Help Clay in his Battle with ALS

On June 2, 2017, after many months of physical and neurological testing for muscle weakness and loss of ability to speak, Clay was given a heartbreaking diagnosis of ALS. ALS is a disease that affects the neurons that control voluntary muscle movement. Overtime movement, speech, swallowing, and finally breathing becomes something he can no longer do without that help of a caregiver, computer, feeding tube and a machine. In order to make day to day life as easy and comfortable as possible there are many expenses that are adding up quickly. Clay now requires round the clock care from caregivers and family. He requires therapy and visiting nurses regularly. There has been the need for many types of equipment from breathing machines, hospital bed, and power wheelchair to the need for a mobility van to allow Clay transportation. All these expenses are in addition to hospital stays, doctors and medications. 

This has been an emotional and stressful time for the Lee Family. Instead of worrying about medical bills and the extra expenses needed to help Clay, lets help the Lee's worry less about that and just focus on quality time with their Dad and Husband. Let's show them the love and support they have so many times shown to others. All funds raised will go directly to the Lee family and will be used for any medical necessities.