All 3 will team up with Jar Of Hope to take on Duchenne Muscular Dystrophy

.@DeonnaPurrazzo & I, alongside @MrsAIPAlisha, are joining JAR of Hope @runDisney 5k this April to make an IMPACT to end Duchenne Muscular Dystrophy!

Please consider donating and help us race to find a cure! https://t.co/D7mvS7Guyb pic.twitter.com/djcgIXRkXP

— Steve Maclin (@SteveMaclin) March 18, 2023

SPECIAL ANNOUNCEMENT

I’ll be participating in the Disney 5K race on April 14 representing @IMPACTWRESTLING and @jarofhop along with @DeonnaPurrazzo @SteveMaclin. Please help us raise money for a great cause and let’s make an IMPACT on Duchenne Muscular Dystrophy. Link in bio 🙏 pic.twitter.com/c7IxH6XkHP

— JUSTLISH (@MrsAIPAlisha) March 18, 2023

What is Duchenne Muscular Dystrophy?

Courtesy of: Jar of Hope

Because no child should have to suffer like this.
Duchenne muscular dystrophy (DMD) is one of the rarest diseases on Earth. DMD is a fatal, muscle-wasting disease you are born with. It occurs once in every 3,500 live births and effects mostly boys. In the United States, with a population of over 330,000,000 people, only about 20,000 children are stricken with Duchenne. And there is no cure.

Our goal is to find a cure for Duchenne muscular dystrophy. With organized fundraising events and support from you, we can continue our mission and turn the dream of finding a cure into a reality.

Duchenne Muscular Dystrophy Clinical Trial 
We have partnered with the University of Florida College of Medicine and RESTEM LLC to to initiate an important trial for Duchenne muscular dystrophy (DMD).

Authorization has been granted to begin Phase 1 of the trial. Here, a “randomized, double-blind, placebo-controlled Cross Over study to assess the safety, tolerability, and preliminary efficacy of Umbilical Cord Lining stem cells (ULSC) in Pediatric patients with Duchenne muscular dystrophy (DMD).”

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