In Georgia the ill and the old are stuck only with themselves. It is very difficult to handle an illness or any disability on one’s own, additionally, solitude together with handicap puts up barriers that cannot be overcome on one’s own. Camillian Fathers have been taking care of such people for a few years. They have two special cars and two teams of reliable people who pay a visit to the houses of the needy. They help them in many ways. The range of care is dependent on a needy person’s health condition. Most often it is cleaning the house, bringing a warm meal, doing shopping but also giving medicines, wiping bedsores, changing incontinence pads, replacing a dressing, bathing, etc. By helping Camillian Fathers in Tbilisi we want to broaden the range of help.
It is widely known that the more possibilities children have, the better their development is. Unfortunately children in Georgia do not have the same possibilities as our Polish children do. The aim of the project is to organize summer camps for children and alternatively school supplies for school learners from poor families coming from Georgian villages. Young volunteers from Poland and other European countries will take care of them at these camps. It is difficult to organize a few centers but the camps are situated in 2 places named exactly the same – Chizabawra. Read more >
The value of the equipment which we provided exceeded PLN200 000 and the cost of transport and repairing amounted to PLN 15 000. It was transported to Georgia as a gift from people not only from Poland but also Germany. Those included, among others, dozens of wheelchairs of various types, rehabilitation standers, crutches, hospital beds, anti-bedsore mattresses ,standing frames and many more. Moreover we sent a large number of toys which went to kindergartens in poor parts in Georgia.
Thanks to TVP3 Rzeszow and Radio Rzeszow we could show that a lot of good and help come from the Podkarpacie region to far-away Georgia , that the inhabitants of our region want to help and get involved in different ways, whether through volunteering or financial support. The most important thing is that we work together above divisions and boundaries. The Camillians delivered and distributed the equipment to the needy in few weeks time, what gives us a lot of joy and satisfaction and certainty that such actions are needed and good. But this would not have been possible without the help of the Donors, thanks to whom we have collected equipment and funds for its transport. The next collection of equipment is the answer to the still existing needs of the disabled in Georgia.
From January to May we will transport rehabilitation equipment given to us from different parts of Poland and Europe and at the turn of May and June 2018 ,we plan to transport it to Georgia. The cost of the entire project is about PLN 20 000. Therefore, we are looking for the donors who will help us carry out and complete the action through supporting us with any amount. We ask from the bottom of heart for help in form of monetary donation. In this way you will join the elite group of Benefactors of ProSpe Foundation and you will have a specific contribution to the Good that changes the world. It will became an investment for the future offering the profits that cannot be measured by any statistics. The payment will be ordinary human gratitude , genuine smile and a quiet ‘madloba’ which means ‘thank you’ and the only measure will be the heart. This will give us the strength to act and help the needy and to build the Good World ,which is our common Home.
1 km- 5 PLN
55 pre-school and school children attend Grandma’s House and classes are conducted three times a week. The annual cost of maintenance an afterschool club is GBP 10,000 which is GBP 850 per month, and one day for one child is GBP 1,50. As part of this amount, children are provided with the help of pedagogues, psychologist, educational aids, books, additional classes, a modest meal, and thanks to Polish missionaries – Camillian fathers, they can learn about our culture and correspond with Polish children.
Helping these children, we give hope … hope for a better future, for a good job, for a decent life, for developing passions and talents, for the realization of dreams. We should not let them stay at the refugee village and live without prospects standing on the threshold of adulthood. They deserve success as well as our children, so let us share what we have to give them a chance for a better life. At the start, they have experienced a lot of evil, cruelty and poverty. Unfortunately, parents often cannot cater for their basic needs, not to mention education at a higher level. That is why we ask for support and help.
Help children from the Grandma’s House and take on a long-distance adoption of one child by paying a monthly fixed amount of GBP 5, GBP 11 or GBP 21 for half a year or a year. You will provide the children with the opportunity to develop and educate, give them a sense of security and the certainty that there is someone who opened their hearts to the needs of others by sharing the good that a fate gave to them.
Five people are currently involved in the project. We want to tell you the story of each of them and ask for financial support, which will be entirely intended for further rehabilitation.
See how we can help them in action -> „Give a kilometer”
With the help of very friendly neighbors and one of the Georgian companies who got to know the history of Vaża, a small building was constructed. The building is currently in a stark condition. It is unplastered, the walls and partition walls are not sectionalized and the floor is only provisional. There is no equipment, no heating, no stove. There is no water in the building. All the „home” equipment consists of two beds, a sideboard, several cabinets, a table and several chairs. The family already lives in this building, however, their financial situation prevents any action from being completed. The family receives 200 lari (approx. PLN 340) of social assistance and 100 lari (approx. PLN 170) for a boy’s pension.
Since year Nikolosi has been using free transport and therapy at the Saint Camil Centre. The center provides him with therapy with a physiotherapist Nino and occupational therapy. Nino tries to strengthen the boy’s hands and correct his posture so that the curvature of the spine does not progress. After one year of therapy, the boy’s mom sees some progress. When Niko feels good he is able to get out of bed himself, he also tries to lift himself up and grab the toys. Due to the spastic hands it is very difficult for him, but he is brave and does not give up. The occupational therapy is very important for the boy. The therapist through various games, plays and using interactive toys and therapeutic aids activates the boy and teaches him basic communication.
(on the left photo of Koba and his mother)
Koba, although he is an 18-year-old boy, looks like a small child because of the illness. He suffers a lot, he cannot eat any solid food (mother usually feeds him semolina or mixed soups). The boy’s body is completely deformed. To a large extent it is the fault of neglect in the rehabilitation and care for the boy. Koba used rehabilitation only in early childhood, later he stayed at home for years, taking only medicines for epilepsy. When we met him, we could not remain indifferent to his immense suffering.
In the centre of Camil, Koba benefits from rehabilitation and therapy with a speech therapist. Due to the very advanced level of disability of the boy, constant rehabilitation and care of specialists is needed. The most important thing now is to postpone the progression of the disease and bring relief to Koba. Koba’s mother noticed that the rehabilitation contributed to the fact that very tense muscles of the boy relax somewhat, especially when boy lies. With the help of mother, he can slowly stretch his right hand, which has always been constricted. During classes with a speech therapist who massages the face of the boy. This is to improve swallowing and chewing. Mother of Koba is very happy with the effects of therapy. She sees a significant improvement, Koba chokes less and less and can swallow with greater ease. Rehabilitation in the Center of St. Camil also fulfills a socializing role. The centre is the only place where Koba has the opportunity to meet his peers. He stays alone with his mother all day, so contact with other people is invaluable.
Karen lives with parents, grandmother and younger sister Lisi. The boy’s mother looks after the children and his father has a part-time job. The Karen’s pension, the grandmother’s pension and social assistance are regular income, which gives a total of approx. PLN 800 for a family of five per month.
Karen’s rehabilitation gives amazing results. Just a year and a half ago, Karen could not walk on his own and he’s doing it today. Systematic exercises have given very good results. Rehabilitator Laura, however, has a cautious approach to the successes in development of Karen. She notices that if her charge does not attend classes for 2-3 weeks, for example due to sickness or holidays, he moves much worse. We are now in a very important moment. We have the first successes but they are still fresh so that it will be easy to lose them. Please, support Karen.
It is impossible to travel to the Rehabilitation Center with public transport using the girl’s current condition. Sofo was in a very bad condition, she started rehabilitation from basic exercises. Step by step, the rehabilitationists teach her new, correct movement patterns, correct posture, work on strengthening the spine and muscles. To our great joy, thanks to the constant care of the neuropathologist, Sopo began to respond positively to epilepsy medication, which makes the attacks rarer and less severe, and also the very embarassing salivation and sleep disturbance stopped. It is very important to continue the rehabilitation and the treatment process for as long as possible, so as not to lose the successes achieved and constantly improve the quality of life of Sopo, thus bringing relief to her great suffering. We also observe with great satisfaction the progress in communicating with the girl. Sopo does not speak , but she is able to answer basic questions through facial expressions or eye movements.
We are asking for financial help so that we can take care of Sopo.
tłum.: Karolina Masłyk