Maceo Carter
@MaceoCarter
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Father, Husband, UNC Tar heels Fan, Sibling, Living with ALS.
Joined May 2017
First it was ALS Arizona to show love. Now, You damn right she's getting recognition from national ALS organizations!! Tell a friend tell a friend. #EndALS.
Our friend Maya Carter wrote a book for caregivers that was "born in the sacred space where exhaustion meets endurance." Maya is a caregiver to her husband Maceo, who has been living with ALS for almost 10 years. Get "The Sweet Between" on Amazon!
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No Hoyer lift means a call to your local fire department non-emergency number so that if you fall you can ask for a lift assist! Personal note – it is weird as hell being able to feel the strength from someone else's arms that you cannot feel in your own body! #EndALS
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IT’S HERE!!!.*The Sweet Between: A Soft Reset* is now available in paperback. Written by my wife, my caregiver, my person — for those who love hard and keep going. This book is a reset. A refuge. A resistance. Order your copy from the link below. Show your love. #EndALS.
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Because being a wife/mom/caregiver/daughter/sister/graduate student wasn't enough my foxy fine wife is now a self published author!! Please support if you can! #EndALS.
amazon.com
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Great night with ALS Arizona during their Boots and Bites fundraising event which raised over $510K!!.#EndALS
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In 2016 the doctors said you have 2 to 5 years to live and get your affairs in order. Well, I made sure to tell my son I'm proud of him before joining the High School Graduating Class of 2025!!.#EndALS
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RT @alsassociation: MUST WATCH: Sen. Durbin to HHS Sec. Kennedy: "Cutting medical research is giving up on the future. You can't do that. T….
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Honored again to have my flag among the other thousands flying on the National Mall!!.#EndALS.
Today, we’re here on the National Mall, steps from the White House & the Capitol, to be visible & spread awareness. We’re planting 6,000 blue flags to represent the 6,000 people diagnosed with ALS each year. #ALSisHere, but #SoAreWe – & we’re not going anywhere until we end ALS.
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With this being–#alsawarenessmonth– Thank You to all the various sports teams that have shown myself and others in the ALS community love especially – @UNC_Basketball .#EndALS
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Never thought I would be cited in a publication used to help make #ALS a livable disease!!!! #EndALS
This week, several leading ALS organizations came together in Washington, D.C. to expedite solutions to advance the fight against ALS in the current policy environment. We have committed to leverage our individual and collective strengths, reduce duplication of efforts, and
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Shout out to the collaboration between.@synapticure and/@TeamGleason and/@BridgingVoice for this new trackball to help me better continue to work!!.#nowhiteflags.#EndALS
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While the rebranding of viral sensations used by others are gaining national attention THIS is the stuff people living with this disease and their families are facing!🤬🤬.@SenMarkKelly @SenRubenGallego .#EndALS.
URGENT: A leaked HHS memo proposes cutting all funding to the National #ALS Registry. This would erase decades of critical research & let down 20,000+ who've contributed. We’re calling on Congress to stop this NOW. Read our letter and take action today:
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RT @SloHoopsFan: VIDEO: Jalen Brunson gets emotional when talking about former Maverick Casey Smith and Heather Mau for the job they did in….
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They never tell you ALS can turn your wife and kids into caregivers and now power wheelchair technicians!.#ENDALS.@alsassociation
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