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- Konstantin Markechko
Total raised
BYN 1 297,79
Total raised (%)
100%
![Konstantin Markechko](/upload/resize_cache/iblock/4d3/rkhl6je1utu6lfi050hx73vuzt51wfqx/375_375_1/Markechko-Konstantin.jpg)
Konstantin Markechko
02/17/2016, Beloozersk, Brest region
Konstantin Markechko
17.02.2016, Beloozersk, Brest region
- Diagnosis: focal epilepsy, with the presence of motor seizures, pharmacoresistant course
- Fundraising goal: genetic analysis
Fundraising is over
Meet the child
Since the age of three, Kostya has been suffering from focal epilepsy. The attacks have become daily after several years. Epilepsy has a pharmacoresistant course, and even after taking the fourth anticonvulsant drug, the seizures persist. To clarify the cause of the disease and the selection of therapy, the child needs to conduct a genetic study - the panel «hereditary epilepsy». The boy was supported by «Chance» program.
To clarify the cause of the disease and the selection of therapy and the selection of therapy, a genetic study is needed - the panel «hereditary epilepsies»
RSPC of Neurology and Neurosurgery
Together we make a difference!
21.03.2017, Minsk
- Diagnosis: neurotrophic keratitis of both eyes
- Fundraising goal: purchase of medication
Amount needed
124 122
We still need to raise
32 578
Total raised (%)
74%
Belarus
- Diagnosis: oncological, hematological and immunological diseases
- Fundraising goal: medications
Amount needed
550 000
We still need to raise
495 134
Total raised (%)
10%