We are a grassroots project. Run by sufferers of PMDD, for other sufferers. We are passionate about raising the standards of care and resources for those suffering from PMDD. We aim to raise awareness in both the general public and health care professionals. We have been running for 6 months and have already been in national publications, liased with MIND charity to create material for their charity and have agreed to work in association with the UK Charity (NAPS - National Association for PMS) and the amazing Gia Allemand Foundation for PMDD (A non-profit which runs internationally)
Funds raised will all go towards setting up a website dedicated to providing specific resources for women - a one stop shop for PMDD information (initially in the UK but once we have that to a tee we will make all information editable so it can be used internationally). Funds will also go into printing costs to provide resources for sufferers.