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.
Since the Flash glucose monitor, the Freestyle Libre was launched in the UK in 2014 I have been watching, following and learning from all that the NHS, Diabetes UK and JDRF UK have done to make sure this revolutionary piece of diabetes technology ends up in the hands of many people with diabetes and not just those who can afford it.
I have just had 4 nights in a row of glorious uninterrupted sleep and the world looks so much brighter. Pleases the Gods I haven’t jinxed it!! Since the Christmas break, my blood sugars were doing a-mazing trampolining and the alarm on my CGM to alert me that my blood sugars are high or low but mostly high.
TIPS FOR PEOPLE NEWLY DIAGNOSED WITH TYPE 2 DIABETES. Diabetes is a complex chronic condition and being told to take medication and watch your diet is not sufficient at all. I feel that’s it’s important that you, the person with diabetes, get the information you need to take charge of this journey and I’ve put together some suggestions for you as a place to start.
