Updated posted by Laura W Gresham 10 months ago
Due to the overwhelming love shown...
Due to the overwhelming love shown towards my sweet Aeidan, I am attempting to establish a facebook page for him. Hopefully, this will streamline awareness, etc. It is still new and suggestions are more than welcomed!! https://www.facebook.com/AeidansAngels
Updated posted by Laura W Gresham 10 months ago
OH wow!!!!!! Thoroughly shocked at...
OH wow!!!!!! Thoroughly shocked at the overwhelming response to my sweet Aeidan boy! If anyone has any concerns or questions about his condition, PLEASE contact me! This little boy has always captivated folks from all walks of life! Any an all donations will go directly towards helping my little Angel receive the quality of life a child so deserves--especially with his special needs. I also promise continued updates and pictures on the progress of this project. Your donations have bought you a vested interest in his happiness. It's only fair for me to help keep you wonderful folks in the loop!
Created by Laura W Gresham on July 5, 2012
Aeidan’s first seizure was when he was 3 years old. One year later he was diagnosed with Lennox-Gastaut Syndrome, the most rare form of Epilepsy that plagues the body with countless seizures, progressive degeneration of the body, along with other serious problems. Our sweet boy is now 8 years old. As of now, his IQ is at that of an 18 mo old, has limited mobility and vocabulary, and has a list of other medical concerns which contribute to his list of 16 medications. Aeidan can go from laughing and playing with his puzzles to being unresponsive and barely breathing in a matter of seconds. Out of all these issues, the problem that plagues him most is not being able to go outside or play with other children—let alone his 2 sisters. His severe sensory issues prevent him from being able to go outside unless it is cloudy. In order for him to remain somewhat stable, we limit visitors and keep his home environment cool, dark and quiet. Studies show this disorder advances quickly, causing life-threatening problems as he grows older. Life expectancy depends on the severity of these issues, which is rarely seen beyond the mid-20’s. At this time, there is no known cure for this debilitating disorder. www.lgsfoundation.org
Recent Donations (27)
$1,915 raised by 27 people in 10 months.
$20.00
Erika Haselhoff
6 months ago
$50.00
Linda and Charlie Sumrell
10 months ago
$15.00
Ron Anderson
10 months ago
$25.00
Rosario Onyekwere
10 months ago
$200.00
George and Melissa Martinez
10 months ago
$25.00
Trevor
10 months ago
$500.00
The Conquerors Assembly / Pastor Ellis
10 months ago
$100.00
Andy Hernandez
10 months ago
$20.00
Laura, Kevin & Audrey Rodriguez
10 months ago
$100.00
Sean Fruge
10 months ago
1-10 of 27 donations
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