About Us

Our core mission is to provide sympathetic support to ME/CFS and FMS sufferers, their family and friends, giving up to date information, advice aand guidance on all aspects of the illness. Through shared experience and united action we are an informed conduit to the medical, social services and other professionals. We promote a wider awareness and deeper understanding of the illness and its effects on all age groups.

The Group is run by a democratically elected Committee of generous and committed volunteers and has acquired a formidable array of patrons over the years.

We hold meetings every three months.

In August each year we hold our AGM and have a birthday lunch - to celebrate the forming of the group.

We also hold other events such as picnics and conferences.

One of our main objectives at present is to interact with our members and give them a voice in our newsletters.  If you'd like to contribute and "Have your say" please email us.

Thanks to the help of Flintshire Local Voluntary Council we are a registered charity (No.1093718)

We do charge a small membership fee which goes towards the cost of the newsletters we produce and we are grateful for the support of Lloyds TSB Foundation for England and Wales which enables us to have a part time administrator work for us and to fund an office.