Total raised
€ 8 800
Total raised (%)
100%
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Dmitriy Yablokov
Dmitriy Yablokov
08/27/2017, city of Minsk

Dmitriy Yablokov

27.08.2017, city of Minsk
  • Diagnosis: primary immunodeficiency
  • Fundraising goal: Defibrotide drug therapy
Fundraising is over
Meet the child
An extremely rare genetic disease of Dima, primary immunodeficiency, manifested itself with the first symptoms when the baby was 1.5 years old. One after another, hospitalizations, examinations followed, the struggle of doctors for the life and health of the baby began; after a while, a diagnosis was made. 

Dima’s disease is characterized by the presence of birth defects that inhibit the immune system, as a result of which the child is more susceptible to various infections, and these infections are treated worse, which can lead to the development of severe chronic infections and inflammatory damage to organs and tissues at any moment. Since January 2019, Dima has been undergoing complex treatment at the Belarussian Research Center for Pediatric Oncology, Hematology and Immunology in Borovlyany, all this time the child is in the hospital. 

Dima expects a vital bone marrow transplant procedure at the hospital. After the procedure, experts predict a high risk for liver veno-occlusive disease. For the treatment of this complication in the transplant period, Dima urgently needs therapy with a very expensive immunosuppressive drug Defibrotide.

Despite his diagnosis, Dima rejoices and smiles, courageously endures difficulties. His whole family hopes for a favorable outcome of the procedure.

Thank you for supporting Dima on his way to recovery!
Together we make a difference!
percent
  • Diagnosis: oncological, hematological and immunological diseases
  • Fundraising goal: medications, MIBG-diagnostic, FMI-test
Amount needed
535 000
We still need to raise
289 169
Total raised (%)
46%
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