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Le Reve Magazine Red Carpet Launch Party Event Benefitting Aniston Williams
Join Le Reve Magazine and celebrity guests to celebrate the launch and Fashion Show event with showcasing designers in the 2012 Dream Team.
Get your chance to meet with a Hollywood Movie Producer and former casting agent Maxann Crotts Harvey, Young Talent Promotional Manager Dani Geddes and welcome our model scout Michelle Johnson from Mama J Management.
Tickets can be purchased on the day for $25.00
Celebrities expected: ALYCESAUNDRA AND GIAVANNA - The Tiara Twins (TLCs Toddlers and Tiaras), PAISLEY DICKEY (TLCs Toddlers and Tiaras) KEYLA CHILDS (The Bay), JULIONNE JOHNSON (ABCs The Revolution), NACHELE JOHNSON (ABCs The Revolution),
JEVON JOHNSON (ABCs The Revolution), SOPHIA RAYNE THOMPSON (Extreme Home Makeover), EMMA BROCK (TLCs Toddlers and Tiaras) and DARRYL WASHINGTON (ABCs The Revolution).
MORE: Featuring a Showcase of our Feature Designers, Melissa Jane, Snooty Booty, The Crown Collectors, E Couture, Purple dotted Zebra, Snowbabies, Mara Skye pageant diva wear, Culver Cutie, Janay's fab Tutu, Todays Boutique Trends, Lu Lu Et Gigi Couture, Cp Pageant wear, Tattoo'd Tykes, Cindy Jeffers pageantwear, Love baby J , Lipstik girls and Glossy Chick
WHEN: Saturday, December 1st 2012
WHERE: Ocean Dunes Resort
201 75th Avenue North
Myrtle Beach, SC 29572,
PRESS CHECK IN: 4.30PM
RED CARPET ARRIVALS: 5.00PM
EVENT OPENS: 6.00PM
About Le Reve Magazine
The first magazine to feature both girls of the pageant industry and models. A magazine that combines talents of the entertainment industry reporting on the latest and most exclusive news and events to all ages.
Showcasing the positive work of both the pageant performers and models that specialises with young talent.
About Aniston Williams
Aniston Brook Williams is the 2 year old daughter of Chad and Kaci Williams, and the sister to 5 year old Dalton. She has brown hair and blue eyes...this is the life that Aniston's mother would have loved to have shared with her since she grew up in pageants and one day dreamed of experiencing that with her daughter if the Good Lord blessed her with a little girl.
At the age of 6 months, the doctors began some research on her because of not meeting her developmental milestones. It was then that they found her to have a chromosomal abnormality that is extremely rare. With this disorder comes many neurological and health issues.
She also doesn't walk or talk and when traveling anywhere she can't travel without oxygen in the event of a seizure outside of the home or the hospital. She takes 10 meds in the morning and 9 in the evening and two others in the middle of the day...just to keep going.
The first issue she had to tackle was tethered cord syndrome, in which she had surgery on at 10 months to release and it wasn't until two weeks after that she rolled over for the first time. Since then, she has had a helicopter ride to MUSC Children's hospital where she wasn't breathing on her own, which resulted in a Nissen Fundoplication procedure and the placement of a g-tube. From that time, she has had several bouts with seizures that cause her to quit breathing and now she is tackling unexplained elevated liver enzymes.
She no longer takes by mouth and is strictly tube fed through the g-tube placed in her stomach.
She has been in the hospital at least once a month since December 2011 with the exception of July. She has sometimes been hospitalized more frequently than once a month. She recently visited a new specialist in Georgia who want to proceed with more testing such as mitochondrial disease and another rare disease called CDG. The chromosomal abnormality Aniston has been diagnose with, as well as the things she is currently awaiting testing for are not curable diseases. Please help support this little miracle and know that her family appreciates it more than you will ever know.
God Bless each and everyone of you and most importantly, please keep Aniston and her family in your prayers, as HE is the Ultimate Physician and we know that He has a plan for Aniston.