Today’s Faces of ALS
The stories featured here help put a name and face with the letters ALS. Individuals who have a connection to Lou Gehrig’s Disease share their hopes when it comes to finding treatments and a cure. Join them and The ALS Association in creating a world without ALS by sharing the stories that most move you to support the fight against this devastating disease.
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AngElina A. | Warwick, Rhode Island
The worst part about ALS is the fact that there's no deadline....Read More
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Ismail T. | Simi Valley, California
I'll never give up my dreams....Read More
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Amy H. | Cleveland, Ohio
Fight until we find a cure!...Read More
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Milton S. | Delandco, New Jersey
My hope is that no one will have to live with this horrible disease....Read More
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Marikatherine A. | Greensboro, North Carolina
I prayed my grandfather would keep fighting....Read More
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Tony C. | Greentown, Indiana
It's very hard to give up my independence. ...Read More
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Connie K. | Elyria, Ohio
Those two months were so hard to watch....Read More
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Rich Z. | Fishers, Indiana
I can live with ALS and will live....Read More
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Carol E. | Richmond, Virginia
I hope sharing my sister's story will inspire readers here....Read More
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Natalie P. | St. Louis, Missouri
Every time I meet a new patient or patient family, my dedication to the cause is reinforced....Read More
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Debbie C. | Akron, Ohio
Neil said everyone has a task in life....Read More
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Alicia P. | Dallas, Texas
She is affected but not defeated by ALS....Read More
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