GENOVARTE
2009 20 June -8 July 2009 from Tuesday to Saturday from 16:30 to 19:00, other times by appointment.
work selected for ArteGenova "I remember my grandmother's" 2008
Thursday, June 18, 2009
Mixed Wrestling Cartoons Glynn
III^ Biennale d’Arte Contemporanea
from Tuesday to Saturday from 16:30 to 19:00, other times by appointment.
work selected for ArteGenova "I remember my grandmother's" 2008
from Tuesday to Saturday from 16:30 to 19:00, other times by appointment.
work selected for ArteGenova "I remember my grandmother's" 2008
Getting Back To Work After Chicken Pox
... AND WHAT THEY ARE ABOUT
After the shift, Dr. Saul Agostini does not forget his patients, even with his wife Beatrice organizes trips and days with them and their parents and colleagues who are willing to join, gather all the days when "his" boys and leads them to spend a day in the full-heartedness and fun.
One thing that occurs twice a year, one day in June and December 1.
key issue is how people look at these guys 'different' physically and have fun and not afraid of veering in the streets and be judged for what they are.
The following will be given a trip made in June
a few years ago, a trip
patrol boat along the Mincio and
cable car on Mount Baldo, and concludes with a dinner at a farm
the area.
You may notice that some of them are in wheelchairs, others walk with crutches, and many of them have the famous (for them!) External fixator. Agostini
The doctor is happy without its coat but still managed to make everyone laugh.
Among the group there are also nurses, the nurse, the hospital chalks.
Among all this we see that everyone is together, socialize, make new acquaintances and re-embraced others are happy to meet again.
In general, hospitals are increasingly seen as places rather negative and very limited to follow the rules, loyal to their duty, with patients who are hospitalized, curative
ie sent home without a lot of confidence.
But here you can read the emotion in the eyes of children, the joy of being able to turn heads high without feeling observed from head to foot.
This led to strong friendships and the doctor Agostini stated that its implementation does not only happen when we work and care but especially when he sees young people who have to endure the hardships of disease and yet are serene and reagiscono.E 'pleased to see the relationship that remains outside the hospital and arranging these output also allows them to meet as provvengono from all over Italy. 
After the shift, Dr. Saul Agostini does not forget his patients, even with his wife Beatrice organizes trips and days with them and their parents and colleagues who are willing to join, gather all the days when "his" boys and leads them to spend a day in the full-heartedness and fun. One thing that occurs twice a year, one day in June and December 1.
key issue is how people look at these guys 'different' physically and have fun and not afraid of veering in the streets and be judged for what they are.
The following will be given a trip made in June
a few years ago, a trip
patrol boat along the Mincio and
cable car on Mount Baldo, and concludes with a dinner at a farm
the area.
You may notice that some of them are in wheelchairs, others walk with crutches, and many of them have the famous (for them!) External fixator. Agostini
The doctor is happy without its coat but still managed to make everyone laugh.
Among the group there are also nurses, the nurse, the hospital chalks.
Among all this we see that everyone is together, socialize, make new acquaintances and re-embraced others are happy to meet again.
In general, hospitals are increasingly seen as places rather negative and very limited to follow the rules, loyal to their duty, with patients who are hospitalized, curative
ie sent home without a lot of confidence. But here you can read the emotion in the eyes of children, the joy of being able to turn heads high without feeling observed from head to foot.
This led to strong friendships and the doctor Agostini stated that its implementation does not only happen when we work and care but especially when he sees young people who have to endure the hardships of disease and yet are serene and reagiscono.E 'pleased to see the relationship that remains outside the hospital and arranging these output also allows them to meet as provvengono from all over Italy.
B4 Delicious Deletion
...
This blog is made public the true story experienced by many children and other adults who had been hospitalized in the hospital Valeggio sul Mincio and were treated by the doctor Agostini Saul.
Within the narrative are explained the little secrets and tricks of the trade that the doctor put in place to buy so much sympathy for his patients and former patients. I would like to specify that
mainly for boys achondroplasia is already heavy for himself to live with this "disease", not only because of the difficulties to perform the most trivial things but also because of the many prejudices and views curious and distressing that people subject to them, Fente that falls into the category of the ignorant!
In this hospital the treatment of patients
is to make them feel at home, without feeling the weight of the reason why we are having to spend whole days inside that structure, personnel (nurses, nurse, doctors, physiotherapists, porters ...) are available in all people, not treating patients as if they were guinea pigs on which to operate, experiment, do analysis, but as people with feelings and sensitivity, and as such are respected and valued.
Making the elongation of arts on children 12 years or more is a very strong shocks, a FASA
particular age and delicate, the staff and the doctor in question are moved to ensure that everything remains a positive experience for them and at the same time to make people understand "normal" that the uvula achondroplasia are common to all people.
In this structure èconsentito parents stand beside their children at any time, except in times of cleaning, medications or other treatments, and if there was any need can stay the night.
Usually in most cases it is known that children are terrified when they come into hospital, but here in Valeggio sul Mincio young patients are natural and have no fear, have formed a strong group of
socialization and encourage and help each other, playing happy though they know they have to undergo surgery or have already been.
The doctor in question enters its orthopedics department always with a smile, always with a word or a caress of comfort, a line in sympathy to snatch a smile to each of his patients.
In an interview granted by him said that his job is to help people to make them feel good and do not put them at ease, also working with them every day and known in their deep and in the private sphere (because that's how every good doctor should work, the interest must be general and complete and also cover the personal sphere of each) and he becomes attached to their work well and feels compelled to help them as best he can. 
This blog is made public the true story experienced by many children and other adults who had been hospitalized in the hospital Valeggio sul Mincio and were treated by the doctor Agostini Saul.
Within the narrative are explained the little secrets and tricks of the trade that the doctor put in place to buy so much sympathy for his patients and former patients. I would like to specify that
mainly for boys achondroplasia is already heavy for himself to live with this "disease", not only because of the difficulties to perform the most trivial things but also because of the many prejudices and views curious and distressing that people subject to them, Fente that falls into the category of the ignorant!
In this hospital the treatment of patients
is to make them feel at home, without feeling the weight of the reason why we are having to spend whole days inside that structure, personnel (nurses, nurse, doctors, physiotherapists, porters ...) are available in all people, not treating patients as if they were guinea pigs on which to operate, experiment, do analysis, but as people with feelings and sensitivity, and as such are respected and valued.
Making the elongation of arts on children 12 years or more is a very strong shocks, a FASA
particular age and delicate, the staff and the doctor in question are moved to ensure that everything remains a positive experience for them and at the same time to make people understand "normal" that the uvula achondroplasia are common to all people. 
In this structure èconsentito parents stand beside their children at any time, except in times of cleaning, medications or other treatments, and if there was any need can stay the night.
Usually in most cases it is known that children are terrified when they come into hospital, but here in Valeggio sul Mincio young patients are natural and have no fear, have formed a strong group of
socialization and encourage and help each other, playing happy though they know they have to undergo surgery or have already been.
The doctor in question enters its orthopedics department always with a smile, always with a word or a caress of comfort, a line in sympathy to snatch a smile to each of his patients.
In an interview granted by him said that his job is to help people to make them feel good and do not put them at ease, also working with them every day and known in their deep and in the private sphere (because that's how every good doctor should work, the interest must be general and complete and also cover the personal sphere of each) and he becomes attached to their work well and feels compelled to help them as best he can.
Wednesday, June 17, 2009
Headache Forehead Spots
AISAC - WHO IS AND WHAT IT DOES WHAT AND WHY
Founded in 1987 by some parents, AISAC Onlus is a non-profit social organization, which has about 800 members and families and conducts its activities in clinical, social and psychological / relational and the rights, involving physicians, mass media, agencies and institutions.
1 - supports scientific research, particularly in the field of molecular biology, as well as research projects, social / psychological
2 - works to promote laws, regulations and effective interventions for people with achondroplasia and their families;
3 - deals with prevention and care;
4 - hosts internships for undergraduates in psychology at the Catholic University of Milan;
Most of the activities that have so far been made possible thanks to the contributions of their members, the Lombardy Region, dellaFondazione CARIPLO of Peugeut Italy, sponsors illuminated for 5 years has supported scientific research in molecular biology. The
AISAC is a non-profit organization that is focused more on general issues arising from the limited stature.
born from the desire of a group of parents who realized the need to create a structure socially and legally recognized.
Completed projects:
projects designed:
AISAC The Association is also registered on Facebook to stay connected anytime, anywhere with those who I am concerned.
Founded in 1987 by some parents, AISAC Onlus is a non-profit social organization, which has about 800 members and families and conducts its activities in clinical, social and psychological / relational and the rights, involving physicians, mass media, agencies and institutions.
1 - supports scientific research, particularly in the field of molecular biology, as well as research projects, social / psychological
2 - works to promote laws, regulations and effective interventions for people with achondroplasia and their families;
3 - deals with prevention and care;
4 - hosts internships for undergraduates in psychology at the Catholic University of Milan;
Most of the activities that have so far been made possible thanks to the contributions of their members, the Lombardy Region, dellaFondazione CARIPLO of Peugeut Italy, sponsors illuminated for 5 years has supported scientific research in molecular biology. The
AISAC is a non-profit organization that is focused more on general issues arising from the limited stature.
born from the desire of a group of parents who realized the need to create a structure socially and legally recognized.
projects:
- L. 266/04: From diversity to exclusion: to break a vicious cycle.
- L. 289/02: no longer alone: \u200b\u200bNeo-parents before the diagnosis.
- L. 285/97: Children "at risk" - To guide, facilitate and coordinate: a path to support parents.
- L. 241/90: family want to become an expert?
- L. 22/93: counter the effects of genes crazy.
- L. 23/99: Diversity is not a handicap training.
Completed projects:
- Cariplo: Why next to the sick child is not born of a sick family: the importance of communication to the first pair of birth defect (handicap or malformation) of your child .
2000 - LR 23/99: The child, the hospital and surgery.
2002 - LR 23/99: Why next to the sick child there is a healthy family .
2002 - LR 22/93: The social exclusion that the stigma of "nano" still requires around 5000 people in Italy. 2 003
- LR 23/99: become great in hospital.
2004 - LR 23/99: A family in shock.
2004 - LR 22/93: The strength of diversity, strength in diversity: a proposed advertising to promote solidarity .
2004 - LR 23/99: A dream destroyed, an unexpected challenge.
2004 - LR 23/99: The network that would say: the value of the experience of families.
2004 - L. 241/90: parents on the phone. 2005 projects designed:
- humanize life in the hospital: a project that protects children hospitalized in surgical wards and / or forced to long-term care
- The child in hospital: achondroplasia protect children hospitalized in surgical wards and / or forced to take long wards
- The social exclusion of a small group of people with dwarfism (rare disease) as a working model for many other
- The knowledge of the families: a proposed mutual aid
- Why a sick child could become disadvantaged
- aid of those who know: a bank of time based on solidarity and sharing
- in the hospital to "grow"
- Guidelines for good care through integrated social and health interventions for people with achondroplasia and their families
- A better future, a future of integration. The AISAC. poses a challenge and a hope.
- For a sick child could become a disadvantage. Break the cycle: disability, social exclusion, abandonment studies, unemployment / poorly paid work, poverty, social exclusion
- Little man big heart
- Why next to a sick child is not born of a sick family
- Become a high to live better? AISAC The Association is also registered on Facebook to stay connected anytime, anywhere with those who I am concerned.
Tuesday, June 16, 2009
Effect Of Water Spill On Memory Foam
I am a graduate of the course of social educator, I chose to do my blog on a "documentary" to address and discuss the issue of hospitalization and the label by doctors and staff on patients with physical ailments that affect the sensitivity of the patients themselves, are ill suited to conduct and aid to healing and health of patients, by "losing" their identity and value as a person.
An attitude is rampant in most health facilities, which has become a routine.
contrast treat the case of a pediatric orthopedic doctor, Agostini Saul, who had the perseverance and willingness to change and affect many of the staff that worked with him, and attracting large numbers of patients who have decided to put in his hands and trust.
He understood the problem that lies at the base and managed to hit the weak point to remedy the situation, putting the game in first person with physical but also moral support for his patients.
This blog has as its goal to raise awareness and support those who want to professionally deal with the health of others, and to understand that what matters is not only a monthly salary and is marked with a gown but also a respect for those who need help and want to be treated as people with names and their life experience, not by weighing them why they are hospitalized, already heavy in itself.
The problem is the lack of consideration of the value of making patients lose their self-esteem, security and identity, since the patient is recognized and called by their number of bed and not his own name.
Orajel Prenatal Side Effects
YOU NEVER HEARD OF PEOPLE ACHONDROPLASIA?
The word achondroplasia is derived from the combination of three words of Greek origin ( to = no, condros = cartilage, Palais = training) and indicates a lack of harmonic development of the growth plate of long bones of the limbs, ie that part of the bone in children is not yet sealed, and allows, through the growth and multiplication of cells located at its Internally, the gradual lengthening of bone.
Achondroplasia affects about 27,000 births and 90% of sporadic cases occurs as a result of a mutation in the sperm or ovum of unaffected parents: the subject achondroplasia arises in this case by a couple healthy unprecedented in families of origin and the possibility of a second affected child is trascurabile.Nel remaining 10% of cases the disease is inherited with an autosomal dominant mechanism, ie one parent affected with achondroplasia transmits the gene responsible for the disease to their children with a probability of 50% for each pregnancy. In that case, then both parents are affected by this disease, there is a 50% chance that the child inherits from one parent and then the gene is affected (heterozygous form ), who inherits 25% from both parents and is therefore affected by a more complex form ( homozygous), 25% who did not inherit the gene from both parents and sano.Riassumendo, if both parents are affected, the chances of having a sick child are 75%.
The altered gene in patients with achondroplasia was identified recently and is located on the short arm of chromosome 4. More specifically it is a "point mutation, an abnormality in the DNA that causes the substitution of an amino acid with another in the protein receptor.
This discovery allows for early prenatal diagnosis for couples at risk (those with at least one partner affection), through DNA analysis, as well as the first step toward understanding the precise function gene and thus for the development of a specific therapy (do not assume, however, soon).
In general terms, then, can we speak of a condition of short stature type of disharmony, with a ratio of truncated limbs altered proportions (trunk and limbs of normal length shorts, with a shortening of the latter that affects parts close to the trunk).
At birth the child with achondroplasia has more or less regular height and weight similar to that of a normal child. The stature and continues to remain similar to that of other children, until the first year of life, and then begins to be visible growth retardation.
The average height you can reach is about 130 cm. The head circumference, higher than normal at birth, grew faster during the first year of life and then stabilized.
With regard to complications - mostly be faced with preventive treatments to prevent the onset or reduce the effect - the most common orthopedic, such as kyphosis, lumbar lordosis and a curvature of the lower limbs. It is rare neurological problems such as hydrocephalus and spinal cord compression in the cervical and lumbar. Finally, it must be said that the achondroplasia not lead to mental retardation.
Currently, the only real option for improving the quality of life for patients is to increase its stature by limb lengthening surgery, surgery that tends to start between 12 and 16 years. The operation involves both the tibias and femurs that the average stress for bone segment is about 10 cm, which may make it possible to reach a height of 150 cm and also to carry out activities before individually precluded, how to use a lift , take public transport and so on.
All the techniques used, however, share the need for long periods of relative immobility, a major physical and mental load for the patient and a major commitment for the whole family.
are normal people, both physically and mentally very sound but with only the misfortune to be small and this makes them uncomfortable in the small tasks that seem mundane to us while they are mountains to climb!
For example, open doors, open a tap, playing the phones, use the kitchen, find the clothes that suit them, get on public transport, drive or even find a job.
But despite all this are very normal people!
What is your reaction if you happen to see one?
Saturday, June 13, 2009
Monster Label Belly Button Rings
family
staging of the family, the wonderful work of Bert Hellinger used in this group allows you to highlight easily field of influence of the family. The way in which we have representatives from the various family members and relationships that occur as the links can reveal hidden secrets of love and orders governing and that the family system that can generate wealth and happiness in it, or suffering and conflict. In recognition of improper and unconscious identifications, in doing honor to the position that every individual occupies within its system, there is a new order based on love and nature. This work full of strength and presence is a boost for the soul and a release for the person. A deep understanding that reconciles us with our roots and makes us free from the past.
The next meetings of family constellations will be held in Modena, Via Pica, on Sundays:
October 11 November 15 December 13
staging of the family, the wonderful work of Bert Hellinger used in this group allows you to highlight easily field of influence of the family. The way in which we have representatives from the various family members and relationships that occur as the links can reveal hidden secrets of love and orders governing and that the family system that can generate wealth and happiness in it, or suffering and conflict. In recognition of improper and unconscious identifications, in doing honor to the position that every individual occupies within its system, there is a new order based on love and nature. This work full of strength and presence is a boost for the soul and a release for the person. A deep understanding that reconciles us with our roots and makes us free from the past.
The next meetings of family constellations will be held in Modena, Via Pica, on Sundays:
October 11 November 15 December 13
Monday, June 8, 2009
What Is The White Stuff Covering My Clitoris
mostra collettiva "Fuori stagione" Milano
the Circolo Culturale Bertolt Brecht in collaboration with
StartArt
Area 2/Via Giovanola 21/C_Milano Tel +39 3397908472 - www.bertoltbrecht.it - MM2 Abbiategrasso
By Vera Carminati
has
Out 2009 season By Lorenzo Argentine
Monday, June 8, 2009 at 18:30
Giulia Accorsi Bonandrini Claudia, Daniela Brambilla, Alessia Carli, Gian Paolo Ciurlo, William Olivati, Zel Ebrity 133, Enrico Francesconi, Silvia evil eye, Luke Best, Maurice Piccirillo, Paola Pigot, Michael Monaco, Enrico Ridolfi, Bruna Anna Ronchetti, Giulio Rossi, Alessandra Rovelli, Hayat Saidi, Joseph Sanpaolo, Donatella Sarchiai, Alvaro & Lori Vallar, Matthew Varsi.
The exhibition will run from Monday to Thursday from 17 to 19 up to 26/06/2009 
the Circolo Culturale Bertolt Brecht in collaboration with
StartArt
Area 2/Via Giovanola 21/C_Milano Tel +39 3397908472 - www.bertoltbrecht.it - MM2 Abbiategrasso
By Vera Carminati
has
Out 2009 season By Lorenzo Argentine
Monday, June 8, 2009 at 18:30
Giulia Accorsi Bonandrini Claudia, Daniela Brambilla, Alessia Carli, Gian Paolo Ciurlo, William Olivati, Zel Ebrity 133, Enrico Francesconi, Silvia evil eye, Luke Best, Maurice Piccirillo, Paola Pigot, Michael Monaco, Enrico Ridolfi, Bruna Anna Ronchetti, Giulio Rossi, Alessandra Rovelli, Hayat Saidi, Joseph Sanpaolo, Donatella Sarchiai, Alvaro & Lori Vallar, Matthew Varsi.
The exhibition will run from Monday to Thursday from 17 to 19 up to 26/06/2009
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