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We've been here twice for the Spina bifida Program, but, I've run into issues along the
way, with, our son, Ethan, and, I was able to phone down and, come see someone, um, within,
within a day of my phone call. So, um, I feel very well supported, in that, I can speak
to someone on issues that are important for his health. You get an idea of what you don't
need to worry about. There is so much information out there that you can get, your imagination
goes wild, and, your kid has everything, and then you come here, and, it's a reassurance
as well. "You don't need to worry about this or that. This is what we're going to focus
on now," and it's very, it's one day at a time, and you don't know these things exist,
until, until you have a, a child with Spina bifida, or with special needs, and you have
to seek them all out, and, these guys help you navigate your way in living with Spina
bifida, and, and it's amazing.