Spinal Muscular Atrophy Type 2
Organized by: Aeriel Jaggard
My name is Aeriel Jaggard. I was diagnosed with Spinal Muscular Atrophy type two from seven months old, and have unwillingly spent most of my 23 years in a rural area of Tye, Texas with very limited disability resources until moving into the city of Abilene in search of more functional accommodations..only to be told by the local APS "specialist" that my circumstances are my "fault" and recommended mandatory placement in an assisted living facility. Being naturally in disagreement with this assessment as a 23 year old proven autonomous and prolific abstract artist and business owner, I'm driven to find the help that is necessary to meet my potential. I am looking for a philanthropist interested in providing funding for some of my specified medical needs such as a robotic arm wheelchair extension and stem cell treatment to hold me over while a cure under development is due to be released in 2018, since I live under poverty level and don't happen to have a spare quarter million in my purse. I am willing to contribute to media as an academic spokesperson if anyone needs such a subject and waive personal information for educational and commercial use where applicable. For further inquiry, here are my contact details: email@example.com ..Thank you!