Events | 2015.03.25
Mom of Three Fights Genetic Disease at Annual Event
Cure HHT, the only US nonprofit organization that supports HHT patients and their families, is happy to announce that Jody and Clay Nissan, mother and father of two children with HHT, will host the 3rd annual Night of Hope. The event aims to educate the public about hereditary hemorrhagic telangiectasia (HHT) and raise funds for Cure HHT, whose mission it is to develop awareness, research, treatment and a cure for people living with HHT.
(PRWeb March 24, 2015)
Read the full story at http://www.prweb.com/releases/2015/02/prweb12536223.htm
For more information, please visit
http://www.prweb.com/releases/2015/02/prweb12536223.htm
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