Notice of Annual General Meeting to be held: On Tuesday 3rd January 2017 At 7pm – Mourne Country Hotel – Members only. Guests welcome to join meeting after AGM finishes at 7.30pm Agenda: 1. Apologies 2. Minutes of the last AGM 3. Chair’s Report 4. Treasurer’s Report 5. Election...
Please try to join us on Tuesday November 1st to hear our guest speaker, Patricia McCrystal CPsychol & AFBPsS, enlighten us about the difficulties (and possible solutions) when dealing with persistent pain.Patricia is a Chartered Psychologist & Registered Counselling Psychologist who specialises in helping patients with persistent pain issues....
A MAJOR demonstration urging more research into M.E. was held at Stormont on Tuesday as part of a global day of action. Protests took part in 25 cities across the world, including Belfast, Melbourne, London and New York. Pairs of shoes were placed at each demonstration to represent the...
For too long Myalgic Encephalomyelitis (ME) has been known as an ‘invisible illness’ with sufferers left with little support and no medical way forward. Across the globe there are millions who live with the condition, and with the knowledge that there is no cure. Those millions feel that they...
It’s been a long time, waiting for an opportunity to improve the image of our group, but we now have our brand new little place on the Internet with our new website. We trust that you will find everything that you’re looking for and remember to check out our...
We are covering two topics this month as below. PIPS offer a number of free help services for anyone feeling desperate or struggling with any issue. They offer a home counselling service for bed bound/ housebound patients. The experienced reflexologist will provide an interactive session, learning us how to...
To celebrate the official office opening of Hope 4 ME & Fibro Northern Ireland, and especially in the light of the recent exciting breakthrough with on the metabolomic deficiencies in ME, our charity is donating £1000.00 to the ‘END ME/CFS Project’ at the Open Medicine Foundation. Quote from OMF...
Northern Irish friends – please will you consider asking your MLAs to support the demonstration at Stormont on 27th September 2016. We have found that MLAs are much more likely to attend events if asked directly to do so by their constituents. Copied below is a suggested letter that...
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