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We are thankful to God for giving
us the dearest of His blessings and that was a wonderful daughter, the late Latreese
Nicole Fagan. She was a strong young lady who faced many challenges, but overcame many
obstacles that stood between her and her goals. Latreese was respected and admired by her
family and friends. She was determined to put her difficulties behind and her lifelong
dreams ahead. She never lost her strong faith in God.
Sometimes we need reminders of
special people who continue to bless our lives. Latreese had a unique personality that was
a treasure to the world. She was sensitive and caring, but very independent and powerful.
Latreese never put limits on herself. She just persevered to the end of her spectacular
life. Latreese would want everyone to know that there is an enduring worth to every
positive step you take, and that the good decisions that you make will come back to bless
you one day. We, her family, pray that Latreeses life story will inspire you to
reach for the stars and to achieve the things that are so important to you.
At the tender age of twelve, our
beloved daughter was experiencing many of the symptoms of the disease Systemic Lupus
Erythematosus (SLE). We were unaware at the time that Latreese was showing signs of a
lupus flare. This meant that her disease was no longer in remission, but it had become
very active. She was experiencing chronic headaches, joint pains, rashes, low-grade
fevers, fatigue and chronic infections. We took her to a pediatrician who was very
perplexed with her multiple symptoms. The physician decided to have her admitted to a
hospital to find a derivative diagnosis. After many questions and tests, the infectious
disease doctors at the hospital gave us a diagnosis of Systemic Lupus Erythematosus. Our
normal reaction was what is lupus?
Lupus is a very serious
autoimmune disease. Our daughters immune system was producing antibodies that were
attacking her healthy tissues. In other words, some parts of the immune system were no
longer protecting her body, but it was harming her vital organs. We were then referred to
a rheumatologist who started Latreese on a regimen of different medications and
treatments. The doctors stabilized her condition on I. V. steroids and oral steroids.
Latreese was never able to be drug free and she was always dependent on some types of
medications. She had to endure many flare-ups that necessitated her going into the
hospital numerous times, missing school, and one time she missed a whole year of school.
She never had self-pity, and she always had her school assignments completed in a timely
manner. Her teachers marveled at her fortitude to get her homework done knowing that many
times she was not feeling well.
Latreese was eventually transferred
to Motts Children Hospital in Ann Arbor, Michigan, due to the complexity of finding
a workable treatment program. We thank God that she was able to graduate from Mercy High
School in Farmington Hills, Michigan, at the top of her class. She was a Phi Beta Kappa
graduate and an honor graduate! She did not graduate with her graduating class due to her
missing a whole year of school, but she did not let that bother her. She was too focused
on getting into a reputable college and getting her college degree. Latreese eventually
was transferred to the adult rheumatology department at the University of Michigan
Hospital. Many great physicians in the rheumatology and hemodialysis departments as well
as other departments saw her on a regular basis. We commend the doctors, social workers,
nurses, caretakers, and others for the excellent care she received.
Latreese was accepted at the
University of Michigan in Ann Arbor, Michigan. She eventually declared her major in
Industrial and Operations Engineering. She successfully completed each year of her
schooling. She worked as a summer intern for Ford Motor Company her freshmen and sophomore
years. She loved the internship program at Ford Motor Company and was seriously giving
thought to becoming a permanent employee after graduation. But she wanted to diversify and
accepted a summer internship position at General Motors. It was during this internship
that her lupus flared again. Her doctors were able to get her lupus under control enabling
Latreese to get back in school. She was so very happy to start her senior year. But her
disease eventually returned to an active stage. She fought hard to complete her senior
year, but she suffered renal failure that was very life threatening. The start of
hemodialysis hindered her plans to return to college, but not her strong desire to get her
college degree. She maintained this desire until shortly before her death. Latreese
succumbed on May 18, 2001. She remained very positive and still was in an upbeat mood
about the future until her untimely death.
Latreese never knew the meaning
of giving up. All of her doctors, nurses, and caretakers marveled at her strength. They
witnessed and saw first hand her life and death struggles to live. She survived numerous
intensive care admissions, intrusive operations, and experiments. She told us that her
doctors called her a miracle and an enigma. They could not
understand how she survived so long with them knowing the severity of her conditions. We
saw her weakening, but she made the most of her remaining strengths. We referred to her as
our little tiger because we could see that she was trying to conquer all of
her limitations. She just refused to stay down, but fought hard to soar like an eagle.
In the long run, the lupus had
harmed every internal organ in her body. It had attacked her skin, vascular system, lungs,
heart, joints, central nervous system, brain, among others. Due to the damage to her
lungs, she became oxygen dependent. The doctors maintained a treatment of mainly
corticosteroids and immunosuppressants. The side effects of these drugs caused her
additional complications such as glaucoma, hypertension, osteoporosis, cataracts, loss of
hair, stomach ulcers, and more infections. She never knew what organs were going to be
attacked next, but she fought each attack with a vengeance. Latreese was a strong warrior
in every sense of the word.
Latreese knew that her strong faith in God sustained
her during those difficult periods. She turned her anxious moments into a positive by
staying in a great frame of mind. She was blessed with many talents. She jumped into her
craft making with a determination to succeed. Latreese has made calligraphy cards, picture
frames, padded albums, seasonal bears, designed t-shirts, socks, tennis shoes, tote bags,
and handmade jewelry, among others. She also has an impressive Beanie Babies Collection.
Latreese believed in looking your best at all times no matter how bad you felt. She set
her goals and methodically accomplished each one.
The University of Michigan
College of Engineering in Ann Arbor, Michigan, granted a posthumous Bachelors Degree
in Industrial and Operations Engineering to our daughter. The graduation ceremony
was held on April 27, 2002 at the Crisler Arena in Ann Arbor. We (her parents) adorned the
traditional graduation cap and gown and walked on stage and accepted her college degree.
We are very proud of our daughters accomplishments.
In memory of our daughter, we
started the Latreese Nicole Fagan Memorial Scholarship Fund, Inc.. Latreese was the epitome
of hard work, strong determination, strong faith and a strong desire to succeed. This
scholarship fund is designed to assist other lupus patients who exemplify the same traits
as Latreese in their desire to get their college education. Latreese realized what it
meant to work hard for something and to reach the goals that she had set. We can stand up
and feel so proud of our daughters legacy. She earned her success!
The longer-range goal of the
Latreese Fagan Scholarship Memorial Scholarship Fund, Inc. is to help lupus patients not
only with their academic pursuits, but some of their personal problems. This is a very
complex disease to fight and it can consume every emotional and physical fiber. We have
asked the Lord to bless this organization so that it can help many more lupus patients. We
need your financial help to enable us to reach our goals. Your contributions are tax
deductible. We need contributors who are willing to donate on a one-time basis as well as
regularly.
God bless all of you.
Edgar & Bettye Fagan
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