**DISCLAIMER**

I do not provide legal advice on this blog. No attorney-client relationship may be established through reading this blog or taking part in a discussion on the blog through the comments.

I also do not provide any medical advice on this blog. While medical conditions may be discussed, it is only for purposes of creating a dialogue and documenting my life and that of my family.

Further, all of the opinions on this blog are completely my own unless noted. This blog accepts no compensation for any opinions, posts, rants, or raves. If I say I like something, someone, an idea, philosophy, or political party, I genuinely like it and I reserve the option to change my mind. Likewise, if I say I don't like something, someone, an idea, philosophy, or political party, its because I don't, but once again, I may be persuaded to change my mind. I urge you to try!
Having a child with a CHD is like being given an extra sense---the true ability to appreciate life. Each breath, each hug, each meal is a blessing when you've watched your child live off a ventilator, trapped in an ICU bed, being fed through a tube. Each minute is a miracle when you've watched your child almost die and come back to you.
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