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2010 CHERUBS Masquerading Angels Ball
October 30, 2010 6:00 pm - Midnight ![]() Formal Charity Masquerade Ball on the eve of Halloween Hiton Durham near Duke University 3800 Hillsborough Road, Durham, NC 22705 Tickets and sponsorships now avalable! ![]() Come join us on the eve of Halloween for a magical
night for a good cause. Celebrity guests, enchanting decor, amazing
music, a casino, silent auction and beautiful attire will make this a
night to remember.
Our
formal black and white masquerade ball encourages men to wear tuxedos
and women to wear white. Dust off your wedding dresses ladies, you are
encouraged to wear it again or you can opt for a black dress or formal costume.
Event: CHERUBS Masquerading Angels Ball Date: Saturday, October 30, 2010 Time: 6:00 - 7:00 cocktail hour, 7:00 - Midnight Ball Location: Hilton Durham near Duke University, 3800 Hillsborough Road, Durham, NC 22705 Beneficiary: CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support. Money raised from this event will go to CHERUBS to fund services to further help families of children born with Congenital Diaphragmatic Hernia. CHERUBS is a 501(c)III international children's charity. Attire: Our FORMAL black and white masquerade ball encourages men to wear tuxedos and women to wear white. Dust off your wedding dresses ladies, you are encouraged to wear it again or you can opt for a black dress. Ladies dresses must be floor length. FORMAL period costumes are welcome, such as the one to the left. Masks are required, some will be provided. Not acceptible; typical Halloween costumes, short dresses, street clothes and scary masks. Tickets: $50.00. Tickets include entry to event, casino, auction, ballroom. It also includes entertainment, hors d'oeuvres, drinks, 2 raffle tickets, 1 bar ticket, 2 casino chips. Age Requirement: You must be 21 years old or older to attend. CHERUBS reserves the right to refuse ticket sales when necessary. Master of Ceremonies: Bob the Blade from 96 RocksSpecial Guests: Miss Raleigh, actress and model, Wendy Petty and Miss Durham County, Jacquetta Taborn Live Band: Will be revealed soon! Casino: Take a spin on the roulette wheel or try your hand at blackjack in our Casino Lounge. Silent Auction: Come browse our auction items donated by celebrities, local artists, local businesses and members of the charity. Photographs: Have your formal portrait taken, a reminder of a wonderful night. Taken by Jim Shaw Photography.
Our Organization: CHERUBS is
a
501(c)III
organization located in North
Carolina.
CHERUBS serves families of children and adults born with Congenital
Diaphragmatic Hernia (CDH). As of April 2008, we have over 2250 members in
all 50
states and 33
countries. Our Board Members include
the founding father of in-utero surgery, genetic counselors,
epidemiologists,
pediatric surgeons and parents of children born with CDH.
We are a volunteer-run organization and a
United States Internal Revenue Service recognized 501(c)III Non-Profit
Organization.
www.cdhsupport.org What is CDH?
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CHERUBS - The Association of Congenital
Diaphragmatic Hernia Research, Awareness and Support. CHERUBS is
the original CDH non-profit organization founded in 1995 to help
families
and medical care providers of children born with CDH.
CHERUBS
is the world's
first, oldest, and largest CDH non-profit organization. We are
truly a grassroots organization - CDH families creating something out
of nothing when there were no other CDH group, information and services
in 1995. CHERUBS
was created to make sure that no family endures Congenital
Diaphragmatic Hernia without support or accurate information. Our Board of Directors
includes CDH parents, grandparents, survivors, nurses, doctors and the
world's top CDH researchers.
CHERUBS is run solely by volunteers and donations. At CHERUBS,
every CDH family has an opportunity to honor or remember our children
while doing good to help others and work together as a CDH community. No other charity in the world has such a
respected, educated or experienced group of leaders who care so much
about the CDH community.
CHERUBS has had many accomplishments and projects in our first 15
years. We are the first charity to promote CDH research,
awareness and support. We created a model organization for
other groups with our services, structure and projects. We
created the first CDH newsletter and the first on-line listservs and
forums for CDH families. CHERUBS is a founding member of
ACDHO. Our CDH Research Database is the largest database in
the world created by CDH families to compare medical histories that
hopefully will assist the CDH research community. CHERUBS
has spoken at International CDH Study Group meetings, given speeches
around the country, given interviews for 20/20 and Mystery Diagnosis as
well many other national media outlets. We hold the
International CDH Conference for families and researchers. Along
with several other CDH
organizations and 1000's of families, we designed the official
Congenital Diaphragmatic Hernia Awareness Ribbon and took a stand
against the trademark on "Congenital Diaphragmatic Hernia
Awareness". We created awareness products, the first
CDH awareness store, logos and we proclaimed the cherub as the official
international symbol of Congenital Diaphragmatic Hernia to represent
those CDH babies who do not survive. And we have done it
all through the hard labor of dozens of caring volunteers who want
nothing more than to make the journey of CDH a little bit easier for
families.
In 2010, as we celebrate 15 years of non-profit service to the CDH
community, we continue our good work through more conferences and
get-togethers, more on-line services and more research. We
have kicked off the year with our "Save The Cherubs" CDH Awareness
Campaign, 2 Congressional Bills to benefit CDH and other cause and
launched our new web sites.
We
are proud to serve over 3100 families in 38 countries and all 50
states affected by CDH since our creation. Through our
dozens of free ground-breaking services and the friendships made within
our member community, CHERUBS has positively affected the lives of 1000's of CDH families and
inspired many new CDH charities and projects who have followed
in our footsteps. We will continue to lead until Congenital
Diaphragmatic Hernia is no more. We are devoted to finding the cause,
prevention and best treatments for CDH.
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