Total raised
BYN 4 342,61
Total raised (%)
100%
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Stepan Rymsha
Stepan Rymsha
03/22/2017, Grodno

Stepan Rymsha

22.03.2017, Grodno
  • Diagnosis: Gaucher disease type 1
  • Fundraising goal: genetic analysis
Fundraising is over
Meet the child
   Stepan is the second child in a large family of Rymsh. The mother found out about the boy's diagnosis during pregnancy - at that time, the diagnosis was made to his older sister. This was the reason why Stepan began receiving enzyme replacement therapy at the age of 6 months.
   Stepan is a very active boy. He goes to school, plays football. However, against the background of enzyme replacement therapy, negative dynamics have been observed. A genetic study is recommended to clarify the diagnosis and select the necessary treatment.
Together we make a difference!
percent
21.03.2017, Minsk
  • Diagnosis: neurotrophic keratitis of both eyes
  • Fundraising goal: purchase of medication
Amount needed
124 122
We still need to raise
92 444
Total raised (%)
26%
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percent
04.05.2010, Zhlobin, Gomel region
  • Diagnosis: acquired three-stage aplastic anemia, superheavy course
  • Fundraising goal: purchase of medication
Amount needed
257 865
We still need to raise
170 393
Total raised (%)
34%
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