Play with a pro! Nyheim Hines, NFL Indianapolis Colts Running Back joins the MDA Let’s Play gaming community on June 12 from 7 p.m. to 8 p.m. for Game Night


Viewers and gamers can look forward to an exciting evening of programming, including gameplay from popular titles Among Us and the Jackbox games, with children and families living with muscular dystrophy, ALS and associated neuromuscular diseases, coming together to create a community.

NEW YORK, June 1, 2021 / PRNewswire / – The Muscular Dystrophy Association‘s (MDA) 2021 national spokesperson, Nyheim Hines, running back for the NFL Indianapolis Colts, will join the MDA Let’s play community of players on saturday 12 june of 7-8 p.m. for the organization’s weekly game night. Hines, whose mother lives with Girdle Muscular Dystrophy (LGMD), joins families living with muscular dystrophy, ALS and related neuromuscular diseases to raise awareness and fundraise for the mission. The prizes offered by Hines include personally signed Indianapolis Colts jerseys. This feed will be hosted by Beaniez, and special guests will be passing through the evening.

“I love the game and I love helping MDA amplify its mission so that we can find cures for my mother and all the families in MDA. Raising awareness and coming together as a community through the game is a chance for everything. the world to connect and energize the mission of funding breakthrough science and care through research, ”Hines said.

Players across the NFL have supported the Muscular Dystrophy Association for many decades, and Hines’ support for MDA in My Cause, My NFL Cleats annual campaign, caught the attention of a 17-year-old Jayston paulson. After a hip injury derailed him in 8e grade, Paulson was diagnosed with Lambert-Eaton myasthenic syndrome (LEMS). Undeterred, Paulson secured a spot on his football team in his sophomore year before becoming 1st all-district team during his junior year. As someone who pursued football despite his neuromuscular disease, Paulson saw Hines’ commitment to MDA and wanted to support the organization alongside him. Paulson will play with Hines on saturday 12 june.

“I am delighted to meet Nyheim! I really like the way he represents neuromuscular diseases as a spokesperson for MDA this year, especially with his custom MDA cleats which first caught my attention!” Paulson said. “After reading more about him and learning what he’s been through with his family, it’s cool to know that there is someone out there who plays the game that I love, who can actually relate to me. in a way. I thought maybe I was the only connection between that disease and playing football. “

Hines’ studs included the names of his grandmother, mother and uncle, who live or lived with girdle muscular dystrophy (LGMD), one of 43 neuromuscular diseases that MDA treats and seeks to cure.

The purpose of MDA’s weekly game night programming, which was launched to keep families connected throughout the pandemic, is to raise awareness and fundraise for the mission of providing the best care, funding clinical trials. and finding cures, and advocating for access for the disabled community. . MDA Let’s Play is now a year round gaming community that meets on weeknights and every weekend for Saturday night gaming evenings.

The community has solidified throughout the pandemic, with MDA families at high risk of COVID-19. MDA provided a safe place for families to reunite and for MDA summer campers nationwide to stay in touch with their friends when the in-person camp was canceled due to the pandemic. To date, over 2,000 people have joined the MDA Let’s Play community on Tic and Discord. You can follow MDA Let’s Play for daily updates here.

“It has been extremely gratifying to be able to keep our families connected through our virtual programming all year round. The game is a great equalizer for people with disabilities and provides a platform for entertainment and inclusion. MDA Let’s Play is one. Innovative gaming platform that connects influential players and streamers with our community. We are delighted to welcome our national spokesperson, Nyheim Hines to the game, ”said Kristine welker, Chief of Staff, MDA.

MDA Let’s Play Background
MDA Let’s Play launch press release
MDA Let’s Play For A Cure Streamathon
In 2020, MDA Let’s Play For A Cure brought together some of the biggest names in gaming, including Zedd, missharvey, Voyboy, Trick2g, JonSandman, Clayster from NY Subliners, and Stixxay and xSojin from Counter League Gaming, among others, and showcased gameplay from Among us, League of Legends, Rocket League, fall guys, Call of Duty and more.

About Muscular Dystrophy Association
For 70 years, the Muscular Dystrophy Association (MDA) has been committed to transforming the lives of people with muscular dystrophy, ALS and related neuromuscular diseases. We do it through scientific innovations and innovations in care. As the primary source of funding for neuromuscular disease research outside the federal government, MDA has committed more than $ 1 billion since our inception to accelerate the discovery of therapies and remedies. Research we have supported is directly linked to life-changing therapies for several neuromuscular diseases. MOVR from MDA is the first and only data center that consolidates clinical, genetic and patient-reported data for several neuromuscular diseases to improve health outcomes and accelerate drug development. MDA supports the largest network of multidisciplinary clinics providing top-notch care in over 150 of the country’s top medical facilities. Our Resource center serves the community with specialized one-on-one support, and we offer educational lectures, events and materials for families and healthcare providers. MDA advocacy supports equal access for our community, and each year thousands of children and young adults learn life skills and gain independence in summer camp and through recreational programs at no cost to families. During the COVID-19 pandemic, MDA continues to produce virtual events and programs to support our community when in-person events and activities are not possible. COVID-19 guidelines and MDA virtual events are posted on For more information visit



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SOURCE Muscular Dystrophy Association

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