[Music]
awareness of the inclusion of
person with down syndrome in society
report of my experiences
Dear ladies and gentlemen
good morning to all I am called you
marques the home is 55 years old had in bagé
ac and rio grande do sul
To dream is to realize the dream is yours.
desire of every human being is achieved
it is wonderful
down syndrome she weaves from the doctor
French generating stirred presented in
scientific congress and 1959
Canada is a disability caused by
a genetic accident from genetics
is not a disease as it was until then
treated with dengue usually occurs in the
for 21 of the chromosomes and today
known as the trisomy 21
I would like to make a call on
the profession of inclusion of the person with
Down syndrome in society remembering
the wise lesson of the teacher and also
She’s her friend too, she’s called Maria.
teresa mantuan that says the inclusion
it is the privilege of living with
difference and eat the important
inclusion in the family at regular school
in sport and work in the life of
whether or not a disabled person is a
act that gives the sense of living you think
you who think what is easy to be
included in regular school in the
work in society is not easy but I
I’m still in the fight if you can think
that I never had asked
only I know how hard it was but never
I settled in accepting the limits
imposed by the doctor and I say no more
let ‘s see genetic has the last
word in your life
thinks it is easy to live in this society
and today I ask you what it is to be
normal that everyone in their different
I remember with pride the importance of
my family in the process including
school at work in society
the firm support of my parents
edson and marilei my marcus brothers
vinicius
He is a surgeon who is not a Maxillo.
facial and viviane speech therapist who
they remind me of my first doll
which reminds me of my first
was the ideologist the priceless doll was
at that time and did not exist for months
huh
in my city this service
the story is that when I had two
years old
My mother bought a doll with phrases.
short
she said that I
it my my muscles
facial and very important speech
activity in my learning
She was one day, she really is not
she is now an adult as I am
as regards my inclusion process in the
regular school
I believe the first student
down syndrome to be seen in the
Brazil a regular school in 1989 of
terry 89 mm in Brazil and at the conclusion
eighth grade in 1995 was chosen by
colleagues from my colleagues in the
four classes
the graduation speaker imagines
gratitude that we feel this moment
I also did the computer course
I went for inclusion in sports
the biggest highlight was in this Olympics
special in minneapolis in the states
United
when I won two gold medals
the coast and the coast of the pitimbu river in the
Brazil in 1991 and already in adulthood
in 1996 it was included in the
I work as a trainee in the
portugal in brasilia
still as intern in the condemned core
by having coordinated by the still as
intern the glue df
coordinated by doctor paulo beck
example of a fight for the guarantee
our rights
in 1997 and 1998 and in 2001 and 2009 and already
professional portfolio I worked with
children in the cross society of malta and
I came to if the court period of
justice the stj where I worked for five
years in 2010 to 2014
I went to work on promotion coordination
disabled person in the government of the
federal district
of 2015 marks the margin of 2016
My dream is my biggest dream is my dream.
greater is in the very near future
because the inclusion of the
placing on the labor market of the
disabled person and even more
woman
as everyone is the path of a bush
Natural
Can you ask me what’s the big deal?
daliane passion there I confess to you
It is my great passion is the theater that
I practice at is at every end of
week in the company of theater nor nando
in Brasilia can still be part of the group
eth and the theatrical collective under the direction
of the teacher Romulus meneses in the part I
I need a cabaret that talks about the syndrome
down
this piece was presented at the festival
national theater of barbacena mm
general elections in 2016 when I received the
best actress of the festival too
participate in events as a speaker
in the schools congresso brazil name of
down in brazil and abroad as the haia
in the Netherlands in 2000 to family members
with down syndrome
my enthusiasm for the cause
on our current board of directors
from our down association is friend cleo
good director of public relations
Another cool project that I’m going to stop.
because generation 21 generation and tells the
life history of 12 young people as the
down syndrome from various parts of the
Brazil
advertising performance
in 2017
I’m a writer, I’ve always had a
dream of writing a book that
will tell the trajectory of my life a
of my life a person with the syndrome
down
various obstacles to winning as the
Prejudice looks mean to ugly face
until it proved that it would be able to give
present in society groups
the book was published in 2004
now i ‘m working now on a
second edition of the book whose
of my book and the woman as all
Campaign to be different is normal in the field
in São Paulo with the presence of the singer
sandy in 2006
the first group was social inclusion
That I lived was with my family.
My brother and my parents never hid and always
I was present everywhere
I was and I say and I say more the yes of my
family is different from your
as its history is different from the
mine and you can imagine how much
My parents fought for me to be accepted.
be it in the regular school of the sport
national and international competitions
participating in children’s dances
When I grew up at parties,
social life
was my participation in the dance of
debutantes of 1988
in bagé my hometown
although I was not moran
but there and I say more if my family
He had rejected denying their part in
my story
would be a void that nobody could
Fill
I’m sure my walk
serve as an inspiration to watch for
other people with disabilities and who
can be included in the company to
exercise their full right of citizenship
I also hope that my story can
help couples who receive their son or
down syndrome necklace to my family
my parents my brothers asking what it is
it’s possible to win we have to win
otherwise we did not do what we 4 in
to have to win coming at the end
happy
I want to thank you from the bottom of my heart.
the invitation of the organizers of this event
and the opportunity they gave me
so I’ll tell you a little about mine here
life history and to finalize a
kiss
and to finalize for us the
reflection to know election i thinker
inhabitants of a cross that says so
nature and it paints for us and after
picture of infinite beauty that had the
eyes meant to live
I thank you all very much.
thanked the jewels
[Applause]
awareness of the inclusion of
person with down syndrome in society
report of my experiences
Dear ladies and gentlemen
good morning to all I am called you
marques the home is 55 years old had in bagé
ac and rio grande do sul
To dream is to realize the dream is yours.
desire of every human being is achieved
it is wonderful
down syndrome she weaves from the doctor
French generating stirred presented in
scientific congress and 1959
Canada is a disability caused by
a genetic accident from genetics
is not a disease as it was until then
treated with dengue usually occurs in the
for 21 of the chromosomes and today
known as the trisomy 21
I would like to make a call on
the profession of inclusion of the person with
Down syndrome in society remembering
the wise lesson of the teacher and also
She’s her friend too, she’s called Maria.
teresa mantuan that says the inclusion
it is the privilege of living with
difference and eat the important
inclusion in the family at regular school
in sport and work in the life of
whether or not a disabled person is a
act that gives the sense of living you think
you who think what is easy to be
included in regular school in the
work in society is not easy but I
I’m still in the fight if you can think
that I never had asked
only I know how hard it was but never
I settled in accepting the limits
imposed by the doctor and I say no more
let ‘s see genetic has the last
word in your life
thinks it is easy to live in this society
and today I ask you what it is to be
normal that everyone in their different
I remember with pride the importance of
my family in the process including
school at work in society
the firm support of my parents
edson and marilei my marcus brothers
vinicius
He is a surgeon who is not a Maxillo.
facial and viviane speech therapist who
they remind me of my first doll
which reminds me of my first
was the ideologist the priceless doll was
at that time and did not exist for months
huh
in my city this service
the story is that when I had two
years old
My mother bought a doll with phrases.
short
she said that I
it my my muscles
facial and very important speech
activity in my learning
She was one day, she really is not
she is now an adult as I am
as regards my inclusion process in the
regular school
I believe the first student
down syndrome to be seen in the
Brazil a regular school in 1989 of
terry 89 mm in Brazil and at the conclusion
eighth grade in 1995 was chosen by
colleagues from my colleagues in the
four classes
the graduation speaker imagines
gratitude that we feel this moment
I also did the computer course
I went for inclusion in sports
the biggest highlight was in this Olympics
special in minneapolis in the states
United
when I won two gold medals
the coast and the coast of the pitimbu river in the
Brazil in 1991 and already in adulthood
in 1996 it was included in the
I work as a trainee in the
portugal in brasilia
still as intern in the condemned core
by having coordinated by the still as
intern the glue df
coordinated by doctor paulo beck
example of a fight for the guarantee
our rights
in 1997 and 1998 and in 2001 and 2009 and already
professional portfolio I worked with
children in the cross society of malta and
I came to if the court period of
justice the stj where I worked for five
years in 2010 to 2014
I went to work on promotion coordination
disabled person in the government of the
federal district
of 2015 marks the margin of 2016
My dream is my biggest dream is my dream.
greater is in the very near future
because the inclusion of the
placing on the labor market of the
disabled person and even more
woman
as everyone is the path of a bush
Natural
Can you ask me what’s the big deal?
daliane passion there I confess to you
It is my great passion is the theater that
I practice at is at every end of
week in the company of theater nor nando
in Brasilia can still be part of the group
eth and the theatrical collective under the direction
of the teacher Romulus meneses in the part I
I need a cabaret that talks about the syndrome
down
this piece was presented at the festival
national theater of barbacena mm
general elections in 2016 when I received the
best actress of the festival too
participate in events as a speaker
in the schools congresso brazil name of
down in brazil and abroad as the haia
in the Netherlands in 2000 to family members
with down syndrome
my enthusiasm for the cause
on our current board of directors
from our down association is friend cleo
good director of public relations
Another cool project that I’m going to stop.
because generation 21 generation and tells the
life history of 12 young people as the
down syndrome from various parts of the
Brazil
advertising performance
in 2017
I’m a writer, I’ve always had a
dream of writing a book that
will tell the trajectory of my life a
of my life a person with the syndrome
down
various obstacles to winning as the
Prejudice looks mean to ugly face
until it proved that it would be able to give
present in society groups
the book was published in 2004
now i ‘m working now on a
second edition of the book whose
of my book and the woman as all
Campaign to be different is normal in the field
in São Paulo with the presence of the singer
sandy in 2006
the first group was social inclusion
That I lived was with my family.
My brother and my parents never hid and always
I was present everywhere
I was and I say and I say more the yes of my
family is different from your
as its history is different from the
mine and you can imagine how much
My parents fought for me to be accepted.
be it in the regular school of the sport
national and international competitions
participating in children’s dances
When I grew up at parties,
social life
was my participation in the dance of
debutantes of 1988
in bagé my hometown
although I was not moran
but there and I say more if my family
He had rejected denying their part in
my story
would be a void that nobody could
Fill
I’m sure my walk
serve as an inspiration to watch for
other people with disabilities and who
can be included in the company to
exercise their full right of citizenship
I also hope that my story can
help couples who receive their son or
down syndrome necklace to my family
my parents my brothers asking what it is
it’s possible to win we have to win
otherwise we did not do what we 4 in
to have to win coming at the end
happy
I want to thank you from the bottom of my heart.
the invitation of the organizers of this event
and the opportunity they gave me
so I’ll tell you a little about mine here
life history and to finalize a
kiss
and to finalize for us the
reflection to know election i thinker
inhabitants of a cross that says so
nature and it paints for us and after
picture of infinite beauty that had the
eyes meant to live
I thank you all very much.
thanked the jewels
[Applause]
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