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Wia dis photo come from, fake images
Foxx once said that he wished Deondra ‘would live her life without limits, as she lives now. Don’t get anything she can’t do. ‘
Hollywood actor Jamie Foxx says that “my heart doesn’t break into a million pieces” after the death of my younger sister at the age of 36.
Foxx says that Deondra Dixon, who has Down syndrome and will be ambassadors for the Global Down Syndrome Foundation, “the sky now dances with her wings.”
Foxx, 52, post: “Deondra … I love you with every ounce of me.”
Along with photos of them together, the Di Ray and Django Unchained star write: “My heart broke into a million pieces … my beautiful and loving sister Deondra didn’t transition … I say transition because she will always be alive. Anyone we know my sister knows how to say that she is a shining light.
“I can’t tell you how many times we have di house parties where she walks on the dance floor and steals the show.”
She added: “Deondra, you don’t leave a hole for my heart … but I’m going to fill it with all the memories you give me. I love you with every ounce of me … the news breaks our family but let’s put di pieces of again along with your love … and you please keep my family in your prayers. “
Di Global Down Syndrome Foundation says Dixon died on October 19.
Wia dis photo come from, fake images
Foxx and Dixon attended the Be Beautiful Be Yourself fashion show last year
The tribute at the top of the Foundation’s website reads: “Deondra came into the world in a loving family and we treat her like any member of the oda family. Dem gives her gifts of full acceptance, trust and knowledge. Dem empowers her. To graduate with a regular high school diploma and take life by storm, if you meet Deondra, she does well.
“Wedon lost our talented, intelligent, feisty, beautiful, kind, caring, caring, pure and generous heart, DeOndra Dixon. Our Down syndrome community did not lose a beacon of hope, a true leader, and a role model we aspire to. always. help the odes. She is like a shining light for our world. “
Dixon’s profile on the foundation’s website reads: “I’m sorry to say I was born to dance. I want to be a professional dancer. My brother didn’t give me a chance to do some special things. I dance for my Blame It video. I don’t dance in the stage for some of my concerts at todo di kontri. And guess what? I don’t dance for the di Grammys!
“I know my family loves me. Dem never set limits and always make me feel like I said I touch the sky.”
- For between 700 and 1,000 babies born, one has Down syndrome, which means they have extra chromosomes and learning disabilities.
- In the 1960s, life expectancy was 15 years, now between 50 and 60
