My name is Robert Himes, I'm 62 years old. Two years ago, I was diagnosed with ALS. The news was devastating, and the disease progressed very quickly. Within six months, I was unable to walk. Within the next year, I lost the ability to eat and speak, requiring a feeding tube. Later in 2024, I developed pneumonia and lost the ability to breathe on my own. I'm now on a ventilator. The average life span for someone with ALS is 3 to 5 years after diagnosis. ALS is 100% fatal.

One of the most difficult challenges is communication being unable to speak . This condition is one that all ALS patients suffer from . The goal of this fund raiser is to provide eye gaze computers to those who can not afford them . If you would like to research the technology you can view at https://www.tobiidynavox.com.

I pray for a treatment and reversal for those who have ALS everyday also. May the Lord Jesus Christ bless us all .

Thank you