Artworks for Charity Auction – 14.04.2018 Poznan (Poland)

I have a pleasure to announce that these two beauties have been given away for a charity auction for little girl named Dorota who suffers from Rett Syndrom. Auction will take place on the 14.04.18 in Poznan (Poland).

Link to an event on Facebook

Stag (Original Watercolour)
Elephant (A3 Giclee Print)

*Rett Syndrom ( brain disorder, symptoms include problems with language, coordination, and repetitive movements. Often there is slower growth, problems walking, and a smaller head size)

charity auction
charity auction


More about Rett Syndrom from Wikipedia:

Rett syndrome (RTT) is a genetic brain disorder which typically becomes apparent after 6 to 18 months of age in females.[2] Symptoms include problems with language, coordination, and repetitive movements.[2] Often there is slower growth, problems walking, and a smaller head size.[2][3] Complications can include seizuresscoliosis, and sleeping problems.[2] Those affected, however, may be affected to different degrees.[3]

Rett syndrome is due to a genetic mutation of the MECP2 gene.[2] This gene occurs on the X chromosome.[3] Typically it develops as a new mutation, with less than one percent of cases being inherited from a person’s parents.[2][3] It occurs almost exclusively in girls.[2] Boys who have a similar mutation typically die shortly after birth.[3] Diagnosis is based on symptoms and can be confirmed with genetic testing.[3]

There is no known cure for Rett syndrome.[3] Treatment is directed at improving symptoms.[3] Anticonvulsants may be used to help with seizures.[3] Special education, physiotherapy, and braces may also be useful.[3] Many people with the condition live into middle age.[3]

The condition affects about 1 in 8,500 females.[2] Andreas Rett, a pediatrician in Vienna, first described the condition in 1966.[3][5] As his writings were in German, they did not become widely known in the English-speaking world.[6] Bengt Hagberg, a Swedish pediatrician, published an English article in 1983 and named the condition after Rett.[6] In 1999, Lebanese-American physician Huda Zoghbi discovered the mutation that causes the conditio




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