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On Thursday April 1 all go to the Plaza de los Dos Congress!!



Hello friends!.
On Thursday April 1 will be an event in the Plaza de los Dos Congresos TGD-Parent organized by Argentina in commemoration of International Day of Autism Awareness.
As you know, here in Argentina, on Friday, April 2 in addition to being a holiday for Easter is celebrated Veterans Day and Memorial Falklands. Whereupon, organize something for this day is impossible. That's why we decided to move the event to this day.
To give more detail about it, I then publish the information which I received by mail through the mail TGD-PADRES:

"Friends

as you guys know on April 2, is the global day of awareness about autism, Resolution No. ° 62/139, adopted by the United Nations on December 18, 2007.

Just like that, last year, PDD PARENTS, your contribution will make the next day Thursday 1 April at the Plaza the two conferences, Callao and Rivadavia Avenue . Since the April 2 meet several things (holidays, long weekend, day Falklands, Good Friday, the anniversary of the death of dr. Alfonsin, etc)

Our proposal is from 12 pm, until 16 pm.

We will make our contribution to society to raise awareness about the disorder suffered by our children, who lead the fight so they can have access to treatments, education and a full social life. We will make a great flyer that contains a brief summary of PDD concept, its main symptoms of alarm and our demands. At 15.30 there will be a release of balloons, and then will say a few words of closure.

also be a good opportunity to gather signatures for our bill, as well as a new opportunity to meet and exchange experiences.

call on all parents, professionals, friends, media, family and neighbors in the city to participate, especially with the presence, albeit 30 minutes or 4 hours, and can cooperate in qeu, flyers, collect signatures, encouraging. also ask the diffusion of the banner attached to acquaintances, relatives, dae media communication, facebook chains, to anyone you know. diffusion that everyone can do will be valuable for everyone.

invite you to take flags or signs that identify us, they can download from the following link

http://www.tgd- padres.com. ar / diffusion. Htm

invite and ask for this via our referring to the same April 1 may be made manifest of this kind in each of the provinces.

remember, and particularly the new sucriptos from the list of all the country you can contact our references for each province in the following link

http://www.tgd- padres.com. ar / contact. Htm

although an awareness day, is also a holiday!

expect them.

SUSPEND OR NO RAIN, NO NOTHING. "


also attached the press release they sent for distribution in any field, especially those who have access to media.
Personally, I took some copies to take to the garden of my son to be distributed, as well as neighboring businesses. Here it is:

Press Release April 1, 2010

So April 1 Plaza de los Dos Congresos: GOING BEYOND!

I'll be there, taking advantage of Valencia's grandparents do not work that day. In this way everyone wins, because I'm going quiet and he has blast with her grandparents, who aware of everything ... best, no?
So to all those mothers of Argentina that could go would be nice if we can find there on this special day. Hopefully we can organize ourselves so that you can give!. My email is posted on my blogger profiled, as well as contact the little sign in the right column Facebook blog. Anything write me and see how we can arrange to meet.

are waiting!

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visit with your neurologist and news in your treatment ...

On Tuesday we visited with Dr. Comas, your family doctor, excellent professional and human being. As I said in other entries, we will always see him every three months to evaluate you and see how they follow from then on treatment. Evaluate whether you need to take another course or if this road we are doing well ... It is super container with us, and very sweet to you.

He was happy, because before entering to his office I told you you had to greet and kiss. So when you came in you said: "Hi Dotor Cobas!, And TAS?." Hahaha!, And he with a huge smile to hear you say those words I returned the greeting with a kiss and a "Hey Valentine!, How you doing?"
This return, in addition to carrying some material with images to see how little by little you improve your language, I decided to take your beloved whiteboard with your bookmarks, because it seemed a good idea to observe how to draw, and as you write single words, being aware of what you write and not doing it "by heart."
His mouth fell open when you took the marker and started write your name, so prolijito, so clear. He said: "how awful!", "For his age is amazing, because even in children without this diagnosis is very difficult to see these achievements."
was laughing when I answered what you asked and until you tell (your way) moments before the reception, we had skidded on the floor and you had fallen flower giving blow in the mouth: "I fell!, flat wrong!, here mouth! "
put us happy to see him so happy with the little steps that you are giving ... and realize that we are on track, or at least I tried. He told us he could see that your language and your connection had improved markedly and the mischief in your eyes was incredible.
Your hyperactivity, often beyond us, but improved a lot, sometimes you have days when you do not stop a second and everything gets boring and any good reason for a tantrum. Your dad let her know your concerns about whether it would be necessary to evaluate the possibility of medicate, to what He said no.
He explained that there are two types of hyperactivity, both of which went hand in hand or were the result of a neurological problem: that which is revealed when the children were making up things or steps in its maturation, which become very restless, bored quickly of all, put anxious and looking to explore and look around all the time and did not stop a second, we said it was inevitable and which had to be filled with patience and set limits. The other is one in which children have an activity "nonsense" walking disconnected from side to side, climbing all over, without showing any interest in any business or any person. That this type of hyperactivity of you had noticed during the first consultation, which did not stay still for a second, I went up to the table, you climb the scale, to the chair, you lowered your, walked from one side to another, try to open the closet doors, the office, at which point should get you so you will not escape. That today this is not the case, he watching you now, to have a dialogue with you, see how you cope, and understand everything, they respond to the slogans and others, sees no reason to think medicate. That relieved me a lot.

also asked me to remind you that room were ... I told him, as did stay in room two in 2009, now with 4 years you were making room 3. He told me to see you wondered why you were cognitively thought for a 4-room quietly. I commented that your bosom Silvi had also discussed the same day of the meeting of parents in the garden. But both were agree that while this is true, there are several aeras where you're still out of date for your age and in my opinion, you feel lost in a room 4. To be in room 3 was going to allow you time to mature and on the other hand, it was good, in a way, you're a little ahead of the rest of your peers in terms of content that works with you Silvi in the room, because this way we avoid frustration on your part.

talked also the theme of this year, I wanted to give it another path to your treatment and stop traveling across both collective and forth every day of the week. It was exhausting for both, but especially for you. So for this and other reasons I decided to leave to the psychologist with whom we work from 2008 until late 2009, certainly on good terms and super grateful for the work they had done with Valen and how much he had been with him. We decided to find a psychologist who could work with you at home.
Your neurolonguista and a couple of moms friends recommended us a psychologist who makes home therapy (CBT) to take into account. We contacted her, and truth, we loved it!. We felt super professional, very sweet and very organized. We really liked the plan of treatment that you want to help implement. So after having a meeting with it and consult with the social work we decided to go this way.
I think this type of therapy is going to come in handy to achieve more.

in brackets, said he never did this type of therapy Valen, because at first I was not quite agree, I thought it would be too. On the other hand Dr Comas we suggested that we start with the professionals that he recommended to us and see how Valencia responded that according to that from then on we would see that course would take.
you are booted to Rachel, you neurolinguist and Silvia, your psychologist, both in clinic, which then add TO and music therapy ... Responded so well to treatment with each of them and although at first it was slow and cost hooked, you did and the progress is going to see over the course of months. Thus decided to continue on this path.
I think with this new professional can achieve many things, and that, obviously, is what we aim for.

The idea is to come (after social work aprube me because until that happens will come less) twice a week two hours each time. Have meetings to guide and control us and also have meetings once a month in the garden with your womb and the principal. Dr Comas
strongly agreed and believes that going barbarian come to polish certain aspect of your behavior with that deal more difficult for us. So we will make a note to introduce social work so we cover all the hours of treatment. Hopefully with this is enough and what they approve.

So this year started with everything. With this therapy Agustina and called the new psychologist who is super sweet with you and goes beyond patience, lol!, And the rest of the therapies that keep doing: neurolinguistics (still with Rachel), TO (with Leo ), music therapy (with Flavia) and spa on Saturday (with Ceci and Flower)., most obviously, integration into your garden with Lucia who hit her with a wave that is very beautiful and tender with you. So

bold mine, we will follow, struggling to see small step for step, loving you as always ... back at you every smile, every kiss, every hug, every look.
Here we will keep fighting melee with autism, to give battle, as every day of our lives. Here we
, celebrating a new word every mischief, each charade, everything that makes us realize that you were more connected with us, with your loved ones in your environment.
for us is to touch the sky with my hands and feel renewed hope and faith is enlarged with every achievement yours, however small, because for some will be small steps, but we are leaps and bounds.

We love you!

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"The Two Faces of Autism" Look Valen! This year are our smiles!

I was speechless when I saw the video with so much love and dedication made Maite, the mom of ...!... Julen It's really a genius! and I'm short of words.

As I told Marina on his blog as a comment to his entry, the videos Maite published in commemoration of the Autism Awareness in 2008 and 2009, reached me after the diagnosis of Valentine.
I saw them through the blogs of other moms who have already visited despite not having yet mine in those days.
Closely watched their smiles, their faces full of mischief, mischief that every child has typical, those eyes that can be complicit in the face of any guy who is happy. They are children, are happy, they are pure is the perfect picture of unconditional love without lies, without prejudice. They are our children, and this makes them unique and different from others. There are autistic, are children with autism. I love this phrase Maite always used, because it reflects our purest reality.
were videos that I left with a feeling strange when I saw them because I was in a period of mourning in which there was no room in my life but why thousands of thousands of questions and thousands of tears in secret. This did not stop me fighting for Valencia from the start, without getting any other goal in sight ... but they were very hard months.
Over time and once I finally decided to create this blog, I describe in greater detail each of the stories I locked each of those smiley faces, as well as the wonderful mothers who are behind those smiles, struggling day after day to see them reflected in their faces.
this year gave me pride to be with Valen between these images, among these smiles, between these stories.
I loved being able to appoint and make known, to everyone with whom I watched this video over and over again, the names of every prince and princess appears, his chest swelled with pride for each of them (as good aunt false , lol!) and each of their brave mothers, whom I consider my friends the destination.

Hopefully this and everything will be done on this day is coming, serve to learn more about this disorder, which everyone realizes, as well Maite says that we are not so different.
I believe that ignorance on the subject is the main culprit that committed so many mistakes in our society, whatever our country of origin. The undertake struggle for the rights of our children is exactly the same.
hope some day we can say that the situation from here on out, compared to here and back changed drastically. THANKS !!!!!!!!!!!!!!!!!!!!!

MAITE

to watch and enjoy this beautiful video:

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Preparing for Day 3 rd World Autism Awareness, 2010


(Excerpted from the website TGD-Padres, Argentina ):

General Assembly 12/18/1907 UN adopted a resolution on declaring Day April 2 as World Autism Awareness , with the aim of warning about this disease, whose incidence has increased worldwide. The text, sponsored by Qatar and backed by 50 other countries, was adopted by consensus at the Human Rights Committee General Assembly.

The document raises a concern about the high incidence of autism in children around the world.

Also remember that early diagnosis, as well as research and appropriate intervention "is vital for development growth."

The resolution highlights also that the Convention on the Rights of the Child stipulates the right of disabled children to enjoy a full and decent life.

The resolution resolves that:

1. Decides to designate 2 April World Autism Awareness, which is observed every year from 2008;

2. Invites all States, relevant organizations of the United Nations system and other international organizations and civil society, including NGOs and the private sector to properly observe the World Day Autism Awareness to enhance public awareness of autism;

3. Encourages Member States to take measures to raise awareness throughout society, even at family level, regarding the situation of children with autism;

4. Requests the Secretary General to bring this resolution to the attention of all Member States and organizations of the United Nations system

PDD-Padres this year is preparing for an event on April 1, since April 2 matches in our country, with the commemoration of Veterans Day and Memorial in Falklands War. In addition to also match Friday. I copy the mail that I received a PDD-parents on this date:

"We are preparing for the day April 1 in the square some gesture of the two conferences. I invite you to agendas that day.

organizing

and calling the respective approvals.

The reason the first is that the day 2 coincides with a) b Good Friday) holiday c) long weekend d) Day of the Falklands.

Therefore we prefer to do it on 1 April

I ask what agenda that day, and will disseminate this information so that everyone can participate. When we have accurate data send complete information.

Moreover through Facebook I received this data and information for those who want to join this cause on that day:

"Light Blue"

In night of April 1, at 21.00 am, the Empire State Building lights up in blue to raise awareness about autism and to commemorate World Autism Awareness Friday, April 2. We are aiming to the world is lit in blue: City by city, town by town - for action to raise awareness about autism in our communities.

Other things you can do to Blue Light It Up

• During April, speak to people about autism, if they ask. (In the photos there is some information that might help)

• Change your profile picture on Facebook of Blue Light It Up logo and label at least 10 of your friends.

• Post on your blog about how this "blue light" can serve to raise awareness of autism.

• Add It Up Light blue logo to your email signature, and write your e-mails in blue!

• On April 2 blue clothing and ask your co-workers, studies and friends who wear blue too.

Take pictures and add them to our gallery.

More information:
http://www.lightitupblue.org/
http://www.autismspeaks.org/press/light_it_up_blue.php


not want to forget, for all blogger this wonderful family and also for those fathers and mothers of children with autism who have no blog, but if you really wanted to participate, the initiative of Maite, the blog "to the moon and back" to this day. Draw from your wonderful blog what it is the same:


... "I suggest two things:
- Work for the" Autism Special 3 "for the literary magazine figuratively. Testimonies, articles, stories, poems, testimonies ... that will compose a reality of the autism puzzle. This year we focused on the theme Inclusion but you can actually write about what you like. In Images can consult and download the 2 issues. The texts can add up the available at the Journal, Figuratively. Right there you can publish or send them to your Anabel (The sound of the grass to grow) to the following address: fiestalemana@googlemail.com Deadline: April 15, 2010 .

- Collaborate on a video. Like last year our chic @ s will be the stars, we show that our children are just that, chic @ s, and that our families are much more than autism. To do this I need to send me a picture, with many of you have contacted through facebook but there are many more with whom I have not yet contacted. And there will be spontaneous not know who also want to join. ! Of course you !!!!!!

Send photo with name of child: hastalalunaidayvuelta@gmail.com Deadline: March 21, 2010.
I look forward to any proposals be gathering there to this day, and I encourage even propongáis who help new ... "


So there is no reason to stay out of this day ... !
Whether or not relatives of a child with autism, you can do much to this day serves to raise awareness in society about this disorder that affects each passing year more and more children.
highlight and prioritize the fact that early detection and intervention are essential for successful development and obtain enormous progress in these children. That
social inclusion and integration at the level of school education is paramount. For that reason, we your parents, we live to fight for their rights are fulfilled, for these things taking place in their lives and ours, but due to ignorance and lack of subject matter and the lack of dedication and willingness by many, ensuring that these rights compliance becomes increasingly difficult. This day does not pass in vain and instead be of much use ... For my son, for you and for each of the children who struggle every day to give battle to this condition, his disability.

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"Mom!, Detonating me dad!"

several days ago that I write about the little steps you were taking this past month.
We enjoyed a great school starts, too many achievements surprised us and made us extremely happy, Dad and me, because no matter how small, for us is infinitely vast. Are these achievements the help us to maintain hope and strength to keep fighting for you and continue to give battle to this enormous challenge that life put us on the road.

Your speech and language are improving day by day.
Now you're talking more, we must find a way to follow giving a sense of communication and your words every time you hear about alone, many times you are performing an activity that reminds you of something you saw on the TV, something they witnessed in the garden or something you did during the day and started talking about it alone, and when we will look at and you say, "What price?", sometimes not seem to listen and keep on your fictional dialogue.
Too many times I hear that to some situation and I answer you wonder to yourself giving in response to your questions the answers that many times we offer you in certain situations. For example, when when we are eating dinner while you crave a dessert or a glass of lemonade (I try to give as little as possible) and which you ask me, saying, "Mommy give me coca po 'favorable?" or "mama post kero po 'favorable'" I answer very firmly, "Not now Valen, if you eat the food as a reward mom gives you, but first you have to eat everything."
Now that seems to retain whatever one says, because as I said on other occasions you have a tremendous memory, when you fancy some of these things and I ask and I tell you: "Valen, later, not now", you look me alone and I say, "Do you want coca ?, eat potatoes and coca give you. " As contestándote wondering to yourself and my usual response.

Despite this, makes us happy to hear you talk and have faith that you will do a little more sense and better singing phrases, as sometimes using a monotone voice when talking or say something, anything it is very normal in children with your diagnosis and what we must keep working.

This effort, to give a sense your words and use them properly, we have seen a lot in recent days.
Without going any further, last Thursday, we could not help laughing with your dad to listen as you told me indignantly that he had challenged you in my absence: as every Thursday, I went home for an hour of my dance class arabe (which I served, by the way, as therapy to release tension, is very productive, lol!) and you will stay with Dad, of course I'm more relaxed because luckily this place where my class teacher is almost in front of my house, into an artistic center.
order not to make too late I came from and start preparing food, your dad bathed that afternoon. But now you have a new skill when doing a "duck water", if a soap falls into your hands, you start to enjoy ice cream like a very confident saying: "Mmm what doctor!" (How delicious!). Of course not let you do that and you remove them again and again, or hide until you finish your bath. That afternoon, apparently we go again with that issue and challenged dad when you put the soap that I was lathering at the mouth. You tell him, "Mom, Mom, I detonated, Mom!". Your father, as is often usual, did not understand what you mean and you just said, "Mom you challenged?", Thinking that you had That meant, to which you, looking at him, not answered.
when I got home, he'd left the bathroom and dad was drying and putting on pajamas. As soon as I saw the bedroom door watching with a smile and greeting you, you told me with a face of indignation: "Mom, my Dad detonation!" "How dared you Dad?!" "And why are you challenged ?! "I said making me amazed at such a declaration, to which you answered me:" Soap mouth, noooo! "," I challenged because you put the soap in your mouth? " I said and you told me seriously: "Yes." I could not hold
laughter when your dad told me what you said in the bath when the incident happened soap and told me tempted to laugh: "Ahh ... I thought you told me what had challenged ... of course!, which I meant was that you would tell me I challenged him, hehehe!.

Another thing that gives me more happiness is that before when I went to get the garden at noon and walk to the bus stop, I wondered, "Valen, Silvi you did today and the kids?", You do not say nothing, still chasing the pigeons in the square when we crossed without even looking at me, like I do not listen.
Now, in your language, your way, told me of what you did in the morning: "Ball, Francisco, beat, and Ariba, which means that you played ball with Matias Francisco and pulling up. Or if you paint or draw I say: "Painting as well!" and show me how to paint with your fingers scribbling in the air. Yesterday
without going any further, as we went by taxi to your music therapy session, when I asked you what you did, you said: "Eteban ball, fell to floor, so (and I threw lying along the car seat) , flat bad bad bad ", which I interpreted as your friend Esteban playing ball with you had fallen to the floor.
makes me happy to share with me what you did in the garden, or things that happened to you or what happened to your friends. That's something I thought hard to achieve. Of course you still have your days in what is not told me anything, and you look to the horizon when I ask. In those days I insitirte a little more for me to look and interpret what I'm asking you, many times we maintain the dialogue, and many do not. But little by little we are getting it.

We must continue working hard to keep giving small step for step, but together little by little we going to do and mom will still be here to continue celebrating sign a new word, every intention you have to communicate with me and with your environment, even if he is your way and more than just mom knows how to join individual words and phrases to understand what I mean.
A year ago these things were unthinkable horrors and suffering they can not get any word from your mouth, despite the stimulation that Rachel, you neurolinguist and we will we took day after day.
Now I can have a dialogue with you, for more triviality, and that is to celebrate and party like we like bold mine: with many kisses, hugs and thousands of:
!!!!!! Okay Valen !!!!!!

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Earth Angels ... Data

God was in heaven watching men acted on Earth. Among them, the desolation reigned ...

"More than six billion human beings are too few to reach the divine magnificence of love," sighed Mr.

The father saw many warring brothers, husbands and wives who did not complete its shortcomings, rich and poor sections, distant healthy and sick, that good day assembled an army of angels and said:

- Have you considered humans? ... Need help! ... You'll have to come down to earth.

- We? asked the angels excited, scared and excited, but full of faith.

"Yes you are indicated. No one else could accomplish this task. Listen!: When I created man, I did my image and likeness, but with special talents for everyone. I allowed

differences between them so that together they formed the kingdom. So I planned. Reach some wealth to share with the poor. Others would enjoy good health to care for the sick. Some scholars and others would be very simple to procure including feelings of love, admiration and respect. The good should pray for those who act like ill. The patient tolerated the neurotic. In short, my plans have met that man enjoys from the earth, the eternal happiness. And to do that, you bajaréis with them!

- What is it? angels asked worried.

"As men have forgotten that I did different in order to complete each other and form the body of my beloved Son, as it seems they do not realize that different want to achieve perfection, bajaréis with free awards. And she gave each one his task:

You have excellent memory and concentration: You will be blind.

You will be telling your body and very creative to express yourself: You will be deaf.

You have deep thoughts, write books, be a poet: You will have cerebral palsy.

I will give you the gift of love and be him, there will be many others like you across the Earth and there is no distinction as to race because you'll face, eyes, hands and body like blood brothers: You will have Down syndrome.

You will be very small in stature, and your sympathy and sense of humor come through Sky: You will dwarf.

You enjoy the creation as I planned for men. You will have an intellectual disability and while others worry about the scientific and technological advances: You enjoy watching an ant, a flower. You will be happy, very happy that love to all and not do any trial.

You live on Earth, but your mind will remain in heaven you rather hear my voice to the men: have autism.

You will be working like no other: You'll be missing arms and legs and all with mouth. And last angel said: You'll be a genius, I'll take the wings before reaching the ground and come down with the back hollowed, men repair your body, but you need to succeed ingeniártelas:'ll mielomeningocelle, which means honey wine sky.

Angels were happy with the distinction of the Lord, but they caused great sadness to have to depart from heaven to fulfill its mission.

- How long we will live without seeing? How much time away from you?.

"Do not worry, I'll be with you day. In addition, this will be only 60 or 80 years land.

"Okay, Father. Will be as you say: 80 years is a moment in the eternal clock. Here we see after a while they said in unison and angels came down to earth moved. Each

reached the womb of a mother. There were formed for 6, 7, 8 or 9 months. At birth, they were greeted with profound pain, fear and distress caused. Some parents refused the task, others took angry, others cast blame to dissolve their marriage and others wept with love and accepted the duty.

Whatever the case, as the angels know their mission and their virtues are faith, hope and charity, among others, all governed by love, they have been able to forgive, and patiently go through life illuminating to anyone that wanted to love. Angels continue to fall to the ground with higher spirits and limited bodies keep coming as long as humanity on the planet.

God wants them to be among us to give us the opportunity to work for them, to learn from them. And work is to serve: serve is to live and live to love, because life gave us for that. He who does not live to serve not serve to live.

If you have an angel in home care for him and learn from him because God has chosen you and not him ... is a valuable gift that few have, but many despise it so you have advantage of the gifts he has and works, it works, lives and loves.

Author: Unknown

Every time I read this text, I was deeply moved ... I'm sure many already know, but it's nice to read it again, and no, expect the enjoyed and that has excited as much as me.

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courses to be held in Buenos Aires, very useful! ...

TCC INTENSIVE IN AUTISM AND PDD:

date: Wednesday March 17, 2010
Hours: 18-21 hours
Place: National Technological University
Address: Medrano 951, 2 nd floor, phone: 4867-7545

Course Description:

Intensive cognitive behavioral therapy in autism and PDD. Doctor charges of psychology at the UBA. Eduardo Cossi. 5 meetings of 18 to 22 hours, five consecutive Thursdays. Incio Thursday 18 March. Quotas limited. Certified

UTN. UTN Reports

capital Medrano 951 (2nd floor-extension) 48677545. PRE-REGISTRATION

acomp_terapeutico@yahoo.com.ar


YEAR COURSE OF THERAPEUTIC SUPPORT

date: Wednesday March 17, 2010
Hours: 10 am
Place: National Technological University
Address: Medrano 951, 2 nd floor, phone: 4867-7545

Course Description:

NATIONAL TECHNOLOGICAL UNIVERSITY COURSE

therapeutic support.

Module I. initiation and module ii. expertise and practices.
Start: Wednesday 17 March, 10 to 12 hours.

Duration 27 weekly meetings.

Objectives: To train an auxiliary therapeutic
able to collaborate and participate in various professional teams in attendance, with strong theoretical and practical tools in a framework defined by the figure of a qualified employee health care, education and field community partner.
Aimed at students, professionals, auxiliary health workers, education, the social community and general assistance, family members of patients and the general community.

APPROVAL CERTIFICATE IS PROVIDED.

National Technological University. BUENOS AIRES FACULTAD REGIONAL
.
Ministry of Culture and University Extension.

Topics: History and Definition
technique of therapeutic support.
concern and basic skills and specific. Delineating the role
Tools and Basics.
Link-Transfer-Monitoring. Organization of work and decision making
's and early clinical intervention.
Dependencies, psychotic disorders, mood disorders, disorders of childhood onset, Third age. Characterization
diagnostic and organizational principles of treatment and intervention of AT.
devices, protocols, consensus. Delimitation
judicial and legal. Ethical principles.
Patient Rights. Legal framework and legal ethics Therapeutic accompaniment (ethics). Disclaimer
.
care and intervention techniques.
social and communication skills.
Troubleshooting and strategies for decision making.
impulse control, anxiety and stress.
cognitive behavioral interventions. System. SPS.
observation and recording.


teaching team: Dr. Eduardo Cossi

. PhD in psychology. UBA. UBACyT researcher. Ms. Veronica

ecossi@psi.uba.ar Recchia. Degree in psychology. UBA. Coordinator.
veronicarecchia@yahoo.com.ar
Space is limited. Pre

by mail: send acomp_terapeutico@yahoo.com.ar full name. ID, contact numbers and e-mail. Medrano

951 2nd floor: University Extension Office. Federal Capital you 48677545.
info@sceu.frba.utn.edu.ar

hope will be useful ...!

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Bloggers OF ALL MY FRIENDS ... A VERY HAPPY DAY!! HAPPY

DAY FOR YOU TO THINK ABOUT WOMEN IN WORDS: GREAT FRIENDS, GREAT MOTHERS FIGHTING ETERNAL, BRAVE, SOLIDARITY, kindness and a big heart.
WOMEN WHO ARE ABLE TO GIVE EVERYTHING TO SEE YOUR OWN HAPPY LIFE FOR YOUR CHILDREN HELP TO FORWARD BY DAY AFTER DAY ... WOMEN
admired and emotions with SIMPLE THINGS EVERY DAY WITH THE THINGS THAT ARE OTHER WOMEN FOR SMALL AND NO SENSE. WHY WE TEACH OUR CHILDREN TO THEM AND WONDERS TO FEEL THAT WE PLAY THE SKY WITH HANDS WHEN THINGS GET SEE WHY pray EVERY NIGHT WITH ALL OUR STRENGTH AND FAITH, HOPE TO SEE YOU ACHIEVE FULL. THANKS

BY GIVING YOUR FRIENDSHIP IN THIS WAY WE TOUCHED TRANSIT.

THE MUCH LOVE!!