Lanxton’s Story

Site created on September 18, 2014

This blog is dedicated to my son Lanxton. He is 14 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  warrior Lanx.

Newest Update

Journal entry by Kota Brown

Yesterday our Lanx had a hematology appt. Unfortunately we still didn't get the results from his Brain Doppler yet which is very nerve wracking. However we did receive his blood levels from yesterday and they weren't as great as we would like them to be which is disappointing. We have alot of work to do to get his numbers better. Lanx hemoglobin for instance is 7.9 his numbers haven't been in the 7s since his splenectomy 5 years ago. We would rather his hemoglobin be in the high 8's -10.7 range. His white blood cells was very high etc. Lanx is now 4'8" and is 84 pound's. Please keep my baby in your prayers. #teamlanx #sicklecellwarrior #myheartbeat
www.gofundme.com/helping-lanx-our-sickle-cell-warrior
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