Helped to pay for diagnostics and treatment. December 2025
Age: 10 y. o.
Residence: Gatchina, Russia
Diagnosis: anaplastic ependyoma of the 4th ventricle (oncology)
Needs: a device to adjust his shunt
Funds to raise: EUR 400
Our long-time care-receiver Alexander needs help in purchasing a device to adjust his shunt. Since the shunt was installed in Germany, a suitable device must also be purchased here. It costs EUR 900, we need to collect the remaining EUR 400
Helped with housing rent. March 2026
Helped with housing during a trip to Germany for treatment. January 2026
We have helped with tickets and the visit to the hospital: april 2025
Age: 13 y. o.
Residence: Moscow, Russia
Diagnosis: Multiple arthrogryposis
Needs: tickets to go home
Funds to raise: EUR 300
Until the age of 5, Misha lived in an orphanage. He has a congenital musculoskeletal condition and, before being adopted, he couldn’t walk or move his arms. Over his 13 years, Misha has undergone many surgeries to be able to live a full life. Unfortunately, he has recently experienced a complication in his foot, that was operated in Germany several years ago. He has now been unable to walk for almost a year.
To determine the cause of the complication, Misha was brought to a German clinic for an examination. A medical board has decided that he would need another surgery. But at the moment, Misha and his mother just need to return home. They need help to purchase the tickets – €300
Helped to buy the medecine, april 2025
Age: 10 y. o.
Residence: Ukraine, Kharkiv Region
Diagnosis: CLOVES Syndrome
Needs: Rapamune medication
Funds to raise: EUR 300
We have helped Sasha and her family multiple times. Alexandra has a rare genetic condition – CLOVES syndrome. She needs to take Rapamune medication on a permanent basis. This time, we need to purchase this for three months. The cost for this medication is 300 euros.
We have helped to pay for the treatment. December 2024
Age: 5 y. o.
Residence: Gomel, Belarus
Diagnosis: cerebral palsy, spastic tetraparesis, grade 4 disability, delayed speech and mental development, limb contractures
Needs: treatment in Switzerland
Funds to raise: EUR 12,200
Ksenia is the first and dearly loved child in her family. During birth, she suffered a severe injury, and since then, her family has been fighting the consequences and her challenging diagnosis. She has undergone multiple rehabilitation courses in Belarus, Russia, and Ukraine, each bringing positive results. A significant milestone in her development could be a stem cell transplant, which has shown promising results. Ksenia is currently in a three-month medication preparation period, ending in November 2024. The family requests help for the stem cell transplant at the LIV Hospital in Istanbul, Turkey. The bill amounts to 25,400 euros, and 12,200 euros are still needed.
We have helped to pay for the reabilitation
Age: 3 y. o.
Residence: Mozyr, Belarus
Diagnosis: SMA (spinal muscular atrophy) type 2
Needs:a surgery in USA
Funds to raise: 1,650,500
A year ago, little Elizaveta was diagnosed with SMA. This is a disease when the muscles gradually break down, get atrophied. A child begins to lose the motor skills already acquired, and slowly, one after another, the body functions begin to fail. There is a way to stop this disease: an injection of the drug Zolgensma. It delivers to a body a working copy of the broken gene. This injection has to be done once in a lifetime, but it is necessary to do this until the child reaches the weight of 21 kg. The cost of this injection is huge: EUR 1,650,500.



