{"id":448,"date":"2018-10-28T17:16:11","date_gmt":"2018-10-28T17:16:11","guid":{"rendered":"https:\/\/wpdev.together-forever.fund\/?post_type=kids&p=448"},"modified":"2025-11-25T13:14:53","modified_gmt":"2025-11-25T13:14:53","slug":"aleksandr-sirivlin","status":"publish","type":"kids","link":"https:\/\/together-forever.fund\/en\/kids\/aleksandr-sirivlin\/","title":{"rendered":"\u0410\u043b\u0435\u043a\u0441\u0430\u043d\u0434\u0440 \u0421\u0438\u0440\u0438\u0432\u043b\u0438\u043d"},"content":{"rendered":"

Sasha was born a healthy and active child. The parents loved their son. At a routine checkup at six months of age, the neurologist was alerted by the baby's slightly strange look. Having received a referral for an ultrasound and CT scan, the parents began to examine the boy. The results were terrible - the doctors made a very serious diagnosis: brain atrophy and mixed hydrocephalus.<\/span><\/p>\n

For a long time it was unclear what treatment Sasha needed. At Tel Aviv Sourasky Medical Center, specialists were ready to conduct a comprehensive diagnostic examination to confirm the diagnosis and prescribe the necessary treatment.<\/span><\/p>\n

Thanks to your support in 2018, we were able to raise 5 610$ for the survey.<\/span><\/p>\n

Parents' appreciation<\/b><\/p>\n

I, Sasha Sirivlin's mom, want to thank Together Forever Foundation for the tremendous help for my son.<\/span><\/i>
\n<\/span><\/i>Thanks to the Foundation and its staff, Alexander and I were examined in Israel, where we were reassured and told that my son did not need bypass surgery at this stage. <\/span><\/i>Thank you all so much and thank you so much!<\/span><\/i><\/p><\/blockquote>","protected":false},"excerpt":{"rendered":"

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