Curs de formare - Terapia 3C - Sesiunea Martie - Iunie 2025

Perioada de inscrieri:  10 Octombrie 2024 - 23 Februarie 2025

Cursul va debuta în:   1 Martie 2025

Durata: 3 luni 

Cui se adreseaza: Absolventi ai facultatilor de educatie fizica si sport, psihologie, medicina, specialistilor care activeaza in autism si parinti ai copiilor cu autism. 

Conditie principala - minim 10 persoane inscrise 

 Zile de curs: Sambata si Duminica Bucuresti : 2,5 - 3.0 h, de doua ori/luna, in weekend, sâmbătă și duminica. 

 Ore de desfasurare: 14.00 – 16.30 

Locatia: str Echinoctiului, nr 41, sect 5, București. 

 Cost – 1300 euro, plătibili astfel: 50% la momentul inscrierii si 50% la jumatatea cursului - modulul de baza.

Cost integral - 1700 euro - contine modulul de baza + modulul de recuperare a deficientelor de orientare spatiala, la copilul cu TSA.

 Platile se vor face folosind urmatoarele date: Asociatia "Clubul Sportiv Guom" Constanta, B-dul Alexandru Lapusneanu, nr. 192, CIF 24260709 contul IBAN : RO41BTRLRONCRT00H6243902, cu mentiunea „Curs 3C-localitatea X” si confirmare ulterioara a platii pe mail: sportautism@yahoo.com. 

Detalii: Cursul va consta in parte teoretica si parte practica si va fi sustinut de prof. Paul Cojocaru, fondatorul metodei 3C. Va fi predat si modulul de aplicare a metodei 3C in mediul online. La finalul cursului se vor elibera diplome de terapeut 3C, in baza carora absolventii vor aplica cele invatate. Noii terapeuti vor putea practica pe cont propriu sau in cadrul asociatiilor de copii cu autism. De asemenea ei vor putea uza gratuit de denumirea terapiei fara incalcarea drepturilor de autor, pe o perioada de un an de la eliberarea diplomelor. Dupa expirarea acestei perioade toti terapeutii vor semna un contract de licenta anuala pentru marca inregistrata. Cuantumul acestei licente este de 100 euro/an. Terapeutii vor putea aplica terapia in orice tara doresc, cu acordul fondatorului. Dupa parcurgerea modulului de baza, terapeutii vor putea participa la celelalte upgrade-uri. 

 Ce este Terapia 3C , pe scurt? 

 Terapia 3C, este un program de optimizare a coordonarilor, in prima faza. Pe parcursul avansarii, abordam construirea gandirii motrice si a inteligentei motrice, scopul final fiind construirea unui comportament psihomotor adaptativ, care sa ofere copilului autist posibilitatea abordarii unui sport individual. 3C inseamna Constientizare, Coordonare, Concentrare. Acestea sunt cele trei arii pe care lucram pentru atingerea obiectivelor noastre. Constientizarea este primul aspect ce trebuie optimizat in procesul de dezvoltare. Copilul trebuie ajutat sa efectueze constient sarcinile impuse. Evident, la copilul cu autism, de cele mai multe ori, nu exista aceasta capacitate. Aici intervine misiunea noastra. 3C SportAutism Program este conceput astfel incat, cu ajutorul exercitiilor de coordonare, tinand cont de sinaptogeneza, sa activam si sa optimizam, cu ajutorul transmiterii impulsului pe calea eferenta, capacitatea de constientizare a propriei scheme corporale si a propriului potential psihomotor. 3C SportAutism Program este conceput pe suport stiintific. Exercitiile vizeaza rescrierea memoriei motrice timpurii si activarea conexiunilor inter-emisferiale, cu ajutorul unor coduri pe axe si campuri. Aceste coduri au rolul de a optimiza gandirea motrica, de a dezvolta inteligenta motrica reducand considerabil deficitul de proprioceptie. Optimizarea capacitatii de coordonare vine ca urmare a dezvoltarii capacitatii de concentrare. Cu cat esti mai constient de propriul corp, cu atat maim ult vei incerca sa ai coordonari eficiente pentru indeplinirea unor taskuri. Capacitatea de concentrare va fi optimizata pe intreaga durata a programului 3C. Secretul consta in numarul de repetitii si construirea exercitiilor functie de reperele enumerate mai sus. 

 Motive pentru care nu poti rata un astfel de curs: 

 1. Ai ocazia, unica, de a invata direct de la fondatorul programului. 

 2. Vei avea ocazia de a-ti insusi o noua perspectiva asupra procesului global de recuperare. 

 3. Vei invata despre un sistem unic de recuperare psihomotorie – recuperarea psihomotorie sinaptogenetica. Acest concept este unic, pe plan mondial. 

 4. Un lucru demn de luat in calcul este acela ca Terapia 3C este premiata de trei ori la Festivalul Mondial de Autism din Canada. Fondatorul acesteia este membru in echipa de consilieri a festivalului mondial de autism, are peste 48 de workshopuri sustinute in tara si 10 pe plan international. 

 5. Terapia 3C, este implementata in Ucraina, Moldova si sunt discutii avansate pentru implementarea in Spania, Luxemburg, Mexic si alte tari, in viitor. 

 6. Terpia 3C este recomandata de majoritatea medicilor care au specializare in neurologie si neuro-psihiatrie pediatrica. 

 7. Terapia 3C nu se adreseaza doar persoanelou cu TSA, ea poate fi aplicata si in alte patologii neurologice. De asemenea, este un bun program de optimizare psihomotorie pentru copiii din ciclul primar. Inainte de pandemie, unii terapeuti au aplicat metoda 3C si in azilele de batrani. 

 Va astept sa va impartasesc bucuria de a lucra si a invata alaturi de copiii cu autism si parintii acestora, dintr-o noua perspectiva si anume 3C.

Este sau nu, autismul, o afectiune psihica?

 

Phelan-McDermid Syndrome - Autismul inteles altfel :)

https://www.massgeneral.org/children/phelan-mcdermid-syndrome 

What is Phelan-McDermid Syndrome?

Phelan-McDermid syndrome (PMS) is a rare genetic condition that causes developmental and speech delays, behavioral problems and a weakened or no ability to feel pain or sweat. Phelan-McDermid syndrome is a congenital condition (condition that is present at birth) that can affect people of all genders.

What Causes PMS?

PMS is caused by a mutation (change) or deletion of theSHANK3 gene (piece of genetic material). In most cases, PMS happens at random. It is not anyone’s fault.

How Can a Person Develop PMS?

There are 4 different ways that a person can develop PMS:

• Simple deletion. This is the most common type of PMS. It is when a piece of chromosome 22(piece of genetic material) on the SHANK3 gene gets lost. This usually happens at random.

• Ring chromosome. This is when chromosome 22 on the SHANK3 gene forms a circle instead of the typical X-shape.

• Unbalanced translocation. This can happen when parents do not know that one or both parents carry the chromosome for PMS.
• Mutation in the DNA sequence (order) of the SHANK3 gene. This usually happens at random.

What Are the Signs of PMS?

Most children with PMS show signs in early childhood. Other children show signs as early as their first 6 months of life. Signs can be different in every person with PMS.

PMS signs can affect development, behavior and physical appearance.

Development

• Developmental delays, such as delayed sitting up, rolling over, walking or talking

• Delayed or absent speech

• Autism spectrum disorder (ASD, or a condition that causes problems with communication, behavior and social skills)

Behavior 

• Repetitive behaviors, such as hand flapping

• Anxiety or nervousness

• Sleep and/or seizure disorders

• Some lower ability to sweat, which can lead to overheating

• Lower sensation or expression of pain

Physical appearance

• Hypotonia (low muscle tone)
• Long head shape with full or puffy cheeks
• Puffy or droopy eyelids with long eyelashes
• Wide, flat nose or face with a pointed chin
• Large hands
• Underdeveloped toenails

Rev. 5/2018. This handout is intended to provide health information so that you can be better informed. It is not a substitute for medical advice and should not be used to treatment of any medical conditions.

3C SportAutism Program - Kitul complet pentru lucrul la masa

3C SportAutism Program Kitul complet pentru lucrul la masa 🙂 Kitul nu contine exercitii. Pentru a lucra cu el trebuie sa contactati un specialist 3C, cu licenta anuala. Pentru comenzi, va rog sa trimiteti mail la adresa sportautism@yahoo.com, cu subiectul Kit 3C.

3C SportAutism Program

3C SportAutism Program, este un program de optimizare a coordonarilor, in prima faza. Pe parcursul avansarii, abordam construirea gandirii motrice si a inteligentei motrice, scopul final fiind construirea unui comportament psihomotor adaptativ, care sa ofere copilului autist posibilitatea abordarii unui sport individual. 3C inseamna Constientizare, Coordonare, Concentrare. Acestea sunt cele trei arii pe care lucram pentru atingerea obiectivelor noastre. Constientizarea este primul aspect ce trebuie optimizat in procesul de dezvoltare. Copilul trebuie ajutat sa efectueze constient sarcinile impuse. Evident, la copilul cu autism, de cele mai multe ori, nu exista aceasta capacitate. Aici intervine misiunea noastra. 3C SportAutism Program este conceput astfel incat, cu ajutorul exercitiilor de coordonare, tinand cont de sinaptogeneza, sa activam si sa optimizam, cu ajutorul transmiterii impulsului pe calea eferenta, capacitatea de constientizare a propriei scheme corporale si a propriului potential psihomotor. 3C SportAutism Program este conceput pe suport stiintific. Exercitiile vizeaza rescrierea memoriei motrice timpurii si activarea conexiunilor inter-emisferiale, cu ajutorul unor coduri pe axe si campuri. Aceste coduri au rolul de a optimiza gandirea motrica, de a dezvolta inteligenta motrica reducand considerabil deficitul de proprioceptie. Optimizarea capacitatii de coordonare vine ca urmare a dezvoltarii capacitatii de concentrare. Cu cat esti mai constient de propriul corp, cu atat maim ult vei incerca sa ai coordonari eficiente pentru indeplinirea unor taskuri. Capacitatea de concentrare va fi optimizata pe intreaga durata a programului 3C. Secretul consta in numarul de repetitii si construirea exercitiilor functie de reperele enumerate mai sus. Inteligenta se construieste in miscare, si trebuie sa dam aceasta sansa copiilor cu autism fiindca AUTISMUL NU ARE COPII, CI COPIII AU AUTISM. Pentru inscrieri va rog sa trimiteti mail la adresa: sportautism@yahoo.com. Multumesc.

Curs de formare Terapia 3C

Perioada de inscrieri: 15 Mai - 15 Septembrie Cursul va debuta in: 2 Octombrie Sesiunea: Octombrie - Decembrie 2021 Durata: 3 luni Cui se adreseaza: Absolventi ai facultatilor de educatie fizica si sport, psihologie, medicina, precum si specialistilor care activeaza in autism si parinti ai copiilor cu autism. -conditie principala - minim 10 persoane inscrise -zile de curs: Sambata si Duminica Bucuresti : 2,5 - 3.0 h de doua ori/luna, in weekend, sâmbătă și duminica. Ore de desfasurare: 15.00 – 17.30 Locatia: Ghencea Business Center, et 4, camera 8. -cost integral - 5500 RON, platibil astfel: 50% la momentul inscrierii si 50% la jumatatea cursului. Platile se vor face folosind urmatoarele date: Asociatia "Clubul Sportiv Guom" Constanta, B-dul Alexandru Lapusneanu, nr. 192, CIF 24260709 contul IBAN : RO41BTRLRONCRT00H6243902, cu mentiunea „Curs 3C-localitatea X” si confirmare ulterioara a platii pe mail: sportautism@yahoo.com. Cursul va consta in parte teoretica si parte practica, si va fi sustinut de prof. Paul Cojocaru, fondatorul metodei 3C. Pentru prima data, va fi predat si modulul online. La finalul cursului se vor elibera diplome de terapeut 3C, in baza carora absolventii vor aplica cele invatate. De asemenea ei vor putea uza gratuit de denumirea terapiei fara incalcarea drepturilor de autor, pe o perioada de un an de la eliberarea diplomelor. Dupa expirarea acestei perioade toti terapeutii vor semna un contract de licenta marca inregistrata. Cuantumul acestei licente este de 100 euro/an. Terapeutii vor putea aplica terapia in orice tara doresc, cu acordul fondatorului. Dupa parcurgerea modulului de baza, terapeutii vor putea participa la celelalte upgrade-uri. Un lucru demn de luat in calcul este acela ca Terapia 3C este premiata de trei ori la Festivalul Mondial de Autism din Canada. Fondatorul acesteia este membru in echipa de consilieri a festivalului mondial de autism, are peste 45 de workshopuri sustinute in tara si 9 pe plan international. Terapia 3C, este implementata in Ucraina, Moldova si sunt discutii avansate pentru implementarea in Spania, Luxemburg, Mexic si alte tari, in viitor. Cursantii au oportunitatea invatarii unei metode direct de la fondatorul acesteia si au acces la ultimele noutati in desfasurarea procesului terapeutic.

Brain damage in premature newborns may raise risk for autism

Brain damage in premature newborns may raise risk for autism BY LAURA GEGGEL / 1 APRIL 2013 Low-birth-weight babies with injury to their white matter — the nerve fibers that connect different brain regions — are more likely to be diagnosed with autism as adults, says a two-decade study published 11 February in the Journal of Pediatrics1. The findings are part of the Neonatal Brain Hemorrhage Study, an effort that began in the mid-1980s. Researchers used cranial ultrasounds to analyze the brains of more than 1,000 newborns weighing between 500 and 2,000 grams (1.1 pounds and 4.4 pounds). They performed these ultrasounds within the first few days of the infants’ lives. Radiologists determined whether the babies had any brain damage, including hemorrhages, ventricular enlargements or lesions in brain tissue. The researchers then assessed some of the participants for autism 21 years later. They found that infants who have any kind of white matter injury are three times as likely to develop autism as those also born at a low birth weight, but without any brain damage. In particular, infants with enlarged ventricles — spaces in the brain filled with cerebrospinal fluid — have a sevenfold increase in autism risk compared with controls. Enlarged ventricles signal white matter loss, says lead investigator Tammy Movsas, medical director of Midland County Department of Public Health in Michigan. “There’s been a lot of controversy among the public and among researchers about whether autism develops in utero or after birth,” says Movsas. “This study gave us a look, at least in a low-birth-weight population, that the risk factors for autism start very early on.” Ultrasound analysis: Movsas points out that not all infants with white matter injuries develop autism, and says her group isn’t suggesting that doctors screen all prematurely born infants for white matter abnormalities. Instead, she says, the study calls for researchers to investigate the link between white matter injuries and autism. Other scientists say the findings aren’t conclusive, pointing to the study’s small size. Although the initial study included 1,105 babies, only 14 were diagnosed with autism as adults. It’s possible the 14 participants developed autism because of another reason, says Charles Nelson, professor of pediatrics at Harvard Medical School and Boston Children’s Hospital, who was not involved with the study. “[It] could be attributed to the prevalence in the general population, and have nothing to do with being low-birth-weight or having ventricular enlargement,” Nelson says. When the study’s participants turned 16, the researchers screened 623 of them for autism2. (The others had died, been adopted or lost touch with the researchers.) When the participants turned 21, the researchers invited back 189 of them — 70 of whom had screened positive for autism and 119 who had screened negative. This was one of the precautions they took to ensure that the sample is representative of the larger group. The researchers confirmed the diagnosis in 14 people (11 from the positive and 3 from the negative group) using the gold-standard assessments, the Autism Diagnostic Observation Schedule and the Autism Diagnostic Interview-Revised. Of the 14, 7 had abnormal ultrasounds, and 4 had enlarged ventricles. Of the remaining 175 participants called back, 41 had abnormal ultrasounds, including 8 with ventricular enlargement. There are a number of reasons an individual could have enlarged ventricles, including hydrocephalus, a buildup of fluid in the ventricles that puts pressure on the brain. But the researchers say that often it’s because the infants have less white matter than do their peers with typically sized ventricles. “The ventricular enlargement represents the fact that the white matter of the brain has less tissue to it, and therefore the holes in the brain look larger,” Movsas says. Hemorrhages do not increase the risk of autism, and neither do tears in the brain tissue in the absence of ventricular enlargement, the researchers found. Weighty risk: Two studies within the past five years have hinted that brain damage in preterm infants is a risk factor for developing autism. The new study uses more rigorous diagnostic tests than the other studies do, says Michael O’Shea, pediatrics professor at Wake Forest University Health Sciences in Winston-Salem, North Carolina, who was not involved in the study3,4. It’s also unusual for a study to follow children from infancy to adulthood, but assessing people for autism at age 21 has its advantages, Movsas says. Although many children are diagnosed by age 3, the average age of an Asperger syndrome diagnosis is 10 years. “By screening for autism at 16 and assessing for autism at 21, we were able to capture all children who developed autism and not worry at the time of assessment that some of them may still develop it later on,” she says. Low birth weight itself is a risk factor for autism, but it’s not clear why this is the case. It is important to learn what increases the risk for autism more: low birth weight or younger gestational age. A number of babies born small don’t gain weight easily, says Alan Leviton, director of the neuroepidemiology unit at Boston Children’s Hospital, who was not involved in the study. “The growth-restricted babies are at increased risk for a number of problems,” Leviton says. “One wants to be able to say that most of what we see [in terms of autism] is not due to that.” The researchers may soon be able to answer this question. They are looking at a variety of risk factors using blood samples and magnetic resonance imaging in another cohort of more than 1,000 premature infants born between 2002 and 2004. References: 1: Movsas T.Z. et al. J. Pediatr. Epub ahead of print (2013) PubMed 2: Pinto-Martin J.A. et al. Pediatrics 128, 883-891 (2011) PubMed 3: Johnson S. et al. J. Pediatr. 156, 525-531 (2010) PubMed 4: Limperopoulos C. et al. Pediatrics 121, 758-765 (2008) PubMed https://www.spectrumnews.org/news/brain-damage-in-premature-newborns-may-raise-risk-for-autism/