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Foundation arranges
meeting with Bush
A wish come true
By J. Scott Trubey
Staff Writer
A 9-year-old Evans girl with a rare
blood disorder had a dream fulfilled recently when the
Make a Wish Foundation granted her the chance to meet
President Bush and tour the White House.
(Read More)
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Mrs. Smith goes to Washington
Lucy Adams
Columnist
No doubt, the gentleman wondered what
Mrs. Smith was doing in the private, men's lavatory
in the White House China Room. No doubt, her unexpected
intrusion made him very, very uncomfortable. No doubt,
he suspected espionage, terrorism, or, worse, that she
wanted to use the stall he currently occupied.
(Read More)
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A
Mother's Definition
I've
been asked to write a brief description of what it is
like being the mother of a child with Glanzmann's Thrombasthenia.
I don't know if it's possible to be brief but I will
attempt it. I have 3 children; my oldest daughter is
11, my son is 4. Julia is the baby; she's 3. Julia was
born with a rare bleeding disorder called Glanzmann's
Thrombasthenia.
(Read More) |

Mom
starts nonprofit to fight disease
By Charmain Z. Brackett
Correspondent
Helen
Smith never thought she'd champion a cause until her
daughter, Julia, was born.
(Read More) |
Mother
hopes her efforts lead to
cure for disorder
By Charmain Z. Brackett | Correspondent
Wednesday, February 1, 2006
Julia,
7, has a rare blood disorder called Glanzmann's thrombasthenia.
Mrs. Smith, through the Glanzmann's Research Foundation,
a nonprofit organization she founded, helps raise money
for research to find a cure.
(Read
More) |
Make
A Wish
White House Visit
(View
Photos) |

Columbia
County Girl Meets President!
By
Trent Butler
Story
Published: Sep 18, 2007 at 9:55 AM EDT
Just
like any other third grader, Julia Smith spends part
of the afternoon in the kitchen finishing her homework.
(Read More) |
| This
is a non profit website. The goal of this site is to
provide the general public, parents, loved ones, and
the medical community with accurate information. All
information is taken from sources believed to be reliable.
No treatment of GT should be undertaken without medical
supervision. Donations should be made to the Glanzmann's
Research Foundation.
All donations are tax deductible. |
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