Friday, May 15, 2015

Diabetes Blog Week - Foods on Friday


Taking a cue from Adam Brown's recent post, write a post documenting what you eat in a day!  Feel free to add links to recommended recipes/shops/whatever.  Make it an ideal day or a come-as-you-are day – no judgments either way.  (Thank you, Katy of  Bigfoot Child Have Diabetes for this topic.)

Thankfully I’ve been in the process of trying to lose weight which for me means writing everything I eat down so this wasn't too hard.

6:30am – 2 packets of Peaches & Cream Instant Oatmeal, a large cup of coffee with sweetener and half & half.

9am – an apple

11:30am – 3 cups of mixed greens with some chopped up cucumber, red peppers, and celery. I also throw in some feta, cooked chicken and dried cranberries for flavour and top it off with low fat Greek dressing. I usually add a yogurt on the side as I need to up my dairy count.

2:30pm – mixed veggies and hummus. Usually some carrots, celery, peppers, and/or cucumber

6pm – Last night I had balsamic pork tenderloin with some rice and brussel sprouts.

Not very exciting. This is pretty much what I eat every day although with variations.

For example, breakfast can consist of 2 scrambled eggs, 1 cup of berries (whatever is in the fridge), and a piece of whole grain toast and butter or maybe pancakes if I’m feeling the need for carbs. Lunch sometimes has chicken caesar salad, or a meat, lettuce and cheese sandwich on whole grain bread with some cut up veggies on the side. Dinner usually consists of some sort of meat choice, a starch and some veggies.

That’s it. Pretty standard. Well except for the wine that makes it in on the weekends J

Thursday, May 14, 2015

Diabetes Blog Week - Changes



Today let's talk about changes, in one of two ways.  Either tell us what you'd most like to see change about diabetes, in any way.  This can be management tools, devices, medications, people's perceptions, your own feelings – anything at all that you feel could use changing.  OR reflect back on some changes you or your loved one has seen or been through since being diagnosed with diabetes.  Were they expected or did they surprise you?

So many choices…there’s a lot about Diabetes that needs to change: a functioning pancreas, the creation of some sort of device that functions like a pancreas, a device that collects all of my data with no input from me – BG’s, food, exercise, insulin given, sleep patterns, stress levels, etc. But I think the biggest thing that needs to change in relation to diabetes is people attitudes.

I’m extremely tired of people asking me if I “should eat that?” or saying that “that’s not good for you”. It’s really no one’s business but mine what I put in my mouth. I get that they’re trying to be helpful but what would be really helpful would be to read up on Diabetes and understand that I can eat anything I want – in moderation and as long as I bolus for it.


The same is true for people without the D. I sometimes wonder how they would feel if every time they were about to eat something that wasn't a fruit or vegetable, I asked them if they would eat that. I’m guessing their response would be pretty similar to mine. 

Rant Over. Look at the Squirrel


Wednesday, May 13, 2015

Diabetes Blog Week - Clean It Out


Yesterday we kept stuff in, so today let's clear stuff out.  What is in your diabetic closet that needs to be cleaned out?  This can be an actual physical belonging, or it can be something you're mentally or emotionally hanging on to.  Why are you keeping it and why do you need to get rid of it?  (Thank you Rick of RA Diabetes for this topic suggestion.

I hoard glucose meters. There I said it. I have at least 20 that I’ve collected over the years. My DNE gives me new ones every few years. Every time I get a new pump, one that links to it is also sent in the box from Medtronic. Family members somehow get them and pass them on to me. I’ve gotten them at diabetes education classes, pharmacy giveaways, and even random doctor’s office.

I have no excuse and no real reason other than laziness for keeping them.

It might even be a sickness. They’re all different brands and types and take different glucose strips. The only thing they have in common is that they don’t have a lancet anymore as I’ve used them up J

I always use the same glucose meter as it links to my insulin pump – Bayer Contour Link. I’m not a huge fan of it as it doesn’t light up in the middle of the night for low BG checks but it sends the data to my pump so my endocrinologist has all of my info in one place. There’s absolutely no point in me keeping them.


Thankfully I’m moving at the end of the month so can use the opportunity to clean out all of my old used meters (as well as the never been used dust collectors). 

Tuesday, May 12, 2015

Diabetes Blog Week - Keep It To Yourself


Many of us share lots of aspects of our diabetes lives online for the world to see.  What are some of the aspects of diabetes that you choose to keep private from the internet?  Or from your family and friends?  Why is it important to keep it to yourself?  (This is not an attempt to get you out of your comfort zone.  There is no need to elaborate or tell personal stories related to these aspects.  Simply let us know what kinds of stories we will never hear you tell, and why you won't tell them.) (Thank you Scott E of Rolling in the D for this topic.)

Wow Scott came up with an extremely hard question for me to answer today as I don’t think there’s anything about diabetes that I haven’t or wouldn't share with the DOC. The anonymity of the internet makes it extremely easy for me to share without fear of consequences.

I do however keep things from my friends and family. I can’t even tell you why as I’m not sure. I didn't even realize that I was doing it until a few months ago. In February, Karen wrote this great post on what it feels like to have a low. It really resonated with me and I sent it to my husband and my mom. My mom called me as soon as she read it and told me that she had no idea that this is what happened when I had a low. I think it freaked her out quite a bit.

I’ve been thinking about why that was the first time I had sent something like that to my mom and I don’t have an answer. I don’t know if sending her stuff like that more often would help her or hurt her more. It definitely something that I will need to ease her into.

I’m probably freer with information with my husband as he’s right there. He sees the all-day highs and the all-day lows. He knows how frustrated I get when diabetes screws with my day or even when I manage to successfully maneuver through the idiosyncrasies of the disease. The only thing I probably don’t share with him is how often I cry when I’m frustrated.

As for friends, they probably know even less.

I guess what I've discovered in writing this post is that it’s really the emotional side of diabetes that I don’t share with people. I've always needed to process my emotions myself before sharing them with others. Since I received my diagnosis when I was in  my early 20’s and was living by myself, I guess I got used to dealing with this on my as well. Finding the DOC and reading about everyone else’s experiences help me deal. I may not be very vocal on twitter or the blogosphere but I’m there and I’m reading. Thanks for posting everyone!

Monday, May 11, 2015

Diabetes Blog Week - I Can


Well it’s time for another year of Diabetes Blog Week. This marks the 6th year that Karen from Bittersweet Diabetes has organized this amazing event. It’s also the 3rd time that I've participated in it. As I mentioned last year, I’m a horrible blogger and as evidenced by the fact that the last time I posted was during blog week last year, really inconsistent. Diabetes blog week gives me a great opportunity to write about something I’m passionate about but lets me not have to think of topics (which is the part of writing that I hate J)

Each day, I’ll take on a post idea that someone else has come up with and link my page to the others that have written about the same topic. Please click on the banner above to see all of the info on Diabetes Blog Week including the participant and post list.

In the UK, there was a diabetes blog theme of "I can...”  that participants found wonderfully empowering.  So lets kick things off this year by looking at the positive side of our lives with diabetes.  What have you or your loved one accomplished, despite having diabetes, that you weren't sure you could?  Or what have you done that you've been particularly proud of?  Or what good thing has diabetes brought into your life?  (Thank you to the anonymous person who submitted this topic suggestion.)

It’s hard for me to think of something positive that Diabetes has brought to my life so I think I’m going to focus my post on something that I've accomplished despite having diabetes. I seem to mention it every time I post but the greatest thing that I've been able to do despite having diabetes is give birth to my amazing son.

I was diagnosed with type 1 in my early 20’s. At the time I wasn't really interested in having kids so it wasn't one of the first things that popped into my head when the Doctor told me what was wrong with me. I was more concerned with the fact that I couldn't just go out with friends, eat a pizza and drink till I had a happy buzz. I actually had to start planning out my food and reduce the amount of carbs I was eating.

It wasn't until I told my mom what the doctor had said that she brought up having kids. When I went in for my first appointment with the endocrinologist, she explained that it wasn't impossible but that like food, it would take a lot of planning and that the risks for something being wrong with the child were a lot higher due to the increased blood sugars.

And boy was she right. It took me two years to get my A1C’s to the right place to consider trying for a baby. It was also recommended to change from being on Lantus (a long acting insulin) because it hadn't had a lot of testing on pregnant women to going onto an insulin pump. Once I did get pregnant, the control that I had to have with my food and testing was amplified by what felt like a million. I had to go for appointments every week between my endocrinologist, obstetrician, non-stress tests, prenatal echo-cardiograms, ultrasounds, dietitians, diabetic educators, and the list goes on.


But at the end, I ended up with the most wonderful, funny, sweet, caring, little boy anyone could have. 



Saturday, May 17, 2014

Diabetes Blog Week - Saturday Snapshots

Back for another year, let’s show everyone what life with diabetes looks like!  With a nod to the Diabetes 365 project, let’s grab our cameras again and share some more d-related pictures.  Post as many or as few as you’d like.  Feel free to blog your thoughts on or explanations of your pictures, or leave out the written words and let the pictures speak for themselves.


Even with this craziness, my BG was 5.5 mmol/L

Friday, May 16, 2014

Diabetes Blog Week - Diabetes Life Hacks




Share the (non-medical) tips and tricks that help you in the day-to-day management of diabetes.  Tell us everything from clothing modifications, serving size/carb counting tricks to the tried and true Dexcom-in-a-glass trick or the “secret” to turning on a Medtronic pump’s backlight when not on the home-screen (scroll to the bottom of this post). Please remember to give non-medical advice only! (Thank you Rachel of Probably Rachel and Kelley of Below Seven for this topic suggestion.)
I Love Love Love this topic! Not because I have any amazing advice to give anyone. Cause I’m really not sure that I do. But because I am so excited to read what everyone else has to tell me. I’m constantly looking for new ways to make my life easier with D.
I do have one thing that I’ve never heard anyone talk about but that I do. I tend to put my infusion sites on my legs. For no other reason than my stomach is so full of scar tissue from 6 years of MDI’s and 2 years of infusion sites. I haven’t worked myself up to trying other spots yet but I know I’m going to have to move to my arms soon. My legs are getting pretty filled with scar tissue as well. As most of you know, having my infusion site on my leg makes going to the bathroom pretty tricky. It’s a constant battle to not pull out my site by getting caught on my pants or underwear not to mention maneuvering around the tubing. To take the tubing out of the equation, I actually thread it under my underwear so that it isn’t an issue when they are pulled up or down.
Now I just need to find something that stops me from ripping out the infusion site ;-)

Thursday, May 15, 2014

Diabetes Blog Week - Mantras and More



Yesterday we opened up about how diabetes can bring us down. Today let’s share what gets us through a hard day.  Or more specifically, a hard diabetes day.  Is there something positive you tell yourself?  Are there mantras that you fall back on to get you through?  Is there something specific you do when your mood needs a boost?  Maybe we've done that and we can help others do it too? (Thanks to Meri of Our Diabetic Life for suggesting this topic.)
Wow this is an extremely hard topic for me. As I mentioned yesterday, I tend to put things out of my mind when I don’t want to deal with them. Don’t get me wrong, I know they exist. I’m not ignorant. I don’t put my head in the sand. I just tend to accept them and move on.
I had a really bad diabetes night on Monday. My BG before dinner was 5.6 mmol/L. I had hamburgers and salad for dinner so it wasn’t very carb heavy. Maybe 30g carbs for the bun. I always let my pump do my calculations for me using the wizard so I know it was right but somehow my BG ended up as 21.5 mmol/L. I think I was in denial cause at first I did a correction bolus using my wizard. Could also be because I’m cheap and I knew I didn’t have to change my pump until the next morning. I checked again an hour later and was at 22.6 mmol/L. I did another correction. Finally 30 minutes later I realised that I was going to have to change my site. The 24.7 mmol/L glaring at me wouldn’t let me ignore it any longer. By this time it was 11pm and I knew I couldn’t go to sleep until I saw the numbers drop. Thankfully about an hour later, it had gone down to 15.5 mmol/L and I knew I was a going to be ok.
The whole time I was going through this I tried exercising. I’ve recently started wearing a pedometer and I had to get some more steps in anyway so I decided to jog around my room. It didn’t work at all. Why is apparent now as it was a bad site but still very frustrating in the moment.
So I guess my way of coping is to try all avenues until I finally accept the inevitable. Once I accept, I’m lucky in that I can forget about it and move onto the next challenge. No magic words here. Just the realisation that nothing lasts forever.
In terms of needing a boost for everything else, nothing brings me up like this guy:

Wednesday, May 14, 2014

Diabetes Blog Week - What Brings You Down



May is Mental Health Month so now seems like a great time to explore the emotional side of living with, or caring for someone with, diabetes. What things can make dealing with diabetes an emotional issue for you and / or your loved one, and how do you cope? (Thanks go out to Scott of Strangely Diabetic for coordinating this topic.)
This post is actually inspired by one that Rick wrote on Monday at TuDiabetes.

It doesn’t matter if I’m happy, sad or angry; emotions always come out of me in the form of tears. As I was reading Rick’s post yesterday (I’m super behind on reading all the DBlog Week posts) I couldn’t help but break down. I don’t think I ever realised before how angry I am that I have diabetes.

I’ve heard a lot lately on how depression and diabetes go hand and hand together. It’s never been an issue that has affected me. I’ve had a lot of people in my life that have struggled with depression and dealt with it either through therapy or medication or both. I’m so glad that those options are available for people that need them. It’s just never been an issue I’ve had to deal with. Most of the time I’m a regular, happy person. I’m just angry.

Before I do anything, my first thought is how it will affect my BG’s especially with all of the big moments. When my husband and I got married, I had to figure out how I was going to give myself a shot of insulin (I was still on MDI) through my wedding dress. I hadn’t experimented on giving myself injections other than my stomach, mostly because I didn’t realise it was possible. I’m angry that my diabetic team at the time didn’t tell me about it. If they didn’t know, why not? They’re supposed to be the experts. Why didn’t they take the time to educate themselves?

When we started thinking about having a baby, not only did I have to educate myself on what having a baby meant but I also had to research what would happen to my diabetes and because I have diabetes, what would happen to the baby. When I got pregnant, my every thought went into “how will this affect the baby?” I’m angry that I couldn’t just be excited that I was pregnant. Instead I spent the whole 9 months wondering and worrying if everything I did was hurting the baby.

I’ve blogged before about my son’s heart issues when he was born. I’m angry that my first thought when I learned that he had ASD and VSD was that it was my fault. Even though the Doctor said that this was not genetic, that it occurs by chance and with no clear reason why it occurs, I was angry that my diabetes could have been the cause. I thank the powers that be everyday that he is a healthy average boy with a tremendous amount of energy and is able to run everywhere he goes. But I’m angry that it’s still a possibility that I caused it in the first place.

I am so angry that as soon as my 2 year old son drinks a higher than normal amount of water, I have to check his BG immediately. My first thought is always going to be “is it diabetes?” It’s gotten so bad that as soon as he sees me advancing on him with my lancet in hand, he runs away from me. He already knows to associate it with pain.

I’m not depressed or sad that I have diabetes. I’m angry.

The second part of this question topic is “How do you cope?” Quite frankly the only thing I can do is try to move on. All stewing about it does it hurt me.

Tuesday, May 13, 2014

Diabetes Blog Week - Poetry Tuesday



This year, Diabetes Blog Week and TuDiabetes are teaming up to bring out the poet in you! Write a poem, rhyme, ballad, haiku, or any other form of poetry about diabetes. After you’ve posted it on your blog, share it on the No Sugar Added® Poetry page on TuDiabetes, and read what others have shared there as well!

It has been an extremely long time since I wrote anything resembling poetry. I went through quite the “dark period” in University where I thought I had to suffer to become the next amazing Poet. Thankfully that only lasted a couple years and I could go back to being my jovial self J. Here’s my attempt at a Haiku about an extremely nasty high blood sugar that refused to go down last night.

Oh blood sugar, high
why do you irritate me
go down, go down now


Monday, May 12, 2014

Diabetes Blog Week - Change The World



Let’s kick off Diabetes Blog Week by talking about the diabetes causes and issues that really get us fired up. Are you passionate about 504 plans and school safety? Do diabetes misconceptions irk you? Do you fight for CGM coverage for Medicare patients, SDP funding, or test strip accuracy? Do you work hard at creating diabetes connections and bringing support? Whether or not you “formally” advocate for any cause, share the issues that are important to you. (Thanks go out to Kim of Texting my Pancreas for inspiring this topic.)

I definitely would not classify myself as a public advocate about Diabetes. I don’t write letters to my public officials about how diabetes needs more funding. I don’t attend diabetes conferences to mingle with other PWD or people who work in diabetes healthcare. I don’t volunteer with JDRF or the Canadian Diabetes Association. Quite frankly I just don’t have time.

I am extremely envious of those that do and that can make it a priority.

I thank those people everyday cause without them; the province of Alberta would not have approved fully funding insulin pumps so that people who don’t have great insurance coverage can have the best care possible. This makes them the second province that includes adults in their coverage.

Without them, the Spare a Rose, Save a Child Campaign could never have existed and children who desperately need insulin would not have access to it.

Without them, we wouldn’t be as close as we are to getting an artificial pancreas. When the CGM detects that you are having a low, it automatically shuts off insulin delivery. While not perfect, it’s a step closer. Karen over at Bitter-Sweet has a really great blog on it.

Without them, there wouldn’t be work going on to look at making glucose meters more accurate.

Without them, there would be no DOC. I would not be able to manage my care as well as I do without the DOC’s support and information. I wouldn’t be able to explain the difference between Type 1 and Type 2 to people. I wouldn’t feel so comfortable experimenting with settings on my insulin pump or trying to different things to make me healthier.

So thank-you again to all those who go out and advocate for Patients with Diabetes. You guys are amazing.

Monday, May 5, 2014

Diabetes Blog Week 2014


The Fifth Annual Diabetes Blog Week is finally here! Last year was the first time I actually participated in it and I had the best time. Karen over at BitterSweet Diabetes created this amazing event 5 years ago. Each week I will be posting about a set topic and linking back to Karen's site. It really serves three purposes for me:

1. I'm a horrible blogger. Real life gets in the way and next thing you know 10 months have past between blog posts. D Blog week helps me to restart myself and gets my creative juices going.
2. People who may not know very much about Diabetes may find some really great information out there.
3. And finally, I get introduced to all of the great D blog's out there and my reading list gets longer :-)

Diabetes Blog week is taking place from May 12th to May 18th this year. Please click on the link above to find out more.

Thanks
Erin

Monday, July 29, 2013

Site Experiment

I've been using my legs for my infusion sites since I was pregnant two years ago and they definitely need a break. I switched back to my stomach about a month ago but have come to realize that there's still a lot of scaring from so many years just using my stomach. This was made glaringly clear to me last week with all of the wonky BG's I was having. On Friday I decided to try out a new site; my lower back. So far it's been really great. My BG's are now back to normal.

The only thing that I really don't like about it is that I'm constantly feeling it to make sure it hasn't become unstuck. I'm so paranoid that I'm going to rub/tear/pull it off. I'm pretty sure that I felt this way the first time that I put my set on my thigh but it feels even more so because I can't see it whenever I want. I have to change it tonight when I get home and I'm really hoping that this area keeps giving me good results. I don't think I'm ready for my arms yet.....

Thursday, July 25, 2013

Wonky BG's

In my last post I mentioned that I was having issue's with my BG's. I checked my BG at lunch and it was perfect so I didn't end up changing my set until the night of the 23rd. Unfortunately the next morning, things went wonky again and have stayed that way. What really confuses me though is this:


5:45 pm - 7.4 mmol/L, ate 60g, forgot to give insulin

7:30 pm - 6.5 mmol/L
8:17 pm - 8.4 mmol/L, , gave 12.4 units for supper

10:40 pm - 9.9 mmol/L, corrected 1 unit
7:00 am - 5.7 mmol/L, ate 75g, gave 21.1 units

9:00 am - 7.5 mmol/L


How can I eat 60 g of carbohydrates, forget to bolus for it and two hours later, have a better BG? I bolused correctly for lunch I had no insulin in my system other than what my pumps delivers for my basal rate. I have no explanation.

Apparently pasta is a magic food?

Monday, July 22, 2013

#DBlogCheck - and other news

I recently just found out about this great idea by Chris at a Consequence of Hypoglycemia. On July 22, 2013 (today) you should post a comment on every blog you read to let bloggers know that you were there. If you don’t have anything specific to say than just say “Check!”. I tend to lurk quite a lot on other blogs but love reading them so this gives reminds me that bloggers really appreciate knowing that others are reading their blogs.
Now onto my news….As usual it’s been extremely crazy around here.

  • My mom has been planning on moving out here for quite some time and has now made the move. She drove out from Montreal a couple of weeks ago after selling her house and within two days of getting here had put in an offer on a great house 15 min from my place. She takes possession on August 1st and should be completely moved in by the 15th. I love having her so close!
  • After 16 months, I think I’m finally getting this motherhood thing down. Which is great as I have been neglecting my crafting like crazy. I’ve finally picked out a quilt pattern for Connor and will be heading tonight to pick out some fabrics. I can’t wait to get started. I’ll be posting pics of the finished product so stay tuned.
  • My BG’s for the last 24hours have been extremely weird. I changed my set yesterday morning at 9am and my BG was 8.5. It then rose to 13.8 at noon. 9.7 at 2:30. 5.9 at 5:30. 5.2 at 7:20. 11.6 at 10pm and at 11:30pm it was 9.3. When I woke up this morning it was 16.4 and now it’s 20.1. I’ve been taking some serious correction blouses but they don’t seem to be getting them down. I have a feeling I have a bad site but I’m so reluctant to change it was my BG’s around dinner were fabulous. I think I’ll wait until lunch and see if I can get it in the normal range. I hate wasting a new set.
  • There are so many wonderful things happening in the city right now and I can’t wait to get out and participate. I’ll try to post a little more frequently for the rest of the summer so that I can share it all with you. Have a great day!


Wednesday, July 3, 2013

Road Trip

Good Morning Father, I have sinned. It’s been three weeks since my last confession..…or blog post. Or more accurately about 6 weeks since I’ve written anything of substance. Work has been extremely ridiculous since I got back from vacation so I haven’t had as much free time as I needed to sit down and finally write a post.

On May 25th, my husband and I took our son and drove down to Omaha for a family reunion. It takes about 25 hours to drive there so we ended up stopping our first night in Great Falls, Montana and our second night in Rapid City, South Dakota. We’ve taken the trip before and had planned to spend a couple of days in Rapid City doing touristy stuff but it was raining the whole way down so we decided to push on and get to Omaha as quickly as possible. We got there on May 27th.
Maps.google.com

If any of you are thinking of spending three days in a car with a 15 month old, don’t. It was not pleasant. We specifically chose hotels that had pools so that we could get as much energy used up as possible before we headed out the next day. It worked for the first day. Unfortunately when we got to Rapid City, Connor had somehow gotten the flu. Thankfully we had already decided to leave the next day as I really pity the poor cleaning crew that had to deal with our room. We used a lot of towels. Thankfully Connor seemed ok the next morning so we headed out as planned and got to Omaha late afternoon.

By the next morning, my husband and father-in-law had come down with the flu as well. Followed the next day by my sister-in-law and her daughter. The worst parts of it only seemed to last for about 24 hours and most of the people were feeling a lot better by Friday.

Most of the week we spent in Omaha was great. We made it to the Henry Doorly Zoo, the botanical gardens, the children’s museum, and to a photographer to get some great family photos.

Having learned from our trip on the way down, we decided to stop by 2 or 3 pm everyday so that Connor could get a lot of exercise in. This made the trip home four days. We finally rolled back into Edmonton on June 6th. While we love road trips, I think we will definitely be flying the next time we head down. 3-4 days in a car son was just a little too much for our son. I think we’ll keep road trips to less than a day away.

As for the Diabetes front, my BG’s were actually amazing. It was a little shocking actually considering we ate out almost the entire trip. I’m talking about McDonald’s, Culver’s (mmmmm…butter buns), pizza ranch, you name it, if it was bad for you we probably ate there. I became very familiar with my dual wave feature on my pump and apparently am now super pro. Yay Me! We also did a ton of walking though as you can probably tell from all the activities above. I’m betting that had some to do with it. It just goes to show that exercise really does stabilize your BG’s. Now I just need to figure out how to add in more activities to my everyday life.

Monday, June 10, 2013

Back from Vacation

After a long two week road trip, I'm finally back and mostly caught up on Facebook, Twitter, Instagram, Pinterest (although I don't think you can ever get completely caught up on Pinterest), Tumbler, and blog reading. Not to mention unpacking, laundry, putting stuff away, cleaning the dust out of my house, etc that goes along with returning home from vacation. I can now focus on writing about my trip. Unfortunately it will probably take a day or two as I still need to get caught up at work. ;-)

I'll leave you with this though.

Gene Leahy Mall

Tuesday, May 21, 2013

Diabetes Blog Week – Spread The Love



As another Diabetes Blog Week draws to a close, let’s reflect on some of the great bloggers we’ve found this week. Give some love to three blog posts you’ve read and loved during Diabetes Blog Week, and tell us why they’re worth reading. Or share three blogs you’ve found this week that are new to you.

I’ve put off writing this post as long as I could with the hope that I would actually finish reading all of the submissions for Blog Week but I wouldn’t put it off any longer. I’ve still only finished reading up to the end of Day 3 so the below are my favourites up until then. As I finish reading the rest of the submissions, I’ll make sure to update.

Favourite Posts

Carey Potash’s and George from Ninjabetic submissions for We, the Undersigned were the funniest posts I’ve read in quite a while.

Heather at Insulin Resilience memory of her daughter attending diabetes camp was so touching.

D-Log Cabin’s memory about her vision and surgery made me realize how important it is to not take my health for granted and to enjoy every minute with my family

Hilary at Rainie and Me reminded me that "I have Diabetes and I'm ok"

Andrea at No Retreat. No Surrender. made me remember why it's so important to keep advocating for Diabetes

In addition to these amazing posts, I’ve also found some wonderful new sites that I had never read before. I can’t wait to start reading their sites from their beginnings.

Saturday, May 18, 2013

Diabetes Blog Week - Diabetes Art Day



This year Diabetes Art moves up from the Wildcard choices as we all channel our creativity with art in the broadest sense. Do some “traditional” art like drawing, painting, collage or any other craft you enjoy. Or look to the literary arts and perhaps write a d-poem or share and discuss a favorite quote. Groove to some musical arts by sharing a song that inspires you diabetes-wise, reworking some song lyrics with a d-twist, or even writing your own song. Don’t forget dramatic arts too, perhaps you can create a diabetes reality show or play. These are just a starting point today – there are no right or wrong ways to get creative!

So I didn't have any time to make anything new this week for Diabetes Art day but I'm rather proud of the project below.

From Left to Right - Oregano, Chives, Basil

As I've mentioned in previous posts, I'm trying to get healthier so as soon as spring hit, I thought I would try growing my own herbs. I thought it might inspire me to cook from scratch more. As I've never really grown anything (I killed a cactus in college) so I am extremely proud of these and consider growing an art form

Friday, May 17, 2013

Diabetes Blog Week – Freaky Friday




Just like in the movie, today we’re doing a swap. If you could switch chronic diseases, which one would you choose to deal with instead of diabetes? And while we’re considering other chronic conditions, do you think your participation in the DOC has affected how you treat friends and acquaintances with other medical conditions?

This was a really hard topic for me to write about. The only Chronic Diseases that I could think of sounded way worse to have than Diabetes. I don’t want Cancer. I don’t want Parkinsons. I don’t want a Cardio-Pulmonary Disease. I don’t want Lupus, Cerebral Palsy, Epilepsy, or Anemia. I’m probably already going to get Alzheimer’s as it runs in my family.

I KNOW Diabetes in all of its unpredictable glory and for the post part I live a completely normal healthy life. Sure it takes some planning to exercise or go out to a restaurant or have a baby, but I can still do all of those things. The other diseases, I’m not so sure. So I’ll stick with Diabetes.

As for my treatment of people with other medical conditions, I don’t think having Diabetes has changed that for me. Unfortunately I’ve known and currently know a quite a few people with other medical conditions. I would hope that I have always been supportive and interested in their condition and not a person that tries to “police” their activities. I’ll have to ask them especially if there’s anything I can do better.