Roxanne Donnell Hall-Kusske
ALS sucks so bad, and no one will know until they go through it. I watched the love of my life waste away to skin and bones, feeling helpless, only being able to take care of him the as best that I could.
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Nikki Rohan
Slow progressing ALS is a blessing and a curse.
Jennifer Barrett Fajardo
Caregiving for someone living with ALS is sort of like the caregiving Olympics. You will do things you never imagined you were capable of doing.
Diane Kideris
It was a privilege and honor to take care of my husband through his illness and death.
Marie Baraldi
I know that Ralph has challenges due to ALS everyday and while he is fighting that fight, I fight for everything else.
Alan Waite
I believe that Connie needed more than ever that hug, kiss, the holding of her hand, or a soft I Love You whispered in her ear at times when it became most difficult.
Jordan Reynolds
I am a mother, wife, full-time employee, and caregiver to a 40 year old husband with ALS. Of all the things we ...
Melody Ward
My husband Frank is an amazing caregiver. This journey has been overwhelming, daunting and filled with surprises. ...
Jenn Maroney
On November 15, just 264 days into our relationship, Gary was diagnosed with ALS.
Nadia Sais
I turn 35 this year and I am beyond grateful for every breath I am able to take.
Kelly Goodman
To help me while grieving, I had songs commissioned about Jason. The songs were created from my memories with ...
Randy Gregory
Despite the impact of ALS on my body, my top priority was/has always been to be present for my children, ...