Lanxton Brown The Disease With No Voice

First post: Sep 18, 2014 Latest post: Nov 30, 2021
This blog is dedicated to my son Lanxton. He is 12 years old and suffers from Sickle Cell Disease (SS).
I want others to understand more about this inherited life long blood disease. I Love my son so very much!! He has endured more then some of us adults. So my goal is to bring about more awareness, education and share the Journey of my brave little person Lanxton.