The Aarskog Foundation achieves Registered Charity Status
It is after much hard work and dedication that we are proud to announce that The Aarskog Foundation UK is now a registered Charity! We are the first of our kind in the world. Michelle Erskine and her team are absoultely delighted to have reached this monumental achievement for the charity.
The Aarskog Foundation becomes a RARE Foundation Alliance partner
Alongside more than 400 other rare disease organizations, The Aarskog Foundation is also now proud to be partnering with RARE Foundation Alliance.
Team Aarskog set to do Skydive to raise money for Findacure
Michelle and Team Aarskog will be bracing themselves for her Skydive on Saturday 25th August, to raise money for Findacure.
The Aarskog Foundation to attend RARE Patient Advocacy Summit
Michelle Erskine of The Aarskog Foundation will be attending the 2018 RARE Patient Advocacy Summit in October, in connection with Global Genes. The Aarskog Foundation are an allied member of Global Genes, whose aim is to provide connect empower and inspire those with rare diseases, their caregivers and the rare disease community.
Speech, reading & translation support with Browsealoud
Here at The Aarskog Foundation we’re delighted to announce that we’ve added speech, reading and translation support to our website with Browsealoud.