The guys got their genetic tests done! Thank you!

Solomon is now 1 year and 9 months old, but he cannot stand, walk, even crawl or sit up on his own. He has no speech either, only babbling. Everything was fine until he was 3 months old, but then his parents discovered that their son started to stretch and nod his head randomly. Later they learn that Solomon has West syndrome, a rare epileptic disorder that affects children under a year old. These seizures are also very difficult to control. Solomon has tried many drugs that do not give a good result. But there is no other choice - he has to constantly try different drugs, because Solomon has no exact protocol for the treatment of epilepsy. The geneticist appointed a qualitative genetic study to identify the specific gene abnormality, to choose an effective treatment to stop epileptic seizures, which would give a boost to the child's development. Solomon and two other children with serious disabilities really need your help! Genetic testing will help each child to understand the causes of their health problems, clarify their diagnoses, and find the right treatment to make their lives happier. Take part in raising funds for these kids. Help them be closer to a healthy childhood!