Positive Meeting with Health Minister re Future of Care for Myalgic Encephalomyelitis (ME).

On Wed 4th December 2019 members of ME Advocates Ireland (MEAI) met with Minister for Health, Simon Harris TD.

Declan Carroll, Irish M.E. Trust with some members of MEAI:
Christine Fenton, Rachel Lynch, Joan Byrne

Background

We had requested this meeting in May 2018 in order to impress upon the Minister what the real lived experience of people with M.E (PWME) is in Ireland today.

Many of you will know that we have consistently lobbied the HSE and Dept of Health in recent years for better medical education, adoption and use of the ICC-ME diagnostic criteria, better supports for PWME, removal of inappropriate treatment protocols (CBT and GET), the need for expert medical supports at Consultancy level, the need for appropriate paediatric supports including transition to adult services, etc.

We have raised numerous Parliamentary Questions through our TDs and have succeeded in raising the profile of Myalgic Encephalomyelitis in the public sphere. Many of the responses to our PQs by the HSE gave incorrect information about M.E. and this gave us an opportunity to challenge that misinformation within our health service.

We have also organised several visibility events outside Leinster House over the last number of years and this has resulted in us building up good relationships with many politicians and key influencers and we would like to thank all M.E. patients, carers, family members and friends who supported these events in any way.

HSE M.E. Working Group

Alongside all this, an independent investigation recommended the HSE create an M.E. Working Group. (We have blogged about this previously).  Through the HSE’s ‘Engaging Patients & Families’ programme, ME Advocates Ireland (MEAI) members expressed their interest and were accepted onto this Working Group. MEAI members ensure we are referencing international best practice to ensure comprehensive guidelines result from the work of the Group to establish what expected best practice should be for those living with M.E. in Ireland.

The investigation recommendations about M.E. essentially became the Working Group ‘Terms of Reference’ which define the remit of the Group.

The importance of including both Irish M.E. Charities was upheld by the MEAI members at the first meeting in May.


 

Meeting with the Minister for Health

We were finally offered a meeting with the Minister for Health, Simon Harris TD, on 4th December and the following gives you an idea of what we discussed at that meeting. Also represented at the meeting were officials from the HSE and the Dept of Health and Noel Rock, TD for Dublin North West.

The Minister was very welcoming, responsive and interested in hearing what we had to say and asked some very key questions, giving us the opportunity to further expand on many of the issues raised.

The following key areas were raised and discussed at the meeting:

·     Diagnostic criteria and the need to use the International Consensus Criteria (ICC-ME) to avoid the potential for misdiagnosis amongst the patient group.

·     The lack of education amongst GPs and other health care professionals about the aetiology of M.E. The role of the ICGP in ensuring appropriate education and training is made available to GPs.

·     The disadvantage patients experience as a result of not having available expertise to treat and support them.

·     The need for the HSE to operate from consistent, correct information on M.E.

·     The dangers of real harm being caused to people with M.E. as a result of recommending inappropriate treatment protocols such as Graded Exercise Therapy and Cognitive Behaviour Therapy

·    The need to end inappropriate referrals to psychiatry.
The disadvantage experienced by PWME as a result of ‘dismissive attitudes’ often resulting in them choosing not to see their GP or Consultant or even attending the Emergency Department.

·     The case for an M.E. specialist consultant.

·     The issues children with M.E. are faced with in Paediatric Services.

·     The role of the M.E. Working Group in ensuring that the HSE carry out a comprehensive International Literature Review of research, as well as including patient experiences, to reduce the HSE reliance on the UK NICE ME/CFS guidelines and the review of those guidelines due next year. In this respect the Minister stated his clear support for the M.E. Working Group. The Minister offered some suggestions about possible measures to safeguard M.E. patients in the interim and agreed to follow up on these.

A powerful video message from severe M.E. patient Noreen Murphy was played to the Minister.

The Minister asked some very key questions and asked for some time to reflect on our meeting and committed to meeting us again after the next M.E. Working Group meeting in January 2020.

We look forward to meeting him again in the New Year and following up on some of the issues discussed.

Thank you to all our advocates whose hard work made this possible. We have something now to build on and we continue to be committed to ensuring that M.E. patients in Ireland are safe from harm and are treated with dignity, respect and correct knowledge by all within the healthcare system.

Piece written by Joan Byrne, ME Advocates Ireland (MEAI)

(For further information about the issues raised, please visit the relevant pages on this blog)

The Barriers We Continue to Face while Living with Myalgic Encephalomyelitis (ME)

It has been just over a year since I wrote about the challenges 

of gaining adequate care to live independently in my home. See here

A lot has changed for the better, 
but the main issue of obtaining PA Services to be supported to leave my home
 has not been resolved. (Yet...)

To recap

In short Myalgic Encephalomyelitis (ME) is not on the Waterford Disability Services approved list of disabilities. I was thus not eligible to get an assessment for Personal Assistant (PA) services.  However I have a Primary Medical Cert, Mobility Allowance, a powered wheelchair from the HSE (our Irish Healthcare System), etc. etc. and my house is fully adapted for wheelchair use. After many emails, and a request from my Public Health Nurse, I did have 5 mornings of 45-minute home care. This was totally inadequate.

After I wrote my account of this senseless and challenging struggle to request to have autonomy over my care the Journal.ie online newspaper took on my story.  Their edited version was scheduled to go out during the Christmas/New Year period. As it happened, I ended up in care the days after Christmas.

Taken into care

I had flagged various departments of the HSE to the fact that there simply was not going to be enough care over the holiday period. Although deemed eligible for weekend care, they kept telling me that there was no funding for this. No weekends mean no Bank Holiday care either. Over the two weeks around he holidays I would have 4 mornings of 45-minute care. Eight days of none. Nothing was done to prevent the inevitable. I became ill a week or so before Christmas and ended up being taken into a local rest home for the elderly the day after Christmas. A totally unsuitable setting for many reasons.

Both the article in the Journal and the blog post written by my ME Advocates Ireland colleague Moira about being in care, gained a lot of attention on social media. They prompted the HSE into action and my care package was increased to twice one hour of daily care, seven days a week.  After nearly two weeks in care I returned home.

Health in decline 

My health had taken a big dip. Over the coming weeks my care package was increased to slightly longer hours in the morning. By February I was so ill that I had great difficulty speaking. It was as if the muscles in my face were unable to perform their basic function. I ended up in hospital with a suspected stroke. I remained there for three weeks. A stroke was ruled out, but I had great difficulty keeping my head up without fainting. Walking even with a walking frame was very impaired. Speaking and swallowing difficulties remained for months.

Unfortunately, one of the assessments I had to have was with a Functional Medicine Psychiatrist, as I was deemed ‘sad’. It cannot be said enough that the biologically debilitating neurological illness ME cannot be successfully treated by functional medicine, and the call for an assessment by a functional medic could only mean that they believed my symptoms were all in my head.

The young trainee psychiatrist with a beautiful open mind totally understood my account of the challenges of life with illness. I am not afraid to show my vulnerability and talk about my life. The medical team must have seen vulnerability as a weakness, and brought me in to see the main psychiatrist. He had no interest in my account of having lived with this illness for two decades and being totally aware of what I am and am not capable of. He drew me a stick figure, a thought cloud and a bolt of lightning.  (I am sorry I didn't ask for this masterpiece…). In a nutshell, I had to push through my limitations and have happy thoughts.

As the hospital is in Cork, and I live in the neighbouring County Waterford, the discharge nurse could not communicate with my Public Health Nurse (PHN). HSE logic. I had to exchange contact details between my PHS and medical team. After three weeks I was discharged, with no idea if I could actually still live independently. Some of the nurses were worried I would end up back in hospital in a few days. A temporary increase in care hours was put in place: Weekdays, morning and evening two hours; and two shorter calls during weekends. Over the coming weeks the evening call was shortened and moved to a midday call. Although my care package is reviewed every few months, these hours are still in place. I am very grateful for the safety this provides and for the wonderful carers I have.

It has taken eight months to regain some level of well being again, but my health is precarious. The numb feeling in my mouth and resulting speaking and swallowing difficulties remained for months. There are many days I spend mainly inside my home, lying in my recliner chair, or confined to bed. There are days I can enjoy the peace of my garden and have my mind focused on creative pursuits. However, I am now rarely able to leave my home. Certainly not unaided.

Which brings me back to the continued request for PA support from Disability Services.

No support to go outside of my home

As outlined a year ago, home care does not involve any care outside the home. My ongoing request for support to go to the shops, to the bank, to GP or chemist, or on a more social and wellbeing level, to go to the library, a café… continued to fall on deaf ears until a month ago. This is still very much a medical model of care. Someone who doesn’t know me decides on what I can and cannot do.

In May I repeated my request, and after many emails back and forth I learned which person in which department would have the ultimate say in whether I would be granted an assessment from Disability Services with the aim to ask for PA support. If successful, the day may come for me to escape my four walls with the safety of PA support.

I never received a response.

In July I forwarded guidelines from the Department of Health regarding Disability Services. These were obtained through Parliamentary Questions on behalf of ME Advocates Ireland.

(abstract:)

  “HSE Disability Services provide personal and social supports based on the needs of the individual, rather than the provision of services base on a specific diagnosis or condition 

The Government is committed to providing services and supports for people with disabilities which will empower them to live independent lives, provide greater independence in accessing the services they choose and enhance their ability to tailor the supports required to meet their needs and plan their lives. 

Over the past year I have received many empty promises. For example:

• 22 January: ‘... in relation to other queries [Assessment for PA], I will make enquiries and will revert back with an update once same is available to me...’
• 18th January: ‘... as previously discussed with Corina the local Disability team plan on undertaking a second assessment with Corina...’ [I never had a first assessment]
• No responses to emails 7 and 23 may.
• 3rd July: ‘... is following up on this matter and will revert to you...’
• I wrote again to ask for an update:
• 6 August: ‘ ... is annual leave until 14th August and we will revert with a response on return. Sincere apologies for the delay in responding to you...’
• I wrote again to ask for an update:
• 29 August: ‘... apologies for delay in responding to your below email. The Head of Service for Social Care is following up in terms of the assessment and we will have an update for you in same soon’.

In September I got fed up with it all. It took me a very long time to totally lose my patience and I contacted the Complaints Officer again. She had been so helpful to put the wheels in motion to get me out of care in January. She suggested that at this stage I would be entitled to contact the Chief Officer, which I did. A few weeks later I received a promise of an assessment with Disability Services.
Thank you.

Disability Assessment at last, after 20 months of asking

In October a Disability Services Liaison Officer came to my house with my Public Health Nurse. We had a very frank, open, and considerate discussion. The many cracks I fall in because of ME not being recognized under disability were identified. She could clearly see how much my illness has impacted on my ability to function. And I should be able to go outside my door…

I truly felt heard. Believed. Understood.

I felt at last that my story is being circulated by someone within the disability services and not just via my emails, and via the limited assessment procedures available to the Public Health Nurse. I hoped I would finally be supported to leave my home. And have control over how I use my care hours, beyond personal care. I am immensely grateful for the excellent home care, but I need to go outside my home at times.

I need the personal support as I need help to get dressed, and when arriving home I would be so tired that I need to be undressed, and put to bed. I prefer not to ask friends to do this.

The assessment was a month ago.

I have not heard anything since, other than yet again a promise of a response, when I made an enquiry last week. No response to follow up email this week.

My thoughts go from: “was this a ticking boxes exercise and thus fulfilled my request for an assessment”. To: “they are taking their time to set up a proper care package, looking at all the identified cracks in the system…”

Maybe, now the Personal Assistance Services Motion has passed in the Government on 19 November 2019, I will finally get an answer?

The perception that living with illness is a privilege 

This year I had to totally re-evaluate who I am. I am an independently minded woman, but can I remain living in my lovely home on my own? Can I continue to enjoy my own space and my newly designed wheelchair accessible garden? It truly is my place of peace and healing. What are my creative abilities at present? Although living with this illness for 21 years, this past year has been one of big adjustments. I had to accept strangers into my private space. I had to accept getting help with basic personal care. I had to accept that I am yet again mostly housebound. I had to accept that I also need support to bring my creative ideas into being.

Some people suggest that I am lucky to have so much time for my creative life. That I am privileged to have my house adapted for wheelchair use, to take ownership of a powered wheelchair and have a loan of a HSE profiling bed (hospital bed). Maybe I feed this distorted image by sharing images of my creative pursuits? Even if these images only constitute a few minutes out of a day, or week? I rather share these visual snippets than the reality of pain, days in bed, at times loneliness. I tell my experiences through my puppets and other creative explorations.

I see myself as an advocate for people with ME and other chronic illnesses and disabilities. My quest for care and highlighting these struggles are not just for my own benefit. I hope to have a tiny say in the way people with ME in Ireland continue to hit brick walls.
I might not have the capability to convey politics surrounding ME, but I hope that with sharing snippets of my personal story and my visuals of my creativity I can make a small difference in the lives of my fellow ‘hermits’.

Thank you for taking the time to read this.

And if I receive news regarding PA support, I will let you know for sure.

Corina Duyn

Founder member of MEAI

PS. Soon, I will be sharing thoughts about my most recent creative explorations in puppetry in more detail on my personal blog. My work can also be followed on Facebook or Instagram

ME visibility action outside Leinster House

Today, Tuesday 14th May 2019 a group of Myalgic Encephalomyelitis (M.E.) patients along with their carers, friends, family members and advocates will be holding a visibility action outside Leinster House on Kildare Street, Dublin from 11.30am to 2.30pm to highlight the neglect and harm caused to some of the most seriously ill of all patients here in Ireland.

The name of this action is #Call4Change4ME

Here are some of the posters we will have on display to make the Government aware (again) 

of your continued fight.

We hope you can join us, but if you can't be there in person, can you please support us via social media?

• Instagram

• Facebook

• Twitter

Many thanks

* Above poster designs by Noreen Murpy.

Our demands in a nutshell.

 Read our press release HERE

Tags like these which give you a snippet into the

lives of people with ME will also be on display.

Many can be read on our Instagram Page

M.E. Visibility Action, Ireland - #Call4Change4ME

M.E. Visibility Action  #Call4Change4ME

MEAI pressrelease:

Tomorrow, Tuesday 14th May 2019 a group of Myalgic Encephalomyelitis (M.E.) patients along with their carers, friends, family members and advocates will be holding a visibility action outside Leinster House on Kildare Street, Dublin, from 11.30am to 2.30pm to highlight the neglect and harm caused to some of the most seriously ill of all patients here in Ireland.

The name of this action is #Call4Change4ME

Many of these patients, some young children, are living lives shut away from the world in dark rooms, too ill to bear even the smallest interaction or movement. They simply would be unable to attend this event, but they will be represented on a display of information tags. The tags will give some information about themselves, where they are from, how long they are ill, etc. 

We hope that these poignant images will bring awareness to the Minister for Health Simon Harris TD, the HSE, the media, the general medical profession and the wider public of how utterly devastating this illness is to children as well as adults.

The theme of this year’s awareness event is ‘Invisibility’. There will be a mask-wearing moment during the Visibility Event where a group of attendees will put on masks to highlight so many of the invisibilities associated with ME.

The invisibility begins with the failure to use the correct International diagnostic criteria, – The ICC-ME, with the result that many people are given a ‘throwaway diagnosis’ of M.E. because clinicians are not following the proper route for testing. This does no favours to those with M.E. or those who may be suffering other conditions but get labelled incorrectly with M.E.

The invisibility continues with the lack of appropriate healthcare pathways, the lack of a national policy on Myalgic Encephalomyelitis, the lack of teaching on M.E. for GPs,  the lack of M.E. aware Consultant Specialists and the lack of other healthcare personnel who are trained in the complex nature of M.E.

Myalgic Encephalomyelitis is an acquired neurological disease (classified under G.93.3 of the WHO International Classification of Diseases) with complex global dysfunctions including pathological dysregulation of the nervous, immune, and endocrine systems and with impaired cellular energy metabolism. In the most severe cases, patients with M.E. are completely bedbound, unable to feed themselves and unable to bear any stimulation such as light or noise. Yet these patients do not have a care plan pathway available to them within our health service as there are no specialist/consultant services here in Ireland.

This appalling situation needs to be rectified and today is another step in our campaign to get appropriate medical services and a consultant led clinic that can carry out the appropriate testing needed to properly diagnose those with the condition.

This protest has been organised from the beds of some very ill people - people who will suffer greatly from the cardinal symptom of M.E. – post exertional neuro-immune exhaustion (PENE). Many of these patients will pay very dearly and may spend days, weeks and even months afterwards bedbound and dealing with a massive exacerbation of their symptoms.

We would be happy to talk to any media about the event and we would really appreciate any coverage you can give us, especially on May 14^th, outside Dáil Éireann.