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News from Buinitskaya Ksenia

Here is some good news from Ksenia Bunitskaya family. Recently we've received a letter from her parents:
"We have inquired in foreign clinics for antibody therapy. And here we've got a bill from the Greifswald clinic (Germany) with the amount of 143,400 € for the treatment. Accordingly we plan her further treatment in Greifswald. It is much less than the amount claimed from the Israeli clinic! We are still asking you to support us with this brave project!"
 
 

Mission "Adeli"

Dear friends,
A lovely young lady Asya applied to our Fund for help. She is a mighty person, a young mother and also a helper to those in need, although she is confined to a wheelchair. Here is her story:
"My name is Asya. I am 23 years. I am a versatile person. I love to draw and do arts and crafts, I help saving cats and organize trips for disabled wheelchaired people to concerts of popular artists. I love traveling. And I also have a three-year daughter.
 
My life would be completely normal if I were not confined to a wheelchair. Because of a vaccination done when I was 7 months I have high muscle tone (spasticity), which can only reduce by physical exercises, massage and horse riding. I can't walk, and take care of myself because of the spasticity. My family and friends help me with all my moves.
 
Now I have a chance to significantly improve my condition. In the clinic "Adele" (Slovakia) they successfully treat people with this kind of disability, where good results are achieved not only children but also by adults. The course of treatment and accomodation cost 8920 euros. This amount is not high, but for me it's impossible to pay. That's why I'm asking you to help me fundraise the needed sum and make a big progress!
 
I hope you can help me with it! Thanks a million in advance to all!!. "
 
We thus ask everyone to support this beautiful girl! Thank you for every help!

Cherven welcomes guests again

 

For quite a long time there were no volunteers to come to Cherven children's orphanage. But recently 2 sisters from Ireland came for a 4-week visit to the children.

There are a lot of impressions, but let's see what the girls say:

"With no previous experience of working with children with disabilities and qualified only in hugs and kisses we were extremely nervous about what was to come, but as always we took it in our stride and with big smiles on our faces we stepped into a place that we would soon come to love!

Unit 6, a palliative care unit where the children have severe mental and physical disabilities with some children fed through nasogastric tubes was the first unit we visited. Although the prognosis for most of the children is not good, a simple walk around the grounds, a trip to the multi-sensory room or balloons and bubbles can really brighten up their day and bring life back into the unit. The moment a child smiles at you or uncontrollably laughs when you tickle them with a feather gives you goose bumps. It really is the small things that make such a difference.

Another unit we worked in was Unit 5, made up of young children with mental and physical disabilities. Some can walk and some are confined to their wheelchairs. One particular boy Victor, has Downs syndrome and as a result, a heart defect. Just a couple of months ago, Pasha another boy with the same condition passed away as a result. Victor is the most intelligent little boy in Unit 5 and when you watch him the realisation that he is a ticking time bomb is extremely hard to swallow.  We spent our mornings bringing all the children on walks around the grounds and bringing groups to the multi-sensory room both of which they loved.

Unit 4, also known as the crazy walkers, are abled-bodied kids who have more severe mental disabilities. At the beginning we avoided this unit because the bad weather meant they were confined to their unit. However, once outside lots of the children enjoyed interacting. We spent time drawing with chalk, playing with balloons that kept bursting because of the heat, bubbles which wouldn’t work because they shook them and loud music for dancing. They loved it, we only wish we had had the opportunity to do it more often!

Unit 3 was hands down our favourite unit. It is made up of older girls 15-25 with physical or mental disabilities. One major issue is that this unit is located on the third floor where the lifts have been broken for over a year and although now fixed have not yet been certified. The girls had not been outside in a year and a half. One of our favourite days was our picnic in the garden where we brought fifteen of the girls outside and sat under the trees listening to music, painting nails, applying stick-on tattoos and eating sweets, chocolate, and crisps for hours. The happiness of finally leaving their unit was palpable and the effort of carrying the girls in wheelchairs down a flight of stairs rapidly disappeared. We spent hours upon hours colouring with the girls in their unit colouring over 300 pictures during our time there.

The ‘older boys and girls’ were another group that we loved to spend time with, they were Units 8, 9 and 11, able-bodied with slight mental disabilities. We spent hours and hours outside playing tennis, table-tennis, bubbles, chalk, Frisbee, and the cone game. One of the nicest things about this group was their ability to share and play with each other. We brought them to the cinema and had a disco for them, where there were games for them to play too. We soon realised that they may like dancing but there is nothing they love more than to play games where there are chocolate coins at stake. We were also able to do an arts and crafts session with the older girls where we made a poster of all their hand-prints not to mention the thousands of stickers then used to decorate their names that we had written out for them. We also had the opportunity to have tea and biscuits in Unit 8. As with most of the activities we pre-organised there was no water to actually make tea, although it did come back after an hour. As two Irish girls we were more than willing to drink tea allowing the boys to show us their photos albums, drawings and their prized possessions.

There are no words that can truly describe what it is like in Cherven orphanage. There are no words to describe the feeling when you interact with the kids. Such small things like bringing a child for a walk or playing music or buying ice-cream can really bring such happiness. Many hailed us a ‘brilliant’ ‘super’ and ‘amazing’ for giving up our time to volunteer in Cherven and yes it is emotionally draining, physically exhausting and at times heart wrenchingly sad, but every single second is worth it! The truth be told it is the most worthwhile, rewarding experience we have had yet!

Aoife & Rachel"

Check out the photos in the album below

Червень снова принимает гостей

 

Довольно долгое время ирландские волонтёры не приезжали в Червенский детский дом-интернат. Но недавно две сесты из Ирландии приехали к детям с долгим визитом, в целых 4 недели.

 

Впечатлений очень много, но давайте посмотрим, что говорят сами девочки:

 

"Не имея опыта работы с детьми с ограниченными возможностями, но полные надежд и любви, мы переживали по поводу того, что нас ожидает впереди, но, как всегда, с улыбкой вошли в место, которое в скорости полюбили всем сердцем!

6-ая группа, где в основном проживают детки с серьезными умственными и физическими особенностями – это первое, с чем мы познакомились в интернате. Хотя прогноз для большинства детей далеко не позитивный, но, тем не менее, простая прогулка по территории, занятия в сенсорной комнате, воздушные шары и пузыри могут действительно скрасить их день и привнести жизнь что-то радостное. Те волшебные моменты, ребенок улыбается вам или задорно смеется, когда вы щекочете их пером, очень волнующие. На самом деле это та малость, которая даёт большую ​​разницу.

Ещё мы приходили в группу 5, где живут маленькие дети с умственными и физическими недостатками. Некоторые из них могут ходить, а некоторые прикованы к коляскам. Мы познакомились с ребятами, с красавчиком Витей, с синдромом дауна и тяжёлым пороком сердца. Виктор самый умный мальчик в группе 5, и когда смотришь на него, то осознание того, что его жизнь – это как бомба замедленного действия, не даёт покоя. Обычно, мы проводили первую половину дня, вывозя детей на прогулки на улицу или в сенсорную комнату, что детям очень нравилось.

Группа 4, - это дом для работоспособных деток с более серьезными психическими отклонениями. Вначале мы не навещали эту группу, потому что плохая погода означала, что дети, ограниченные стенами небольшой игровой комнаты, могут быть легко возбудимыми. Однако, как только погода улучшилась, мы отлично играли на улице, наслаждаясь их компанией. Мы рисовали мелом, играли с воздушными шарами, баловались с мыльными пузырями, танцевали под громкую музыку.

Группа 3 – без сомнения наша любимая группа. Она состоит из девочек от 15 до 25 лет, у которых физические или умственные недостатки. Одной из основных проблем является то, что этот блок расположен на третьем этаже, где лифты не были запущены долгое время. Хотя в настоящее время они отремонтированы и сданы под использование. Из-за этого девочки выходили на улицу не чаще одного раза в год. Самым запоминающимся стал день, когда мы вывели девочек в сад на пикник: мы сидели под деревьями, слушали музыку, ели сладости, шоколад и чипсы, играли. Счастье девочек было безграничным, что несомненно затмило нашу нелёгкую работу по спуску их с третьего этажа. Много времени мы проводили за рисованием, а ещё наделали 300 фотографий.

Также мы любили проводить время со старшими мальчиками и девочками из групп 8, 9 и 11. Большинство из них трудоспособны, однако имеют некоторые умственные особенности. На улице мы организовывали игры в большой теннис, настольный теннис, играли с мыльными пузырями, рисовали мелом, играли в фризби. Приятно видеть, что ребята делятся друг с другом игрушками и играют вместе. Мы сводили их в кино и на дискотеку. Там с ребятами организовывали игры с призами, но больше всего им нравится танцевать. Мы также организовали занятия по декоративно-прикладному искусству со старшими девочками, где мы сделали плакат отпечатками рук всех детей, а также тысячами наклеек, которыми они украсили свои имена. А ещё мы устроили чаепитие для ребят в 8-й группе. Как и большинство мероприятий, всё было спланировано заранее, но когда мы пришли, то воды в интернате не было, и нам пришлось ждать целый час, пока она не появилась. Мы пили чай, ребята показывали нам свои фотографии, рисунки и их ценные вещи и много болтали.

Трудно подобрать слова, которые действительно могут описать, что это такое, Червенский детский дом. Трудно подобрать слова, чтобы описать это чувство, когда вы общаетесь с детьми. Такие мелочи, как прогулка или музыка или мороженое действительно могут принести такое счастье детям. Многие говорили нам: "супер" и "здорово",  что мы уделили наше время Червеню, но это тяжело, это - эмоционально осушение, это физически изнурительно, и порой сердцу мучительно больно, но каждый миг, проведённый там, стоит того! По правде говоря, это самый бесценный опыт, который мы когда-либо переживали!

Ифа и Рэйчел"

Больше фото внизу в альбоме

Sofia Markevich is looking for you support

Dear friends,
 
We are pleased to share the news of Sophia Markevich! The girl is making a good progress, but she needs your support once again.
 
Sofia's mom says:
"In December 2015 and April 2016 Sofia did a course of treatment in the neurological center" Prognoz ", St. Petersburg. After the two rehab courses in St. Petersburg, my daughter finally started speaking some words, building short sentences of three words. Although Sofia can not pronounce some letters yet, we're working on it. We hope to go on the next trip scheduled for September 30, 2016. The cost of the enxt course is 4,400 Belarusian rubles (44 million in old currency). So we ask for your help, as we are unable to pay for the treatment ourselves. Sonia has a good chance for recovery. So please, help us make a difference for our little angel. A huge thank you to all who will respond to our request. "
 
Banking details for the treatment of Markevich Sofia
opened in a branch of OAO ASB Belarusbank 413/07, Lida, branch code 696
Belarusian rubles - № 000069, transit account 3819382104109
Euro - № 000020 transit account 3819382105717
 
EasyPay No: 31751847
Thanks a million to all and one!

Please support Olya Listratenko

My name is Irina and I’m the mother of Listratenko Olga, from Cherikov, Mogilev region.

I have never asked anyone for help before, but now I have no other choice. Our girl is already 14 years old. She has cerebral palsy, spastic diplegia. All these years we have been working hard to improve our daughter’s health, so that she could be more independent. This is our dream. Olya had a lot of the surgeries (11 in total) and I just not tell, how much pain and suffering she’s been through all these years. All Olya’s life is constant rehabilitation, operating, treatment, recovery. And we have invested all we had into it. And now we are out of funds, that’s why we need your support.

We have recently returned from a trip to China Clinic for treatment and rehabilitation. And thank God, she made a huge progress: she strengthened back, neck muscles, learned to crawl, to walk without splints with a walker, to sit with straight legs. For us, these are Olympic achievements! But most importantly, the chief doctor of the clinic has encouraged us to come back to the clinic at the end of September 2016, to consolidate the improvements, because as the girl matures and there won’t be much time left to help her. The treatment will take 2 months and the cost is $ 8,000.

We are asking all caring people to support us with anything! Every little helps and we'll be grateful for any amount you can contribute towards Olya’s better quality life!!!

The banking details are in the album under the story!

Rehab for Amelia

My name is Alesya Matveychik and my daughter’s name is Amelie (born she was 28.07.2014)

Diagnosis: CP,  spastic plegia more pronounced in the right limbs, with severe motor impairment. Convultion syndrome in remission stage since March 2015

Amelia has s good rehabilitation potential, but we need your support as we cannot cover the cost of the rehab due to the poor financial situation as we constantly go on rehabs and all the money goes for it.

For the rehabilitation in "Spring" center of St. Petersburg, we need 200 thousand Russian rubles (about $ 3,000) before the 4th of July.

I’m kindly asking you to help Amelia have a better quality life, have a chance. Thank you for all .....

Charity accounts opened in branch 402- Volkovysk, Sovetskaya, 20, UNP 500054844, MFO 152101689

-Bel rub-Transit account 3819382100569 for the charity account 000038 in branch 402, unlimited

- US dollars -Transit  account 3819382105607 for the charity account 000049 in branch 402, unlimited -- - Euro-Transit account 3819382105607 for the charity account 000013 in branch 402, unlimited

-Russian Ruble-Transit account 3819382105607 for the charity account  000020 in branch 402, unlimited

Irina Povroz needs a surgery

Irina’s story!

Diagnosis: The speech development disorder; dysarthria; mental retardation; Cerebral Palsy of average degree, Tonic-clonic form. Ira was born on 14.12.2007, at the 36 weeks of pregnancy term. The ultrasound at 35th week showed that the child had lack of oxygen. The doctors decided to induce labor, stimulated, and on the second day after stimulation our long-awaited girl was born! In the hospital everything was ok. But a month later we noticed that Ira was developing very poorly. For the next 2 months she didn’t show any singes of proper development, not even trying to hold her head up. The ultrasound of the head showed that Ira had hydrocephalic syndrome. So we started active treatment at home and in hospitals. At 6 months Ira began holding her head, 7 sounds appeared, she smiled at us, tried to pull the handles to sit down, as if everything was fixed. But at 8 months of age in the hospital Ira was given a large dose of diuretics and she got worse. Ira deteriorated to the level of a one month old child ... We went to the center "Mother and Child" in Minsk, and there Ira was literally put on her feet. Gradually she began to smile, then there appeared the first words. Since then our baby already had about 10 words: Mom, yum-yum, woof-woof (we had a dog) dad, uncle .... We were happy to hear every new word and continued to treat and strengthen her physically. At 1 year and 3 months we were on a regular course of treatment in a hospital, there Ira got ill with high fever, had some kind of infection (we do not know what it was). But having returned home, we noticed that she lost all her words, every day we were trying to remind them, but our girl was silent ... In 1 year 9 months she was diagnosed with CP. It was another terrible blow ... We knew that tears of sorrow wouldn’t not help. Again, we fought for the health of our girl. We were constantly undergoing treatments in different hospitals: injections, medications, physiotherapy, massage, exercise therapy, electrical treatments, laser, acupuncture, speech therapist, psychologist, music lessons, etc. ... But there was no response. She was on rehab courses in Minsk; St. Petersburg; Sanatorium "Belarus" in Druskininkai; 3"Dolphin" courses. The treatment gave results- Ira learned to walk, got stronger physically, began to understand more, but unfortunately, she is lagging behind in development and cannot speak.

Now Ira is 8 and a half years. This is the time when kids go to school, but health does not allow her to sit with the other children at the desk. We do not despair and look for possible ways of treatment. We did courses of treatment and rehabilitation in China, Foshan "hospital maternal and child", in 2014 for 4.5 months and in 2015 - 9 months. After the assessment in China Ira was diagnosed with atrophy of the frontal lobe brain petals that are responsible for speech and intellect. On 15 November 2015 in China's Urumqi, Ira had a surgery for implanting stem cells (in the head). Half a year passed since the surgery. Stem cells are well settled and began to function. As per advice of doctors, we are constantly loading Ira with daily sessions with a psychologist, speech therapist, motor skills, dancing ....

Those results we saw encouraged us and inspired to further action.

For Ira to live without constant assistance, perform a simple self-care skills, communicate with others, we need to take the next step. And this step  is stem cells (second implanting). We understand that without it we won’t be able to restore brain function, develop memory, attention, thought, speech.

We ask you, our dear friends, PLEASE HELP US !!! We really want to see our Ira smart and independent!!!!

The operation is scheduled for July 2016.The amount to be collected 12000$

We need to continue the treatment, but the family money is not enough for permanent treatment courses of our girl ... Please help us heal our baby! We won’t cope on our own ... Thank you to everyone who will respond and will not pass by our troubles!

Here are the banking details to help Ira:

Belarussian rubles - charity account number 000053.

Bank: OJSC "Belarusbank" branch 413/07 JSC "Belarusbank", Sovetskaya Street, 17, Lida, Belarus. Transit account 3819382104109

US Dollars - charity account number 000075.

Bank: OJSC "Belarusbank" branch 413/07 JSC "Belarusbank", Sovetskaya Street, 17, Lida, Belarus, Transit account 3819382105717

Russian Rubles - charity account number 000019.

Bank: OJSC "Belarusbank" branch 413/07 JSC "Belarusbank", Sovetskaya Street, 17, Lida, Belarus. Transit account 3819382105717

Fundrasing for Ksenia Buinitskaya

 

We are asking you to help save our child - 3-year-old daughter Ksenia.

 

Like everyone else, we just lived, were happy and never thought we would have to seek help of strangers. Only your humanity and mercy is the only way to save our baby !!!

My daughter was born on time, healthy and strong. She only had flues, all vaccinations are done on time. Cheerful, smiling, lively, sociable and very inquisitive, our girl was going to go to kindergarten. No signs of trouble, but one day Ksenia had pain in her leg, there was a slight limp, just a week after she was complaining of unbearable pain. We went to the emergency room, where she was diagnosed with a preliminary diagnosis - children's arthritis. We went for treatment in the 4th Children's Hospital in Minsk. A full examination on abdominal ultrasound revealed a tumor of the right adrenal. Then she was sent to the State Oncology Centre Borovlyany where on the August 14, 2015 Ksenia got terrible diagnosis - stage IV neuroblastoma of the right adrenal with metastases in the para-aortic lymph nodes and bone marrow. It was like a death sentence. CANCER. Our world collapsed in an instant ... How could this happen to a perfectly healthy, cheerful and always active child?

Faced with such a grief, our life has changed dramatically, divided into "before" and "after." The meaning of our lives was to save her daughter, at any cost!

Ksenia had 6 chemotherapy blocks for tumor removal operation, MIBG-therapy, high-dose chemotherapy with auto transplant of peripheral stem cells.

The treatment gave a positive result, which confirms the conclusion of MIBG-scintigraphy, traversed 31.05.2016g.

Our treatment approved in Belarus is almost completed. But in countries such as Germany, England, Israel and the United States for patients with positive dynamics in the underlying protocol treatment, antibody therapy, they have a practice, which helps the body to completely destroy single cancer cells, preventing the risk of recurrence, which is common for the disease.

We contacted several foreign clinic for antibody therapy. Israeli hospital Schneider agreed to take us for the treatment. The total cost for treatment in the hospital is 355 700 $.

We understand that it is an expensive treatment and we can’t cover it ourselves. But we must do everything possible to save her child !!!

Therefore we ask you and ask you to provide any possible assistance and support the dreams of a little girl -  just to live !!!

Sincerely, Buynitsky family.

 

Location: Republic of Belarus, Minsk, st. Casimir, 27, kv.36

Phones: +375 (29) 577 22 October Tatiana, Ksenia’s mom

                    +375 (29) 315 87 80 Denis, Ksenia’s dad

 

Banking details:

Charity accounts opened in branch 510 Belarusbank - Minsk, Kuybysheva Str, 18; UNP 100633430; MFO 153001603:

- Belarusian Ruble - Transit account 3819382100008 for the charity account  000006 in branch 510/421, unlimited

- Russian Ruble - Transit account 3819382103249 for the charity account  000002 in branch 510/421, unlimited

- US Dollars - Transit account 3819382103249 for the charity account  000004 in branch 510/421, unlimited

- Euro - Transit account 3819382103249 for the charity account  000002 in branch 510/421, unlimited

Payment purpose: for treatment of Buynitskaya Ksenia.

MTS +375 29 5621066 Buynitsky Denis Petrovich

EasyPay 46142156

PayPal Denis.belarys@gmail.com

Help Polina Khristiuk

Dear all,

My name is Julia Nikolaevna Khristyuk. I am a mother of two children with disabilities – Polina and Maria. I will begin with the story of her eldest daughter Polina. Polina was born on 07.05.2009 prematurely - at 33 weeks with a weight of 2 kg. After a visit to the neurologist and several rehabilitation center "Tonus" she was diagnosed with: cerebral palsy, severe spastic hemiplegia in her upper limbs.

At that time it seemed that Polina was sentenced for life and for all of us who are around her and loves her. Polina has been in the rehabilitation center in Brest for children with intellectual disorders "Tonus" and in other centers of Belarus since she was 4 months old. However, for the full recovery it was not enough.

At the age of two years Polina does the first year of intensive neurophysiological rehabilitation at the International Clinic of Rehabilitation in Truskavts. Correction of the spine and a variety of procedures were carried out there: physio therapy, massage, light therapy, facial massage, reflexology, mobilizing exercises, Apitherapy, vibroekstenzor. After the first course Polina started turning around in different directions, crawling a little, muscle tone decreased, there appeared more words. Pauline was in that center four times. Today, Polina can crawl on their belly, sit on the floor, walk with support at both hands. She began to say simple words, simple sentences, but not always clear. Unfortunately, due to the strong spasticity in her upper limbs, Polina can’t not hold a spoon in her hand, and can’t eat independently, draw or write. My daughter is 7 years now. She is very smart and pretty. In March, May and December 2015 we went to Warsaw to the rehabilitation center "Olinek", where Polina was treated by method "Tomatis", as well as with a course of massage, exercise therapy. Two weeks ago we took Pauline to Tula for the tendon release operation. A month or two after the surgery it is necessary to continue active physio. Polina is scheduled for a rehabilitation course at the center of "Olinek" from August 8, 2016 and for a course of rehabilitation and social adaptation of the Institute of Conductive Education in Budapest on September 5, 2016. We have always paid for all rehabilitations and travel cost ourselves. And never complained. We know that there worse cases. In June 2014, we had twins, Alexander and Maria. Everyone was happy. However, it turned out that Masha got an intestine infection, and on the fifth day after birth Masha had her first operation and got a stoma in her belly. In intensive care in Brest Masha and I spent about one and a half months. Then in Minsk within three weeks she had complex operations on the intestine in the Republican surgery center. And then three long months in intensive care. But in spite of all the efforts, the problem is not solved. Masha was discharged from the hospital for a few months so that she could go home to meet the family and get prepared for the next operation. The first time Masha got home when she was almost 5 months. We were all very happy. Two months later, Masha had the last surgery and it was successful. We could not believe that it was over!!! But our joy was short-lived. We began to notice that Masha does not always respond to sounds. After all investigations Masha was diagnosed with hearing loss of the 4 degree on the right ear and the left ear - 2-3 degree. So far, none of the doctors can say for sure, why Masha lost her hearing. But all agree that the most likely numerous courses of antibiotics and led to the complications. We wanted to make an urgent operation on the establishment of a cochlear implant for her. Operation cost 26,500 Euro and 850 Euro Advance Diagnostics. The operation was scheduled for September 2015. And we got help !!! The necessary amount was collected in three months. Masha had surgery in September. We still have a long way to go with Masha, because the intensive care after surgery took so long. She will turn 2 in a few weeks time!!

And now back to our older daughter to Pauline. After the operation, as I wrote above, we have planned several exchange rate rehabilitation. In "Olinek" they provide the therapy in a suit "Adeli" and hand therapy. The second course is scheduled for September, we had planned to go to the Institute of conductive Pete Pedagogy in Budapest, where children try to learn to adapt to the social environment.

Unfortunately, rehabilitation and accommodation costs a lot of money. All our money spent on maintenance of the auditory processor and hearing aid youngest daughter. According to the latest rates the rehab in Olinek center is about $ 1,700 and $ 500 for accommodation. And in the course of the rehab institute Pete is 1200 Euro and 1100 Euro for accommodation. The returned flight to Budapest is about 15 million rubles. Please help raise funds for two rehabilitation center "Olinek" and the Pete Institute for our eldest little daughter Polina. Course in Warsaw is around US $ 2,200 and a course in Budapest is about 3000 Euro.

With great respect and hope for help, Julia Khristyuk

Charity accounts opened in branch No186 No.100 of the branch of OJSC "Belarusbank", Brest, Cosmonauts blwdr, 94; UNP 200246676; code 246

Belarusian rubles: No.000085

(Transit account No3819382124630 - indicated for Transfer of funds by legal entities or the transfer for other banks apart from Belarusbank)

Euro: No.000053

(Transit account No. 3819382104878 indicated for Transfer of funds by legal entities or the transfer for other banks apart from Belarusbank)

Russian ruble: No000059

(Transit account No. 3819382104878 indicated for Transfer of funds by legal entities or the transfer for other banks apart from Belarusbank)

US dollars: No. 000141

(Transit account No. 3819382104878 indicated for Transfer of funds by legal entities or the transfer for other banks apart from Belarusbank)

Payment purpose: fundraising for treatment of Khristyuk Polina.

Accounts opened in the name of Julia Khristyuk

WebMoney:

US Dollars: Z151678901585

Euro: E313824550796

Ru rub 147849812388

Home address:

224020, Brest, Masherov Avenue, d.39, kv.135

Recipient: Khristyuk Yulia Nikolaevna

Contacts:

+375 29 729 12 74 - Julia (Polina’s mom);

+375 29 728 40 24 - Maxim (Polina’s dad);

8 0162 51 88 77 (home)

Stiftung «Dobra tut» — ist eine Wohltatigkeitsorganisation. Ihre Prioritat ist die Aufrechterhaltung des Wohnkomforts in unterschiedlichen Pflegeheimen fur behinderte Kinder und Erwachsene. Wir unterstutzen Pflegeheime und ziehen Voluntare furs Helfen beim Spielen mit den Kindern oder Arbeit mit Behinderten hinzu.  

Wie konnen Sie unsere Stiftung unterstutzen: des Geld auf unser Konto uberweisen, oder Voluntar werden und den Kinder und Erwachsenen direkt helfen.

Sie konnen den Rechenschaftsbericht an unsere Tatigkeit gelesen.

Контакты

Address:
Angarskiy pereulok, 117, Minsk, Belarus, 220137 
E-mail: dobratut@gmail.com
Phone/fax: +375 (017) 246-26-39
http://dobratut.by
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