Winter Blues.

Uni goes back this week after a Winter hiatus. While I haven’t exactly been looking forward to it, thankfully week one is just a ‘go through the unit outline’ kind of a week. Which means a few more relaxed nights catching up on Australian Survivor.

At the beginning of my break, I stared into the depths of my wardrobe where my diabetes gear is housed, contemplating change. Did I want to take a pump break? Try that new meter? Or put my new faster acting insulin to the test? I got as far as a different meter, but after a few false readings was quickly reminded of why I love my AccuChek Guide so much and shoved it back into a drawer.

The more that I stared at the contents of my wardrobe, the more I realised that I no longer desire change in the way that I manage my diabetes. Which is weird, because for the greater part of the past three years, I’ve genuinely wanted change to help me to better cope with diabetes at that specific point in time. Perhaps it meant seeking out an insulin pump to give me more flexibility in managing my blood sugars. Or subsequently taking a break from the pump to simplify things and alleviate the mental burden of navigating pump settings. Or hassling AMSL Diabetes to cough up a #TslimForFrank so that I’d have something more modern and wearable to look at.

Yet now, I feel comfortable with what I am doing. I feel comfortable with what I am using. I also feel confident that what I am doing and what I am using allows me to manage my diabetes in the best way that I possibly can – for the time being.

In the midst of a crazy intense year, I think my real focus is minimising the burden of diabetes on the rest of my life. At the moment, I don’t have the headspace to deal with the hiccups that may come from adjusting to different tools. I need that brain space for my studies, for my work, for my family and for my life.

So I guess for me right now, minimising the burden of diabetes doesn’t involve paying attention to the diabetes itself, but moreso the things around the diabetes.

I’ve been getting more organised with my meals through the day over the past couple of weeks. When I’m more organised with my meals, I eat better than when I’m not. When I eat better, I feel better. See: this post. I’ve added a few more recipes to my brekky/lunchtime/snack repertoire. I’ve also been consciously trying to eat more veg and drink more water.

I’ve got alarms set on my phone to remind me to change my infusion sites and refill my cartridges. I’m in a pretty good routine of changing my site every 3.5 days, so that changeover falls every Tuesday afternoon and Saturday morning. Cartridges get replaced and filled with half of a penfill on a Saturday, and topped up with the back half on a Tuesday.

I’m also hoping to give myself a little more structure in my studies this semester. It often became far too easy to sit pondering over a problem for far too long, when it could be more easily solved with a fresh set of rested eyes. I know that when there’s more balance between study and free time, my mindset is better – which is equally pertinent when diabetes is strapped along for the ride.

Speaking of mindset, sunny Winter weather of late has also given me more time for this.

I’ll be honest – the past six weeks have been weird. I’ve quite possibly been consumed by everything that I want to get done in the back half of this year at times.

It took a while to get here, but I’m happy to report that I’m feeling the most refreshed that I have been over the past six weeks. Here’s hoping that my second semester is easier now that I know what to expect.

The Not-So-Serious Stuff.

When I first started writing here on my blog, I remember seeing lots of the more serious stuff from the diabetes orgs. That diabetes is the leading cause of this, and puts you at a greater risk of that. I can still remember seeing all of those messages, and wondering where all of the positive stuff was. In a small way, I just wanted to show a different side to diabetes. A more positive side.

I can remember wanting to write about things like Climbing the Sydney Harbour Bridge, graduating from uni and blowing out the candles on my birthday cake. I wanted to churn out those positive messages about people with diabetes being superheroes, able to do absolutely anything that they set out to do. Because after all, why shouldn’t we?

At the time, living with diabetes was hard. I had no peer support. I didn’t feel confident navigating this condition around my life. I didn’t even know what the hell I was doing. This crazy journey has also taught me for a second time that living with diabetes is hard.

It’s hard playing pancreas. It’s hard finding the mental space and physical energy to manage this condition. It’s hard to give myself encouragement when I’m so invested in the numbers and only have myself and my long term health at stake. It’s hard not to be consumed over how well placed I am to continue to be able to afford my diabetes care into the future.

Diabetes is serious. As I’ve began to take my condition more seriously, I’ve come to appreciate the importance of getting all of those annual screenings. I want to be aware of those things that diabetes might put me at risk of developing. I want to engage in some of those more difficult conversations. In 2019 people are still dying from missed diagnoses and the exorbitant cost of insulin abroad.

Diabetes tools and tech have also come a long way in the short time that I’ve lived with it. I remember my diabetes educator requesting a special USB cable and software from Abbott just so that I’d be able to see my BGLs on a computer screen back in 2010. Today those readings send wirelessly to the mySugr app on my iPhone for instant review. Then there’s things like NovoPens, insulin pumps, Libres, CGMs, faster insulin and closed loop. Phew!

So, I guess the point of this long winded post is that the world of diabetes through my eyes has become this great big complex, serious and even political thing over the past few years. While that’s never going to go away, I guess I’d like to be reminded of some of some of that not-so-serious stuff more often as well.

Like this poster that I was reminded of earlier this week, a few days too late after National Diabetes Week. And the frame above it sitting proudly on my wall, both bringing a smile to my face when I think of them.

The Fifth ‘T’

Earlier this week, I was finally able to put a face to someone whom I’d only ever known through the DOC. This person was probably one of the very first people I’d connected with when I first started writing here on my blog a few years ago. Despite living in the same city and perhaps being in some similar circles, we hadn’t quite been in the same place at the same time up until now.

He very generously gave up his time to speak to myself and fellow Young Adult Diabetes Committee members, sharing his own story of a flexible diabetes management regime that suited his lifestyle. One part of this was a DIY closed loop system.

I listened intently as he explained the ins and outs of this system, watching his blood sugar rise ever so slightly while the system automatically delivered micro boluses to correct. When question time rolled around, I asked him what sort of time commitment was involved in setting up such a complex system like his.

He told us about the many different online communities there were available to support him in setting up this system. About the ‘build parties’ where groups of like minded people got together to learn off of each other. How he was happy to accept messages and offer support to people who might be thinking about building a similar system.

‘It’s much easier when you have the community to help you’ were his exact words.

This really has nothing to do with DIY closed loop. So please don’t ask me questions, because I would hardly be able to answer them. But my new friend’s sentiments could be equally applicable to almost any subset or interest group within the diabetes community.

The diabetes community supports each other 24 hours a day. Whether it be through Facebook groups, Tweet chats, information sharing, storytelling or meeting up in person, this community is truly one of the most genuine things that I know of.

I mean, why else would you meet up with a total stranger from the other side of the world who’s been backpacking through Australia? Or tell someone you barely know that they can come to your door to borrow some much needed diabetes gear?

For the most part, we don’t do it to get famous or build followings or make money. We do it because we genuinely want to feel connected, informed and supported – and we want our peers to feel exactly the same as we do.

If you’ve been paying attention to National Diabetes Week, you’ve undoubtedly heard about the four ‘T’s of diabetes. Being tired, toilet, thirsty and thinner. However, I still think that there’s a ‘T’ missing from those four.

It’s not necessarily a symptom of diabetes like the other four ‘Ts.’ But to me it’s something that’s synonymous with diabetes. I can’t think about diabetes and not be reminded of this word. A word that’s been so life changing and such a vital ingredient in being able to cope with a complex condition so well.

For me personally, that fifth ‘T’ of diabetes would undoubtedly have to be the word ‘tribe.’

As the old saying goes, find your tribe and love them hard.

They really do make diabetes suck a lot less.

The First ‘T’

Happy National Diabetes Week!

If you haven’t already seen the flurry of posts circulating on social media, Diabetes Australia are running a third iteration of their ‘It’s About Time’ campaign, calling on earlier detection of both type 1 and type 2 diabetes.

For type 1 diabetes, the focus is on the first ‘T’ that we noticed when we were diagnosed. Once again, I’ve filmed a vlog to mark the occasion. Look out for the bit where I forget one of the four ‘Ts.’

Please do share the campaign materials with your family, friends, colleagues and networks who might not be aware of those symptoms this week – because that’s really what this campaign is all about.

It’s About Time we all knew the signs and symptoms of diabetes.