It’s time for last Autumn Internationals #MatchDaySorted 🥳🎉
Follow & RT for a chance to win:
2x Tickets to Ireland v Australia match on Nov 30th in AVIVA
4x Pints of @Heineken_IE
2x Match Day Burger
Winner announced lunchtime on Thursday!
It’s time for another #MatchDaySorted 🥳🎉
Follow & RT for a chance to win:
2x Tickets to Ireland v Fiji match on Nov 23rd in AVIVA
4x Pints of @Heineken_IE
2x Match Day Burger
Winner announced lunchtime on Thursday!
Good luck everyone!
Here we go again with another MASSIVE #MatchDaySorted 🥳🎉
Follow & RT for a chance to win:
2x Tickets to Ireland v Argentina match on Nov 15th in AVIVA
4x Pints of @Heineken_IE
2x Match Day Burger
Winner announced lunchtime on Nov 13th!
It’s time for another BIG #MatchDaySorted 🥳🎉
Follow & RT for a chance to win:
2x Tickets to Ireland v New Zealand match on Nov 8th in AVIVA
4x Pints of @Heineken_IE
2x Match Day Burgers
Winner announced lunchtime on Nov 6th!
#matchdaysorted
📢 AV Room Briefing - Leinster House
This is more than a look back—it's a call to action for the future of paediatric spina bifida and scoliosis services in Ireland.
We’ll address the past 10 years of challenges but, more importantly, we’ll push for the urgent reforms needed to ensure that no child is left waiting for life-changing care.
🗓 Date: Wednesday, 25th September 2024
🕓 Time: 4:00 PM
📍 Where: AV Room, Leinster House
Speakers:
👤 Amanda Coughlan, Co-lead of Spina Bifida & Hydrocephalus Paediatric Advocacy Group
👤 Úna Keightley, Co-lead
👤 Claire Cahill, Co-founder of Scoliosis Advocacy Network
👤 Michelle Long, Co-founder
🌟 Please request your local TDs and Senators to attend and show their support.
#BackUs #TimelyCare @SBH_PAG #HealthCareRights #ScoliosisCare #SpinaBifida #FutureOfCare
An email sent to An Taoiseach @SimonHarrisTD this morning. I’ll keep you all posted if I hear back ❤️
Hi Simon, I am writing to you as an incredibly concerned parent of an 8.5 year old boy, Harvey. Harvey has Spina bifida and scoliosis which in itself is challenging, but when those conditions are coupled with a lack of access to therapy, a hospital that is potentially misappropriating funds, and incredibly long wait lists for urgent and life changing surgeries, then it becomes impossible to adequately care for your child.
Harvey had an Xray in January 2024 that showed his scoliosis curve is at 110°, if you have read in to scoliosis then I am sure you are aware how this is at a point where it is detrimental to his health and quality of life.
Harvey was under Connor Green and was listed for urgent surgery in February 2022 after repeated pneumonia infections, 30 months later he is still only on the surgical list under Connor Green as he does not have a surgeon willing to operate.
The task force you hold in such high regard has not made contact with my family, nor is there any details online of how to contact them to enquire as to when your child will finally be treated.
You continually tell families like ours that you care, and you have been promising to fix this since 2017. 2017 was the year we were told that Harvey’s ribs were crushing his lungs and controlling his scoliosis was life and death.
Here we are in 2024 and nothing has changed except we now have a surgeon under investigation, longer wait lists, more children waiting, a still not complete hospital, and funds not being spent as intended and no answers yet as to where the money *we* fought for went.
You say you care but your actions have left us feeling anything but.
We as a family also have a child facing open heart surgery next month and this is just more stress and concern that we do not need.
Another summer has just passed and Harvey has spent the majority in his room, often needing to go back in to bed because he is in so much pain. Is that the life you think the children of Ireland deserve? Would you accept that if it was your own child?
Can you imagine being told your child has a potentially life threatening condition but that it will be years before it would be treated?
We need actual action, not more empty promises.
You need to engage with all advocacy groups, not just those that are currently working with the task force. There are very valid reasons why the other groups have chosen to not engage and they need to be heard.
We need contact details and open dialogue with the task force so that we can actually feel its existence.
We need answers as to where the funding for scoliosis and spina bifida services went.
Most of all, these children need to get their quality of life back before their whole childhood passes.
I look forward to hearing from you.
Kind Regards.
Gillian Sherratt
my current olympics obsession is henrik christiansen, this swimmer from norway who’s obsessed with the chocolate muffins in the olympic village and can’t stop making tiktoks about them
It's time for #MatchDaySorted 🥳
Follow & RT for a chance to win:
2× Tickets to Ireland v Scotland on the 16th of March
at The Aviva
4× Pints of @Heineken_IE
2x Match Day Burgers
1× #MatchDaySorted
Winner announced lunch time this Friday!
#IrelandVScotland
It's time for #MatchDaySorted 🥳
Follow & RT for a chance to win:
2× Tickets to Ireland v Wales on the 24th of February at The Aviva
4 × Pints of @Heineken_IE
2× Match Day Burgers
1 × #MatchDaySorted
Winner announced lunch time this Friday
#IrelandvWales#SixNations
It's time for #MatchDaySorted 🥳
Follow & RT for a chance to win:
2× Tickets to Ireland v Italy on the 11th of February at The Aviva
4 × Pints of @Heineken_IE
2× Match Day Burgers
1 × #MatchDaySorted
Winner announced lunch time this Friday
#IrelandvItaly#SixNations
Huge news for @HyperemesisIE and all those who campaigned for Cariban to be reimbursed because of the *crazy* cost it added to pregnancy https://t.co/OpE4FnsQdN