hours and compensates for the tiny trickle of insulin that your pancreas releases even with diabetes.
I only use one type of insulin and that is Novolog.

12-How many time you use to measure your blood sugar on daily basis?

I check my blood sugar anywhere from six to ten times a day. I check before meals, when I wake up, and before I go to bed.

13- In the school or in a party or in a hiking with friends, do you measure your blood sugar?

Of course I do. I would rather not, but I think stoping to test my bloodsugar is better then feeling miserable if I hadn’t tested.

14- Do you think if you do not have diabetes then Claire without diabetes is more successful and happier than Claire with diabetes?

What an interesting question! Diabetes is such a part of my life that if I suddenly woke up one day and didn’t have it I would probably be a little lost. I can imagine myself reaching down to give myself insulin, and then realizing that I wouldn’t have to do that.

15- Did you visit our website “”?

I just did. And it looks cool, but I can’t read it.

16- What was your feeling when you have received an email from, your Iranian friends?

I was thinking that it was an amazing offer and that I would be stupid not to take it.

17- We would like to hear your suggestion in order to improve our website?

Like I said before, it looks cool, but I can’t read it. Sorry that I can’t give you more suggestions.

18- Please tell your message to your Iranian friends who have diabetes.

Keep going! You aren’t alone. And know that you now have a diabetic friend living in the United States. I wish everyone the best of luck in controlling their diabetes.


So I now have new friends in Iran! It is so cool! Thanks to Masood Hasannejad for giving me this wonderful opportunity!


Claire Montgomery

Related Posts:

Fan Mail: Leiren

Fan Mail: Aimee

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. 😀

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:

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.

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.

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.

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 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!

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

Related Posts;

Fan Mail: Leiren