Wednesday 9 May 2018

Podcasts of Interviews by Members of ME Advocates Ireland (MEAI)














This page includes podcasts of interviews by members of 
ME Advocates Ireland (MEAI) 











Corina talks about the article about living with ME during Covid-19 restrictions as well as the two year fight with the HSE to gain proper care and PA support.





In this second interview from her bed Noreen Murphy chats with Ray Dolan to highlight M.E. in an effort to get recognition, support, care and treatment from our government, HSE and Health Minister and, of course, to get our GPs taught about M.E.  




Christine Fenton was invited to talk about ME by a local radio station in Castlebar, Co Mayo. Christine chatted on CRCfm with Angela Faull on Thursday  Jan 10th, 2019 about ME in general and about her own illness. 






A very clear interview about what M.E. is, how it affects people, especially those severely affected. Including paralyses.  And details about the ME Awareness Protest in Dublin 10th May, and why we are out there.








Interview from her bed- with Ray Dolan to highlight M.E. #MillionsMissing demonstration outside Leinster House Thursday, 10th May, from 11:30 until 2:30 in an effort to get recognition, support, care and treatment from our government, HSE and Health Minister and, of course, to get our GPs taught about M.E.




"On the show Presenters Bernadette Phillips and Stan Phillips spoke with Author Corina Duyn about the 'reality' of living with M.E. and the aftermath of travel. Also about the upcoming M.E. #MillionsMissing Event in Dublin hosted by M.E. Advocates Ireland happening on 10th May which is part of a global campaign for M.E. health and Equality." Also  8th March 2018  & November 2017 reality of M.E. and society's views on disability.












"I suddenly started losing the use of my legs, my arms...and my body stopped functioning."
Myalgic Encephalomyelitis (M.E.) patients - who experience severe, persistent debilitating illness, held a peaceful awareness protest outside Leinster House today to highlight what they claim is the utter neglect of ME patients in this country.








  • A Mullingar woman with severe ME has set up an online petition for the drug, Ampligen, to be licenced and made available to treat people with Myalgic Encephalomyelitis (ME). Noreen Murphy says the treatment is available in the US but not in Ireland. Noreen has been telling Keith Shanley on the Midlands Today Show that she has written numerous letters to the Department of Health.




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