Showing posts with label #DiabetesTechnology. Show all posts
Showing posts with label #DiabetesTechnology. Show all posts

Thursday, 23 June 2016

Advocating Together We Can Make A Difference



I felt very 
​honoured
​ and proud to be given the opportunity​ to
​go
 to Leinster house as part of a team Advocating for a National Diabetes Strategy with a multi-year resource plan. 
The work involved in getting this together in a few short weeks was a huge task but Kieran from Diabetes Ireland 
​with his experience pulled this together perfectly. 
 
Together we were strong, and together we were firm
​, ​
It felt strangely powerful 
​!​

It all started after hearing about minister Harris imposing a hiring freeze on the HSE.  I was fuming followed by action. Putting my feelings about this in writing and emailing as many TDs as I could find email addresses for, yes I had a good old rant.

Frank O Rourke
​ the 
TD
for my area
​ (North Kildare)​
 wrote back to me quickly and in a phone call the next day he suggested we ( my colleagues & myself ) come to Leinster House and present our case on a national level to the ministers, all of which he would invite to attend. 
​now how exciting did this sound ?
Yep said I, seemed like a good idea and so the plan was hatched. Not in my wildest dreams could this Advocacy Project happen with effect without professional facts, figures and backup.
​ ​
My next phone call was to Grainne at Thriveabetes for advice and then Diabetes Ireland to talk about how best to go forward with this opportunity which had literally fallen in 
​m​
y lap.

I'd been given a job with huge opportunity but
not 
in my Wildest dreams could I do that job, well not alone anyway.
​ ​
Kieran was the person in Diabetes Ireland I spoke with and the support I received was instant.
​ ​
Kieran enlisted the help of the Clinical Leads for paediatric and Adult services and it all started to come together.
Every single step of the way Kieran keep us in the loop and made sure what was happening was with our approval.
After only a few weeks to plan it all the pressure was on to make sure everything was covered and then finally the day arrived ! 

I met Grainne, Rebecca, and Liz at Heuston Station and together we met the rest of our team
​ ​
across from Leinster House for coffee where a last chat
​ and briefing​
 could be had among ourselves and Frank O Rourke before being brought across
​to Leinster House.

It was a very well attended meeting by TD's and Senators, and both Clinical Leads talked about the lack of Diabetes Services nationwide but particularly In the SouthEast where services seem to be particularly bad.

Rebecca and I both spoke about living life with type 1 diabetes, Rebecca from the point of view of a parent of a child with type 1 and me from an adult point of view. 
​Any​
 lack of service
​ we were experiencing in our Diabetes clinics was highlighted​.
 

I never knew before exactly what the crew at Diabetes Ireland did, I knew 
​they worked on​
 lots of 
​campaigns​
 but I'd no 
clear idea of what those campaigns​
were​
.

After today I understand a little better what their job and their role in our lives is.
I also understand that we as patients can shout from the rooftops advocating and raising awareness
​in our separate groupings​
 but unless we work with our peers as a united team we are unlikely to be heard by those that truly matter to our lives as people with type 1 diabetes.
There is no "i"
​ in the word
 team, certainly advocating as a small body will make noise but if we want changes we have to all pull together with the one agenda and as one body.

​Today was a special day and we need to say thank you so much to Frank O Rourke TD, for giving us this opportunity also Kieran O Leary and his team from Diabetes Ireland​, their patience and support was endless and invaluable, and im sure it will continue to be so as they continue to work with us and also on our behalf.

The support we recieved from our community was overwhelming as the days grew closer to the briefing and if i had a message to everyone now, it would be that there is strength in numbers, it is very important that we stand together and united as people with type 1 diabetes, to campaigne for a better and healthier future together. 

Feeling the love .......
Davina πŸ’™




Saturday, 6 June 2015

Seriously Loving The #Technology & #Accessories us #T1Ds Use ....... #CGM Today's Gonna Be a Good Day, Ye Today's Gonna Be a Good Good Day .....





Seriously Loving The #Technology & #Accessories us #T1Ds Use ....... #CGM Today's Gonna Be a Good Day, Ye Today's Gonna Be a Good Good Day .....


Sometimes no matter how attentive we are to our T1, it just seems to do its own thing. After counting carbs, calculating and bolusing correctly to see a BG higher than it should be can be so bloody disheartening. It's like working hard for absolutely no recognition and no pay off at the end of the job. 
It's easy when things don't work out to think to ourselves "why bother" but then the thoughts of all those complications set in, and my drive to stay between the lines continues through good days and bad. Whether in feeling great or absolutely rotten.

Anyone who knows me will know about Misty, Grace and Princess Kate.
My 3 amigos..... My Pets .......
Princess Kate is only 4 and 1/2 months old, fully trained and nearly talks to me but every now and then despite all my efforts she will do something either good or not so good that just leaves me speechless.

I think I see my #T1 a bit like my other pet. I'm constantly watching, training, guiding, managing, and sorting it out 24/7/365 ( you'll notice I don't say controlling ) because I believe we manage but we never control and if you think you do, then just look back through your records at that day you did everything right, everything the same as you always do, but had a BG reading above or below what you planed for. ( we manage, but our body's control )

It was after this realisation that I began to feel I needed something other than just a BG meter and a finger pricker. I needed to see if my BG was climbing or dropping before it was at crisis point. I needed an alarm to say, "hey Davina pay attention your about to break the speed limit" just so I could put the breaks on before I hit a wall. 

I found something that could do all that, my CGM ( Medtronic Guardian ) 
Yes I still finger prick, but only every 12 hours and enter my reading to keep the CGM on track ( to calibrate it ).

I wake in the morning and I can see if Iv had any highs or lows through the night, and if I see that over those 6-8 hours through my nights sleep Iv "flat lined" lol ---------- meaning my BG has hardly budged either way, I'm awake and I'm between 5 and 6 then I know as the Black Eyed P's would sing..... Today's Gonna Be a Good Day 🎢🎢🎢 Today's Gonna Be a Good Good Day 🎢🎢🎢
Lovin my CGM and can't imagine life without it. My BG bouncer, My Door Man, My Security Guard-ian.

O FYI Iv called her "Jelly Bean" yes HER .... Well she does multi task ! 
Sorry guys ......

Just a T1 with an opinion

Davina