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We want to hear all our warriors’ stories. Send us your or your loved one’s story for a chance to be the warrior of the month and be featured across Deanna Protocol’s social media and emails.
Meet the Warriors
Greg is a 64-yr-old high school softball coach. He was diagnosed back in October of 2009 and has been on the Deanna Protocol since 2013.
He loves the NY Yankees, the Rocky series, and the song, “You Say,” by Lauren Daigle.
In addition to that, Greg comments that his progression has slowed down considerably since taking the Deanna Protocol, and he has been able to remain active with the help of his walker.
Dave was diagnosed in 2013 with Bulbar onset ALS, but his symptoms started a year prior. He has been taking Deanna protocol since summer 2022 and has stayed on it ever since!
Although having to use a wheelchair to move around, Dave loves being outside and rolling around town with his family and friends. He also enjoys movies, music and watching the world news. He has been inspired by Deanna and Steve Gleason and they inspire him to keep fighting!
Dave's goal is to enjoy his life and cherish his precious memories.
Cori is 58 years old and she was diagnosed on May 2022, she recently retired to spend time with family. Her husband is her inspiration and thanks to his efforts and proactivity with research, she was able to start the protocol soon after her diagnosis.
She loves to cook and bake for her family and friends, but also enjoys hiking with her husband and silver Labrador, Riley!
Cori has mantras that she begins her day with, such as: I am a warrior, everyday is a fresh start and treat every day as a gift. Hope these help inspire other warriors.
Terry was recently diagnosed with ALS in 2021 and has been using the protocol ever since. It has helped him reduce muscle spasms, he used to be an avid woodworker and make musical instruments, but due to ALS had to stop.
His wife is his biggest inspiration as his main caregiver and he's amazed on the way she stepped up the plate to support him.
Jerry, was a firefighter for 29 years before his diagnosis in 2016. He started the protocol 3 months before being officially diagnosed, and still takes it to this day!
He's a family man, supported by his wonderful wife, 3 daughters, their husbands and 10 grandchildren! He loves listening to Christian music and spending time with his loved ones. He shares he's had a happy life and looks forward to keep enjoying his loved ones for much longer.
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More from our Warriors
“The Deanna Protocol has given me (physical) strength and has kept me out of a wheelchair!”
“My mother was diagnosed with ALS 6 years ago. The disease started in her legs and went to her arms 6 years ago. Now, my mother is still taking the Deanna Protocol and is doing very well!”
“In only a few days, I noticed improvement in my voice. I experienced less muscle fasciculations and I wasn’t as tired.”
“I love this product. When I skip a dose, I really feel a difference.”
“I noticed a big difference in my concentration.”
“After going off the Protocol for a few days, the tremors became very very bad. After going back on it again, they went away very soon after.”
“I can definitely think much clearer on the Deanna Protocol. The brain fog is gone and it’s my first week on it. I’m hoping I see more of a difference as I continue to take it.”
“I’ve been taking the Deanna Protocol for 5 years and the product has had a wonderful impact on me physically.”
“This has been a God send! It has improved my swallowing, speech, mental clarity, less brain fog, les fasciculation! I wish doctors could recommend this!”
“I got on the Deanna Protocol right after I was diagnosed and have barely noticed any progression of my ALS in the past 3 years. I’m also treating the borrelia infection, as Dr. Tedone recommends. I feel I’m doing better than people I have spoken to who wait until they have advanced stages of ALS to take it.”
“The Deanna Protocol helps me physically. I think it’s the reason I’m not in a wheelchair. My ALS was progressing pretty quickly before I got on the Deanna Protocol. I feel more mentally alert too. That’s a relief.”
“Catching ALS early and starting the Deanna Protocol soon is so important. I started immediately after diagnosed and I’m still walking, talking, eating, dressing and showering on my own. It’s easier to preserve function than to get it back and I’m so glad I started when I did.”
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