I'm being sincere here. I am surprised and excited to see interest in this. Someone very close to me has no discernible cerebellum and no one we've seen or known has ever considered it medically interesting.
I felt the same way when I saw this article. My cousin's daughter was recently diagnosed with cerebellar hypoplasia (a missing or smaller than normal cerebellum), and it's been pretty terrifying for them. They live in a rural area where no one has ever dealt with the problem, and they're spending insane amounts of time and money on therapy (in a city an hour away) to help her learn basic skills. She celebrated her 3rd birthday this week and she can't walk, talk, or even stand unassisted.
On one hand, this article thrills me to think that at some point, her daughter might lead a relatively normal life. It's heartbreaking to see the way she suffers right now - like there's more going on in her head than she can tell us, and you can see the frustration on her face when she tries to do things or get her point across. On the other hand, I'm hesitant to send the article to my cousin because I know everything related to her daughter's problem is deeply depressing to her as she's dealing with a frustrated child who makes very little progress from day to day.
On one hand, this article thrills me to think that at some point, her daughter might lead a relatively normal life. It's heartbreaking to see the way she suffers right now - like there's more going on in her head than she can tell us, and you can see the frustration on her face when she tries to do things or get her point across. On the other hand, I'm hesitant to send the article to my cousin because I know everything related to her daughter's problem is deeply depressing to her as she's dealing with a frustrated child who makes very little progress from day to day.