We are expecting yet another increase in the price of prescription charges in England any day now. The Hughes Syndrome Foundation is pleased to be one the original members of the Prescription Charges Coalition who is launching an online petition, calling on the government to end unfair, outdated and arbitrary prescription charges for everyone with a long-term condition ... including APS/Hughes syndrome.
The petition, hosted by the British Heart Foundation is easy to fill in. Just click here to add your support and please forward to family, friends and colleagues too:
campaigning.bhf.org.uk/ea-a...
Remember that petitions do work if we can all pull together. Thanks for sharing if you can
Appeal for APS specialists in the UK (sorry - rest of the world will follow at a later date!)
Half-marathon run. 2nd March 2014. Llanelli, Carmarthenshire. 2 Sisters & Friend running in aid of Hughes Syndrome - Mum so Proud
