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

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)

Great start of the volunteer summer season 2016 was put by our friends from Burren Chernobyl Project in Gorodische children's orphanage. Now kids from units 3,4 have their own verandas. Huge thanks to all who have contributed not only the funds, but the warmth of their hearts. 

And already this evening we're welcoming a new group from Ireland and are looking forward to some new interesting and touching moments!

Dear all!

I’m Diana, and I’m asking you to support my special child Eugene

Lagutko Eugene (5 years), Baranovichi

The diagnosis: cerebral palsy, double hemiplegia, spastic tetraparesis, learning disability

Born at the 30th week of pregnancy. For two weeks he was on artificial lung ventilation and ate through the tube. Having started breathing independently, Eugene was transferred to Children's Hospital, where he subsequently became worse – started having frequent apnea episodes. The child’s deteriorated sharply.

Now Eugene is five years old. And for all five years we’ve been on constant treatment sessions, also taking expensive medications. We‘ve been on many rehab courses in "Mother and Child", centre "Turpentine", "Tonus" centre. Also were treated in the clinic Kozijavkin (Truskavets), in Lithuanian sanatorium "Belarus" and had two courses of rehabilitation in China (Funds “Planet of Good” and “Opeka”helped raise funds).

Eugene fights for his health, he is a very strong, patient and grateful child. He has a good progress: started crawling, recently has started tolerating sitting for a short while (of course with support, but we are very happy). He has even started talking (saying mom, dad, baba, ded, go, aw-aw, yes, no). But now our main problem is Eugene’s hands, they are very tight. And without the help of the hands it is not possible to learn to crawl, sit, stand and then to walk. Hands play an important role in this process. After all, in life, every minute we make something with our hands, the whole future life requires precisely coordinated movements of hands and fingers such as dressing, eating, and performing a wide variety of everyday activities. Even sitting in a wheelchair a person can be socially adapted, if he can manage moving with their own hands. At the moment, all my focus is on rehabilitation in this direction! I'm doing everything possible to organize a proper treatment! But, unfortunately, I cannot pay for the treatment he needs. I'm officially caring for a disabled child, which I’m getting paid for, but the money is not enough of course. And I also have another child and no partner to share my responsibilities. The main part of the income is spent on treatment of Eugene. Currently he needed money for surgery to help to reduce tension in the muscles and relax them, and it costs 25,000 Russian rubles. And in September, we are expected to go to the rehab center  for children with cerebral palsy (in Beijing), for the course of 2 months at the cost of $ 8500 (with the flight). For us it is a chance to teach Eugene to sit independently, and to start looking after himself. I kindly ask all caring people to participate in the fate of my child and help him have a better quality of life!

With respect and hope for help Lagutko Diana!

+375 29 802 01 80 Lagutko Diana. (Eugene’s mom)

+375 16 362 55 41 (home phone)

Banking details:

Charity accounts opened in №802 branch of OJSC "Belarusbank"

UNP 200369858; MFI 150501245

Belarusian rubles:

Transit account number 3819382109656

Charity account number 000054

US Dollars:

Transit account number 3819382112542

Charity account number 000098

Euro:

Transit account number 3819382112542

Donation account number 000016

Address:

Baranovichi, Domeyko st., 25-41, Zip Code: 225405

You can also transfer funds:

-EasyPay № 44939025

-yandex money 4100 1405 9096 694

- WebMoney.

Ruble: R120154220757

Dollars: Z470127546636

EURO: E414775473440

Our stories and updates could be found in here and here and here

Hello, we are writing to you with a huge request for help! The beginning of our history can be found here 

"Our Yanais 6 years old. Very slowly, but still she is developing thanks to daily work. But I would compare Yana’s development with the children’s mobile that parents hang over the babies’ cribs when it’s winded up, it goes round and sings, but gradually it runs out, and the music is getting slower and slower until it is stopped. Same story with Yana: good rehabilitation gives her a proper push to the development and our work with her. She learns well that it allows us to go on with our domestic classes that also give a greater feedback, but gradually, like a carousel, the "charge" comes to an end, and further work does not bring an adequate response. Therefore, she needs to go on the rehabilitation courses to give the child another push and the ability to further development and for us parents a way to communicate with specialists that suggest where we have to improve our work with the child. Thanks to all caring people we have been on rehabilitation with Jana in Russia and China. China has given us very good results: Yana started crawling on all fours, to say "yes" or "no" when asked, now our her communication is based on leading questions about what she would like or check educational methods that can be answered "yes" or "no." Yana began to ask going on a potty, mostly showing gestures, which is also very important for us. Now Yana can walk a little, holding to a stick, or with support at her pelvis. Now we would really like to have that rehab course done in the Polish intensive rehabilitation center "Olinek," where many Belarusian kids had good results in the development. Mainly due to the treatment by the method of Professor Tomatis many nonspeaking children begin to talk. Jana really wants to learn to speak, as the communication with  "yes" and "no" level is not enough for her now, she gets very upset when trying to say something to us, but we do not understand. Regular sessions with a speech therapist has not given such an opportunity, she needs a push from the inside. The condition for treatment by the method of professor Tomatis is a block of at least 4 courses with an interval between the first and second course of no more than 4-6 weeks, so we ask all concerned people to support us and to get to the treatment center for intensive rehabilitation "Olinek." So that it becomes the push to wind up her little mobile and get her started on the proper speech.

The estimated cost of the treatment of 8,500 euros.

Contacts:

(+37529) 744-28- 48 - Anastasia, Yana’s mother

(8-017) 221-52- 02 - home number

Banking details:

Charity accounts opened in №614 branch of OJSC "Belarusbank" - Minsk, Karbishev str, 13, - 2

UNP 600052608

MFO 153001520

- Belarusian rubles - transit account №3819382106084 to the charity account №000002 in branch number 614/61

- Euro - transit account №3819382118580 to the charity account №000001 in branch number 614/61

- Russian rubles - transit account №3819382118580 to the charity account №000001 in branch number 614/61

- US dollars - №3819382118580 transit account to the charity account №000001 in branch number 614/61

Payment: To be admitted to the charity account in the name of Anastasia Yaruta for treatment of Yaruta Yana

Million thanks to everyone in advance!!!"

Varvara not for a second allowed the thought of failure to cope with the disease and she always believed she’d be the winner in the unequal battle with the severe disease. This little girl immediately realized that only unconditional faith in herself would help to conquer cancer cells.

Now Varya is an ordinary child who really wants to believe in her bright future.

Varvara Stasheuskaya 9 years, Minsk

Diagnosis: right adrenal neuroblastoma combined with damage of paraorthal lymphnodes and lymphnodes of vascular pedicle of the left kidney T3N1M0, Stage 3, after the comprehensive treatment - remission. Varya was diagnosed with it in November 2010, in cancer centre in Borovliany, Minsk district.

Initial treatment was carried out in Borovliany clinic - 6 chemotherapy blocks. Since there wasn’t a possibility to perform a surgery in Belarus, we went to an Israeli hospital Schneider, where the tumor was removed by 98%.  After Israel she underwent 4 more chemotherapy, beaming and 8 months of dry chemo (Roaccutane). There was a long-awaited remission in 2012!

 The children with this diagnosis should have preventive assessments every six months for 5 years.  Thus we need to go back to Israel to fully examine and check Varya’s condition!!!

Neuroblastoma is the most poorly studied and insidious form of pediatric oncology. Very few survive. Our girl is the lucky one! But cancer is dangerous and may recur. We are all fighting for Varya’s life, this is our mutual victory! Now is very crucial moment - a 5-year remission threshold and half way to healing is passed.

His example proves: Cancer is curable.

For the assessment we need to fundraise 16 120$ before 01.07.2016

Please, help us to make sure that the disease does not go back!!!

Banking details:

Charity accounts opened in branch №614 of OJSC “ASB Belarusbank”- Minsk,

Karbysheva Str , 13/2, UNP 600052608; MFIs 153,001,520.

- Belarusian Rubles - №3819382106084 transit account for charity account №000009 in branch #614/143

- US- Dollars - №3819382118580 transit account for charity account №000013 in branch # 614/143

- Euro-№3819382118580 transit account for charity account №000011 in branch # 614/143

- Russian Rubles - №3819382118580 transit account for charity account №000010 in branch #614/143

Payment Purpose: For treatment of Varvara Stasheuskaya

Mother’s phone no: +375291291803

EasyPay  number 20704518

WebMoney account:

B362147008659 - Belarusian rubles

E910381695119 -Euro

R389147790069 -Russian rubles

 Z391150365233-US Dollars

 U167258283227 - Ukrainian hryvnia

Address:

220066 Minsk,

Tashkentskaya Str.12-43, Minsk

Recipient - Davydova Elena

                       (DAVYDAVA ALENA)

details for Schneider clinic.

 Kindly

transfer the money - to the following bank account:

 Payable to:

Schneider Children's Medical Center of Israel

 Bank: HAPOALIM

 Branch: 552-Beilnson

 Address: 1Denmark Street, Petach-Tikva, Israel

 AccountNo .: 220442

SWIFT OALILIT

 IBAN IL69-0125-5200-0000-0220-442

Patient Name:

Stasheuskaya Varvara ID number at the hospital: 8291110197-0

* Varya's help group

* Details

* Varya's story

* Documents

CONTACTS:

Mother - Davidova Elena +375291291803

 manikulia@mail.ru

Many sencere thanks to everyone!!!

        ‘Fragments from the nuclear explosion fallout at Chernobyl station which blew into the sky on 26^th April 1986 landed on us. At first we heard only of rain clouds bringing devastation, of animals contaminated by radiation. We were told – ‘don’t go there, not if you are young, or pregnant, or ever want to be pregnant; not unless you want to come back with two heads, several cancers and the likelihood of more. Don’t go there!

But we went anyway.’ (From ‘Fallout’).

         In the quiet and dark of the night – of this night – thirty years ago as we all slept quietly, the world changed. For some it was just a news story the next morning on their news channel.

         For others, it was in their lives, in their bodies, in the very air. And no one told anyone! Nobody really knew how much damage was being done. The beast released into the night air could not be recalled, could not be brought back. The genie was out of the bottle – with an evil that spread quietly and gently and deeply into the lives, into the minds and bodies of people – of children – we have come to know and love.

        Thirty years on and we are still involved, still making that journey to Belarus. We go there not because of nuclear power or contamination. We go to meet those who are now our friends, our pals – and we go because we enjoy going there, we love going there.

Let us hope that tonight is a quiet night in the world;

that whatever evil that is about to be coughed up on top of our beautiful world will somehow be contained this night and not released.

Let us hope that something beautiful may be released into the night air this night,

Something to make the world a better place,

To make us all a little better.

         Let us hope for something. Something small. Something beautiful. Something that will grow and creep like a rambling rose over the wall into our neighbours minds and hearts and souls around our beautiful world.

Let us hope this night for something beautiful.

Let each of us be that something small.

Something small and beautiful which will spread out from this night, in the quiet,

In the darkness,

Without anyone being told.

Liam O’Meara

Another heartbreaking story and another request for help. Little girl Darina really badly needs your attention and support.

" Hello!

My name is Anastasia Kolonitskaya, I am the mother of a special child Darina.

Daryna was diagnosed with cerebral palsy. She is 2 years now, but she can not hold her head, sit or talk and eats through a tube. But despite all the difficulties, we do not lose heart and fight for a better quality life for our girl every day.

In 2015, we fundraised money for a trip to The Institutes for the Achievement of Human Potential (Italy). With the help of caring people we were able to take the baby for a visit and get a competent examination.

The specialists of The Institutes for the Achievement of Human Potential Darin examined Darina, noted a positive change (Daryna’s hearing and vision improved) and developed a rehabilitation program for the next six months. We have a program of various methods including usage of respiratory masks, learning to communicate with Darina on the board of choice, hearing program, vision and tactile stimulation, three types of patterning and we also increased the number of sliding down on sloping floor. And as the child progresses the constant adjustment of the program is needed often, so  we have another appointment for July 4, 2016.

Visit price: 5250 $ and 3155 € +  travel costs.

We’ve also fundraised money for a trip to Moscow for the introduction of umbilical cord blood cells in KrioTsentre. It took us a long time to study this procedure, we considered the opinions of parents, who had already tried this method, communicated with experts and we realized that this is our chance! This is the chance for our daughter to see the outside world, the chance of a significant reduction in spasticity and hyperkinesias and to improve physical activity. We hope that this will become a new impuls to Darina’s development .

The cost of one implant is 77,000 Russian rubles. We need to make 6 implants: first 2 with an interval of 2 weeks, then every 3 months. Thanks to the funds collected, we have already made 2 implanting procedures, the next one is expected in July.

Miracle happens, where he was waiting for! We are looking forward to, hope and trust and ask for help from all of those who care!

You can follow the news on Darina’s improvement in  VKontakte social network http://vk.com/club91244744

The required amount is 6150 € + 11 200 $. We have already fundraised 1050 €, 5672 $.

Still need: 5100 €, 5528 $

Details to help Kolonitskii Darina

Charitable accounts opened at branch # 511/290 of "Belarusbank", Minsk,Okhotskaya str, 135 K.3, UNP 100349858; MFO 153001815

- Belarusian rubles - №3819382103561 transit account for the charity account №000002 in branch № 511/290, unlimited

- Russian rubles - №3819382104993 transit account for the charity account №000002 in branch № 511/290, unlimited

- US dollars - №3819382104993 transit account for the charity account №000003 in branch № 511/290, unlimited

- Euro - №3819382104993 transit account for the charity account №000002 in branch № 511/290, unlimited

Payment purpose:  treatment and rehabilitation for Kolonitskaya Darina

Web Money

E310557593832 - Euro

R259910918217 - Russian rubles

Z212272752924 - USD

B165000538148 -Belarusian rubles

For postal money orders:

Minsk, ul. Okhotsk d.95 / 15-1, 220137 , Kolonitskaya Anastasia (mother)

Yandex money

410013146132881

Easy Pay № 27908419

Here is a video story of Darina http://vk.com/videos-91244744?section=all&z=video-91244744_171783602%2Fclub91244744%2Calbum-91244744%2Fpl_-91244744

Contacts:

Kolonitskaya Anastasia V. (Darina’s Mother) +375 291 192 674

Thank you very much for all your support!!!"

Dear Friends, 

This is really a unique situation, so please help baby Camellia. The friend of the family Svetlana Kurochkina writes:

"My friend’s family has a great misfortune! Their daughter Camellia, 1 month old, was diagnosed with retinoblastoma. This is eye cancer. The family did everything possible to take the baby for medical treatment to Germany. They are already there. The treatment costs 50,000 euros. A lot of people have responded to trouble from everywhere. The family is also supported in Germany, some people have alreadycontributed EUR 5,000 and the hospital has also provided them with a free room as it is a unique case. Camellia is the only newly born child with such a disease in the world. She is now with her parents in Berlin in clinic Charite. Please, support Camellia and let her see this beautiful world and the people who have not passed by and helped her !!!

Charitable accounts opened at office 215 of Belarusbank - Orsha, Lenina Str, 81; UNP 300460375; MFO 150801647:

- Belarusian rubles - transit account 3819382302077 for charity account 000035 in branch 215 / operating service, unlimited

- US dollars - transit account 3819382303669 for charity account 000029 in branch / operating service, unlimited

- Euro - transit account 3819382303669 for charity account 000012 in branch / operating service, unlimited

- Russian rubles - transit account 3819382303669 for charity account 000018 in branch / operating service, unlimited

Payment purpose: To be admitted to the charity account opened in the name of Kopysheva Taisiya for the treatment of Camellia Demchenko.".

Thanks a million in advance!!!

Dear friends, 

Please, read the story of little Matvei. He is a brave fighter for his life, so let's support him:

I am a mother of three children, one of them is Matvei - a child with disabilities, he has a diffuse lesion of the midbrain, congenital heart defect (trisomy of chromosome 21), and other conditions.

In July 2014, I visited the American courses, held in Moscow on "What to do if your child has brain damage." In September we were in Philadelphia, thanks to family and friends (they bought the tickets) and all the people who donated money. Taking into consideration his diagnoses we put together a program for six months. In March 2015, we paid a second visit there. This program changes as the child achieves the certain development objectives. The cost of travel 10 000 Dollars, taking into consideration the payment of the lectures course for parents and teaching methods of the rehab, tickets, visas and accommodation.

A trip to the rehabilitation institutions Glenn Doman in Philadelphia - is not a whim, it's a chance for Matvei to restore the lost brain function. The program, in which we are engaged on a daily basis is very difficult, not every parent is ready to accept the way of life for the sake of their child, in spite of the good result. It is very difficult, but the result is fantastic.

How it happens is a mystery of nature. Our child is becoming smarter day by day, he makes us happy with his success, and this gives us the strength and confidence that everything will be fine. It is necessary to continue and not give up.

We consistently treat the main cause of Matvei’s problem - the diffuse lesion of the midbrain. Every day we undergo physical, intellectual, manual, physiological and respiratory program. The entire program is created for Matthew by experts and it became the way of life for us!

He still doesn’t speak, sensory is damaged as well as the motor skills. The possible reason why he doesn’t speak is lack of oxygen supply to the brain, as well as problems with the hearing. Only specialists of the Institute can help Matthew to achieve a good level of development, they have designed a unique technique that really helps the children with such diagnoses to develop normally. No organization here is willing to deal with such Matvei’s  problems in complex, but we of course still desire to help him as soon as possible. We see the results! Matveyushka can look after himself, he understands and tries to be helpful in the family and is actively involved in domestic affairs, he has viewed by over 3000 encyclopedic facts, read more than 400 books and passed all arithmetic tasks as the part of the intellectual program. He also started improving physically. The everyday programme consists of physical and intellectual tasks. Respiratory program consists of respiratory patterns. All this is to oxygenate the brain and to show it how to breathe correctly. We just carry a tactile and auditory stimulation. All programs are designed for the damaged areas of the brain. Brain is a muscle, which is growing in its active use.

We ask you to support us in this long marathon to raise funds needed to continue treatment that was begun! We need not only material, but also information support! Do not leave us, please!!!

Charity account is Belarus bank are to be found here http://belarusbank.by/ru/30394/blagotvoritelnost/3081

You can also find us in social networks

 https://vk.com/club74183862

 http://ok.ru/aniskovmat  
 

And you can also help through these services: 

QIWi 79203020877 
Pay Pal grudetskaya@gmail.com for Matvei
 Yandex money 410012356139708 
 МТС +7 910 760 82 81 
 Beeline +7 968 688 41 43 
 Megaphone +7 920 302 08 77 
 Sberbank 4276 8801 6757 4015 (Orlovskaya Elena, Matvei’s mom) 
 EasyPay 00114397 
 WebMoney. 
 Rubles: R635464811669 
 Dollars: Z817935844573 
 Bel rubles: B606264298751 
 MTS +375 29 886 44 05 
Visa Card of Belarusbank 4266200038282604 Orlovskaya Elena (Matvei’s mom)

Thanks a million in advance!

Friends,

As you can see, there are many requests coming to us from so many families, but we are kindly asking you to take part in the fate of these wonderful little children. Your every help will become a step on the way to recovery. Here is the story of a little Nikita that requires rehabilitation. It is not expensive, but it can significantly improve the child’s health:

"Hello, my name is Oksana, I have a son - Nikita.

Nikita is 3 years old, his main diagnoses are cerebral palsy, spastic hemiplegia, post-hemorrhagic occlusive hydrocephalus (a condition after ventriculoperitoneal shunting).

 Nikita is able to talk now. But his musculoskeletal system is impaired (tight right hand, low physical activity, the left hand is active – he can take things, attempts to eat independently). While walking with support on two hands he intends to tip-toe and then step on the whole foot but with legs crossed. He can not sit for long without support, and he cannot sit down independently.

Nikita was born prematurely (30 weeks), on the 4^th day he had a brain bleeding, which caused hydrocephalus. He had a surgery  at 1.6 months. For a long time Nikita was on artificial lung ventilation (about a month). He was discharged home at 2 months with psychomotor retardation, and then every 2 months we went for the rehabilitation to the Republican Scientific and Practical Center * Mother and Child * (4 times),  Since he was 1 year we are undergoing  on the rehabilitation courses in Minsk city center of medical rehabilitation for children with intellectual disabilities (were there 9 times), we go to the rehab centre Zhivitsa (Gomel regional Hospital), and do regular courses of massage and  physio in the community clinic, also we regularly go to the pool.

As the time goes by, the dynamics is positive, but it is very slow. We decided to take Nikita in the specialized sanatorium for children with cerebral palsy in the Czech Republic for the first course of rehabilitation treatment, which costs 4470 euros. It is not possible for us to save such an amount in 3 months, so we are asking you for your support!

Charity accounts opened in branch 511 of Belarusbank - Minsk, Dolgobrodskay st, 1; UNP 100349858; MFO 153001815:

- Belarusian Ruble - Transit account 3819382103561 for the charity account 000007 in branch  511/197,

- US Dollars - Transit account 3819382104993 for the charity account 000016 in branch  511/197,

- Euro - Transit account 3819382104993 for the charity account 000006 in branch  511/197,

- Russian Ruble - Transit account 3819382104993 for the charity account 000008 in branch  511/197.

Payment purpose: for treatment Yaroshik Nikita.

+375 29 7887709 – that’s the number that you can top up, and the family can withdraw the funds towards treatment.

Home address:

223060, Minsk region,

d. Large Trostenets, street Youth, 3/2, kv.62

contacts

MTS +375 29 7887709 mama Oksana,

 oksanka418@mail.ru"

Thanks a million in advance!

Dear friends,

We are asking you to help this wonderful boy:

Little Timur Zulfalievu was born a perfect child. And neither his mom nor specialists noticed anything special about him in the maternity house. But later on his mom Veronika started noticing that Tsimur doesn’t breath regular. First their doctor said it was just a flue. But then after some more check-ups he was diagnosed with spinal muscular atrophy Verdnig-Hoffmann type 1. The family tired various clinics to help his condition, but the child was only getting worse. Now he needs a ventilator to help him breathe.

The family has managed to collect 6333.75 euros of the required amount of 10460 euros. But they still need 4 126.25! For those who could understand a bit of Russian here is their social network page, where one can see the updates!

Below, you will find the accounts to transfer funds:

JSC "Belarusbank"

Charity accounts opened in OAO 'Belarusbank' CPU 416 of the branch 413 'Belarusbank' '. Location: Novogrudok, Mitskevicha Str, 22a. UNP 500191715, 152101696 MFI:

Belarusian rubles: account number 000009

Transit account 3819382104109

Euro: account number 000003

Transit account 3819382105717

USD: account number 000017

Transit account 3819382105717

Russian Rubles: account number 000003

Transit account 3819382105717

Accounts opened in the name of Zulfalieva Veronica Y., Address: Belarus, Grodno Region, Novogrudok,  Mendeleev Str., 26B-2

Payment Purpose:  for the treatment of  Timur Zulfaliev and the purchase of medical equipment

We thank you very much in advance!

From the bottom of our hearts let us wish you a happy St.Patrick's Day!

May it be a truelly enjoyable day!!!

Special greetings to our friends, partners, volunteers from Ireland - Burren Chernobyl Project, Chernobyl Children's Trust and to everyone else! Hurray!

Yours,

"Dobra tut"