Thursday, May 6, 2010

Missed Anniversaries and a New Project

Well, I did it. I actually forgot something I have celebrated every year for the past 3 years...until this year. On May 1, 2006 I became an insulin pumper for the first time. I took my mother down to the CDE’s office with me because they suggested that I have someone else to drive, since I would basically be starting from scratch on basal rates. My mother was more than happy to go with me. That day changed my life. To me, it was a chance to make a change. It was a time to start over.
I had started taking semi-decent care of myself in order to meet the requirements to get an insulin pump in the first place. But I wasn’t where I needed to be and I knew it. And I knew pumping would give me the motivation to take this hand I’d been dealt and actually play it like it should be played. I had the chance to make up for years of poor and semi-poor care.
I won’t say I’ve always done what I am supposed to, since starting to pump. But I am treating diabetes differently. And I feel like I have better control.
After I started pumping, I began to seek out more information about living life as an adult with Type 1 diabetes. Internet searches led me to dLife and their message boards, and also to Kerri’s blog (Hi Kerri!). Kerri pre-engagement, pre-marriage (Hi Chris!), and pre-baby (Hi BSparl!). Like so many of my fellow bloggers, Kerri inspired me to start my own blog. So in April of 2007, I stumbled my way onto blogger and started my first ever post.
And the rest is history. This community has grown by leaps and bounds since I began my blog. I went from trying to read every blog (there weren’t so many of us back then….), to just trying to keep up with what I can. I’ve had the chance to meet some of my fellow bloggers, which has been so fun. I’ve gained friends. People that I know will be there if I need them and who will understand my day to day struggles and victories with diabetes.
Even when I went from blogging only about diabetes, to blogging about other aspects of my life, my fellow bloggers have been around and made my life more wonderful.
I wonder what my life would have been like if I’d never started pumping. I wonder what it would be like if I had never stumbled across Six Until Me. I know I would be a different person.

So, instead of forgetting TWO of my anniversaries (because I totally FORGOT!), I've just decided to celebrate a little bit late. :)

Also, in case you've been living under a rock, there is a new project getting ready to happen in our wonderful on-line community. Karen from over at Bitter-Sweet Diabetes, has come up with a wonderful idea and wants all of the community to get in on it. Quite simply titled "Diabetes Blog Week", Karen has come up with topics for us to blog about each day. In essence, we'll all be blogging about the same thing every day so we can get an idea about how we all feel about the same subject.

I, for one, thing Karen is fantastic to come up with this idea. And apparently, so do 59 other bloggers because at last count, there were 60 of us signed up. What? You've not signed up yet?!?! Go! Now! Join us. :)

Now....I'm off to start early drafting my posts for next week.......

Tuesday, May 4, 2010

Update on Tennessee Flooding


I just got off the phone with the Middle Tennessee chapter of JDRF. They wished for me to express their gratitude at the inquiries about those needing diabetes supplies. They also said that they have had NO calls or questions about people needing supplies at this time. (AMAZING! And wonderful!) But they did take my e-mail address and phone number, so I will be passing along any info I get, if something does come up.

The lady I spoke with said that the most devastating damage is downtown and along the Cumberland River in Nashville. These are the touristy areas. The areas that generate a VAST majority of revenue for the city. It sounds like the effects will be more economical and long term.

However, there are many, many people who have flooding in their basements, homes, etc. And these are the ones that we are currently worried about. They are currently in shelters across the state and some are not sure when they will be able to get home, as roads and bridges are washed out and homes unlivable at this time, due to water damage.

For now, this is the info I have for you, if you want to help out:


- My previous post has all the Red Cross info. It came directly from Middle Tennessee's Red Cross page. They need all the donations they can get, I'm sure.


-Check out Nashvillest.com at THIS page for more places to offer help. Supplies, donations, etc. They have a very comprehensive list.




Also, please read THIS blog post by a hockey blogger. "Hockey?" you may say. Yes, hockey. This post is not about hockey. It's about the spirit of Nashville and Tennessee in general. And the disappointment I know many Tennesseans, including myself, feel about the lack of national media coverage of this epic disaster. It's touching. And it will remind you not to forget about the damage and those who are and will suffer because of this disaster. Tennessee is made of of mostly strong, independent, loving people who will do anything they can to help those around them. I just hope that others remember that and lend a helping hand to us.


Thanks for reading guys. It means a lot to know you read, even when it's not diabetes related.

Update....

I've had a few question about the possibility of diabetics needing supplies in the Middle and West Tennessee areas. I currently don't know anything, but am in the process of finding out what I can. For now, I can offer you this info:

Middle Tennessee Red Cross
The Nashville Area Red Cross is in need of financial support to continue providing relief to victims of local disaster flooding. The American Red Cross is not a government agency. All disaster assistance is free, and is funded solely by local donations.
There are several ways to give:

•Visit www.nashvilleredcross.org and click DONATE NOW to make an online gift
• Mail a check to the Nashville Area Red Cross2201 Charlotte Avenue, Nashville, TN 37203
• Call (615) 250-4300 to make a donation by phone
• Text REDCROSS to 90999 to make a $10 donation on your mobile phone

Monday, May 3, 2010

Sadness: Flooding in Tennessee



Typically, this is my music post. Today, I'm just going to share my feelings. As many of you may have heard, Tennessee was hit with record rainfall over the weekend. I'm fine, as is my family. Although we got a lot of rain, it was nothing compared to other areas and there was little to no flooding anywhere around me.

Downtown Nashville

However this was not the case with many other parts of my state. Nashville, which is where I go to my endo, see concerts and plays, and shop, is pretty much under water. There are areas that are not, of course, but historic downtown is pretty flooded. The beautiful Opryland Hotel is closed until further notice because of the flooding inside.



I-24 On Saturday


Other areas of the state, further west, are also suffering major flooding and damage.


Cars in the aftermath of the flood waters


As I have watched this all on television, it is eerily similar to watching the horrors of Katrina. I know the damage will be no where near as bad for Tennessee. But the pictures bring those same scared, frustrated, angry, and helpless feelings out in me. And maybe even more so, because Nashville is a town I know so well. And Tennessee has been my home for my entire life.


Inside the most beautiful hotel I've ever been in: The Opryland Hotel & Resort Lobby


My thoughts and prayers are with those who have been effected by this flooding. And I can only pray that recovery is swift.

Inside the Opryland Hotel & Resort. The Delta Portico

Thursday, April 29, 2010

By the Glow of the Pale Pump-Light

I awaken to a shrill beeping sound. In my head, I know what it is. But I'm tired. I reach down and push the buttons on my pump to make it stop. Just like it was an alarm clock with a snooze button.

In my sleep-hazed mind, I know I should look to see if it is informing me of a high or a low. I unclasp my pump from the waist band of my pajama bottoms and lay it on my stomach. Almost too tired to even bring it up to my face.

I lay there drifting, I know, back to sleep. But I shake myself and push the "down" button, knowing it will turn on the pump back-light. My CGMS says 80. But I can tell from the drastically dipping trend line, that I'm probably much lower.

I could roll over and turn on my bed-side lamp. But I don't. I don't want to wake up. And I know where everything is anyway.

I grab for my meter. Using my pump as a dim light, I test my blood sugar. 64.

I don't even zip up my meter case. I just push it to the edge of the bed and grab the juice box that I know sits by my alarm clock.

I down it quickly and roll back over and drift back to sleep.

I wake up with my still unzipped meter next to me. I turn off my alarm clock. I test again. I'm 114.

Monday, April 26, 2010

Music Pick of the Week

This week's pick:






My new motto: I wanna go live in Glee-land.
Cause in Glee-land....you have cool things happen......like this:


Thursday, April 22, 2010

I Wonder....

I wonder..... if people see me and think of me as the diabetic who's name is Cara, or as Cara who happens to have diabetes


I wonder..... if people see me and think if I lost weight and exercised, my diabetes would go away.


I wonder..... if people think of me as sick.


I wonder..... if people pity me.


I wonder..... if I'll end up with complications that will drastically alter my life.


I wonder..... if I will ever not wake up.


I wonder..... if there will ever be a truly closed loop system so I can live my life with less worries and stress.


I wonder..... what it is like to work doing a job you love, and not a job that give you great health insurance.


I wonder..... if I'll ever meet all of my blogger friends.


I wonder..... if people that I love worry about me in regards to my diabetes.


I wonder..... if I can take that worry away from them.


I wonder..... if I'll ever get over the guilt of making my mother's cry.


I wonder..... if being my friend is harder that being someone else's friend.


I wonder..... what I would be without diabetes.


I wonder..... if I'll ever figure myself out well enough to know what I want to do with my life.


I wonder..... if diabetes will be part of that.


I wonder..... if there will ever be a cure.

Wednesday, April 21, 2010

Birthday Cuppies

Fourteen years ago, my life changed forever. I spent the first 15 years of my life with only a MUCH older brother in the sibling department. My half-brother was 19 years older than my and had already left the home when I was born. But fourteen years ago, as of Monday, I was blessed with a baby sister.
Rachel and I are as different as night and day. With so many years between us, we often disagree. And with so many years between us, there is a fine, fine line between sister and parent for me, which drives her exceedingly crazy.
But she blesses me so much. I'm so crazy about her. She's growing into a fine young lady. She has her moments (what 14 year old doesn't?), but overall she is smart, funny, out-going, and truly cares about people.
When I asked her what she wanted for her birthday cake, all she would tell me was that she wanted light blue and light pink and chocolate cake. So, I had to get creative. This is what I came up with:



My sister loves music.



She sings like an angel.


She has recently taken up bowling, and plans to be on the bowling team when she goes to high school next year.

And she ALWAYS has her crazy pink iPod stuck in her ears (and turned up WAAAYYYY too loud).


She loved the cupcakes and the other small gifts I got her. And I was happy I was able to make her birthday a little more special, just like she's made my life more special.
I love you, Rachel.

Monday, April 19, 2010

Late Post on Endo Visit....

I went to the endo last Monday. I was supposed to post this last week. But sadly, my week was spent doing nothing but working and baking/decorating cakes. So there were no blogs. Sigh.
I love my endo. I am a patient at Vanderbilt University's Diabetes Center. The office is huge. There are many doctors, nurses, nurse practitioners, CDE's, etc. When I first transferred to this center, I was concerned that I might feel like a number, or like I never saw anyone I knew.
That was not the case at all. I am on my 4th (5th?) visit if I'm not mistaken. I have seen the same endo, nurse practitioner, and CDE every time I've been there. The office staff seems to been the same (I recognize faces when I go in). Every time I've had lab work done, the same guy has done it. Until this visit, the nurse who checked me in was the same lady. This time was the first time I'd had a different nurse.
I like that. It makes me feel like I'm part of something. Even though I'm sure the doctors and nurses may not remember me every time I'm there, I know that the chances of them remembering me are higher, simply because I see the same person every time. That in itself is a comfort to me.
At this visit, I was scheduled to see the CDE and my endo. I was looking forward to it. I had a list of question to talk with the endo about (one of which was Symlin) written down before I even got there.
For the past several visits (almost a year), my A1c has been stuck at 6.9. Everyone was really happy with that number, but having seen a 6.3 (and held it for 6 months), a 6.9 had been very frustrating to me. The first thing they do when they check me in is my A1c and vitals. It takes about ten minutes to get results back, so I was in the exam room waiting by the time the nurse got my results back. She knew I was anxious to know the results so she stuck her head in the door and said "6.6".
My joy knew no bounds. I'm quite positive I looked like a total idiot as I cheered for myself. But I really didn't care. And still don't. That 6.6 was so much nicer than the 6.9 I'd been glued at for so long. I feel like I had been working somewhat harder at getting that number down, so it was nice to see somewhat of a payoff.
When the doctor came in, I started off by discussing my morning spikes in blood sugars. Almost every day when I get up, my blood sugar is in range. I don't eat anything. I am not a "first thing" eater. I have to wake up some. So I get up around 6:00 and get ready for work. I usually grab something to eat as I'm walking out the door to work at around 8:00. And almost without fail, between 8:00 and 8:30 I start to spike. And it tops out in the 200s before coming back down.
It doesn't matter what I eat, when I eat, or even if I eat. It happens 95% of my work mornings.
Weekends aren't the same. I typically don't have that spike. If I do, it's rare, and not as violent increase or decrease.
This leads me to one conclusion: Work causes my blood sugar to rise. Or more specifically, the stress I feel when going to my job and while I'm working. Don't get me wrong, I'm beyond thankful for my job. But it's high stress, not something I enjoy most of the time, and not something related to my field. But, when a diabetic has great health insurance and a steady paycheck....well, let's just say I don't want to rock the boat.


*cue Glee version....*






During the discussion, I bought up Symlin. My doctor gave me some information on it and told me to think about it and we'd discuss it at the next appointment. I was glad she said that. I wasn't sure I wanted to go on it. But I did want to learn some more about it and wanted to know if she thought it could be something to help me. We also did some adjusting to my basal rate during the week. We increased my basal around the time that I am spiking in the morning and hoping this is something that will help take care of the spike so that I don't have to go on any other medications at this point.
I also asked her about my eyes. As I shared not long ago, my regular eye appointment showed some bleeding in both of my eyes. I was worried about what to do and how to handle the situation. My doctor immediately confirmed that I needed to not only make an appointment with a specialist, but that I didn't need to wait 6 months. She suggested that I make an appointment fairly soon. She basically said, just in case, it's better to have a specialist look at it now and to keep seeing a specialist in the event that I ever needed eye surgery. So, even though I've not done it yet, I will be making that appointment within the next week. I'm hoping to get in to see someone in the next month.
Next up was meeting with my CDE. I <3 my CDE. She actually listens to me when I talk. The first meeting we ever had, I told her flat out that I was NOT a record keeper. All my insulin info and blood sugars are in my meter and pump, so why bother? And as for a food diary, that's laughable. I might keep one for half a day. And then I forget to write something down, I get frustrated and I quit.
When I told her that, she listened. She, instead, worked with what my pump and meter had and talked to me about the types of foods I eat and when and what I snack on. I love that she didn't try to push me to keep records. It can be really frustrating when doctors or CDEs keep at you to do something that you know you aren't going to do anyway.
I shared with her what the doctor had said about my morning spike and she agreed that the spike was more than likely emotionally based.
Then we started looking at the few mornings when I have an above average blood sugar. Typically they only happen when I eat late at night. After she asked me some questions, she (and I) came to the conclusion that the high blood sugars aren't from anything other than me miscalculating doses and insulin to carb ratios because I'm afraid of dropping too low in the night (I live alone, after all).
All in all, she said that I didn't need to do much. But "if I have to pick on something, I'd say quit eating so late at night. It makes your blood sugars go crazy." :) See? I <3 her. Overall, I was pretty pleased. I have another appointment in a few months. Let's hope that these changes in basal rates take care of my morning spike during the week. If they do, maybe I'll be back at my 6.3 (ohhhh....happy thoughts!).

Sunday, April 11, 2010

gLee



Tomorrow night. I've been waiting for months for this. Now it's time.




Wednesday, April 7, 2010

New Creation, New Method

You all know I live in the South. :) And while many of the things you hear about the South are nothing but myth (YES, we have indoor plumbing. And shoes. And some of us even have college degrees! LOL), other things you may hear lean more toward being truth, than myth.
One of those things (at least where I grew up) is the plethora of camouflage that takes residence in the closets of most of us in the South.
Hunting and camo are pretty regular things in my area. I even had a teacher in 8th grade that actually took the first day of hunting season off work. Totally not lying about that. :P
Anyway, for sometime now, I've wanted to do a camo cake. I had seen some that I liked and some I didn't, but I'd never had anyone to make one for. Most of the people in my family aren't hunters. We have more fishermen.
A couple of weeks ago, I had an "emergency" text from a friend requesting a last minute cake for a child's birthday. And by last minute, I mean VERY last minute. It was about noon on Saturday and they needed it Sunday morning. Luckily, I had a free evening and the desire to bake, so I said yes and asked what kind of things the child was interested in.
As soon as the word "hunting" came out of her mouth, I knew what I wanted to do. Camo cake, here I come!

I understood the basic concept of getting the icing on there. I have learned almost everything I know about cake decorating from the website CakeCentral. I highly suggest it if you are at all interested in learning the art that is cake decorating.
I made my 5 icing colors (I am missing one of the bags in the picture) and got started. Basically, after filling the layers, and adding a crumb coat (a very thin layer of icing that you decorate over), I put the cake in the freezer for about 15 minutes.
When I took it out, I took the 4 camo colors and iced over the whole thing. This is what it looked like at that point:


Not very pretty, huh? I didn't think so either. LOL. I then used a method called the Viva method to smooth the icing out all over the cake.
And no camo is complete without hunting orange accents. So I took orange decorator gel with a small amount of red gel to give it the proper color. A put an orange border and letters on the cake and this is how it turned out:



It was surprisingly easy to make and everyone seemed to be really happy with it. So, mission accomplished. :)






Tuesday, April 6, 2010

Broken and Scraped

Yesterday was one of those days. You know the kind, right? The kind that makes you want to crawl in bed and suck your thumb and hold your blankie in the other? Yeah, that's the kind of day I had yesterday.

It started out with knowing that my car needs new breaks. In fact, I need them YESTERDAY. My mechanic (i.e. my wonderful step-dad) is currently under the weather, so for now I'm driving my car as little as possible. This isn't too difficult for me, considering that I live a total of 0.2 miles from work. The weather has been beautiful for the past couple of days, so I've taken advantage of that and I've been walking to and from work. It's really something I should do more often.

Then, work yesterday was pretty much stress to the max. I try not to complain too much on this blog about my job. I'm thankful for it, even when it's stressful. But yesterday I left work with knots in my back from being so tense. I hate days like that.

Monday nights is community choir practice for me. It's something I can do without being featured (since my voice isn't that great, but not horrible either) and it lets me explore my love of music. When I got to choir practice, I caught my pump on something and SNAP! I broke my pump clip. I use my pump clip all the time. In fact, the only time I don't use it is when I have a dress on and am using the thigh holster or storing it in my bra. And if you know me, my dress wearing is minimal at best.

My pump, and therefore my pump clip, have been through a lot with me in the past (almost) 4 years. I'm not the most graceful person. I even fell down the last couple of steps of my apartment and fell ON my pump one time. And the clip didn't break. But if you look closely at the picture below you can see the scratches where that happened.

But after last night, I was pretty sad about my clip. I can get by, most of the time, with sticking my pump in my pocket, but at night, I clip it to my pajama bottoms, and that's impossible without a clip. So last night I broke out the larger, more bulky holster clip. I hate it. So first thing this morning I ordered another clip. Thank goodness for speedy shipping, courtesy of MiniMed. It should be here by the end of the week.

Well, when I got home from choir practice, I logged onto Twitter to complain about my broken clip, but before I could do that I was tossed into the mix with the many of us in the D-OC who found out we'd been "scraped". Until last night, I didn't know this term, but basically, it means someone was taking out blog posts and posting them as their own with no credit or link back.

To me, this is the ultimate betrayal. It's stealing something from me that can't be replaced. It's someone stealing my WORDS. I was furious, as were many others in the OC. I was switching back and forth from Twitter to Facebook and talking with several other people in the OC. We were trying to figure out who to contact to report the problem. After a while, it was apparent that most of us had done all we could. But I was still upset and it was nearly midnight before I could go to sleep.

I could go into all the reasons why being "scraped" made me feel violated, hurt and angry. But I won't. I'm sure those of you who are reading were probably right there with me. I will just say that this morning, when I got up, the site had taken down EVERY post and posted an apology (in very poor English, but an apology nonetheless).

I had hoped it was the start of a better day. And it turns out that it was. Thankfully. After a day like yesterday, it was nice to have a more calm Tuesday.

Monday, April 5, 2010

Life Choices

A few days ago, Lee Ann, over at The Butter Compartment, posted a blog about being in the minority of people who have chosen not to have children. As I read her blog post, I got fairly emotional and wanted to comment. But then I realized how much I had to say, so instead I talked with her and decided to post my own blog on this very sensitive subject. And while my ideas may vary some from Lee Ann's, I understand her views and I encourage you all to read her post. It is truly moving.


I was diagnosed in 1986. I was never told (that I can remember) that I shouldn't have children, but it seemed to always be a silent understanding that I might not live a long life and that having children could be very hard on me (hello, Steel Magnolias).




I'm a kid person. I love babies. Even when I was 12 and 13, I was helping out in the nursery at church. I went to school to be a teacher. I worked in child care for several years. Even now, I teach a Sunday School class at church to get my "kid quota".
I always remember wanting children, but just automatically saying that I wasn't going to have them; that I would adopt instead. Adoption wasn't a big deal to me, since I was adopted. I never thought twice about it and never really felt like I was "missing out" on anything.


My mother didn't have a biological child until I was 15 and my baby sister was born. I never felt any different being adopted. And I just thought that I'd get my children a more non-conventional way.


When I was in high school, I was terrified of getting pregnant. Therefore, I escaped high school "unscathed," so to speak. It was always in the back of my mind. I had a dream when I was a senior in high school that I was married. I couldn't see who the person was, but I knew his name. And I was crying because I'd found out I was pregnant. I was so scared. In my dream, I remember Mr. Mystery Man telling me that everything would be okay and that we'd get through it fine.


For a girl who doesn't dream on a regular basis and NEVER remembers it, I can still tell you how I felt during that dream and after waking up. I wanted to be strong. I wanted to be happy. But I was scared. And for someone who is decidedly pro-life, my dream self even entertained ending the pregnancy (although I know I wouldn't do that now).


For someone who is fairly young and in decent health, I have seriously considered having my tubes tied. I haven't done it for the simple fact I've not felt the need to push it when I've not been in a serious relationship where I felt pregnancy could become an issue.


I'm creeping toward 30 (I say creeping, since I want to hold off on the big 3-0 for as long as I can ;P ) and as I've gotten older, I've thought more about having a biological child. Until the past 3 or 4 years, I didn't even entertain the idea of having my own child. But being an active part of the D-OC, and having friends who are diabetic and have had children with no problems, I let myself play with the idea a little more.


I don't have many of the health issues that Lee Ann has dealt with, but I share many of her fears. I spent a childhood with semi-decent care (not the best, not the worst). But my teen and young adult years were sketchy at best. I rang in several A1c's that would make any endo cringe. It wasn't until I got out of college that I really took control and made a serious effort to control my diabetes. For a long time, I thought I might have actually been blessed enough to avoid any serious complications from that time in my life. But with the occasional tingling in my feet and my recent eye doctor's visit, I realize that poor care or not, I'm 24 years into a disease that slowly damages every major organ of my body.


Currently, I'm glad that I didn't get my tubes tied when I first decided to. Mostly because I want the option there. But I'm not sure I actually want to have children of my own. And until I'm sure of how I want to do this, I don't want to make any life-altering decisions. My new endo's profile on their website states that she specializes in diabetic pregnancy. And while this comforts me, should the need ever arise, I still am uncertain about how I want to do things.


And I guess I don't need to make any decisions since I'm not even in a relationship at this point in my life. But so many things from Lee Ann's blog resonated with me.


How do you approach NOT having children in a new relationship? While I want to leave the option open, I also don't want to give anyone any false ideas about my becoming a biological parent, when I may chose not to take that route.


Why would I want to cause my body any more damage, risking leaving a child without a mother and a husband without a wife (and a single parent to boot)? Part of that fear may come from having lost an aunt due to uncontrolled T2 diabetes. This left my uncle a single father, and a small child without a mother.


And what if my child developed diabetes? I know you can't control that. To my knowledge, T1 diabetes didn't run in my biological family (although I don't know anything about my biological father). But it is still an increased risk of passing diabetes on. And to be honest with you, I don't know if I could live with the guilt of knowing my child developed diabetes. I had a friend who told me that my adopted child could get diabetes. After all, I did. But at least I would know it wasn't my DNA and my genes that were part of the reason.


Like Lee Ann, I've dealt with many well meaning people who think I've lost my mind. I have a very dear friend who has said to me on several occasions, "You should have at least one of your own. You should experience pregnancy at least once. It is so wonderful." And I'm sure it is. I have several close friends with children. They talk about the wonders of pregnancy. But I may not take that road. Does that make me "weird?" Maybe. Does that make me less of a woman? I don't think so. Because I choose not to have biological children of my own doesn't make me any less of a person. It simply means I've chosen another way.


People make their life choices for a variety of reasons. I've not made a set-in-stone decision at this point. But I believe people should remember that everyone should make the choices that are best for themselves. And that includes whether or not to have a biological child, or even to have children at all.


Tuesday, March 30, 2010

Alarming

Sunday night I ate a semi-late dinner. I typically eat no later than 7:30, maybe 8:00. Sunday I got busy and wasn't really hungry. Most times like that I would just skip the meal altogether.

This time, I didn't. Instead, I ate around 8:30. I bolused and by bedtime (around 11) I was clocking in fairly well in the mid 100s with some insulin still on board.

I have had problems in the past with not hearing my CGMS alarms at night. Typically it gets to the point where my pump has started vibrating. But, still, it wakes me up.

Sunday night, I didn't have such luck. Or better yet, my "luck" included me turning off the alarm every time it went off, and never doing a thing about it.

This is what my sensor alarm history looks like:

11:35 pm - 172 (I have my high alarm set at 170)

12:34 am - 242

1:35 am - 252

2:34 am - 190

3:35 am - 198

4:34 am - 228

5:35 am - 258

6:34 am - 212

My Insulin Bolus History shows no action was taken until I was awake at 6:00 am. I tested and was in the high 100s. I corrected and continued about my day, hoping for a better grasp on the blood sugars. Sadly, that didn't happen. I chased highs all day long until I began rage bolusing and bottomed out at around 3:00 pm.

However, my rage bolusing is not the subject of this post. My lack of action on the high alerts is my problem. I vaguely remember hearing one alarm. All the others I must have turned off in my sleep.

So far this has never happened to me before. My concern is what if it had been a LOW alarm, instead of a high alarm? That could have been bad. Very bad. I got my CGMS partly because I live alone, and I like the security.

So, I guess this is a call to MiniMed: Make the alarms louder. Or give us the option to make them louder (for situations like this).

Cause, maybe if they were louder, I wouldn't turn them off in my sleep without really waking up.

Monday, March 29, 2010

iPod Challenge: Part Deux

I hadn't done this in a while, so I thought I'd start it up again. A meme of sorts. :) Plus, I wanted to compare it to my list from last time. Oh, and just a disclaimer: I don't actually own an iPod. I have a Zune, which I love very, very much. It's just that everyone pretty much has an iPod. And I wanted a title that could be recognized.
So, put your iPod (or other mp3 player) on shuffle and list the first 25 songs that play....

1.) There's No Buisness Like "Show Business -from OBC of Annie Get Your Gun

2.) Just Might Make Me Believe -Sugarland

3.) Cold As You - Taylor Swift

4.) Friends - Band of Skulls (from the New Moon Soundtrack)

5.) Story of My Life - Bon Jovi

6.) Trani - Kings of Leon

7.) Crazy Ex-Girlfriend - Miranda Lambert

8.) Complicated - Carolyn Dawn Johnson

9.) I Thought She Knew - 'NSYNC

10.) One of These Nights - Eagles

11.) Let's Fall In Love - Rod Stewart (from the Great American Songbook collection)

12.) Long, Long Way From Home - Foreigner

13.) Does the Wind Still Blow in Oklahoma -Reba McEntire w/ Ronnie Dunn (from Brooks & Dunn)

14.) Leaving You - Nickelback

15.) Don't Rain On My Parade - Lea Michele from Glee Soundtrack

16.) God Must Have Spent A Little More Time On You - 'NSYNC

17.) Last One Standing - Emerson Drive

18.) Big Blonde & Beautiful - Hairspray Original Broadway Cast

19.) Cold Desert - Kings of Leon

20.) Endless Helpless Hoping - Josh Gracin

21.) Woke Up This Morning - Nickelback

22.) The Way You Look Tonight - Rod Stewart (from the Great American Songbook collection)

23.) All I Wanted Was a Car - Brad Paisley

24.) Time With You - Billy Currington

25.) The Woman With You - Kenny Chesney


The only justification on any of these songs is my 'NSYNC. My only excuse is that I dug them out to try to cling to my youth. At least I didn't break out the Britney. :P

So, join me. Try this for yourself. And give me some suggestions. I'm always about widening my musical horizons.

Thursday, March 25, 2010

Mamma Mia!

Theatre Thursday is here again folks! Lately I've been to see several shows, so I should have a Theatre post for the next few weeks in a row.
Back before Christmas my mother and I watched Mamma Mia!, the movie. We both thought it was thoroughly cheesy and we both loved it (If you know us, you'd know that both thoughts are completely possible at the same time...).

Through my wealth of useless knowledge about all things Broadway related, I knew that Mamma Mia! the Broadway touring production was coming to the Tennessee Performing Arts Center (further known at TPAC) in the spring of 2010. Immediately, my mind went to Christmas gifts, and what a great gift it would be to take my mom to see the show.

My mother has never been to New York. She's never seen a Broadway show before. But she spent a lot of time growing up doing plays at school and singing show tunes in choir. In fact, she sang me more show tunes than lullabies when I was a child. She is basically the reason I love musical theatre so much.

After confirming that I could get tickets before Christmas, I knew right away that's what I was going to do. I also purchased the movie, unwrapped it (and let's be completely honest, I watched it, too) and put the tickets inside the DVD case.

She was thrilled when she opened her Christmas present. And I knew that I'd not only get to hang out with my mom (which I don't do nearly enough anymore), but I'd also get to see a show. And what's better than a show? Sharing it with people you love, of course!

This is a few weeks ago now, so I figured it's time for the theatre critic in me to come out. First of all, I'd like to say that both my mom and I, along with a great friend of mine that went with us, had a fantastic time. Second of all, I'd like to say the the show is every bit as cheesy and fantastic as the movie. Actually, a little more fantastic, just because it's live theatre and not a movie.

Mamma Mia! has been on Broadway for several years now. It's currently playing in the Winter Garden Theatre (where Cats was for so many years!). The poster even says "The Global Smash Hit". And it really is global. The show currently has productions in London, New York City (of course), Norway, and Mexico. There is also a North American Tour, an International Tour, a Dutch Tour, a Spanish Tour, and an Australian Tour. Whew! If that doesn't say "Global Smash Hit", I don't know what does.

Now, onto my review:
For those of you who have never seen the movie or the musical, I'll give a brief synopsis. The show is about a young woman, Sophie, who is about to get married. She has been raised by her single mother, Donna, never being told about her father. In her desire to meet her father, she discovers that her mother doesn't even know who it is; there are three possibilities.

So, without Donna's knowledge, Sophie invites all three men to her wedding, hoping to discover who her true father is.

Of course, hilarity ensues, especially upon the arrival of Donna's old friends Tanya and Rosie, and her three ex-beau's, whom she's not seen in twenty years.

Throughout it all, Sophie learns that family is what you make it, and Donna learns that sometimes it's okay to ask for help and that love doesn't always go away.

And the greatest part of the show: every single song is an ABBA song. I wasn't born when ABBA was popular, but like most people (at least people with good taste in music ;)...) I've learned many ABBA songs over the years. And I can assure you that nearly every song that you would know by ABBA is in this show, from the title track, Mamma Mia, to Dancing Queen. There are 22 total songs in the show, and I knew about 80% of them going in.

All the actors and actresses did a good job, but Rachel Tyler, who played the role of Tanya, and Kittra Wynn Coomer, who played the role of Rosie, stole the show. Their comedic timing was impeccable and they were probably the most talented of all the actors and actress in the show.

So, is Mamma Mia! the greatest musical ever written? No way. Not by a long shot. But it's fun, and funny, and is something even a non-musical lover could enjoy, if for nothing more than the songs. There seemed to be a large number of women enjoying the show with friends, especially women who were young during the ABBA reign. And I know that I enjoyed every second of it.

Wednesday, March 24, 2010

My Adoption Story

I realized, in the past few weeks, that many of you don't know that I'm adopted. Some of you may. It comes up in my conversations (especially when relating to diabetes) quite a bit. Since Elizabeth Arnold, who I've gotten to know on Twitter, and more recently, in her new blog, is adopting, I thought I'd share my story with all of you.
To save on confusion in my story, any reference to mom, dad, or parents refers to my adoptive parents. Any time I am referring to my biological family, I will use the term "birth" or "biological".

My parents met, and were married in southern California. Both had spent a majority of their childhood, and all of their adult life in California. When they married, my dad already had a son from a previous marriage and my mom and dad were unable to have children. My mom wanted a child.

At the time, they were attending Calvary Chapel in Downey, California. Calvary had just started an adoption ministry called House of Ruth. Years later, I would write to the director, Karyn Johnson. She told me I was one of the first adoptions that House of Ruth helped to facilitate.
My mom and dad never hid the fact that I was adopted. I always knew. My mother had a cross-stitched picture that she kept on my wall in my bedroom. I still have it. It was of a mother holding an infant. The poem under it reads:

Not flesh of my flesh
Nor bone of my bone
But still, miraculously, my own
Never forget for a single minute,
You didn't grow under my heart
But in it.

That's how I always felt. My mom and dad told me how special I was. Because they got to pick me. That someone loved me enough to give me to my mom and dad, who could take care of me better and love me more. As a child, that made me feel wonderful.

As I grew older, I learned a more about the story behind my adoption. It's never that simple, is it? When we are children, a child-like terminology can explain it all. As an adult, the story and details behind it make it so much more special.

My parents signed up on a list of adoptive parents through House of Ruth. Shortly after that, my parents moved to Tennessee. My father had spent his early childhood in Tennessee and still had family here. He and my mother moved and began their lives here, while waiting to hear something about a baby.

My mother had prayed and believed that God had promised her a baby girl. But it was 3 years and several let downs before I would enter the picture. And even my entrance was filled with drama. My mom tells me there were several birth mothers who pulled my parents' profile. They would be all excited....up to the point they found out that the baby would be living in Tennessee. I'm not sure, but I think there were people who still believed that there was no indoor pluming here.... and that we never wore shoes. (Totally not true, by the way...I have had indoor pluming my whole life. And we do wear shoes...most of the time ;P )

But my parents kept praying. And my mom kept believing that she'd get her baby girl.

When my birth mother and her family contacted House of Ruth, I believe the fact that I would be far away from California was a positive for them. My parents had little time to prepare for me, if I have it timed correctly in my head. My birth mother was in her 6th month before she told anyone she was expecting.

The the surprise. I came a month early. I was sick. Very sick. When the doctors called my parents, they told my mother not to bother flying to California because I wasn't going to make it. I had a valve in my heart that wasn't working properly. They were flying me from Los Alamitos General Hospital in Orange County, to Long Beach where there was a more capable NICU.

After talking with the doctor, she told him that she'd be on the first plane out of Nashville because God had promised her a baby girl and she wasn't going to lose me now. She said "God's working through your hands, doctor. She'll be okay."

The story goes that the doctor, a known atheist, got on the helicopter and informed the flight nurses that they'd better get a move on because "Ladies, God is apparently working through my hands today. Let's go take care of this baby." My mom said when she finally got to the hospital in California, that all the nurses came out of the back to see "the lady that had made the atheist doctor talk about God." I've always just thought it was a wonderful example of my mother's strong faith in God.

At the hospital, they were trying to use a new drug to get my heart to start working correctly. If that failed, they were going to have to do heart surgery. But the drug worked. I was in an incubator for 17 days. In the hospital for a little longer than that. The picture below is of me at 3 weeks old. The bear next to me was a gift from my birth mother. I still have it. I always thought I was an UGLY baby. My head was HUGE and kind of wrinkly. I think I looked like a little alien. Mom says I was beautiful (of course) and that I grew into myself very quickly.


My parents took me home to Tennessee. I am pretty sure that my mom sent pictures a few times. And when I was 4 years old and diagnosed with diabetes, my mom said she contacted someone to find out if T1 ran in the family. To their knowledge, it didn't.

For a long time, I don't think there was any contact. Then, when I was about 15 or 16, my mom was contacted about my birth mother wanting to meet me. My sister was still a baby, and I wasn't going to go on my own. But by the time I turned 18, we were contacted again. I agreed to go. I spoke with my biological grandmother on the phone and she sent me a collection of pictures of my birth mother, my aunts, their husbands and children. Some were of my birth mother and her sisters when they were younger. It was interesting. I could see myself, somewhat in those pictures.

I started college in the fall of 2000. For my fall break, I flew to Idaho (where the family was now living). It was only my second time on a plane (not counting my flight from California to Tennessee when I was a baby). It was my first time ever flying alone. My dad was a little worried about me going. My mom wasn't. I'll never forget the conversations I had with both of them that day.

That morning, I had a complete melt down. I was terrified. Of what? I'm not sure. I lay in my bed crying. I begged my mom not to make me go. She said to me, "You've blessed my life for 18 years, Cara Elizabeth. I'm your mother. I'll always be your mother. But you need to go be a blessing to these people too."
I went. Willingly. My dad drove me to the airport. This was all pre 9-11, so my dad went with me to the gate. He sat in the chair and didn't say a whole lot. He usually doesn't say a whole lot. But that day he said, "Promise you'll come back. I don't want you to go out there and not come home." All I could do was hug him and let him know I'd be back. I'm my daddy's baby. I had to let him know no one could take his place.

I spent 4 or 5 days with them (I don't remember exactly; it's been 11 years!). Stepping off the plane walking into the arms of the people who I share DNA with was surreal. Over the time there, I met my birth mother, her mother, my two biological aunts, their husbands and 3 first cousins. All along, I found little things (and big things) that were like them. Some things I would have never considered genetic and after meeting them, I think they might be.

I'm a lefty. There were other lefties in the family (although my dad and niece are lefties, too, so that could go w/ genetics, or learned...). There were two teachers (I have a degree in education). My biological grandmother and I had a very similar taste in books and colors. At night, I take a bottle of water, or something to drink w/ me and sit it by my bed. Sometimes I may drink it. Sometimes I may not. But its there if I want it. I found out that everyone in my immediate, biological family does the same thing. In my family, I don't know of anyone who does this.

Overall, my trip was wonderful. I learned so much about my "other" family. It was a fantastic experience in so many ways and is something I will never, ever forget, or regret. I've not been back to visit since, but I stay in contact by phone with my biological mother, and on the internet with other various family members.
Many people have asked if I consider my biological family as part of my family. In many ways I do. But my true family, the family that I will always consider my family is the family who raised me. They took me in willingly. They loved me. They cared for me through this lovely chronic illness we call diabetes. They've continually supported me in everything I've done.

I just happened to be a lucky one. I have two great families. And I love them both.

Tuesday, March 23, 2010

Dentists and Eye Doctors, oh my....

Today I had 2 different appointments. I set up my dentist and eye doctor on the same day to basically get them both out of the way. I was overdue for a dentist appointment and a little late for an eye doctor appointment. Getting them both in one day helps with work also.

I chose to put the dentist appointment first because I knew, after eye dilation, that I would be useless for the rest of the day. My eyes take an abnormally long time to return to their original state.

At the dentists, it was discovered that one of my fillings had chipped. This means another appointment to get it fixed. Also, I apparently have a wisdom tooth coming in. I didn't know it. And I've not had any come through before. The dentist said since it's not bothering me that we'd not worry about it for now.

A good cleaning and fluoride treatment later, and I was ready to go. No new cavities. Nothing major, other than the chipped filling. I have to say, I left feeling pretty good about myself.

I asked my mom to drive me to the eye doctor. I've been going to the same eye care center since I was about 15, save for a couple of appointments in college. During my time there, I've only seen 2 eye doctors. One of them, sadly, passed away when I was just starting college. The second doctor had been there every since.

Today, I found out there's a new eye doctor. Apparently the other one moved on. When I saw the new doctor, I nearly fell over. I went to high school with him! He was YOUNGER than me! And he's an eye doctor. Okay, that makes me feel really old. I don't think he remembered me. Which is fine. But I have to say, I almost yelled, "Oh my GOD! You're my DOCTOR???"

However, he did a good job and was very professional. It's just a little weird having someone younger than me, be my doctor.

Sadly, when he was done with my eye exam, the bad news came.

I have bleeding. In both eyes.

After 24 years of diabetes, and only 1 other time of having any bleeding at all (which was gone the next time I went in), I have bleeding in both eyes.

He was very positive about it. The right eye, he expects could be gone at my next eye exam. It's that small. The right eye, he sounded like he didn't expect it to go away. He did say it's on the outer area of my eye, so it's not an issue at this point, as far as vision goes. He even said it could possibly get better.

But he didn't sound like he expected it to go away.

I have an endo appointment next month. He planned on sending my report on to my endo. He also said he didn't really thing that I needed to come in for a 6 month appointment. His words were, "It's such a small issue right now, unless you have a change in vision or some other problem, I don't even feel like we need to see you again for a year. Six months is not necessary."

But I'm scared. I know it's not a big deal. I know, after 24 years of living with diabetes, my eye issues are minimal compared to what they should be. But I'm still scared.

Some people with diabetes fear loosing a limb. My greatest fear is losing my sight. I could figure out how to deal with being in a wheel chair or on a walker. I could figure it out.

But being without my sight is so very scary for me. So many of my joys and hobbies depend, almost totally on my sight. Reading, cake decorating, watching Broadway shows, blogging. Even my sign language. They all require my sight.

Could I do it? Could I live without my sight? I'm sure I could. God won't ever give me anything I couldn't handle. I meet people every day that say they couldn't have diabetes. But until you have it, you don't know what you can do. But I have to say, I hope I don't ever find out what it's like to live without my sight.

And knowing I could do it, doesn't make me any less scared of actually having to do it.

Monday, March 15, 2010

Choices, Choices, Choices...

I grew up in a really, really small town. Most of you would be amazed at how small my town really is. Until I was 8, we didn't even have a Wal-Mart. And when we got one, it was so small that they didn't build one any smaller. Ever.
I remember when it opened. My dad and I went in and I headed (like I always did...and still do) to the stationary section. I have always been obsessed with pens and pencils and notebooks and stationary. I don't know why. But I have. I'll never forget my dad saying, "There are just too many choices. How are you supposed to chose?"

I'm pretty sure he was joking. But I remember silently agreeing with him. How was I supposed to pick a new pen when there were so many to chose from? Different colors. Different sizes. Different inks.
Part of me is still that way, even though we have a bigger Wal-Mart now, and I've seen the wonders of Staples and Office Max in other places. Part of me still wishes, to some degree, that there were only 2 or 3 choices. Then it wouldn't be such a hard choice. You'd get what you'd get and you'd be happy with it. Or, as one of my Sunday school kids says, "You get what you get, and you don't throw a fit."


Maybe I'm indecisive. But I also feel that way about insulin pumps. I began pumping on May 1, 2006. Which means four years is just around the corner. I'm (for the most part) happy with my MiniMed 722. I am (for the most part) loving my CGMS. But my warranty on my pump will be up in May. And my CGMS warranty has actually already been up for a while.


But sometimes I want to try something new. I wonder about other CGM Systems. I wonder about other pumps. And I wonder why I can't try one, really try one, without risking being stuck with something I hate for the next four years.

You know the grass is always greener on the other side....until you get there. And like I said before, I'm not UNhappy with my MiniMed system. But sometimes I just want to take some others on a "test drive". To see if the grass really is greener on the other side, or if I need to stick with what I know works. With what makes me happy and what works and what my insurance pays for.

So, my question today is, do you guys ever feel that way too? Do you wish you had more options? Or do you think you have too many options?

Wednesday, March 3, 2010

My Latest Creation


I've not been caking much lately, but the next couple of months will have more due to several birthdays and holidays coming up. Here's the first of my new string of creations:

Enjoy!

Monday, March 1, 2010

Elliott Yamin

Diabetes and Music Monday meet.

Elliott Yamin was on American Idol a few years ago. He was one of my favorites and he finished third. He is also a Type 1 diabetic. I know a lot of people talk about how American Idol uses the back story to promote different people. Some people like it, some don't. You would think that having diabetes would make for a great story. But I don't recall hearing about Elliott having diabetes until almost the end of the season. And I watched EVERY EPISODE. He had already become one of my favorites, but after hearing that we had diabetes in common, it quickly sealed my love for Elliott.

He has worked some with JDRF that I know about and I'm sure he's done other things in relation to diabetes.

Last night I found out that Elliott was in Chile when the 8.8 earthquake hit. I read about it on some news site (I don't remember which). I immediately went to his Twitter feed. I found out that he had been tweeting consistently since the earthquake and was doing some interviews with different media outlets.

I also found out that he was running low on insulin. Very low. He stated on his twitter account that they had only planned to be in Chile through Sunday and that he hadn't brought much more insulin than that. (He has been traveling quite a bit in the past weeks, all over the globe.)

The thought that Elliott (or anyone for that matter) would be caught in situation like that brought fear to my heart.

Two different times he Tweeted about being low on insulin. Then, earlier today, he tweeted an SOS message asking media people who were traveling out of the country if there was any way he could go with them since he was running so low in insulin. Again, I was scared for him.

He tweeted that they were telling him they could leave Wednesday. Then Friday. Then they weren't sure.

All I could think was that if he was running that low on insulin, he wouldn't make it to Wednesday or Friday.

Just a little while ago (around 5 CST), he tweeted that he was now doing okay on insulin and there was no need to worry.

I sighed in relief.

Knowing he had insulin made me a little more calm

I know some people may say "Why would you get so upset about someone you'd never met?" My only answer is that I can only imagine the fear that I would be feeling. The panic that would set in, if I were in that situation. I realize that in the event of any natural disaster, a lot of people can die from lack of medical care. But people think about lack of medical care regarding injuries, most of the time. They don't think about lack of medical care in regards to people with chronic illness. Elliott just put a face on that.

I wish Elliott a safe rest of his time in Chile, and a safe and speedy trip back to the States.

Lesson: Always pack extra times 3

Statement: Never yell at me for packing waaaaayyyy too much stuff when I got on vacation. There's a reason I have a suitcase big enough for myself to fit in....

Thursday, February 25, 2010

Wasting Money

Sometimes we waste money. No surprise there. We buy clothes we never wear, or make-up we never use. Or a CD or DVD we only watch once. I try not to do that very often. But sometimes it just happens. Even more, sometimes we buy things *gasp* we DON'T REALLY NEED! Ekkk!

I did just that last week. And my frivolous prize came in the mail today. Gratefully on a day when I really needed some retail therapy. I'm feeling much better now, thanks. :)

I have written before about my obsession with theatre and all things musical. Since today is officially my Theatre Thursday, I am combining diabetes with theatre...again. Most of you (yeah, I'm talking to you Kelly!) know about my love of Wicked the musical, although any type of musical theatre will feed my addiction.

I just was Wicked (for the first time) when it came on tour to Nashville. I bought my tickets more than 3 months in advance. That's how excited I was to see it.

Well, Minimed (diabetes enters, stage right) offers skins for their insulin pumps. My pump is clear. I did that so it would match anything I wore. I bought a skin a couple of years ago from them and kept it on my pump for quite some time. I loved it, but got tired of it and took it off after a while. Since that time, Minimed has extended and offers a place where you can completely personalize your skin. Using a picture, or clip art, or whatever you want, you can make your skin look like whatever you want.

Although it's completely dorky of me, I went Broadway. Better yet, I went Wicked. Below are pictures of my new "wicked" pump.
The picture I started out with.

The top of my pump.







The bottom of my pump.

My pump. Yes, I know it looks upside down...

but I did it that way on purpose so I could see the full title on the bottom. :)

Wednesday, February 17, 2010

Diabetes and Fear

I know there are a lot of people who sit around and worry and fret over their future in relation to diabetes. What if I loose a limb? What if I have to have an amputation? What if my kidneys fail?

While these are all very real possibilities, they are by no means something I sit around thinking about. If I did, I'd worry myself straight into the grave long before diabetes ever even got it's chance.

Instead, I live my life to the best of my ability and let God take care of the rest. I do the best I can do at any given moment to take care of my diabetes. Sometimes my blood sugars are good. Sometimes they aren't. Either way, it's just that single moment in time. I fix it and move on.

I do have fears though. But they are more immediate fears. The right now, so to speak.

Here's my example:

I have a dear friend of mine who is a single mom. She has 2 young children and not a lot of family around to help her out. We do have a fantastic church family that is always willing to step up when needed, but as some of you may know, it's nothing like having family or a significant other around to help out when you need it.

The other morning my friend called me. She was very sick with a stomach virus. She was needing help and asked me to come over and help her with her children. My first reaction (on the inside) is "Sure! I'll be right over." But my second reaction wins out.

Fear. What if I get this virus? What if I end up in the hospital from it? (It was entirely possible as one of her children already had it and had to do to the hospital) What if, what if, what if?

I told her no. But I offered to help her find someone to come instead. She called some other people and got the help she needed.

That fear made me sad. It made me angry. And it made me realize what a great community we have here in the D-OC. I tweeted my frustrations about not being able to help my friend and had 2 different people (from 2 different states faaaarrrr away from me) want to know where in Tennessee I was because they had friends/family that might have been able to help out.

I hate that I have to be scared of getting sick. I've not been in the hospital in about 6 years. I've not been in the hospital overnight since I was....wow, I think I was about 7 years old. But that fear is there. The fact that I can get sicker, quicker and worse than a lot of my healthy friends makes me angry. Because earlier this week, it interfered with my being able to help a friend.

The immediate fears are there. No, I don't think about them all the time, but they are in my mind when I'm making decisions about when to test, when to eat, when to call a doctor, and apparently when to help a friend or not.

Do you guys have fears like that? Immediate fears dealing with the right now instead of the far off future?

Friday, February 12, 2010

Phantom Pains and Diagnosis Dates

I've been off the blogging for a few days because I had company in town. Originally she was only supposed to stay for a long weekend, but it turned into a long week because she lives in the northeast and was snowed OUT of home. I loved having company, but it made it hard to find time and inspiration to blog. But I'm back today with two seperate topics.


First up: Phantom Pains.


You know how people that lose limbs to amputation will sometimes have phantom pains? Well, I have infusion site phantom pains. You know that feeling when you have a slightly sore site from your infusion set or sensor? Or you are right toward the time when you are going to be changing sites and it starts to get a little sore?


Well, I sometimes get those same feelings in spots where I don't currently have an infusion set or sensor. Like today, I have a sensor in my left thigh. It has been in the same spot for around 3 days. But my right thigh (where I had my last sensor) occasionally has a phantom pain.


And when I went to push on the area to see if it was sore from the previous sensor, it wasn't the same spot and the spot where the pain had been wasn't even sore.


I also have that happen occasionally with infusion sites. Do any of you have that happen, or am I completely weird?


Next topic: Diagnosis dates.


Last Friday I blogged about my celebration of my diagnosis date. During this time, I noticed several other bloggers who had diagnosis dates very close to my own.


Allison, Katie, Rachel, Kathy and Sara all have diagnosis dates within a couple of weeks of mine. I also have a friend who is not part of the online community that was diagnosed in February. I wonder if it is the time of year... with our immune systems so comprimised and sickness triggering it and all that. I suppose that could be a plausable theory. I'd like to take a survey of when people have diagnosis dates.
When's yours?

Thursday, February 4, 2010

This Date In History

February 5, 1986. I'm sure there were lots of things going on in the world. I don't know what they were. I'm sure there were treaties being signed, or rock stars dying, or someone famous that was arrested. Maybe not. Who knows.

But February 5, 1986 was a day that my world, and the world of those around me, changed forever. After being very sick for a while, having nightmares, drinking water til it poured out the corner of my mouth, and wetting the bed several times a night, my mother took me to my family doctor. I'm sure there were other symptoms. I don't know what they were.
That morning, in the doctor's office, Dr. Joshi didn't even take my blood sugar before looking at my mother and telling her I had diabetes. A blood test verified it. As for the exact number, I don't know what it was. But my mother has always said that Dr. Joshi looked at her and said "How fast can you get her to Cookeville?" I'm sure they could have put me in an ambulance. But mom took me herself. The doctor told her not to even stop at home for clothes. Just to get me there.

I was in the hospital for several days, but you've all read this story before.

Instead, I want to talk about how much diabetes has given me. It's given me strength. It's given me friends. It's given me something that I think kept me out of trouble as a teen (nothing like the fear of getting sick to make you not was to party as a high schooler). Diabetes has given me sympathy for others and understanding that I don't think I would have otherwise.

It's been with me through thick and thin. Keeping me company, in a weird way. Present at every holiday and birthday. On every vacation. At every class I've taken. It was with me when I graduated college and when I paid off my first car. It was with me when I had my first date and my first kiss. And until a cure happens, it will be with me at every other major event (and minor event) in my life.


Boston Cream Pie Cake

So today, 24 years to the day after my world changed forever, I am going to have cake. And eat it too. I'm going to test and bolus and correct as needed. And have a wonderful time doing it.

This is the cake I really wanted....but, alas, it was made by Charm City Cakes and A) I can't afford it and B) it's too far away. Sigh. Someday.

Wednesday, February 3, 2010

TMI Post-Men, You've Been Warned

Okay, as most of you know I'm typically not a person who writes highly emotionally charged posts like I did on Sunday night. I was just feeling very frustrated and highly annoyed. However, it now makes sense. My monthly visitor came today. And as all of us women know, PMSing is one of the most emotionally charged times of our month.

Over the weekend I was fighting horrible high blood sugars. I assumed it was because I was constantly snacking and not doing alot because I was snowed in. However, hind sight's 20/20, right?
Typically, for 2 to 3 days before I start my period, my blood sugar runs crazy high. If I am thinking straight and I know it's coming, I'm prepared and I raise my basal rate by 10-20%. This usually works quite well.

Then, the day I start, my blood sugars plummet. I mean, non-diabetic type plummet. Yesterday around 6 p.m. my blood sugar leveled out at around 100. And it stayed there. All night long. I even tested in the middle of the night. I was 113. This morning, I woke up 93. By the time I got to work, I was 96 (this almost NEVER happens. My dawn phenomenon hits around 7:30 and I'm raising rapidly by the time I get to work at 8:00).

All day long I ate. I ate bad stuff. I ate food that I didn't bolus for. And I never got above 144. All day long. According to my pump, my daily average was 111. My daily sensor average was 96.


It's ironic really. That on a day when I truly feel like I've been hit by a truck (possibly a truck full of penguins....who knows) and I'm tired and cranky, that my blood sugar chooses to behave. Perfectly.


It must be Mother Nature's way of giving the diabetic chick a break. "Hey, since you have to feel like crap from your period once a month, I'll let the diabetes give you a break for a day or two. How's that? Will that work for you?" Well, Mother Nature, it would work better if I didn't feel like crap....and I didn't have diabetes in the first place. But hey, beggars can't be choosers, right?