Saturday, 24 June 2017

Diabetes, gastroparesis and weight loss





Hi everyone! As some of you may have noticed I have been AWOL for quite some time on social media and although I am trying to keep up with my diabetes activities I'm finding it a bit of a struggle. The main reason for this is the sudden and (currently) unexplained lack of energy I have been experiencing which has left me with little to no "get up and go" to do the extra work that I used to do on my blog. I say it's unexplained, but there are a few reasons which stand out to me such as being unwell with gastroparesis which had caused me to vomit almost daily for around 3 months now, sometimes up to 4 - 5 times a day. Sexy, right?
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Tuesday, 4 April 2017

Insulin pumping 4 years on


To begin this blog I must send out an apology. It would appear it has been 6 months since I last posted on here and although I have regular thoughts on blogger topics that I'd like to share, my time and energy levels have taken me away from my previous health-related brain dumps. I'd like to say that I can now go back to blogging as I had before, however working as an actual real life nurse now (I know, it's a scary thought) is far more physically and mentally demanding than I could have ever expected. That's not to say that I don't love my job, I absolutely adore it in so many ways, I just now need to summon enough energy and motivation to get back to my old advocacy and social media ways. It would appear that people have, sadly, lied to me, and coffee does not provide adequate support in summoning these blogging essentials.  
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Wednesday, 23 September 2015

Gastroparesis: From The Top





It has been over 7 months since I was diagnosed with Gastroparesis, so I thought it’s probably about time that I started attempting to get my confused, fuzzy brain around it. For me this means getting all of my thoughts out onto paper (ahh fresh internet paper) in order to make some sense of something that is utterly confusing and something that I’d much rather ignore. Unfortunately Gastroparesis doesn’t like to be ignored though! (Cont)

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Sunday, 29 March 2015

The unpredictable side of Gastroparesis and Diabetes Management




“I heard you”, Mr T said.

“What did you hear?” I asked.

“I heard you being sick again. Why were you sick?”

This morning I’d woken up feeling nauseous. I got out of bed, leaving Mr T asleep, and pottered around the house, tidying and chatting away to the degus. I took an anti-sickness tablet and made myself some ginger tea – someone had suggested drinking it when nausea sets in. Not long after the kettle had boiled I was in the bathroom bringing up last night’s dinner. I had eaten 12 hours ago yet there it was, clearly it had been sitting in my stomach overnight, not heading anywhere. I instantly felt better after emptying my stomach, brushed my teeth and went back to my ginger tea. It was a relief to have the undigested food out of me and the nausea settled quickly, but it wasn't healthy, I knew that, I worried about the damage that was being done after years of vomiting on and off. 

I checked the screen on my insulin pump and looked back over the CGM (continuous glucose monitoring) trace for the past 12 hours. I could see that my pump had suspended my insulin around 45 minutes after I had bolused for my evening meal – the pump does this when the CGM picks up that I’m heading for a hypo. This must have been because the insulin started working before the food had digested. Throughout the night I could see that my glucose levels were unusually flat, with no post meal rise at all. This wasn’t surprising now that I know my food didn’t really leave my stomach (or the majority of it anyway).

This, compared with other days, has been a relatively easy day. For the past few weeks since I’ve had the CGM and been able to see exactly what my glucose is doing, I’ve become increasingly frustrated and scared when seeing my glucose levels. I have lows not long after eating and highs much later, this is due to stomach emptying as described above. I have tried to adjust to this by taking my insulin after I have eaten and spreading the delivery out over an hour or so. Sometimes this is effective, sometimes it isn’t. My stomach will, at times, empty like it should, meaning that I then have a high followed by a low, due to taking insulin later.

It’s almost impossible to take insulin to cover food as I never know when or if my stomach will empty. How can I predict that? I can’t. It’s opening up a whole new world to me and along with that come more and more questions. How will I manage this when I don’t have CGM in 3 weeks time? What will my a1c be like? Will I be able to have an a1c that will be safe enough for me to have children? Will this cause my retinopathy to progress? Will this cause me to have further complications related to uncontrolled glucose levels?

Taking it each day as it comes seems to be the only option with something this unpredictable. I’ve started medication as prescribed and I’m self-managing as best I can from information I have found on the internet. I had always thought that I quite liked spontaneity, not planning ahead and seeing what the future brings. One thing I have learnt over the last three weeks is that when it comes to my health, this is the opposite of what I want. It’s frightening, it’s depressing and it’s still something that comes as a huge regret.  


Take care of your diabetes as much as you can, and hopefully it will take care of you.


Ninjabetic x 
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© Ninjabetic

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