Ataxia Telangiectasia (A-T) Trial Launch

March 23, 2022, marks the official launch of the Ataxia Telangiectasia (A-T) trial.
Thank you to the multidisciplinary efforts of Dr David Coman, Professor Martin Lavin and their teams for their tireless pursuit to find a new treatment option for children with A-T.
To the families impacted by this genetic condition and organisations such as BrAshA-T Ataxia-Telangiectasia and Rare Voices Australia - this is for you!
Greg Hunt MP, we are grateful for your heartfelt support and the $2.46 million grant received from the Medical Research Future Fund.
None of this would be possible without all of you.
Find out more about A-T and the ongoing trial: ow.ly/JmHA50IpVsG
Or support us by making a donation today: ow.ly/fbt950IpVta

[@RavinderSingh-nh7hb]

My son is suffering from AT and I pray to god something positive will come out of this trial … please save all AT kids … This is Ravi from India …

[@umadevi9615]

Me babu age yantha andi yala unadu babu ma babu ki same problem

[@ZubairBashir-rw3yo]

My daughter is suffering from (A-T).is there any updates to how this trial is performing.if it's proving to be successful or not? Plz any update? highly thankful to u.

[@mannyduran6107]

Is there any updates to how this trial is performing? If it’s proving to be successful or not. Please any update would be greatly appreciated.

[@sadiamoin5791]

I have 2 child they both are AT positive my son is not in this world in the age of 6 .6 he death My daughter is 10 year old she can't move her self she is on IVIG injection plz cure for her

[@etteseb]

Is there any updates on this