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Cystic Fibrosis

Social Media Changes Lives

The other day, I received an email from a kid named Robert:

Hey Chris, you may not know me. I just recently started watching your live feed. I’m nineteen years old. I was born with a lung condition called Cystic Fibrosis. I am on the transplant list at University Of North Carolina. I will have to move up there with my dad for about 8-12 months. The insurance company covers the operation but does not cover living expenses and etc. I am currently taking donations and was wondering If you can do anything to help. Here is the link for donations.

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