There are lots of people on social media doing their bit for diabetes awareness, and this is fantastic. However, raising awareness seems to be a big buzzword these days, but what does that really mean, and how do we raise awareness of something effectively? Should I do it by sharing a random image on my Facebook feed that doesn’t tell any of my friends anything at all? Or should I use my social media to share information?
In this post, I will provide a short summary of the information revealed from parliamentary question responses on how many people in Ireland use insulin pumps, what clinics provide them as a treatment option and how many new pump starts are done each year.
My diabetes diagnosis shattered my confidence in my ability to take care of myself, and my plan quickly became to just get through the rest of the term, move home for the summer to my previous summer job and figure the rest out over the summer. Adjusting to my new normal of living with diabetes began while I was still in hospital, or did it?
I realised last year that in all the blog posts I’d done these last 13 years, I have never shared my diagnosis story, so here it goes. My diabetes diagnosis is not unique; many of my friends with diabetes share similar experiences; however, some people end up very ill and may have spent time in intensive care units in hospitals. Thankfully this was not the case for me, but I did feel like I was dying.
The purpose of the document is to provide an estimate of the number of people who are using HSE-funded Flash and CGMs in Ireland and to prompt a discussion around access equality. I believe we need to talk about how fair it is that so many are approved for HSE funding and why some people are still being made to pay.
Every year, when I write my Christmas cards, I include a letter with a bit of a summary of what our family has been up to. When your family lives on two continents it’s important to keep the connection in this way.
It was while I was writing this letter that I realise just how much has happened to me this year because of blogging and volunteering. Here is some of my favourite highlights from 2019;
I’ve been psyching myself up for the next chapter of my life for….., at least…..., two, three, ok more years. Totally psyching myself up. Em, yeah, totally. I am dusting off my CV, getting motivated about starting a pension plan (not so much) and trying to figure out (again) what I want to be when I grow up.
Thriveabetes exhibited at the Diabetes Ireland national conference recently to spread the message about the Power of Peer Support in diabetes. It was brilliant! We met so many people and exchanged so much of our lives with diabetes with so many strangers who we hope will find their own support locally. So what is so powerful about diabetes peer support?
