Keenan Kahill and San Francisco Giants’ Players Perform Dynamite [VIDEO]

Youtube / Social Media sensation Keenan Kahill is joined by World Champion San Francisco Giants' Players Cody Ross and Brian Wilson in his newest viral video.

Keenan was diagnosed with a rare genetic disease at the age of one called MPS Type 6 (see full description below). Keenan underwent a bone marrow transplant in 1997 to slow down the progression of the disease, which required Keenan to live in a isolation for almost one year to prevent infection. Keenan has since had multiple surgeries including a surgery to relieve pressure on his brain. Keenan has overcome all of these obstacles to finally achieve two successes.

Keenan has garnered international recognition for his videos and with his recent appearance on Chelsea Lately it has become a game changer for Keenan. Keenan is living each and every day hoping to show the world that talent no matter how much adversity its presented with will always overcome all obstacles.

Keenan and "Ross the Boss" will unveil a new video at a game on May 25th, with a portion of all ticket sales helping to benefit causes dear to both Cody and Keenan.  Here is their promotional video to promote the big night.

Watch as Keenan Kahill performs "Dynamite" with the World Champion San Francisco Giants' Cody Ross and Brian Wilson.

MPS VI
MPS VI is a rare inherited lysosomal storage disorder estimated to occur once in every 340,000 live births. As a result of a deficiency of the enzyme N-acetylgalactosamine 4-sulfatase (arylsulfatase B), individuals with MPS VI are unable to breakdown substances known as glycosaminoglycans (GAGs), which are found in connective tissue throughout the body. The GAGs accumulate in the lysosomes of cells, leading to multi systemic abnormalities and numerous clinical manifestations including respiratory and cardiovascular complications, gastrointestinal symptoms, joint stiffness and restricted movement, and a loss of vision and hearing. MPS VI is a progressive disease and leads to severe disability and a shortened life span in virtually all cases. There are less than 1,100 people worldwide who have the disease.

To learn more about Keenan or about the special night in San Francisco, check out the following links.

http://www.keenansroom.com

http://www.sfgiants.com/specialevents