OACS Ireland receives no state funding whatsoever and relies on it’s Chairperson and members of the board many who are parents of children impacted to voluntarily run the organisation.  The workload is becoming increasingly demanding especially since the launch of the Inquiry. The figures on Ronan Glynns report on Valproate should be better highlighted to give more credence to our cause so to speak if you will.  Between 1975 and 2015 he estimated 3126 Irish babies were impacted in the womb.

To Make a Donation to OACS via idonate please visit or share this link

https://www.idonate.ie/fundraiser/OACSadmin

Where Your Money Goes

Funds raised through the I-donate OACS Ireland  Fundraiser page will assist our Voluntary OACS Group with the ongoing Admin cost of operating the group.  

In particular we need funds for our Office Admin, Printing, Phone, Internet / Website and Social Media Costs to help us build awareness and to offer support to families affected by  Foetal Valproate Syndrome/Spectrum Disorder.

Organisation for Anti-Convulsant Syndromes Ireland (OACS Ireland)

OACS Ireland is a voluntary group, we provide support, help and advice to other families, whose children have been affected by Foetal Anti-Convulsant Syndrome (F.A.C.S) in Ireland.