We have been told it is unrealistic to expect treatment for Grace this side of Christmas. After such elation in June we didn't think it was possible to experience the depths of despair we currently are 💔💔 #Spinraza#devastated
https://t.co/0FLgKmHU9Y
Last June, 25 child patients in Ireland with debilitating SMA (spinal muscular atrophy) conditions, were told funding had been approved for ‘miracle drug’ Spinraza. @SMAIrelandCom. https://t.co/AfLeZPwCAb
@SimonHarrisTD @MichaelRingFG thanks for taking the time to talk with us today. Grace was so happy to finally meet Minister Harris - "he's quite tall in real life!" We look forward to progressing things with you sooner rather than later.
#Spinraza was approved 18 weeks ago, we had hoped Grace's trreatment would be well underway by now but to date Grace hasn't even received a date to begin treatment. The elation deflation cycle continues...@HSELive@SimonHarrisTD Winter months are detrimental pleae stop the delays
Spinraza approval greeted with relief as Friends of Grace delighted with HSE approval after a long and arduous campaign
Full story here: https://t.co/1ygLOFyP8u
We are so delighted that our little Grace will get her best chance at life and we couldn't have done it without you. So from the bottom of our hearts a huge "Thank You" to you all.
Have we won an Oscar! First the delight, now the fear of forgetting to thank someone. Thank you to every single person be they family, friends, media, politicians or just lovely people who heard our story, for all the messages of help and support over the #Spinraza campaign.
@SimonHarrisTD Thank you Simon, this means everything to Grace and all the other sufferers who will benefit. It was a long hard road and we appreciate the work put in on your side.
Great day for all the families & friends of #SMA children. Heartbreak, emotion, the meetings, false dawns, broken promises...just to to get to today. This news brought a tear to my eye, and delighted for @grace_friends and all the other kids. #Spinraza is a #LifeChanger