IN-FACT – Independant Fetal Anti Convulsant Trust


All original content copyright Emma4facs 2012 – 2014

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IN-FACT (Independent Fetal Anti Convulsant Trust) was formed in November 2012 by myself and colleague Janet Williams. Both ourselves have children affected and diagnosed by the exposure to Sodium Valproate (Epilim)
Janet has 2 children diagnosed with FACS Syndrome and I myself have 5 children all diagnosed with FACS

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IN-FACTS OBJECTIVES

IN-FACT have been noted through Government as the Official National Campaign Group

IN-FACT has been set up for the purpose of giving relief and assistance to all persons whose disablilities were caused by the fact of their mother taking an Anti Convulsant drug during pregnancy to treat her condition.

To support by means of payments to the beneficiaries to help with the cost of care, welfare, treatment/education supporting them with their injuries

With intentions to pay sums of money to help and support submitted through Government or Pharmaceutical Company donations

The Trusts work entails providing long term support for those affected by Anti Convulsant medications during pregnancy, and working with a wide range of professionals and organisations in raising awareness of Fetal Anti Convulsant Syndrome (FACS) within Government and Health Agencies

PLEASE NOTE : ALL BENEFICIARIES MUST BE PERSONS BORN WITHIN THE UNITED KINGDOM

ADVISED AND SUPPORTED BY

The Thalidomide Campaign Team

Nick Dobrick
Guy Tweedy
Mikey Argey

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IN-FACT work side by side with The FACS Syndrome Association so that when the time is right for financial support, people will only have to register once.

Please click on the link to register on our National Databse :  https://www.surveymonkey.com/s/9JH33ZR

All information is held confidentially

FSA - FACS SYNDROME ASSOCIATION

FSA – FACS SYNDROME ASSOCIATION

One thought on “IN-FACT – Independant Fetal Anti Convulsant Trust

  1. Pingback: IN-FACT – Independant Fetal Anti Convulsant Trust | Emma4facs

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