If you follow me on Facebook and Twitter you'll know that we are just back from a couple of days in Newcastle which I'll tell you about later. When we arrived back in Dublin we had to head to Tallaght as Jono had a hospital appointment. They always seem to call everyone in at the... Continue Reading →
The Waiting Game
I'm sure if you live in Ireland you will know all about the huge waiting list for children with scoliosis to be seen by a consultant. Jono had his spinal surgery in 2009 and it was a battle back then. Sadly things haven't improved at all over the last 8 years. You can watch Megan... Continue Reading →
Tuesday
T is for Tuesday. Only one photo today, I'm lacking in inspiration at the moment in photos and the blog. Hence why it's just Tuesday 🙂 It was a busy enough day today. I had a meeting about a project I'm going to be helping out in...more about that in the weeks to come. I... Continue Reading →
Dublin in December
Another long overdue blog. We had two trips to Dublin last month (one after the other...always the way). Not for pleasure, both hospital visits. One for blood tests for Lucy and I...to see if we have a bleeding disorder (we have to go back next month for further tests). The other for Jono's spinal check-up.... Continue Reading →
The weekend
Well it's been a bit of a week with one thing and another. The photo was taken from our drive on Thursday morning, I love to see the sunrise....we don't see that many of them though. On Tuesday Andy wound up in hospital. He only went to the doctors for a blood test, he's been... Continue Reading →
Give the children their SNA’s
It's said that school days are the best days of your life. Try telling that to the children with special needs and their parents. Due to the cutbacks most, if not all, of the children that had full-time SNA's (Special Needs Assistants) now have to share them or in some cases only have 'access' to... Continue Reading →
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