Receiving detailed DNA information from your parents is the base of your life. It stores essential genetic codes necessary to begin your life. These genetic codes pass life forming information to your cells and make them learn on how to reproduce, grow, ensure good health, and build essential proteins. DNA is actually a blueprint of your life.
But, sometimes, the DNA that makes your life possible can carry defective genetic codes to the cells, which make cells behave abnormally and contribute to several deadly diseases. The onset of Sickle cell Anemia is a result of such a kind of faulty DNA.
The Blood With Sickle Shaped
A healthy red blood cell typically acquires a rounded shape and supplies adequate oxygen to the body tissues. But, when you are diseased with Sickle Cells, many of your red blood cells change their shape like a crescent moon.
When this happens, a sickle-shaped red blood cell falls short on oxygen and consequently fails to supply sufficient oxygen to your organs, resulting in widespread organ damage.
These sickle cells can’t move freely into tiny blood vessels and clump together, causing the blockage of the life-saving flow of Red Blood Cells. The blocked path of RBC sparks excruciating Pain, and if pain medicines don’t mitigate the condition, you may end up in an emergency department.
Healthy red blood cells live up to 90 to 120 days, but cells resembling a sickle have a shortened life span of about 20 days. The early deaths of sickle cells cause a severe form of Anemia. In the worst scenario, Sickle cell disease can cause a sickle cell crisis where stroke, acute chest syndrome, recurrent infections, vision loss, and premature death are common.
This disorder predominantly affects people of black ancestry. In America alone, nearly 100,000 people are fighting this pesky disease, most of whom historically belong to African origin. About 80 percent of all SCD patients live in Sub-Saharan Africa.
Why Early Diagnosis Of Sickle Cell Anemia Holds Merit| Dr. Sebi Journal
Sickle cell Anemia comes with significant risk factors if undetected and untreated. According to a report from CDC, Sickle Cell Anemia causes a considerable reduction in your total life expectancy – perhaps more than 20 years. Sickle cells can impair nearly all your body’s vital organs, including the heart, lungs, kidneys, eyes, liver, gallbladder, and brain.
In other words, Sickle Cell Anemia is deadly. Early diagnosis gives you an opportunity to access early treatment, and the early treatment of SCD can dramatically prevent premature death and the onset of dangerous complications. With the proper treatment, most children live into adulthood without any complications.
This is why experts advocate screening every newborn for Sickle Cell Disease. The early screening of SCD is done with a simple blood test called high-performance liquid chromatography (HPLC). Some other means of diagnosis methods are applicable to diagnosing Sickle cells – Click here to see them.
The Occurrence Of Symptoms | Dr. Sebi Journal
The symptoms of sickle cell anemia normally appear for the first time when a newborn reaches 5 to 6 months of age. Every individual reacts to the disease differently, so the signs, the degree of severity, and the relapse frequency greatly vary from person to person.
To better understand what symptoms people usually have during the crisis of Sickle Cell Anemia, Dr. Sebi Journal interviewed Hehleena Cardosa, a top Sickle cell expert in Washington. She helped us understand how symptoms of Sickle cell Anemia manifest. Here’s some parts of the interview –
“I always feel agonizing whenever I see an SCD patient approaching me with a wild pain,” – she recalls. It is so heartbreaking. In my 23 years of being an SCD expert, I have observed that Pain is an everyday struggle in most SCD patients.
Adding further to it, Hehleena says: “Let me tell you, most SCD patients who come here deal with a great degree of
welling on their hands and feet. Pale skin is also common, which indicates the presence of Jaundice. Fever is another symptom people usually get during the crisis of SCD.
She told us in her interview that patients with sickle cells are anemic and debilitated. If your child relatively has slow body growth, it may be a sign of Sickle cells. Frequent relapse of infection is also common in SCD patients.
What Is Even More Concerning
The hard-to-tackle pain is not a mere concern for patients with Sickle Cell Anemia – the standard set in the society makes it a stigmatic disease. Sickle cell disease is in no way contagious, yet most SCD patients face social exclusion. People consider them untouchable, and because it is strongly associated with the black community, racism is almost always the issue.
The havoc of societal stigma substantially challenges the mental stability of SCD patients; no surprise if they fail in their battle against SCD stigma. Fear, Guilt, and Mental crisis make it even harder to deal with the condition. It hinders access to the proper care and funding help.
According to a report by the National Library of Medicine, the chance of funding support for SCD is eight times less likely than getting funding for Cystic Fibroids (A genetic disease common in white people).
There is an increasing need to take appropriate steps to curb the irrelevant stigma around SCD.
Sebi Stands On Sickle Cell Anemia
Dr. Sebi narrated Sickle cell anemia as a disease that can manifest if a person is deficient in Iron. Dr. Sebi testifies that when a person is poorly deprived of Iron, the blood plasma is broken down into a sickle shape and causes dozens of complications.
You may be Iron deficient for a bunch of reasons, but the top factor that contributes to iron deficiency is not eating Iron rich foods. Dr. Sebi believed that getting the proper nutrition from food can cure any disease, and Sickle cell Anemia is not an exception.
Dr. Sebi claimed to have a cure for Sickle cell Anemia, and he proved it before the apex court. He highly advocated the intake of Iron Phosphate to treat Sickle cell Anemia.
How Effective Is Natural Treatment For Sickle Cell Anemia?
A bunch of evidence advises the use of Herbal supplements against Sickle Cell Anemia. Scientists have identified certain anti-sickling herbs that have been in use in African regions as a primary treatment for Sickle cell Anemia. The naturally occurring local herbs in West Africa, like Utile, Mexican Tea, and Petiveria, are scientifically proven herbs to tackle complications of SCD. These herbs are now the center of attraction for global scientists to develop effective holistic remedies.
The Nigerian National Institute for Pharmaceutical Research and Development has prepared a drug called Niprisan, which Nigerians use to heal Sickle Cell Anemia. It is good to know that Niprisan is a combination of indigenous herbs that significantly improves the life of SCD patients. Different scientific findings indicate that the use of Herbs for Sickle cell Anemia holds excellent merit.
Dr Sebi broadly advocated the assimilation of herbs to counter Sickle Cell Anemia. Burdock root holds an incredible amount of Iron and other substances essential for healing Sickle Cell Anemia. So Dr. Sebi used this herb in conjunction with other plants to cure this disease. According to a statement made by Dr Sebi, all plants that concentrate on Iron can help through the process of healing SCD.
Experts from India who are well-versed in Ayurvedic healing systems believe that herbs have divine powers of healing blood related disorders including SCD. B P Tamrakar, conducting research with the All India Institute of Medical Science, claims that Ayurveda can cure 9 out of 10 Sickle Cell patients. Herbs not only cleanse the body but also eliminate the root cause of disease by working at a molecular level.
We have ample evidence that suggests if we use herbs appropriately, we can significantly prevent the complications associated with Sickle Cells. Even if you are on prescription drugs, you can still use herbs to better manage and possibly cure SCD. It will also lessen the adverse effects of chemical drugs and take part in nourishment of your cells.