Help Hardy beat Cystic fibrosis!

Hardy was diagnosed with Cystic Fibrosis* at birth and after a surgery to repair his intestines and 16 days in the hospital Mommy was able to bring him home. He has spent the first year of his life being an amazing, inspiring little man as he is just a happy little guy despite everything this horrible disease has put him and his momma through. Hardys mom is a very hard working single mom. She eat, breaths, and dreams Hardy.  Unfortuntately, Being the most hard working, dedicated mommy I know hasnt been enough. Hardy's medication co pays and specialist visits are very expensive and although she is managing  we are  starting this campain  because Hardy is finally big enough for a vest**. A vest is a very expensive tool used as a treatment technique for CF.
The vest will help Hardy tremendously as winter is coming and he is already having alot mucus build up. But his mom's portion of the cost is $3600.  We really hope that we can help Hardy and his Mom so that she can get his vest shipped and get her little man some relif so he can keep kicking CFs Butt!!!

*Cystic fibrosis (CF) is a life-threatening genetic disease that primarily affects the lungs and digestive system. An estimated 30,000 children and adults in the United States (70,000 worldwide) have CF.

**High-frequency Chest Wall Oscillation also is called the Vest or Oscillator. An inflatable vest is attached to a machine that vibrates it at high frequency. The vest vibrates the chest to loosen and thin mucus. Every five minutes the person stops the machine and coughs or huffs.