Isay Isay is a 32 year old gamer living in Columbia, SC. I cut my teeth on the early Sierra/Lucasarts adventure games and honed my skills on the Genesis. I'm a proud poppa of 2. You might already be aware of my style of PUN-ditry
Currently Playing DS - Final Fantasy 6 Advance
PSP - Tactics Ogre: Let Us Cling Together
PS3 - Asura's Wrath
On the Queue Assassin's Creed
Assassin's Creed 2
Assassin's Creed: Brotherhood
Batman: Arkham City
Beyond Good & Evil HD
Call of Duty: Black Ops
Deus Ex: Human Revolution
Fist of the North Star: Ken's Rage
Hard Corps: Uprising
Ico/Shadow of the Colossus Collection
Metal Gear Solid 4
No More Heroes 2
Red Faction: Guerilla
Sonic's Ultimate Genesis Collection
Warhammer 40K: Space Marine
What's in a name? So where does Isay Isay come from? Well to amuse myself, I name all my characters I say so whenever someone talks to them they sound like Foghorn Leghorn or what I thought English people sounded like when I was little. Needless to say, I'm easily amused.
Cystic fibrosis is a devastating genetic disease that affects tens of thousands of children and young adults in the United States. Research and care supported by the Cystic Fibrosis Foundation are making a huge difference in the lives of those with CF. My wife was diagnosed with CF when she was 13 and it is something that she deals with everyday. A year ago, we met Noah who is the same age as my daughter. He was diagnosed with CF at birth, but is a shining example of how far treatments have come. In the time between my wife’s diagnosis and Noah’s. there have been numerous new treatments which have increased the life expectancy for those with CF.
This year, I'm walking in the Great Strides walk at 2013 Columbia - Saluda Shoals, Riverbirch Shelter on 05/18/2013. Please help me meet my fundraising goal of $200.00 by sponsoring me. Your generous gift will be used efficiently and effectively: approximately 90 cents of every dollar of revenue goes to support vital CF programs.
If you would like to donate, you can do so here. Every little bit helps.
To learn more about CF and the CF Foundation, visit www.cff.org.