About Myalgic Encephalomyelitis (ME)

Sunday, 7 April 2019

'Call 4 Change 4 ME' - Myalgic Encephalomyelitis (ME) Awareness Event May 2019








Myalgic Encephalomyelitis (ME) May Awareness Event 

Tuesday May 14th, 2019

11:30 am - 2:30 pm

Leinster House





The May ME Visibility Event takes place during ME Awareness Month on Tuesday May 14th outside Leinster House, Kildare Street, Dublin at 11:30am - 2:30pm

At this year’s Visibility Event, being organised by ME Advocates Ireland (MEAI), patients & advocates, families & friends will once again be raising awareness of Myalgic Encephalomyelitis (ME) & the thousands of people with ME in Ireland who are invisible because of ME & Government inaction.

We will be calling for change to the situation of ME in Ireland & are giving the Visibility Event the name - Call 4 Change 4 ME










We will be using the hashtag #Call4Change4ME on social media, and calling on the Irish government, the Minister for Health, and the HSE to plan to change the situation for people with ME in Ireland who are currently invisible to them. People with ME are invisible not just because of this debilitating neurological illness but also because of lack of Government action.

People with ME suffer from a lack of friends & family, career & hobbies because they are so unwell and house-bound, too ill to maintain relationships, which eventually break down. And they are too ill to work. Very severe ME patients who lie paralysed, tube-fed in darkened rooms are rendered even more invisible. They are not physically out in the world - no one knows they are there.

There is a disparity between how one feels living with a chronic illness, versus how imperceptible that experience is to the outside world. This incongruence presents many challenges that can confound illness. ME, an invisible illness can be met with scepticism, others think you look well and don't look sick at all.

ME patients suffer multiple invisibilities. Currently ME is invisible because there’s no national policy for ME, no healthcare pathway, no consultant, no ME-aware medics, no training of medical students & professionals, no criteria adopted & no treatment.

Conversations do not begin with invisibility. Change won't happen there. The potential for change can only be found with visibility, so we are coming together and calling on the Irish Government and HSE to have a conversation to begin the change to the neglect of people with ME.



We Call 4 Change 4 ME because in the eyes of the Irish Government & the HSE people with ME in Ireland are invisible  













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Prevalence rates, based on international rates, for ME patients in Ireland in 2019 are between 10,000 and 19,000


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WHAT'S HAPPENING AT THIS YEAR'S VISIBILITY EVENT?

• We will be talking to Gov Reps, TDs, etc again.

• We will have a group of people in attendance wearing white face masks to highlight the invisible nature of ME & the invisibility of ME when it comes to Government policy etc. 
The masks will be worn for a short time during the visibility event to signify that we are still being ignored & are invisible to the Minister for Health & HSE.

• We will capture the mask-wearing moment on a live Facebook feed.

• We will involve you who can't attend in the mask idea. See details on the masks below.

• We will have last year’s Information Tags on display, as well as any new tags you send this year.

• There will be a ‘Tree for ME’ event during the main event where we will plant a tree in memory of all who have died from complications with ME and we will add small tags with the names of ME patients who have died.

• We hope to have press & media in attendance, as we did at the two previous visibility events in May 2017 & 2018.

• We hope that everyone who attends the event will wear blue clothing. The colour blue represents Myalgic Encephalomyelitis (ME).

• We will provide blue ribbons to wear. Blue ribbons represent Myalgic Encephalomyelitis (ME)












Event Page

Please see the Call 4 Change 4 ME event page & let us know if you are interested or can attend here














HOW CAN YOU BE PART OF THE CALL 4 CHANGE 4 ME EVENT ON TUESDAY MAY 14TH?


• You & family, friends & carers can attend the event outside Leinster House on May 14th or invite others to attend on your behalf. 

Please use the event link to ask others to attend & share widely here


• You can be part of the mask-wearing event this year by sending us an image of you wearing a mask to represent the fact that you are ‘missing’ - missing life, family, friends, career, social life, good health, appropriate healthcare pathways, etc, & to represent the fact that when it comes to the HSE & the Government there are a lot of things invisible e.g. ME policy, appropriate care pathways, diagnostic criteria, ME-aware medics & trained health professionals, treatments, etc.
(there are more details on the mask idea below)







The Mask represents Invisibility, this year's theme for the ME Awareness Event






• You can be represented at the Call 4 Change 4 ME event by having an Information Tag with information about you on display at the event.
See images below showing the Information Tag Display board & tags we used at last year’s event.
(there are more details on Information Tags below)

• Share the Call 4 Change 4 ME event page on social media- on Facebook, Twitter, etc to encourage others to attend on May 14th.
The more people who attend the better so that we can use our collective voices to call for change to the situation of ME in Ireland.
See link to event page here.


• Invite your local TDs to this year's Call 4 Change 4 ME awareness event to come out and chat to those attending - to patients, advocates, friends and families of those with ME. See link to TD list below






DETAILS ON MASKS & INFORMATION TAGS BELOW: 


MASK

Keeping up with the invisible illness & invisibility theme we are planning that people in attendance at the Call 4 Change 4 ME event will wear masks for a short time during the event to signify that ME patients are still being ignored & are invisible to the Minister for Health & HSE.
(We will be organising the masks for a group to wear at the visibility event.)
We encourage you to be part of the mask-wearing event this year by sending us an image of you wearing a mask to represent the fact that you are ‘missing’ & please send a brief piece about you - about who you are, how long you have had ME, what makes you feel invisible, what changes you’d like to see made by the Government & HSE. Just a few lines to add when you send us your photo.




How to organise a photo of you wearing a mask at home:-

- Order a mask online, buy one in a local shop, or make one, or have somebody make one for you using a sheet of paper/cardboard. If you buy a mask or make a mask it doesn't have to be exactly like those in the images but as close as possible, i.e. white and blank.
- Take a selfie of you wearing the mask or get someone to take your photo.
- Add the hashtag #Call4Change4ME to a photo of you wearing your mask as in the pics attached below.
- Send the photo to us to share on social media.
- Send some information about who you are, how long you have had ME, what makes you feel invisible, what changes you’d like to see made by the Government & HSE to make ME visible. Just a few lines to add when you send us your photo. See sample information below.



Mask to represent invisibility & blue ribbon to represent ME


Example info:

Invisible for 12 years with Myalgic Encephalomyelitis (ME). Invisible from my life - my friends & family, my career & hobbies. Invisible because there’s no national policy for ME, no healthcare pathway, no consultant, no ME-aware medics, no criteria adopted & no treatment. In the eyes of the Irish Government & the HSE I am invisible #Call4Change4ME 












NB There are a few ways to send your mask image & information.
Send by email to info@meadvocatesireland.com
Or send by pm to the ME Advocates Ireland Facebook page via the message button. Page link here


NB- Sending your image & info means you are happy for it to be posted on social media eg FB, Twitter, Instagram.




INFORMATION TAG

We are using the Information Tag display that we used at last year’s event again this year. The display contains information tags which have information about patients who sent info & a photo to us last year.
(Please see images from last year’s display below in pics attached)


Information Tag Display Board at the 2018 ME Visibility Event





To involve as many people with ME as possible in this year’s event, the organisers would like to invite people with ME or their carers to send us an Information Tag - a brief piece of information about you & your illness, or about the person you are caring for, & a photo too to be displayed as an Information Tag at the Call 4 Change 4 ME visibility event.
(NB There is no need for those who already sent Info Tags to us last year to send again as we kept your tags)

Your Information Tag will be displayed for others to read at the Call 4 Change 4 ME visibility event, e.g. TDs, attendees, & passers-by. The Information Tag will represent you if you cannot attend the event.

If you'd like to make your own information tag, see how to do that below.
If you would like us to make your information tag, please send us your information and your photo to our email address: - info@meadvocatesireland.com
Or
Send by pm to the ME Advocates Ireland Facebook page via the message button. Page link here

NB-Sending an information tag means you are happy to have your image & info posted on social media and displayed at the visibility event.






How to make the Information Tag yourself at home or have someone you know make one for you.

- Write a brief piece about yourself or the person with ME on an A5 sheet of paper,

e.g. name, how long ill, what is missed in life, what difficulties you face having M.E., what changes you would like to see in healthcare, etc. There won’t be a lot of space on an A5 page so please be brief.
(NB - A5 size is half A4 size and the dimensions are 5.8" wide by 8.3" long)




- We encourage you to attach a photo of yourself above or below your information piece. The photo can be any photo you have that you don’t mind giving away. You can add a photo that best represents how unwell you are.

- Please add the hashtag #Call4Change4ME somewhere on your tag.

- Laminate the tag if you can. 


The tags will be hung in portrait orientation (longways) as in image above. 






EVENT REMINDER 
What: - Call 4 Change 4 ME - May visibility event
Where: - Outside Leinster House, Kildare Street, Dublin                                   
When: - Tuesday May 14th, 2019                                                                       
Time: - 11:30am – 2:30pm
Event link: - here














Sunday, 10 March 2019

Press Conference about ME and Fibromyalgia - MEAI member Christine Fenton speaks about ME



On February 21st 2019, ME and Fibromyalgia patient-advocates attended a press conference in Buswells Hotel, Dublin, organised by Gino Kenny TD and Rachel Lynch of FibroIreland, to call for change for 1000s living in Ireland with these two neglected illnesses. While Fibromyalgia was well represented by Ursula Hakman, Marissa Appel, John Maher and Adrienne Dempsey, ME was represented by Christine Fenton of ME Advocates Ireland (MEAI). Gino Kenny TD hosted the event and Dr Shelagh Wright opened the talks. The press in attendance included RTE and the Irish Times who published reports on the event.





Christine Fenton of ME Advocates Ireland, far left




The press conference was organised as a response to inaction by the Irish Government and the HSE after a call for change to the neglect of ME and Fibro patients was made at a presentation on ME and Fibro in front of TDs and other Government representatives in the Dáil in January 2018 here .
At the follow up press conference in Buswells Hotel patient-advocates explained their own situation with illness and talked about Government inaction and the ongoing lack of support for those living with Fibromyalgia and ME.





Christine Fenton, centre, with members of MEAI & FibroIreland
in the AV Room in Leinster House Jan 2018



Christine Fenton, member of ME Advocates Ireland, was one of those who spoke at the 'Call for Change' presentation in the Dáil last year. Christine made the trip from her home in Sligo to Dublin to highlight the inequalities faced by Irish people with ME here *
As nothing had been done in the last year and despite being very ill, Christine made another trip to Dublin to remind our government about what needs to be done to provide ME patients with more appropriate healthcare. Christine called for much needed change.








Christine Fenton (MEAI) speaking at the press conference





Link to Christine's press conference speech below:-

Christine's Speech



Full Press Conference available on FibroIreland's Facebook page at the following link: -

Full Press Conference on ME and Fibromyalgia














Thanks due to Rachel Lynch and FibroIreland for providing the recording of this event.
Many thanks to Gino Kenny TD and Rachel Lynch of FibroIreland for giving ME Advocates Ireland this opportunity to raise awareness about ME issues.






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Other presentations re ME & Fibromyalgia made at the Call for Change event in the AV Room in the Dáil in Jan 2018 below:-





(Joan Byrne's presentation here)







Rachel Lynch & Clodagh Lawlor re Fibromyalgia



Sunday, 13 January 2019

Radio Interview -Talking about Myalgic Encephalomyelitis (ME)






ME - 'a condition that is often misunderstood'


Recently ME Advocates Ireland (MEAI) were contacted and invited to talk about Myalgic Encephalomyelitis (ME) by a local radio station in Castlebar, Co Mayo. Christine Fenton, one of our members, offered to do the interview and she chatted with Angela Faull on Thursday morning, 10th of January on CRCfm about ME in general and about her own illness.

The presenter was well aware that ME is a condition often misunderstood and recalled reading a book about an American doctor who had a role in teaching and helping people suffering from AIDS, and 'who found it more difficult to sustain her ME patients than it was to sustain her AIDS patients'.

Christine talked about the cardinal feature of ME, Post Exertional Neuroimmune Exhaustion (PENE), which can be caused by any amount of physical or mental activity, eg having a shower, talking on the phone.

Christine highlighted the lack of support for ME patients in Ireland especially from the HSE, despite a recent recommendation from a report from the HSE to set up a working group to bring about guidelines.
She referred to mixed attitudes among HSE personnel where she has met staff who want to do their best but she has also met other staff who are totally dismissive.



 'There is no culture in the HSE that understands it [ME]'. 



Here is the link to the complete interview below.




Compiled by MD

Saturday, 5 January 2019

Nobody Should Have to Live like This - I Need Care to Live Independently

ME patient Corina Duyn reflects on the challenges of having Disability Services in Waterford accept her as having a disability.




One of ME Advocates Ireland (MEAI) co-founding members, Corina Duyn, a ME patient/advocate, is currently trapped in a care home because she cannot live in her own home without the necessary homecare she requires, and her disabilities are not recognised by the HSE as disabilities in the area where she lives. Her illness Myalgic Encephalomyelitis (ME) is however recognised as a disability elsewhere in Ireland where other patients have been provided with home care packages to suit their needs.



Post code lotteries have become a real issue when it comes to seeking help from the HSE in Ireland. Corina, who needs daily care, is currently looking for homecare that will enable her to live in her own home. She has written to HSE's 'Have Your Say', HSE Community Care, Head of Primary Care, Disability Services, the Public Health Nurse and a Senior Complaint Officer. All are aware of her ongoing situation but so far Corina has not received concrete answers or a solution. Her pleas for help via regular emails and phone calls have fallen on deafened ears and she is now ten days in a care home for the elderly.

Corina who is 56 years of age was forced to go into the home for the elderly over the Christmas period because of a worsening of her health and an inability to care for herself. Corina's greatest fear is that she would have to remain in the care home and won't be able to return to her home. 






Tweet from Chronic Illness Inclusion Project




An article published by TheJournal.ie on January 2nd, and written shortly before Corina deteriorated in her own home during Christmas, highlights the importance of recognising all forms of disability and judging them on their own merit. Sometimes categories of disability do not work and as a result people fall through the cracks in the system. Link to article 
Compiled by MD