Posted in: Blog by chirocare on October 22, 2010
A few months ago we shared the story of the Akin family, close friends of Dr. Gina’s.
We wanted to engage and educate the public about a very rare blood disease called HLH or hemophagocytic lymphohistiocytosis. The Akin’s lost their sons Matthew and Andrew to this disease. Now, they have started their own foundation promoting awareness and community surrounding their beautiful children and others affected by HLH.
Please visit the website; Matthew and Andrew Akin Foundation to learn more about the National Marrow Donor Program, Histocytosis Association of America and the Cincinnati Children’s Hospital.
Thank you so much and please feel free to copy this link…Tell your friends and family about the Akin family and how we can all be a part of the cure!
Comments
Wow this is a great resource.. I’m enjoying it.. good article
Comment by autism symptoms on December 21, 2010 at 1:55 am
Nice site, nice and easy on the eyes and great content too.
Comment by Medical Billing on December 23, 2010 at 4:25 pm