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My son who has Arnold Chiari Malformation
$120 raised
12% of $1k goal
3 contributors
0 days left
Ended Apr 3, 2014
My son William Taylor was born with a brain defect - Arnold Chiari Malformation with Syringomyelia. He had extensive brain surgery at the age of 17 because of oncoming paralysis and host of other dibilitating symptoms.   He was told after the ...

My son William Taylor was born with a brain defect - Arnold Chiari Malformation with Syringomyelia. He had extensive brain surgery at the age of 17 because of oncoming paralysis and host of other dibilitating symptoms.  

He was told after the surgery that the type he has was really bad and that he would not be able to work.  William being the person he is did not take that advice and worked anyway.  However, it was his last employment that really harmed him the most.

He worked for the American Red Cross and everything he was not supposed to do - he did, such as driving long stretches of time and lifting heavy cots and machines for blood drives.

It took its toll on him and now he is having the blindness, Nystagmus, dizziness and severe headaches, along with gait issues and more.  13 years later, again William is being told he cannot work. All of this took place in November 2013 and continues today. 

Please help me help my son.  He has doctor’s appointment he cannot afford the co-pays or gas to get to and from and he needs medical help.  He just need a little bit more help than I can give them as his mother. 

Friends and family PLEASE help me help him.

Thanks you

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