The title was quoted to me by Steven and it fits the last week perfect. As you guy's may have noticed I have not been around. Our little guy has been in the hospital. He has been diagnosed with Central nerves system apnea complicated with reflux. This basicly means he stops breathing and spits up alot. We where admitted for a few days for testing and returned home yesterday. He is on a heart lung monitor indefinitely. His condition seems to be self correcting so far. We havent needed cpr to revive him from epesodes(3 or 4 a day). I have excellent insurance & we have in home care visits along with 24 hour tech support on the equpiment. A nurce comes out to the house and uploads the data and will deliver it to the apnea center once a week. As data is observed our usage on the equipment can be adjusted but for now he is on it 23 hours a day.
We are lucky to have such a good support system and we keep in mind many many parents have it WAY worse than us. That being said I should be back to hanging around and being a PIA very soon
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Just figured I blog a bit.
Tom
We are lucky to have such a good support system and we keep in mind many many parents have it WAY worse than us. That being said I should be back to hanging around and being a PIA very soon

Just figured I blog a bit.
Tom
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