My 11m old was just diagnosed with central sleep apnea. It wasn’t a giant shock because we thought he had something going on because of his dwarfism. But it was surprising to find out he has central sleep apnea instead of obstructive. Basically surgery can’t fix it and it’s a life long diagnosis. Does anyone have experience with this? I know I make mountains over mole hills, but I’m freaking out. It feels like my little guy is losing all parts of normalcy. How do you go to scout camp with a cpap machine? 😭😭😭