Angela Blair

Worship and Praise in the NEW YEAR 2026 Live with one of God’s Anointed Vessel’s Lady Angela Blair, NYE at Amity Bible Church - 7pm.

Pre-NYE Fellowship begins at 6pm.

cc: Angela B-Jeffries

Please help us wish our CEO and God’s Anointed Vessel, Angela B-Jeffries a very BLESSED Birthday today!

May the Lord continue to grant you all of your heart’s desires in the coming years!

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“Happy Birthday Angela” 🎂🎈🎁

~ From the ABJM3LLC Family

DALLAS and Surrounding Areas, Get your tickets for where “Gospel and Hip Hop Meets Classical”, featuring some fantastic artists like Erica Campbell, Gaye Arbuckle, Zebulon Ellis, Tatiana Barnett plus a special “50 years of Hip Hop” tribute featuring DJ Spinderella, Leon Lacey, Norris Johnson, Robert Sput Searight, our very own Angela Blair-Jeffries! You do NOT want to miss this event.

Come out and support this amazing event produced by Toska Medlock Lee, Tenth Child Inc & Project Unity.

Tickets are available at Dallas Symphony Orchestra, dallassymphony.org.

Angela Blair-Jeffries
ABJ Music, Media & Management LLC

Hello Angela Blair Family! We have been working extremely hard loving on people the way the Lord intended for us to love.

This holiday season, I am personally asking for my friends to please help Malachi’s dream come true! He is a HUGE Cowboys fan. We have ONE Dallas Cowboys Home Game left and I want to get him there! Will you help me?

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Meet Malachi Boyce. Date of birth 12/15/2004. A vibrant and loving 17 year old boy who loves the Dallas Cowboys and happens to have been born with Hunter syndrome.

What is Hunter syndrome?
Hunter syndrome or Type II Mucopolysaccharidosis is a lysosomal storage disease which is caused due to iduronate-2-sulfatase(I2S) enzyme deficiency. This enzyme is needed to breaskdown complex food molecules called glycosaminoglycans.

How rare is Hunter syndrome?
The prevalence of Hunter Syndrome is 1/100,000 – 170,000 of male babies. Hunter syndrome is an X-linked recessively inherited disease, therefore, it occurs, almost exclusively in males.

What are the symptoms of Hunter syndrome?
A child with Hunter syndrome may look normal up to the age of 2-4 years old. Facial and physical changes as well as intellectual disability can be seen by the age of 2-4 years old.

No cure is available for Hunter syndrome. The most severe cases can be life-threatening, with life expectancy typically between 10 and 20 years.

**He turned 18 on 12/15/22, a miracle alone. He lightens up when he sees the Cowboys and will even mum a little. He doesn’t speak but he does smile. Can we help him smile before his family moves out west in a couple of weeks so that he can receive better treatment.

Whatever you give will be given towards tickets for the Cowboys vs. Eagles game on Christmas Eve or flood him with any Cowboys related and we will meet to pick it up for him for Christmas.

You may give financially through our charity, LifeChangersNPO, Inc via CashApp - $LifeChangersNPO or Zelle - [email protected].

Merry Christmas and thanks in advance!
Let’s change a life, One at a time!

Love,

Angela Blair-Jeffries
Life Changers NPO, Inc
Exec. Director