<div>My name is Robert Himes, I'm 62 years old. Two years ago, <strong>I was diagnosed with ALS</strong>. 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. <strong>The average life span for someone with ALS is 3 to 5 years after diagnosis. ALS is 100% fatal.</strong>
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<div>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 <a href="https://www.tobiidynavox.com" target="_blank" rel="noreferrer noopener"><a href="https://www.tobiidynavox.com" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.tobiidynavox.com</a></a>.
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<div>I pray for a treatment and reversal for those who have ALS everyday also. May the Lord Jesus Christ bless us all .
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<div>Thank you
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Alyssa Mandarino

Martin Harper

Zach Michael

anna czech

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