30. My Fiancé and her T1D

When I first met Niki I had no idea she had Diabetes, not that it mattered to me of course, but it wasn’t long before I found out when we went for a coffee at the café and she took insulin for it. Some of my family members have Type 2 Diabetes and I’m ashamed to say that I never really took the time to find out more, all of that changed the minute Niki whipped out her insulin pen within an hour of meeting her. I have a greater understanding of Type 1 and Type 2 Diabetes, I now understand what it takes to manage this condition on a day-to-day basis and the many thought processes involved. I understand that there are many dangers and I watch my fiancée keep herself alive every day, that’s not scary anymore, it’s the reality for her and she does it so well.


Aside from being the worlds foremost expert in Niki’s T1D she also has the most amazing human qualities which she readily extends to strangers. One of my favourite examples of this is when Niki took infusion sets to a complete stranger one evening because they’d travelled to Oxfordshire and had forgotten their spares. Niki didn’t hesitate to do this for someone she’d never met before and this is typical of the caring and nurturing person she is. She’s the most caring person I know and this also shows in the social media family she’s part of. There’s masses of support to be found there and Niki is very prominent in making sure people can find that. The friendships that have been made there are many, and I’m so glad I get to count these people as friends too now. (Not to mention my relief that they all approve of me).



After just 5 weeks of being with Niki, we travelled to London to get her first insulin pump. It was a stressful day for me, I knew the hopes and fears she had for this method of managing her T1D and I didn’t want her to be disappointed. All those concerns disappeared upon seeing the tears of joy roll down her cheeks as she officially began pumping insulin, I knew in that moment the relief she must have felt at having the ability to calculate her boluses more accurately and the freedom she hoped the various functions would give her. Sadly, that first pump hasn’t always made life easy for Niki and my heart has broken watching her struggle and breakdown because of it. There are always other considerations in addition to the standard daily thought processes Niki has, where to place the cannula, how to dress to accommodate it, what to wear to be able to access it. The Kaleido has already eliminated some of the pump related clothing issues for Niki; she suddenly owns dresses…without pockets!! I’m seeing her begin to feel more confident and comfortable in her own skin, especially around her Diabetes Management and it’s so good to see that again.


I see the Kaleido has the chance to give Niki the freedom to choose how she lives her life, because even though she is absolutely amazing at everything she does, especially keeping herself alive everyday, this will go a long way to helping her actually live it.


Written By Matt – Fiancé to Niki & Dadda to Moomin


This is a series of blogs I will be writing about Kaleido. In the interest of being open and transparent I wanted to share with you all that I’m excited to have become a Kaleidoer. This means I am fortunate enough to get to trial the Kaleido Insulin Pump. When they announced their UK release was imminent, Kaleido asked for Kaleidoers and having been keeping a close (and very interested) eye on them for some time, I got in touch. I feel really lucky that they’re also letting me use their platform to share my experiences of living with T1D whilst preparing for my wedding day. These blogs will be shared on my own site also.
If you have any questions, please feel free to DM me.

All images copyright Author and Kaleido


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