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ABOUT SICKLE CELL — AND WORK TO CURE SICKLE CELL DISEASE

November 7, 2021 / by Dr. Carl Smit / in General Health



A NONPROFIT CORPORATION WORKING TO CURE SICKLE CELL DISEASE




ABOUT SCCF

The Sickle Cell Cure Foundation, Inc. (SCCF) is a nonprofit corporation
registered in the State of Oklahoma. Its 501(C) (3) status has been approved by
the Internal Revenue Service of the United States as of February 12, 2007. Thus,
all donations to the Foundation are tax-deductible. The date of SCCF’s
incorporation was July 28, 2006.


SCCF PURPOSE

Sickle Cell Disease (SCD) affects more people in the world than any other
genetic disease. Globally, almost one-half million babies die from SCD each
year. They have discovered a treatment that promises permanent relief from the
suffering, pain and premature death caused by SCD. Sickle Cell Cure Foundation
have devised a strong global plan for delivering this treatment. Female Viagra
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GLOBAL MISSION

Sickle cell disease (SCD) is a global problem. As the most common genetic
disease in the world, SCD touches the lives of millions and affects many more.
People of at least five racial groups and numerous ethnic origins have inherited
the sickle gene. SCD is correctly classified as a “tropical disease”. Kamagra
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MALARIA – SCD

HbF (fetal hemoglobin) suppresses the expression of sickle cell disease. In
addition, a recent literature review by the imminent Dr. David Weatherall
suggests that HbF protects infants from malaria during the first year of
life,until HbF levels decline to modest levels through a normal developmental
transition as quoted below: In vitro studies. Viagra 100mg in Australia for
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DOSAGE AND RECOMMENDATIONS


ACCOMPLISHMENTS IN 2013

The SCCF and EpimedX, LLC together developed relationships with additional
partners. The international company that manufactures the chemical used in
treatment has provided over $300,000. to further research. In mid year,
Analytical Edge Laboratories, also located in the University of Oklahoma Health
Science Center Research Park (formerly Presbyterian Health Foundation Research
Park) agreed.

 


FACTS ABOUT SICKLE CELL DISEASE (SCD)

In the United States, SCD affects primarily people of African descent. But this
pattern of prevalence is changing, with increasing numbers with SCD being found
among Hispanics, Native Americans and Caucasians. SCD affects a large percentage
of people in Central America as well as significant numbers in the Carribean and
in South American countries such as Brazil. In the Mediterranean countries, SCD
is found in people of Portuguese and Spanish descent, as well as in French
Corsicans, Sardinians, Sicilians, mainland Italians, Greeks, Turks and Cypriots.
Prevalence is increasing in other European countries such as France, Germany,
and the UK, due to both to newborns (new incidence) as well as migration from
African countries. Sickle cell disease also affects large numbers of people in
Middle Eastern countries, Indian and Asia. And approximately 70 percent of the
global number of SCD cases are in Africa. SCD is the most frequently occurring
genetic disease on earth.

Approximately 1 in 12 African-Americans are carriers of the Sickle Cell Trait.
Many more are afflicted worldwide.

The average life expectancy of someone who suffers from SCD in America is about
40 years. Where treatments are not readily available, they often die in early
childhood. In underdeveloped countries, 60-to-80 percent of babies`with SCD die
before two years of age.

SCD causes lung tissue damage, pain episodes and stroke. The blockage of blood
flow caused by sickled cells also causes damage to most organs including the
spleen, kidneys and liver.

People who suffer from SCD have mostly hemoglobin S, an abnormal form of
hemoglobin. However, all people are born with hemoglobin F, or fetal hemoglobin,
which does not sickle. Normally, by six months of age, hemoglobin F expression
switches to hemoglobin A, normal hemoglobin, or in the case of someone who
suffers from SCD, hemoglobin S.

The Sickle Cell Cure Foundations’s cure is based on introducing a protein that
causes a reversal of this switch, from HbS back to HbF. There are some people in
whom this occurs naturally, and they do not suffer any of the symptoms of sickle
cell disease.

http://www.bu.edu/sicklecell/research.html

> Home




CONTACTS

The Sickle Cell Cure Foundation, Inc.
601 NW 13th Street
Oklahoma City, OK 73103
Telephone: (405) 706-5802




DR. CARL SMIT

Carl Smit, born on October 22, 1970 in the city of Dallas, Texas, was trained in
the area of gynecology, beginning his studies at the University of Atlanta with
a student award granted for his good grades, after graduating from a general
practitioner He specialized in the area of gynecology, doing his internships at
the Piedmont hospital, after opening specialized, he obtained his master 3 years
later to enter the study of his life, which he defined as the evolutionary
process of the embryo until time of delivery To date.


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