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Class Administrator: Lori Stanford
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Class News
9/26/2007
PHOTOS!!
PLEASE SEND ANY OLD AND CURRENT PHOTOS OF YOU, FRIENDS, AND FAMILY TO [email protected] SO I CAN START COLLECTING FOR THE SLIDE SHOW. MAKE SURE THEY ARE SMALL ENOUGH TO SEND!!
THANKS,
LO
. . .
Continued
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Message
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nicki shealy rogers |
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hi everyone!!
i know that i moved befor |
Mon 6/30/2008 10:36 AM |
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HOTEL INFORMATION
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Lori Stanford |
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SO, I LIED!! HOTEL INFORMATION WILL NOT |
Tue 6/17/2008 9:11 PM |
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MEET AND GREET
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Lori Stanford |
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ON FRIDAY, JULY 11, AN INFORMAL MEET AND |
Tue 6/17/2008 9:09 PM |
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Jessica Johnson (Maiden Name-Rudd)
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Jess |
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Hey everyone! Well, updates! I married |
Sat 1/26/2008 9:15 AM |
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REUNION DATE-JULY 12
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Laura Barber |
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Hi Everyone,
An official date has been |
Tue 1/8/2008 3:11 PM |
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In case you missed the memo...
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Geno, GQ, Gene |
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Joined the peace core in 99'. Helped re |
Sat 7/28/2007 12:58 AM |
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Gwendolyn Gibson (Record) |
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hello everyone. Lets see whats been goi |
Mon 7/24/2006 11:06 AM |
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Lori Stanford Wynkoop |
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Please let everyone you know to update t |
Fri 7/21/2006 9:34 PM |
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Today's Featured Biography
Traci Dorman High
I graduated from FSU-PC in 2002, the same year I married Aaron. We moved back to his hometown (Duluth, MN) for 9 months before he decided to go active duty and apply for a pilot slot. We decided we would rather live anywhere than endure another Minnesota winter. We moved to Texas for training, to the smallest town ever on the Mexican border. His current assignment is Charleston, SC. We had our son Maximilian on 11-14-06. On 9-27-07 Max was diagnosed with a rare, fatal, genetic disorder called Spinal Muscular Atrophy Type I/II (neuromuscular disease). There is no treatment or cure for this illness. At first we just thought he was a low muscle tone child, but then he completely stopped progressing physically. He will continue to regress until his muscles completely give out on him. SMA is the #1 genetic killer of infants and toddlers. Up until the time Max was diagnosed we had never heard of this disorder. My goal now is to spread the word. This disease is considered an orphan disease (very little funding for research). It effects 1 in 6000 babies born in the U.S., but the fatality rate is so high there are very few living with the disease. If you would like more information on this illness you can visit www.fsma.org. Aaron and I are in the unique position of realizing what a precious gift he is every day. I spend my time managing his care, which entails multiple appointments per week and trying to make life interesting for him.
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I had a baby girl Ashlynn Kay on April 10, 2005 an
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3/29/2008
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I married Kris Johnson in 2000. He also joined the
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7/24/2006
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