UNCRPD – Getting Ready to Ratify (2)

Like mentioned last Friday, I went to a conference on the hopefully soon-to-be ratified UN Convention on the Rights of Persons with Disabilities (UNCRPD) and this Friday, I will attend a second conference about this. Before I received both invitations, I was unaware of the CRPD. My first thought was “Oh I thought there were already rights in place for people with disabilities?” Not so, and I have tried to learn about conventions and optional protocols since then. It’s testing though, remembering article 1 by the time I’ve arrived at article 2 is a bit of a challenge, but challenges don’t scare me. On the contrary.

Human rights, oddly so, and especially rights for people with disabilities is not common knowledge just yet. Sure, we all know that you should not kill your neighbour because of his/her gender, religion, sexuality etc, but how much do people really know about rights for the disabled? As a person with a disability myself, I should be in the loop n’est-ce pas?

However, the first thing I heard about UNCRPD was two weeks ago when an email landed in my mailbox with an invite to a conference. ‘Fancy,’ I thought, ‘that is definitely something I am interested in,’ especially if it’s about the opportunity for people with disabilities to take part in public and political life on an equal basis with others. When a week later the MS Society were stuck for someone representing them at the UNCRPD – Ready to Ratify conference, I heard about Ireland’s slow move towards that very ratification.

What stood out on Friday – politicians beware – was the intent everyone carried with them, from the main speaker to the very last person who attended. They showed the necessity people with disabilities have to be recognized by their own government. Ireland, as Ireland goes, is working ever so slowly towards this, and has signed but not yet ratified the convention (together with only two other states in Europe… shame on you Ireland!). Hence the visit of the CRPD to Dublin. And could you blame them?

Present were John Dolan, CEO of the Disability Federation of Ireland who started by giving a short overview on the history of the Convention and how we as a society need to start looking after people, emanating late teenager Dónal Walsh’s wishes. Dónal, who stepped into the limelight shortly before passing away due to terminal cancer, went public about his anger at teenagers who commit suicide. While he wanted to live so much, other people were giving up without thinking about the life they were leaving behind. We need to care so, we need to look after other people.

Also at the conference was Theresia Degener, Professor of Law and Disability Studies at University of Bochum in Germany. Theresia is also a member of the United Nations Committee on the Rights of Persons with Disabilities and who could be better placed than her to tell everyone what the challenges are like to have the convention ratified.

Martin Naughton represented the Disability Federation of Ireland and he inspired me no end; I hope I will remember his words for a long time to come.

Agnes van Wijnen, MSc and Independent Developer and Advisor on Disability Policy & Strategy and Researcher in Disability Studies gave an overview on how The Netherlands are trying to get the convention ratified by using interesting ideas to inform civil society about the rights for persons with disabilities.

Finally, Professor Gerard Quinn, Director of the Centre for Disability Law and Policy at the National University of Ireland, Galway School of Law gave an overview of the laws that need to be abided to by Ireland if they were to ratify the convention.

If Ireland were to ratify… ‘If

No more ‘ifs!’

Ireland needs to ratify now. Do not tell us you will ratify somewhere in 2015, ‘we need a date now, minister.’

“As disabled people, we have to step up and our expectations need to change. We will not refer to ourselves as disabled anymore; we want the same rights as anyone else.”

Those were words spoken by Mr Naughton and clearer his language could not have been. He called disabled people to action and said that disabled people need to be given back their voices. Also, the capacities of a person with disabilities need to be recognised and people need to be put in the driving seat of their life again.

John Dolan said that every letter, call and email is a form of protest and that the impact will be how organised we are (use good intelligence before protesting) when we contact our local TDs and government. We can use the conference as a driving force forward, to build on how many people were present and we must spread awareness about the Convention on the Rights of Persons with Disabilities.

We must educate Irish and foreign citizens living in Ireland about what the convention would mean as disabled people, what it could mean to people waiting on a diagnosis to put their minds at ease. Unaware yet of their future on a medical level – they should be comforted by the idea that Ireland is doing what it possibly can to respect their rights.

We, as already disabled people, must check with our government and find out what the value of our life and as people are to them. Are we only as important as the money we put into their bank account or are we as important as healthy people, as valuable as them and do we not hurt enough already without being treated unequally by the people who should protect us?

Ireland is still in the top 20 of the richest countries in the world, using austerity and recession is not a legitimate reason not to ratify the UN convention. Failing to do so is to disgrace disabled people by not acknowledging their human rights.

What I wanted to bring in this blog post was the view from a person living with a disability, not one trying to explain what conventions and protocols mean. Explain it as someone who thought her government had already ratified this ever so important document. I had the opportunity to visit the conference on the impending ratification and I will forever be grateful to the Irish MS Society for once again thinking of me.

I am claiming my voice back.

UNCRPD world map

© Willeke Van Eeckhoutte and Ireland, Multiple Sclerosis & Me, 2011-2013. Unauthorised use and/or duplication of this material without express and written permission from this blog’s author and/or owner are strictly prohibited. Excerpts and links may be used, provided that full and clear credit is given to Willeke Van Eeckhoutte and Ireland, Multiple Sclerosis & Me with appropriate and specific direction to the original content.

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Quirky, tenacious and neurologically compromised female expat living in Ireland since 2002 ◾ MyTherapyApp Best MS Blog for Simplicity 2018 ◾ Everyday Health Top 10 MS Blog of 2018 ◾ WEGO Health Patient Leader Award Nominee 2018 ◾ Feedspot Top 50 MS Blog 2017, 2018 ◾ Ireland Blog Award Finalist 2014, 2015, 2017 & Shortlisted 2018 (competition ongoing) ◾ Contributor to the Novartis MS blog Living Like You ◾ Contributor to MS Ireland’s blog MS & Me ◾ Contributor to The Mighty ◾ Guest contributor to MyTherapyApp.com

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