Brad Hauer Fund

Brad Hauer has recently been diagnosed with an extremely rare autoimmune disorder called Stiff Person Syndrome (SPS). 
This disorder is so rare that chances of getting SPS is only  1 in 1-million.  SPS affects the central nervous system, causing extreme muscle spasms and nerve pain. In turn, it disrupts daily life from "routine" simple task to major movements such as walking and the ability to drive.  Brad has been and continues to be in constant pain.  THERE IS NO CURE FOR SPS.  Brad can only receive treatments to assist him.  He has already received 5 plasma transfers and medication.  This only helps control symptoms, but again will not cure him.  Brad needs and will continue to need 24 hour care.  His wife Margo, has made the tough decision to quit her job to care for him and their 6 kids.  This means losing a second income.  This is a life changing event for the Hauer's.   Anything you can assist with financially will be greatly appreciated.   Also, Brad welcomes visitors at his home for any friends or family that would like to stop by.  God bless and thank you in advance!