Kira K.

The collection is over. Thank you!

Age: 7 y.o.
Diagnosis:stadium 4 retroperitoneal neuroblastoma, relapse
Needs: immunotherapy in Spain
Funds to raise: EUR 200,000

Kira was diagnosed in 2016, in the age of 3. This was followed by a severe, aggressive treatment: Kira underwent 6 blocks of chemotherapy, an operation to remove a tumor, and bone marrow transplantation, that had heavy consequences.
Owing to the help of caring people, they have managed to go timely to Greifswald clinics, Germany, for a treatment with antibodies (immunotherapy).
But there was a relapse in April of this year.
Now Kira needs to undergo transplantation, immunotherapy and other important treatments. Kira gave a good response to the treatment she has already received, and she has every chance for a full recovery. A clinic in Barcelona is ready to accept the girl. The cost of treatment is EUR 307,000. The family has managed to collect € 113,000 on their own. Kira, like any child, has her own wishes. She wishes simple things: to go to school with other children and celebrate her birthday at home with family and friends.
For the wishes to become true, she urgently needs to start the treatment. And for this they urgently need about 200,000 euros.

Almost all parents of our care-receives are heroic people! They withstand the trials that a normal person in peacetime can hardly imagine. To survive, they need our support.
But there are also the parents who, despite being immersed in their difficult situation, can think of others and make better the world around.

Polina K.

The collection is over. Thank you!

Age: 9 y.o.
Residence:Kharkiv region, Ukraine
Diagnosis: spinal muscular atrophy (SMA) and grade 4 neuromuscular scoliosis
Needs: surgery in Germany
Funds to raise: EUR 50,500

The SMA has weakened the muscles throughout her body, she cannot walk or even stand on her own. From the age of 3, her back began to deform. All day long Polina has to wear a tight corset to support her spine. However, the disease is progressing and now the girl has severe scoliosis with a lateral arch of more than 90 degrees. This causes serious breathing problems, impaired blood circulation, heart displacements. Polina requires an urgent surgery to correct the scoliosis. Taking into account the severity of the underlying disease, the doctors have recommended installing a magnetic structure MAGEC System in Germany. This design can be adjusted without surgery as the child grows, by expanding the structure using a special magnetic device. The procedure has to beperformed 2-3 times per year in a clinic.
The sooner the operation is done, the more chances are there to save Polina. Such surgeries are not performed in Ukraine. The German clinic in the city of Bochum is ready to accept the girl. The price tag is EUR 70,500. At the moment, it remains to collect EUR 50,500.

Leyla B.

The collection is over. Thank you!

Age: 3.5 y.o.
Residence: Kazakhstan
Diagnosis: juvenile myelomonocytic leukemia
Needs: stem cell transplant in Turkey
Funds to raise: EUR 93,000

At the age of seven months, the girl was diagnosed with a terrible disease – juvenile myelomonocytic leukemia, blood and bone marrow cancer. Since then, the struggle for the child’s life has not stopped for a month. Leyla has undergone stem cell transplants twice: both times the transplant was rejected. The girl suffers from concomitant diseases. Kazakh doctors recommended the treatment abroad. However, the authorities of the republic did not find money for Leyla … Now the only hope is the third transplant, in a Turkish clinic Medipol Mega. The cost of treatment is EUR 93,000. Parents are borrowing and fund-raising. Please help Leyla!
Update: Leyla got worse. She has to fly urgently to Istanbul with her parents.

Leyla’s page at GoFundMe

Ekatherina K.

The collection is over. Thank you!

Age: 7 y.o.
Diagnosis: Facioscapulohumeral muscular dystrophy (FSHD).
Needs: rehabilitation in Germany
Funds to raise: EUR 6,000

7 years ago, Katerina’s parents learned that their daughter is terminally ill. She is doomed for atrophy of the muscles of the face, arms and legs. She will lose of the ability to walk.
In 2016, the girl has underwent a surgery in Paris. Owing to this, she has a chance for the continuing body functioning, chance to walk independently and to self-care. But for the body to continue to function, rehabilitation courses are necessary.
Despite her illness, Katerina is a volunteer in kindergarten where she teaches English to children. She is a kind, intelligent and responsive girl. She dreams to start learning marketing next year. Katya wants to live like an ordinary person, to have a profession and be useful.
For the rehabilitation course in the German clinics Tera Reha Zentrum, EUR 2880 is required.

Nikita G.

The collection is over. Thank you!

Age: 7 month old
Diagnosis:organic brain damage, persistent vegetative state, epilepsy
Needs: treatment in Germany
Funds to raise: EUR 10,000

Nikita was born this spring. The birth was difficult, the baby had severe asphyxia. All this lead to serious consequences for his health. The baby lacks a number of vital reflexes: he cannot eat, breathe, or swallow on his own. Nikita breathes with an oxygen concentrator through a tracheostomy tube. In Belarus, doctors cannot provide any qualified help. There, the child was given a disability status and the palliative care was recommended. The parents have found a German clinic Helios, where the doctors are willing to help. Long-term medication and brain stimulation are needed. The cost is EUR 105,000 euros. EUR 10,000 remains to be collected.