O nama/About us

Ovo je moje BLAGOMOJE DETE SA POSEBNIM POTREBAMA moje najveće blago Ukratko: Rodila se 7 nedelja pre vremena, ostala bez kiseonika posle rođenja (HIE - hipoksično ishemična encefalopatija - oštećenje mozga usled nedostatka kiseonika), dobila bakterijski meningitis i sepsu sa samo 7 dana. To je ostavilo mnoge komplikacije: krvarenje u mozgu II/III stepena, proširenje moždanih komora (ventrikulomegalija), manji obim glave (mikrocefalija), povećan tonus mišića (hipertonija), usporen proces mijelinizacije u mozgu, strabizam, epileptiformne promene EEG-a i najnovija dijagnoza Spastična parapareza (podvrsta cerebralne paralize). Nije sve baš tako strašno, moje blago hoda samostalno od 2,5 godine, i još uvek uči da priča. Zove se Valentina, i ima 8 godina. Ovaj blog su priče iz života deteta sa posebnim potrebama, i svim izazovima koje život u Srbiji donosi samohranoj majci deteta ometenog u razovoju.
MY SPECIAL NEEDS CHILD my greatest treasure She was born 7 weeks premature, had HIE (Hypoxic ischemic encephalopathy) brain damage due to perinatal asphyxia (lack of oxygen right after birth), than had bacterial meningitis and sepsis when she was only 7 days old. That caused also: bleeding in the brain (that led to PVL), enlargment of brain ventricles (ventriculomegaly), smaller head circumference (microcephaly), high muscle tone (hypertonia), delayed myelination in the brain, strabismus, Epilepsy-like changes of EEG, and her final diagnosis Spastic Paraparesis (type of Cerebral Palsy) and Moderate mental retardation. It's not all that bad as it may seem, my treasure walks independantly since 2,5 years old, and still learning to talk. Her name is Valentina, and is now 8 years old. This blog is a set of true life stories of a special needs child, all the challenges that living in Serbia brings to a single mom raising a special needs child.