FACS AssociationFetal Anti-Convulsant syndrome
Welcome to our website. FACSA is a support group for families and children who have been affected by AEDs during pregnancy and have a diagnosis of FACS Syndrome (FVS)
Without the help and dedication of the founding members, we would be at a real loss of which route to take to care for our 3 daughters affected by Sodium Valproate. Thank you so much, ladies
Our Key Pages
This site will include a lot of information, here are some shortcuts to some of the main things you may be looking for. If you are looking for something else try the SiteMap
Fetal Anti Convulsant syndrome is an Umbrella Term for a host of different Epilepsy medications taken during pregnancy that have had an effect on the baby in Utero.
New warnings and guidance on prescribing sodium valproate to girls and women with epilepsy have been issued by the MHRA (Medicines and Healthcare Products Regulatory Agency).
Download our Educational Materials for you to print. If you would rather receive free original copies please contact us
Please get in touch if you have any questions, information, want to know more, or if you would like original documents sent to you by email
Some of the Places we have been featured in
BlogLatest News, Information & Updates
This is a devastating blow for the Irish Valproate Campaign. It took us months of work at The National Archives going through hundreds of files and thousands of papers to find the Government evidence on Valproate. Without these documents we now have with our...
Our downloadable and printable leaflets and information booklets are now available on the website.
Following last weeks Valproate Stakeholder Network meeting, we contacted Andrew Dillon Chief Executive of NICE (Clinical guidelines) as we were under the assumption that the current NICE guidelines did NOT include the new PREVENT programme for Sodium Valproate. Today...
A new research out from Denmark confirms all AED's are associated with Neurodevelopmental problems when used in pregnancy. We have said this for the last 6 years of Campaigning, Action now needs to be taken from MHRA.
About Our Founders
We won’t stop fighting
Janet Williams and Emma Murphy founded FACSA in 2012 after the collapse of Product Liability Litigation against Sanofi. Their aim was to represent affected families in the UK and implement change with regards to the prescribing of Sodium Valproate and to ensure justice for those affected by the medicine and to be the main port of call for families harmed by Epilepsy medicines.
Both Janet and Emma have Epilepsy and children affected and diagnosed with Fetal Valproate Syndrome