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Today, I’m seeing blue everywhere I look. Admittedly, that could be becuase I am wearing blue jeans, a blue shirt, a blue ring, a blue necklace and, terrifyingly, blue mascara. 
And I can’t help but notice how much blue there is in our world. Today, the Melbourne skies are a particularly bright blue which made me smile as I opened the blinds in my bedroom. Even Mother Nature is celebrating Blue Fridays and raising diabetes awareness!
My daughter’s school uniform is dark green, but today she has soft blue ribbons tying up her ponytail and a blue circle pinned to her school dress. And she’s more than ready to explain why to people. ‘It’s about diabetes awareness. It’s important people know about diabetes’, she told me earnestly. Sure is, kid.
Cherise Shockley is the founder of the Blue Fridays campaign. She’s one of those people whose passion and commitment to diabetes is incredible. And she’s an amazingly nice person as well. Read all about the campaign here.
Wearing blue on Fridays throughout November is an easy way to get people thinking about diabetes, but you need to do more than just throw on a blue scarf (oh yes – I have one of those with me, too). You need to tell people why you are wearing blue, what it means, why it’s significant to you. Post a photo on your Facebook page and tell people why you’ve put it up there. Tweet a photo with the tag #BlueFridays. Ask people at work to adopt Blue Fridays for the rest of the month. By doing these things, people will be talking about diabetes – it’s a way to get diabetes front and centre of people’s minds, for them to think about donating to diabetes causes, to think about getting themselves or a family member checked for type 2 diabetes, to think about the symptoms of diabetes.
Next week on World Diabetes Day, the world will be lighting up in blue as monuments across the globe take on a blue hue. You can read about it on the IDF website. Keep an eye out for iconic buildings in your city.
Go get your blue on! And get talking!
Today at Diabetogenic Paul Buchanan is guest blogging for me. A couple of months ago, Paul asked me to guest blog for him. You can read that here. Paul has lived with type 1 diabetes since January this year and because he’s not the type of guy to sit back and wait for things to happen, he set up the #GBDOC Twitter and Facebook pages and a website, too. A couple of months ago, Paul asked me to guest blog for him. You canead that here. I was lucky to meet Paul at the EASD European Bloggers Summit earlier this month. There were lots of girly squeals (both of us) when we met. Take it away, Paul!
Ok, so I was diagnosed in January 2012 with T1 at the age of 44 – a bit of a shocker – but then it would have been a shock at any age. And another thing, I’m a grown up! I’ve had to deal with some pretty serious things in my life so far, work, travel, relationships – I’ve got a few scars, I’ve been around the block a few times, so dealing with ‘the D’ shouldn’t be too tough, right?
I mean, I really am a lucky guy, ‘cos almost immediately I found the #doc (the Diabetes Online Community) and wow – talk about support! There isn’t a question I can’t ask, there isn’t an issue I can invent, there isn’t a problem that exists that the #doc hasn’t got an answer for. When I say “an answer” I really mean a thousand voices all crying out with advice and love and empathy!
And another thing, talk about technology! 2012 and I’m on these tiny weeny little 4mm 32 guage needles that mostly I can’t even feel going in (there is the odd ‘screamer’n’bleeder’!), I’m queuing up for a pump and will get CGM just as soon as those tight-fisted buggers at the NHS realise how much of a difference it makes in quality of life and start to fund them properly over here.
I’ve got mobile apps that help me track, well, everything really! I can email and text my Nurse Consultant (she is a goddess amongst HCPs). I’m back in training having now done my first triathlon, I’m signed up to do a 70.3 ‘half’ Ironman in 2013 and life is good!
So, yeah, bloody lucky!
Being a ‘grown up’ with a few years under my belt I don’t give a stuff if other people are offended by me testing or injecting in public, in a restaurant or in the shops! I have no issues with telling people or answering questions, probably ‘cos it gives me chance to show off how much I’ve had to learn in the last six months, and I have never had to be a child with D. I have never had to feel different, never had to be treated differently, never had to worry about ‘being just like everyone else’. To all of you who were diagnosed as children, I salute you. That you not only ‘survived’, but that you are all now a part of the #doc and so willing to help others is a testament to one of the demonstrable upsides of living with a chronic condition – you are all better people than nearly everyone I have ever met, and I am proud to be a part of the family.
Lots of Love
@T1HbA1c
Thanks, Paul! You can read more from Paul at his blog here. The #GBDOC Twitter chats take place on Thursdays at 7.00am AEDT. You should sit in – they’re a very amusing bunch!
The app mentioned above in Paul’s post is MySugr. I had a look at it when I was at the European Bloggers Summit and can’t wait for it to be launched here. It’s great to see a diabetes data tracking app that has been developed by folks who ‘get-it’. I’ll let you know once it’s available in Australia.
Last week, I sat glued to my Twitter stream watching the tweets from two separate events that had a strong diabetes consumer (or, if you prefer, patient) presence. Firstly, there was the Roche Diabetes Summit (#RDS12) which brought together 34 diabetes bloggers from across the USA. You can read some terrific reports about the summit here and here.
Immediately following the Roche Summit was the American Association of Diabetes Educators (#AADE12) Conference. Once again, the Twittersphere was full of commentary about the different sessions, blogs were written and Facebook pages provided reviews and photos from the conference. I learnt a lot about what was going on, what new things were catching the attention of members of the diabetes online community (DOC) and I noted things that I want to speak with my endo about next time we meet.
Coming up later this month is the Australia Diabetes Educators Association/Australian Diabetes Society conference. I’m going which is pleasing on a number of levels, not the least of which is that it is on the Gold Coast which will mean some slightly warmer weather. The main reason I’m excited though, is because I will be able to ‘report back’.
How many consumer advocates will be attending the Australian conference next week? I’m guessing not too many.
You may ask why it’s important to have people with diabetes at these events. It’s a valid question. I mean, the events are for health professionals to do some professional development, some networking and find out the latest in the diabetes world. The sessions are not designed for consumers, really.
And that’s all relevant and true. But how does the information presented at these conferences then get filtered through to people living with diabetes? How do we find out about the latest and greatest, the new research, the new studies? In all honesty, how many of us have health professionals who relay this information back to us?
My endo is one of the few that actually does. We speak about conferences she’s attended and new things presented. In fact, part of my screening (read: interviewing) process when I look for health professionals is to ask what conferences they’ve attended recently and what they’ve found interesting. It gives me an idea of how up-to-date their knowledge base is. But more importantly, it gives great insight into how well they then pass on that information.
So, let me ask again: Why is it important to have people with diabetes at these events? It’s critical, because it means that the information gets passed on to us – the people living with it. Which better informs us. Which helps us make decisions about our care to improve outcomes.
There needs to be a shift in Australia. People with diabetes need to be part of the planning of conferences. If we are (or diabetes is) ‘the problem’ then we need to be part of – actually, leading – the road to the solution. I wrote about this last year, but as each year passes, and as I see more and more evidence of consumer involvement in other countries, I wonder why we seem to be so behind the times.
We need to be there in numbers and we need to be recognised as a way to get messages out. It’s a revolution in terms of the place of consumers. But our rightful place is front and centre at information sessions talking about the condition with which we live. And the time is now.
So, with this in mind and knowing that I’ll be at the ADEA conference later in the month, what is it that you want me to report back? Have a read of the program and in the comments section below let me know if there is anything you want more information about. And I’ll try to get to the sessions, tweet and blog about it.
This is the tale of the time I took myself of to Accident and Emergency (A&E). This is not a decision I take lightly as there are a million things I’d rather do. Like saw off my own leg, puncture an eardrum or attend a meeting of an anti-vax conspiracy club. But I’m writing about it because it was a crap experience all around and I’m interested to hear how others have dealt with similar situations.
So, here is the good thing about having type 1 diabetes. I walk into a heaving A&E waiting room. There is blood (the guy in the corner holding his head), guts (a woman near the front throwing up hers), tears (the old woman with her daughter) and silence (most of the other people). I tell the triage nurse the situation which sounded something like I have type 1 diabetes, I have been vomiting for the last three hours, I have ketones of 4.8 and my last BGL was 12.8mmol/l. The triage nurse takes one look at me and opens the door to let me in. Like it’s 1991 and I have a gold medallion to the Underground nightclub. Straight into the VIP room!
Unfortunately, this VIP room is lit with unflattering lighting and instead of comfy lounges I lie on a trolley. I am seen by a couple of brilliant nurses who put in an IV line and ask sensible questions and say sensible things like ‘Of course you can check your own BGL. Would you mind telling us what it is when you do it?’ I have two new BFFs and I want to take them out for ice cream – perhaps I’ll wait until the ketones have cleared, though. I tell them that, according to my sick day protocol, I have upped the basal rate on my pump and have given myself a correction bolus which is already working as my BGL is now down to a stellar 7.6mmol/l. Brilliant BFF nurse #1 says ‘Well, obviously your protocol is working. Are you happy to check again when the doctor comes in and let him/her know how things are going?’
Emergency doctor comes in after a mere 25 minutes (seriously VIP) and starts asking me what’s going on. I repeat the story, report that I’ve just checked my BGL again and I’m down to 6.9mmol/l and he starts by asking the usual questions about diabetes starting with ‘How’s your diabetes’. I never know how to answer that question. ‘Um, good thanks. How’s your father?’
The next thing he says is ‘We are going to need to disconnect your pump’ to which I respond, ‘That’s not going to happen’. He looks surprised and repeats a little louder what he said. This time I answer with ‘Not an option. Come up with another idea’. Now, I know that I am a nightmare patient. I know that at this point in time the doctor was wishing that I was actually unconscious. But I also knew that my pump was working (see: BGL dropping at sensible rate for proof). I also know that I was polite. Assertive; but polite.
It was then I summoned the immortal words of one of the presenters from a Type 1 in the City event and said ‘I would like to see the endocrinology registrar. Now. Please.’ Trump card! It’s kind of like lawyer-ing up!
The endocrinology registrar has much more of an idea until this question came out ‘What’s your blood sugar usually?’ Huh? Usually when? At what time? When I’ve done what? When I’m feeling how?
How is that a question? There is no answer. My blood sugar is usually variable. That’s called diabetes.
What happened next was me refusing to disconnect my pump (again) followed by a demand (from me) that the registrar contact my endocrinologist, which she really didn’t want to do. I held my ground and promised that I would disconnect my pump if recommended by my endo.
Five minutes later, the registrar returned to my room, muttered that the pump could stay connected and then she left. I didn’t see her again. I fell back against the pillow, exhausted, emotional and, despite getting my own way, I felt defeated.
I am sometimes accused of making diabetes look easy. It’s not. And when something like this happens, it reminds me just how difficult it is. The outcome of my visit was rehydration, blood tests to check all sorts of levels, monitoring of ketones (which were gone in about three hours) and then I was sent home. Mind you – I did tell the endocrine registrar (much to her astonishment) that I was leaving at 6.30pm, so she only had until then to get me sorted. (The reason for this was that I had to emcee a diabetes information session at the hospital’s conference centre.)
So, apart from five hours in A&E, not too much of an inconvenience.
But the aftermath hit me like a lead balloon. Firstly, I rather arrogantly was upset that I had found myself in that position. Gastro leading to ketones and dehydration is not the most unusual thing in the world, so I’m not sure why I should think I’m above it all. I’m not.
The second thing that upset me is this, (and again, I hope this doesn’t make me sound arrogant). If I have to battle so much at a relatively easy visit to A&E – if I have to pull every trick to ensure that I get what I want the way I want it, how do people who don’t have the same understanding of the system manage? The people who don’t know the tricks. Surely being heard is a basic right in circumstances like these.
I need someone to explain to me how it is possible that it’s OK that every minute of every day I am the one who makes all my own diabetes decisions and yet the minute I walk through the doors of a hospital I am not equipped to do so.
Do you have any experiences in A&E that leave you feeling a little cold? How have you dealt with them?
