Mia’s speech to FN
Denne teksten er et blogginnlegg, og er ikke skrevet av Downs Syndrom Norge.
Ønsker du å dele dine erfaringer? Da kan du sende det inn her.
Hello My name is Mia, I’m 28 years old and I’m from Norway. It is a great honor for me to share my experiences and thoughts about CRPD. This is my first speech in English ever. Good language is very important. Without language, it is difficult to participate in society and decide over one’s own life. I was lucky. In kindergarten and primary school, I received very good language training. We worked systematically according to something called the Karlstad model. I learned to speak, read and write. That is why I can stand here today.
In Norway, it varies how good language training children with Downs Syndrome receive. Not everyone gets the same opportunity as me to develop their abilities.
In high school, I studied health and care. The first year was theory, then I was in practice at a day center for the elderly. There I got my job. I look forward to every day at work!
It is very important for me to be able to make a difference in society. I know many people with disabilities in Norway who do not get to develop and use their abilities either at school or at work. I have bought my own apartment in the center of my city. I would rather do everything myself, but I understand that there are some things I need help with. Many municipalities want people with intellectual disabilities to live in the same building in order for the help to be more effective. They want to save money. I don’t think it’s right that someone should be forced to live in a certain place to get the help they need. Nor can it be right for others to decide who you will live with.
I want schemes that can give me exactly the help I need to be able to live as equal a life as possible as everyone else.
The CRPD has not yet been taken into the laws of Norway. Our organizations are working to ensure that the CRPD is included in the Norwegian Human Rights act. They say that it will give us the strongest power.
In September, we have election in Norway. I have the right to vote, and will vote for the party that supports us best. Because one thing is clear: Better support, better life!
Thank you for your attention.
Det er organisasjonene Downs Syndrom Norge, Landsforbundet for utviklingshemmede og pårørende (LUPE) og Norsk Forbund for Utviklingshemmede (NFU) som sammen har forespurt Mia om hun vil tale for FN.
Se Mias tale her (26:33 – 33:25)























Skriv om dine erfaringer
På bloggen vår ønsker vi å høre dine erfaringer og historier. Bli med og la oss sammen skape et mangfoldig bloggsted.
Siste blogginnlegg

CRPD inn i menneskerettsloven: Hvilke verdier vil vi etterlate neste generasjon?
Ved å innlemme CRPD i menneskerettsloven vil vi som samfunn sende et tydelig signal om at alle er like mye verdt og har rett på det samme. Når du stemmer, spør deg selv: Hvilket samfunn vil jeg være med å bygge?

Når rettigheter møter virkeligheten – hvorfor CRPD kan gjøre en forskjell
På papiret finnes det lover som gir rettigheter til individuell tilpasning, medvirkning, og å bli hørt. Men i møte med kommunen oppleves det som en mur – en mur av dårlig økonomi, mangel på kunnskap og, noen ganger, ren diskriminering.

Demokratisk kraft for Downs – CRPD må tas på alvor
Nå har vi en unik mulighet til å sette rettighetene til mennesker med Downs syndrom og andre funksjonsvariasjoner på dagsorden.