Two days ago, my young son was diagnosed with congenital heart disease. Within 24 hours, it became apparent that I would need a means of working through the cognitive and emotional turmoil due to my baby's condition. Additionally, I would like to keep family and friends updated and shed some light into Baby G's disease. Answering the same questions over and over is very draining.
A blog seemed like the perfect solution. Keeping a record of our journey is therapeutic for me, and it can serve as a resource for our support network.
Please excuse my poor grammar and writing. I don't have much time to write and edit these posts; I would rather be playing with my little baby. Any questions can be directed to the comments section. They may not be answered immediately, but I will do my best to reply in a timely manner. Once again, I would rather be playing with Baby G.
The following posts will deal with G's heart murmur, his achievements, and the amazing treatments available to him.
And here we go...
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