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On May 22, 2000 a news story I completely revolutionizes life. I went for an ultrasound control and the first image that appears is the chubby face of a child. I am nineteen weeks and fortunately the baby is at least as good results from the first images.

What a thrill and terror I felt at that moment. I'm 24 and expecting a child but not
is certainly the best moment of my life. I spend the rest of the pregnancy may be thinking how difficult the life of my child without a father at his side. I guess his future with me and takes its first steps
, kicks a ball, ride a bike and all I can think is more beautiful when you are pregnant.

On September 13, Matthew was born 35 weeks and three days via a Caesarean section because I have a fever, so my gynecologist decided not to risk over time and an hour from my shelter my child is already born
. Everything seems normal.

The first year of life passes quickly, but Matthew does not meet any of the early evolutionary stage
.

September 11, 2001 there was the attack on the Twin Towers, September 12, 2001 there was the attack on the serenity of a young mother. Very coldly and without ever seeing the child, the psychiatrist tells me about
brain injury. The total cattle invade my mind and tears in my eyes ...... I can not imagine anything. Two weeks after I bring the child, other harsh words I enter the mind and heart: "It 's palsy"
All this diagnosis without examination. We begin the process: encephalogram, CAT scan and MRI. The overall picture is full of inconsistencies, but no one explains the situation well. They tell me: "Matthew has a spastic quadriplegia caused by fetal distress and Arnold Chiari malformation type I in the cerebellum. Something I do not square because the hospital where I gave birth, when I present the situation of my son, the pediatrician who has resigned, and my gynecologist deny this fetal distress. We started out 'the pilgrimage from different doctors and all I confirm the diagnosis: the case of spastic quadriplegia.

In October we start physical therapy in neurospischiatria but not enough for me.
so I submit to a physical stress that Matthew only a person with a strong will can stand. We're going to Bergamo for speech therapy, physiotherapy in Cremona for personal initiative, in Milan for a pseudo speech sent by the psychiatrist and in the meantime the child is also attending the nursery school, is free from any commitment on Sundays only.

the age of 3 years and 4 months, undergoes the first operation adductor groin Foligno and 4 years and 2 months and faces the second operation, this time with a flexor that forced him to stop at least a month because i have to chalk
both legs.

Matthew endured with a smile and a determination to be envied.
But what happens after intervention? The child has urgent need to resume physiotherapy for not ditching the result of the operation but unfortunately this does not happen. After six months and resume in another department in another hospital. We pass by the area of \u200b\u200bneuropsychiatry at the physiotherapy hospital in Brescia Montichiari. Within a year Matthew went from making coffee to park their cars and play with the first physical therapist to walk with a
quadripode he called Ugo. What a change !!!!!!!

With the new physical therapist, I am aware of the true clinical picture of Matthew: while reading the reports of the examinations, he says: "If I had seen before I would have said gliesami \u0026lt;lady can not do anything, I'm sorry>. I do not understand what you are telling me and instinctively I sit as if I were to receive yet another blow. Finally someone explained to me the two pages of MRI in a few words saying that Matthew would be a vegetable, essrer should not be able to do anything but in reality the child is doing the work
very few brain cells alive and even hyperactive.

And to think that I believed that what they told me my son was on the pathology of all. I had to wait 5 years and a physiotherapist to learn the truth.

On 14 November 2008, at dinner Matthew completed his first and only three steps alone and the tears flow from wild my eyes.

Since March 2009 we unfortunately ricapitati for bureaucratic decisions under the Neuropsychiatry and Matthew is no longer with Hugh and walked with no other help.
After 9 years of struggle and to live according to my son, I can say with absolute certainty that there was no better name I could give him. Matthew means gift of the Lord, and I think it's just 'cos. In spite of all he is peaceful, tranquil, cheerful, aware of his situation, but most fighting is my benchmark, my strength and my light.

Mat THANKS TO EXIST !!!!!!!!

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The History of The History of Leonardo Mariavittoria

My name Mariavittoria Benedetta, I was born in Udine January 10, 2008 at week 26. At birth I weighed just 502 grams. My mom was sick for some time, but her gynecologist had not noticed that I had some serious problems of growth, later diagnosed in hospital as a serious case IURG.
On 1 January 2008 my mother was in Slovenia, one of the many stations of well-being, to try to remedy problems caused by serious problems with blood flow and functioning of the kidneys, the doctors were referred to 'obscure. The evening of that day he had a detachment of the placenta and, after fighting one night in a small hospital mountain, we were transferred by helicopter to hospital in Udine, the closest place to the Italian border, there are the same in his belly for 9 days, trying to strengthen my expansion box, which, given my non prematurity were not ready. The doctors were puzzled, given the state of my heart when I was still strong pain in my stomach. Every three hours a nurse came to check if there was, then one night my mother was very ill. In the morning the doctors decided they could not wait any longer, because otherwise I had to come get me and my mom would not have survived ...
At birth I surprised everyone with my vitality and my efforts to breathe, but unfortunately my lungs were not working yet .. so I was intubated for more than three months, during which I faced many infections that persecutes expansion box on my sick, but me and my mom we never gave up, even in moments when it seemed that there was no hope
.. Slowly I recovered and got the weight of 2.2 kg are returned home May 24, 2008. In early July, I finally removed the oxygen respiratory assistance. My
meant that conditions of extreme prematurity I was severely hypotonic and I brought a delay of several months in brain development. I went then stimulated both from the point of view Physiatric that from the standpoint of psycho-motor to allow the brain to the muscles and finally to complete their development.
One year I was sitting with the aid of a pillow, I was unresponsive to external stimuli, and had poor muscle strength so that I could move on its own. After a moment's hesitation, my mother had the good fortune to be directed to the physiotherapy hospital in Montichiari, thanks to frequent weekly sessions where I could strengthen my muscles and I learned the reactions necessary balance and fall the journey as well as to manage the space.
Today, at the age of 2 years finally walk. I'll never stop to thank those who have been able to stimulate my potential, giving me a hand in trying to deal with that mental and motor retardation that I bring from my birth, because my organs and the brain had not yet finished their training process. Now I'm struggling with the psycho-motor skills, cognitive learning to prevent problems that may arise with school age. I think for me as a serious premature prevention and stimulation is crucial, since we are still "textbook cases" before 2000 and that children like me would not have survived the birth. We act as sort of "edge" to be "guinea pigs" and end up in the manuals of international medicine .. my mom and I never stop believing in medicine, therapy and prevention of any damage that may arise.

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Now that you have searched for years, finally discovers she is pregnant.
A pregnancy with some snag a TN too bad checks, but checks that everything seems to go well. Echography you see that you're a nice boy, your name immediately Leonardo x your will to fight despite the low amniotic fluid and should be born first.

born with the Sept. 13 with five weeks in advance, I realized that everything that I believe does not exist, that life is not a fairy tale.
At your birth you do not cry .. why? is not happening so the programs I've seen, something is wrong but the doctor tells me not to worry ... I get off after 4 hours in intensive care because that is where did they get there and that it remains for 39 days attached to those tubes.
but I wonder why us? Lots of life and death, your kidneys become blocked as strong as a lion, but you exceed 48 hours and then the diagnosis ... me and your dad the world collapses, you have a brain malformation called agenesis of the corpus callosum but something else is wrong, talk about the syndrome.
But now you're here and we want to help you, you have to fight the tears ended.

At discharge your diagnosis: respiratory distress, prematurity, partial agenesis of the corpus callosum, cromosopatia rare partial monosomy of 9 associated with a partial trisonomia of 10, these words still echo in my ears,
\u0026lt;\u0026lt;His son may be a vegetable>> ... then I'll compare you to a flower that must be cared for, nurtured and loved ...

You surprised us all with your progress, slowly blossoming and you tell Leo to those doctors that a small flower has taught us so much, even if they do not do your peers, your mom and your dad are growing and learning, you're LEONARDO!

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The story of The Story of Gloria Elena

PEARL ....... MY GLORY.
The day I heard the news that I become a mother was the happiest day of my life, like the nine months spent waiting for this little creature.
The day of delivery arrived and I am unaware of what was happening, I gave birth, by Caesarean section, my daughter.
climb out of surgery just to see the girl I asked the nurse if we could see her, but she said that she had been transferred to another hospital because she was born underweight. But from that moment I felt inside me that something was not wrong, my husband and my parents at every visit that I received were behaving strangely.
For several days I kept asking what was wrong the child, accuse them of not telling me the truth, but their response was always the same: underweight.
After four days, the doctor sat down next to my bed and started to explain what actually happened to the child.
"Madam, I'm sorry but her daughter was born with a malformation of the spine, is celebrolesa and serious."
I will never forget that day, the confirmation of my questions, it was as if the whole world comes down on me in these situations, the first thought is always, "because she just had to happen to us?" When I heard that Your daughter has a disability, is a painful awakening Suddenly, you're unprepared, you have before you a future of uncertainty and difficulty.
Finally after 8 days I can go see the baby for the first time, that little creature in the incubator with all those tubes, I did not know whether to laugh or cry, I was not aware of what awaited me, of what doctors I would have said about their health situation.
In fact, after one month, the doctor appointed by us tells us what his colleagues say about the situation of the girl: "I'm sorry, but you have to be strong for the things I am going to say doctors do not know if you can take home the child because the situation is very critical, do not know how to survive. "
We burst into tears, I could not understand why God, I had "won" a disabled daughter and now will not let me, to me, so believe in him, he could not make me do that.
For a month after birth the child brought home and from there began his battle for life ", numerous hospitalizations, surgeries, therapies ... ..
During these years I found myself many times to cry, thinking about things that would never have done or said like other children, but eventually I stop making comparisons and begin to see "my daughter," to work with her, I I do as an intermediary between you and the world, so see it grow every day, always With her smile, her eyes speaking, his warbling ... in short, what about ... these disabled children will give more satisfaction to those of children with disabilities, when they come into your life you can not do without, and is also why I try not to discourage me, to be strong for her, to make it grow in a peaceful, not to make them miss anything, even the little things that mean so much to you, I can feel a valued commodity. (it is) Any
his goal is for me a refill, I feel stronger, I feel like to convey my satisfaction to others, encouraging them to tackle any problem presented itself, but also make myself available of those who are beginning to experience similar experiences.
Now I can say that these past 13 years with ups and downs, joys and sorrows, sacrifices ... are evidence of the will to live that you love that forward, but especially for the love he receives.

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Hello, I am Helen, I have six and a half years and my condition is suffering from a spastic diplegia perinatal that big words ... Wow! Neither do I know what it means, but my problem is especially noticeable when I walk. Occasionally I stumble, I fall down and cry, and, as my mother, I do some 'the piattolina
... The only thing that I know is that I do not miss the fun, they are reckless, and I like to do everything I can ...
When I was in the belly of my mother, I slept more, and apart from the hiccups, which I still carry around, not doing much . In fact I was so quiet that I was born the beauty of twelve days after the date: "His belly is a swimming pool lady, her daughter is too good in there!" Were the words that she heard my mom every time he went to x do an ultrasound to check that the liquid is diminished ...
Note that there were about 35 degrees outside, who made him take me out to the scorching heat?? So in the end they did
so that forced me to come to light, 17 June 2003, my reluctance.
Unfortunately, it is a strange thing happened: I was x see the light, when they realized that I could not get through, my little heart from the effort has begun to slow. In the end I was so tired that when I was born I have not even had the strength to cry.
I rested five minutes and then I decided it was time to make me feel, but I thought I should finally see my mom, she was gone and in its place was a strange man dressed in white. I do not like and so I cried, then you are determined to bring the arms of my mother .... Hey, but there was also my dad ...
Finally comes the time of the food and presentation to the grandparents. Ugh I have a Banana with those little hair I had, but where have the imagination!
We went home and who was waiting for me? A mega cagnolone all black that I smelled right under the chair.
Everything goes well except that I was always hungry!!
At six months, however, the mother noticed that I can not sit well, even x it must always put a pillow behind my back. He says that the pediatrician
diminish his concern by saying that I was a bit 'lazy and that I would have started later. Spend another three months ... and so when we hear "... but really it is time that the lady is a child sitting alone now, "decided it was time to change doctor!
Let's go to a lady that I view the whole new (and who had never made a visit as well!), And after seeing the booklet issued by the hospital, tell the mother that perhaps there has been a pain in childbirth and that I may have the muscle tone of the back is not very developed compared to my age.
Cabbages and what does this mean?
the beginning of a series of visits, leading to an initial diagnosis: suffering from perinatal hemiparesis.
So I suffered while I was born there was no need to tell me, I already knew, I made the effort!
And then?? Start
physiotherapy, not without tears (and tears), and after about two weeks they can crawl, something I had never done before.
After about a month I try to get up attachment to things, but a hand is always closed.
Mother points out that this particular therapist becomes suspicious and makes me do another control.
the end, the final diagnosis was spastic diplegia suffering from perinatal
All ... after about 18 months after my birth !!!!!
short time it took to discover that during delivery I received a brain injury! And no one in hospital had said anything to my mum and my dad, when I brought home.
After five years, thanks to a therapist who made me work hard, I can say that a disabled person "skilled" in everything I want ...
grow up I'd like to make a skater, but who knows!! For now I think to play and finish school, which I love. I'm also going to the pool to improve my balance, my breathing and my autonomy
... Maybe next year I can swim like my dad, without him to keep me.

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Lupita - The first choice

After letting us know that Pita had suffered permanent problems, doctors from the NICU before and those of the NPI then gave us a very general indications of what could be our child. They said it was impossible to establish a precise diagnosis even then, that in time we would have .. or rather they would know more. Our Neuropsychiatrist suggested we wait for it to pass the first year of life before to stamp any kind of therapy.
In the meantime we began to throw across your network fossennata of information, searching, hoping to understand what to expect. So we happened on the site of an association of Verona, where a psychiatrist, tries in every possible way to pass the message that early detection in CP is essential and that, above all, it is critical to intervene immediately with rehabilitation.
so we went to Verona and at the age of two and a half months Pita begins rehabilitation.
I still remember this puppy of less than three pounds more than a child who looked like a piece of marble as was his hypertonicity.
Clearly the first to inform you of our decision was the psychiatrist who told us not to overdo it does not stress a child so small. And he was kind enough to suggest that in Montichiari at the hospital was a training ground to childhood and then maybe we could try them instead of going to Verona.
So we decided "to the shortest path "and since then Lupita is followed in Montichiari, with many small and excellent results.

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The story of Lupita

One morning in May, we were in 2006, I discovered she is pregnant ... I could not believe, in short, Fabio and I had just suggested to try that was already in a Baby!
Of course we were happy even if a little frightened, in short our lives as children were concluedento to make room for those parents.
Of course we did not expect the series of "surprises" that we already had the pregnancy.
eighth week I learned that expecting twins, a case of twins rare as monochorionic and monoamniotica, so having to make weekly checks because high-risk pregnancy.
Twins? and most at risk! Despite everything, however we have always been calm, I've been feeling well and even went so proud of my belly that would have kept me forever.
were hospitalized at 28 weeks by caesarean section planned for 32. The doctors said that given the particular case had my little safer out of the belly. But at 32 we arrived, the very day of the completion of 31 weeks monitoring has detected a heartbeat coming down, always remember that morning, and remember with gratitude the midwife who did everything to keep me quiet until I rushed to the delivery room for an emergency Caesarean ...
and here they are ... two little little frogs immediately transferred to NICU. Fabio remembers two small little creatures in one cradle Terme and runway.
Ruby has now breathed by itself, but instead Lupita was just saved by a miracle and intubated immediately. Despite the concern of doctors and their timeliness, our little Lupita reported permanent brain damage, diagnosed with spastic quadriplegia PCI.
When we were informed, after 20 days in NICU, I did not understand anything more, I sincerely thought that by now we had done it ... and in a moment the world has changed .. all the certainties of the first to go missing in a world made entirely of questions without answers. How many tears .. As much distress and anger .. but the days went by and our kids were ready to come home at last, so, with so much strength and courage and also with so much fear, we wiped away the tears and we brought home our girls to start our lives together. There is nothing like you expect it especially if you have a disabled child, the first year we went home x only bring us to carry out checks on checks. I hardly remember it was so hectic. But slowly, slowly, everything becomes routine .. It is not easy and sometimes the discomfort is felt, the difficulties are many, but not spring moller and not ever.
One of my certainty is that there are no certainties, there is no possibility of a path "normal", but this can be Verame a positive note, because every little thing is a great gift. Our road has just begun but what I know today is that I want my little girls are both happy, each with its own strengths and weaknesses.

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TORINO - TURIN






The Medieval Borgo and Rocca of Torino constitute the set of a museum - albeit sui generis - the particular architecture of a particular historical period, just one of the Middle Ages .

The village is in fact more like a monumental archaeological site and was born in the Parco del Valentino as Hall 's International Exhibition which took place in Turin from April to November of 1884 .

for breaking up at the end of the International, became the city museum in 1942 .

This is a fairly faithful reproduction of a typical late medieval village in which they reconstructed streets, houses, churches, squares, fountains and decorations of the time surrounded by walls and fortifications and dominated by a fortress . It is accessed through a tower-door.

are also present in the village since 1884 craft shops .

La Rocca has four floors: the basement that houses the prison, but the ground floor entrance lobby, the courtyard, the soldiers' dormitory to house the mercenaries, the kitchen and the dining lunch, the first floor home to the room of the guardian who controlled access to the drawbridge, the vestibule and the baronial hall, the bedroom inspired by the room of the King of France Castle Issogne , the oratory, the room the damsel, and the chapel.

The town was built between 1882 and 1884 by a group of artists and intellectuals coordinated by ' architect Portuguese Alfredo d'Andrade .

The Medieval village of Turin is a museum together even if the particular nature of the architecture- the Middle Ages . It was built between 1882 and 1884 by a group of artists and intellectuals coordinated by the Portuguese architect Alfredo d'Andrade .

Both

borough as rocca are inspired many castles of Piedmont and Aosta Valley : the courtyard of the rocca is a true copy Castle Fenis , the source of Castle Issogne , the village church of the Church of Avigliana, etc.

The village is more like an archaeological site, monument and was born in the Valentino Park and pavilion of the international exhibition to be developed in Turin from April to November 1884 .

destined for demolition at the end of the international exhibition, became a civic museum in 1942 . This is a reproduction of a typical late-medieval village which has been reconstructed streets, houses, churches, plazas, fountains and decorations all the time surrounded by walls and fortifications and a height rocca . It is accessed through a gate tower.

The village is also from 1884 groups of artisans and teachers.

La Rocca has four floors: the basement prison stay, the first is the income, the atrium, the courtyard, the place for soldiers destined to host the mercenaries, kitchens and dining rooms, the second floor Curator is the bedroom which controlled access to the drawbridge, the lobby and the room of baron , the room inspired by the King of France Issogne Castle, the chapel, the room of "Damigella "and the chapel.

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Medieval Village - Ceres

The Monte dei Cappuccini is a hill that rises behind the city of Torino on the right bank of the Po near the bridge Piazza Vittorio Veneto .

This hill was used for defensive purposes since ancient times as one of the above crossings Po The first news of the presence of a church dating back to XIII century .

The name "Monte dei Cappuccini" comes from the grant to Capuchin use of this area by Savoy in second half of the sixteenth . Also at that time the Savoy commissioned the construction of a church with the convent.

The works for the Capuchin church, which was dedicated to Marian devotion , were started in 1583 , the original project Ascanio Vitozzi based on a centrally planned building in a Greek cross, was then made by the engineer mannerist Giacomo Soldati . The painter Isidoro Bianchi of Champion Italy you created numerous paintings over the years 1630 - 1633 . The main altar is the work of Carlo and Amedeo di Castellamonte .
The project was completed in 1656 , the year of consecration of the building. In seven hundred were then added some valuable paintings.

During the Napoleonic period, with the suppression of monastic orders, the monastery was temporarily used for other purposes and restructured.

Nell ' eight hundred the dome was built in the octagonal as well as can be seen today.

Severely damaged by bombing during the WWII , the complex has been recently restored.

Currently, besides being back seat of a convent, houses the National Museum of the Mountain and the headquarters of the Italian Alpine Club Turin.

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Monte dei Cappuccini - Torino - the railway bridge

The Turin-Ceres is a line railway of Province of Turin currently managed by Gruppo Torinese Trasporti (GTT) in the past was run by the company SATTI , successor to the FTC in 1981 (Turin, Northern Railway) in 1967.

History.

The line was built gradually: starting with Turin, 18 April 1868 was inaugurated the first stretch of railway between the station of Porta Milano and Venaria , 1 December 1868 you arrive up to Caselle and 28 February 1869 reach Cirié , for a total of 21.343 km and 5 stations: Madonna Country to 3.239 km, Venaria (7.252 km), Caselle (13.270 km), San Maurizio Canavese (18.317 km) and Cirié ; station Borgaro (9.260 km) will be built only in 1870 As the town of Borgaro Torinese had not initially paid contributions for the construction of the line, while the Turin Dora station (2.236 km) was only one stop. In

1876 (August 6) the line is brought up to Lanzo Torinese the presence of the President of the Council of Ministers and Depretis 1913 Eng. Alberto Scotti finalizes the design of the railway to Ceres : thanks to the collaboration of Austrian prisoners of war in June 1915 the railway reaches Germagnano and 17 June 1916 completes the entire line mountainous with stretches maximum gradient of 35 ‰, curves of 200 m radius and total length of about 44 km.

On October 6, 1920 the Turin-Ceres was the first Railways Organization in the world to adopt electric traction DC High Voltage (4000 V).

A special feature of the railway line is that all stations in the mountain section, from that of Lanzo to that of Ceres were built between 1886 and 1918 in Swiss style with a rectangular , the waiting rooms of the first and second class accommodation for the caretaker in the first and second floor and roof with four slopes.

Four stations are larger ( Lanzo, Germagnano , Pessinetto and Ceres) and the other 4 ( Funghera , Traves, Losa and Mezzenile ) are smaller, while maintaining the same characteristics with regard to plant (no double waiting room), facades and roofs.

Another peculiarity of the line is a single view of the viaduct with 50 m of reinforced concrete on Stura di Val Grande to Ceres, 190 meters long.

Until 1988 the line runs from the station of Turin Cirié-Lanzo located in Corso Giulio Cesare close of Porta Palazzo and along the route branched racordi several rail companies: one for the Arsenal in Piazza Borgo Dora, one for the gasworks (hereinafter Italgas ) in Corso Regina Margherita 52 (plant reached with a bridge over the Dora Riparia ), together with those of Mont Cenis and TMJ Workshops Course Tortona, for the company and the company Gilardini NAFTA): This connection will be discontinued February 5, 1968. Other connections along the line are those for Ferriere FIAT (at the Madonna di Campagna ) for SNIA Viscose and Manufactures of Martiny Venaria for the Manufacture St. Maurizio in San Maurizio Canavese for the mill of Bosso Mathi, for amiantifera of Balangero for the mill Germagnano and that for the talc mine of Pessinetto . In 1967 he was also made a connection which, just upstream from Madonna Country led to the municipal slaughterhouse in via Traves. The freight ceases in the mid-eighties and now the line is crossed only by passenger trains. In 1967
with Ministerial Decree the line was taken directly to the government commissioner Management and 1981 passes in the management SATTI .
the late '80s the line has been extensively renovated and buried in the town of Turin ; concurrently work was abandoned the station in Torino Cirié -Lanzo and the terminus was moved back to the station turin Dora, built for the occasion as well as that of Venaria Rigola- Stadium.

As of September 22, 1993 the railroad was discontinued and only traveled by train to Germagnano after the flood that hit the Valli di Lanzo broke down the bridge of Cornalè Pessinetto and severely damaging to those Sabbione Mezzenile and one near the cemetery Pessinetto . Following the work of Passante di Torino is now separated from the network RFI. .

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