Te dashur miq - MAASBesa po fillon nje fushate per ngritje fondesh per Katerinen. Katerina (Kate) Zguri u lind ne 17 mars 2009 ne Shqiperi. Ajo ishte nje foshnje e shendetshme, se ciles i pelqente muzika si dhe te luante me femijet e tjere. Fatkeqesisht tani Katerina vuan nga nje semundje neurologjike e panjohur, shenjat e para te se ciles u shfaqen pasi ajo mbushi 2 vjec. Pas nje vaksinimi rutine, ajo filloi te ndieje mpirje te gojes, humbje te shpeshta te ekuilibrit, dhe lodhje. Gradualisht simptomat u perkeqesuan dhe tani ajo nuk mundet me te flase, te ece apo dhe te buzeqeshe. Gjate ketyre 2 viteve familja e saj eshte perpjekur deshperimisht per te gjetur nje sherim, por deri tani kjo nuk eshte arritur. Mjeket ne Shqiperi nuk arriten ta diagnostikojne dhe te gjejne shkakun e semundjes se Katit, gje qe e shtyu familjen e saj te ndermarre nje udhetim te mundimshem e te gjate neper spitale dhe mjeke te ndryshem ne Europe dhe Amerike ne kerkim te nje kurimi qe do t’i kthente Katit fjalet, te ecuren dhe buzeqeshjen. Prinderit e saj, Dhimiter dhe Nerida, kane shfrytezuar te gjitha kursimet e jetes se tyre per te mundesuar vizitat nga mjeket me te mire neper spitalet e Greqise, Zvicres dhe Italise. Lufta per te gjetur nje kurim te pershtatshem ka patur pasojat e veta dhe tek vajza e tyre e vogel, pasi deri tani ajo ka zhvilluar mjaft testime dhe analiza dhe akoma nuk eshte bere e mundur te gjendet nje kure. Pas kalvarit 2 vjecar dhe vizitave te shumta neper spitalet europiane, familja u keshillua ta sjelle Katin ne Children’s Hospital ne Boston, si nje nga spitalet me te mira pediatrike ne bote. Kati eshte paciente e Children’s Hospital qe prej muajit korrik, por semundja e saj akoma po mbetet nje enigme. Ne si shoqate kemi vendosur te ndihmojme familjen e vogelushes dhe po ndermarrim nje fushate per ngritje fondesh per familjen. Por si gjithmone kemi nevoje per mbeshtetjen e komunitetit qe ka qene shume e rendesishme ne fushatat e meparshme. Cdo shume qe do mund te dhuroni mund te ndihmoje prinderit e Katit meqe ata nuk munden te punojne dhe kane shpenzuar te gjitha kursimet e tyre. Momentalisht ata po banojne ne Philoxenia House, ne lagjen Jamaica Plain, por ky eshte nje strehim i perkohshem. Se shpejti do t’ju duhet te kerkojne nje strehim te ri, megjithese nuk kane kurrfare te ardhurash per te mbuluar shpenzimet e perditshme. Katerina po vizitohet nga mjeke te ndryshem dhe duke pare perkeqesimin e situates, prinderit e saj mendojne se do t’ju nevojitet edhe nje makine. Per me teper prinderit e Katit po presin nje femije qe duhet te linde ne fillim te nentorit, gje qe e ben te veshtire qe nena e Katit ta mbaje ne krahe per ta shoqeruar ne spital. Ne kemi krijuar një faqe në internet nga ku secili prej jush mund te dhuroje aq sa ndjen per t’i lehtesuar sado pak dhimbjen dhe stresin Katit dhe familjes se saj. Ju lutemi klikoni në linkun e meposhtem dhe ndiqni udhëzimet. Per te bere donacion per Kate -- icanhelp.maasbesa.org/ Gjithashtu, lutemi te mos hezitoni të na kontaktoni nese hasni ndonjë problem me procesin e dhurimit. Ju faleminderit shume per ndihmen tuaj per Katerinen dhe familjen e saj. --------------------------------------------------- Dear friends - MAASBesa is organization a fundraising campain for Katerina. Katerina (Kate) Zguri is a four-year-old girl from Albania who suffers from a very rare form of neurological disorder. The first signs appeared when she was two years old. Kate was continuously losing her balance and later experienced muscle and spasm seizures. For the last 2 years, her family has been on a desperate search for a cure. Doctors in Albania were not able to diagnose and find out the cause of Kate’s disorder. Thus, the family began their difficult journey traveling from one hospital to another in various European countries. Her parents, Dhimiter and Nerida have gone far beyond their means using all of their life savings to make sure Kate was seen by some of the top doctors in Europe and the United States. The search for a cure has come with the price of their little 4-year-old daughter undergoing hundreds of tests and procedures with no answers and improvement in her condition to this date. Kate was hospitalized in Greece, Switzerland, and recently in Italy. After the two-year journey traveling from European hospital to the other, Kate was referred to Boston Childrens Hospital in Boston as one of the top pediatric hospitals. Although a patient at Childrens Hospital in Boston for the past two months her diagnosis still remains an enigma. Kate’s condition continues to deteriorate and she can no longer talk or walk. We are reaching out to ask for your help. Any donations for Kate would make a big difference, since neither Dhimiter nor Nerida are allowed to work in the USA, and they have exhausted all of their savings. They are currently living at Philoxenia house in Jamaica Plain, but this is a temporary housing solution. Soon they will be looking for a new place to stay while they have no money for their living expenses. Kate is going back and forth to the hospital for more tests, and given her grave condition the parents feel a car is a necessity for them. Moreover, Nerida and Dhimiter are currently expecting another child who is due in early November. This makes it harder for Nerida to carry Katerina in her arms -- especially without a car. MaasBesa is organizing a fundraising for Kate. We have created an online page from where you can easily donate to help Kate and her family. Please click on the link below and follow the instructions. To donate for Kate please visit -- icanhelp.maasbesa.org/ Please do no hesitate to contact us should you encounter any problems with the process. Thank you very much for your support for Kate and her family.
Posted on: Tue, 29 Oct 2013 23:17:37 +0000
Trending Topics
Recently Viewed Topics
© 2015