Advancing Daily Nutrition for Sickle Cell
Our New Product For Sickle Cell
Our New Product For Sickle Cell
Our New Product For Sickle Cell
With over a decade of research and studying natural alternatives to help people with sickle cell preventatively with their additional daily nutritional needs.
This is the first product from my new supplement company, "Mazz Formulaz" in honor of my father "Tarramazz" aka Terry, who recently passed away in 2023. I have worked in the natural health, vitamin and supplement industry for about decade and cared for my 29 year old son with sickle cell who also had a stroke, his entire life.
My product has 14 ingredients that are natural and can help those who have sickle cell. It is being developed in a facility that is equipped with the latest technology and equipment, allowing us to conduct groundbreaking products and make new contributions to the sickle cell community.
We are in the production phase and will have samples that we will give away. Our GoFundMe will help with the first batch and also give many of the donors an opportunity to contribute to a great cause and groundbreaking product. All donations are appreciated and we are working in many directions with many great partners to get this product going.
ONLY 14 INGREDIENTS
Our New Product For Sickle Cell
Our New Product For Sickle Cell
The experience and research combined with me being passionate about advancing medical science and improving patient outcomes through innovative research for SICKLE CELL (SCD). I created my product with 14 ingredients that can be helpful for the daily health of people with sickle cell.
My ingredients include the clinically researched L-Glutamine which can help repair damage caused by the blockages of the sickle cells and more. My goal is to provide a custom formula for a specific need, with the ingredients that can help with daily health and nutrition for someone who has sickle cell and have specific challenges and deficiencies due to their condition.
This is not to replace medical treatment or medication. It is like a multivitamin and superfood blend for the sickle cell wellness. I encourage understanding ingredients, reading labels, taking vitamins, eating well, exercising along with that but many have a problem taking multiple things and I found that good simple ingredients gives you more of what you need and that could help you preventatively in so many healthy ways.
Hello
Merchandise to Support Sickle Cell Kidd
Support #sicklecellkidd with merchandise, to encourage better living with sickle cell where we work collaboratively to develop innovative solutions to bring awareness Click link and put in a custom order to get options of merchandise sent to you .
Advancing SCD Research Natural &Medical Science
Sickle Cell Kidd G6PD Research
We are a natural medical research and development company for SCD life coaching and living well with sickle cell advocates who are dedicated to improving patient outcomes through innovative solutions. Our team of natural and medical experts works tirelessly to develop new technologies and treatments that can help people lead healthier, happier lives. Whether you're a healthcare provider, a patient, or a researcher, we are committed to advancing the field of medicine and making a difference in people's lives. Our purpose of this research and review is how both G6PD and Sickle cell both cause hemolysis and often occurs in individuals of African decent and effects males. These disorders co-occur often and possibly interact changing clinical outcomes in SCD patients.
" G6PDs stands for glucose-6-phosphate dehydrogenase. G6PD deficiency is a genetic disorder that affects an erythrocyte (red blood cell) enzyme and may contribute to anemia. The severe form of the deficiency is called FAVISM, which causes more symptoms and poses more risks than other types of G6PD deficiency.
Those with G6PD deficiency can experience increased hemolysis, or destruction of red blood cells, due to a defect in the glucose-6-phosphate enzyme. This interferes with the ability of red blood cells to bring oxygen throughout the body to tissues, causing a variety of symptoms related to anemia such as weakness, fatigue and common in sickle cell.
There are more than 400 genetic variants of the G6PD deficiency that have been identified. But just because someone inherits a genetic variant does not mean that they will become ill and deal with symptoms. It’s possible to be a “healthy carrier” and overall have a good quality of life. According to the G6PD Deficiency.
With G-6-PD deficiency you can have a perfectly normal life, provided you avoid the drugs and foods. It is therefore of great importance to learn whether you, or your baby, suffer from the deficiency, so that you can watch your diet and drug intake, and warn your physician or pediatrician and important to also know if you have a sickle cell trait which can be discovered in the newborn screening early on in life.
As mentioned above, people who have G6PD deficiency develop hemolytic anemia, which, according to the U.S. Department of Health & Human Service’s Genetics Home Reference page, occurs when “red blood cells are destroyed faster than the body can replace them.” Anemia is defined as “a condition in which the body does not have enough healthy red blood cells.” There are a number of different types of anemia depending on what’s causing it. When someone has hemolytic anemia their red blood cells, which are produced inside bone marrow, are destroyed more rapidly than usual. In people without anemia, this is normally about 120 days after they are produced.
Hemolytic anemia in people with G6PD deficiency is usually due to reactions caused by a bacterial or viral infection. It can also be due to side effects caused by taking certain medications or drugs, such as antibiotics or medications used to treat malaria. In the U.S., 1 in every 10 African-American males has the defective gene that causes G6PD deficiency. While many people with G6PD deficiency don’t have any symptoms at all and live a healthy life, some have more severe cases. When they do occur, symptoms can include those tied to anemia, such as weakness and fatigue. We want to identify it's ties to sickle cell the sickle gene which leads to elevated levels G6PD deficiency."
Learning how to avoid triggers in diet, stress , pain management and how the G6PD enzyme effects SCD patients are prone to hemolysis due to the shape of their red blood cells and how if they are deficient in G6PD the hemolysis may start to escalate. Our team at Sickle Cell Kidd will continue to follow the progress in this research and will continue to look for natural ways we can prevent the hemolysis for the SCD community.
- Latoya Harris, Author, Natural SCD Life Coach and Researcher
Reference:
https://draxe.com/health/g6pd-deficiency/
Our Services
We offer a wide range of services, including natural and clinical trials, product development, and consulting. Our team has years of experience in the SCD community and industry and is dedicated to helping our clients achieve their goals. Contact us today to learn more about how we can help you.
SCT and Getting Tested for Diabetes Inaccurately
Transforming Medical Research with Sickle Cell Kidd
At Sickle Cell Kidd, we are passionate about transforming the medical research industry. Our team of holistic herbalist, researchers, medical professionals, and previous scientists/engineers we research from and reference all work together to develop cutting-edge technologies and treatments that can improve patient outcomes. We believe that by pushing the boundaries of what's possible, we can make a real difference in people's SCD lives.
" A person with SCT {Sickle Cell Trait), hemoglobin A1C might be falsely low or high when certain test methods are used to measure hemoglobin A1C. Therefore, for persons with SCT, a normal hemoglobin A1C might not provide assurance that diabetes is absent. Healthcare providers who obtain hemoglobin A1C tests on their patients with SCT should determine from the laboratory which test method was used in order to have confidence in their patients’ hemoglobin A1C results".
According to the "National Heart, Lung and Blood Institute 2023, more than 2 million people in the United States live with the sickle cell trait. This is NOT the actual the disorder those who have the trait (SCT) only carry 1 copy of the altered hemoglobin gene and rarely have any medical symptoms related to SCD (sickle cell disease). Those with SCD carry two copies of the altered hemoglobin gene and those two copies cause a person with SCD to have reoccurring pain episodes and may have life-threatening complications that causes brain damage, and damages organs. bones, kidneys, liver, lungs, and heart."
SICKLE CELL DISEASE is most common in the people of African, Middle Eastern, Mediterranean, Central and South American and Asian Indian cultures and decent. These cultures especially African decent also have a high rate in diabetes which is why the correct test is important to prevent misdiagnosis and wrong treatments. Here at Sickle Cell Kidd we research all relating to SCD life and prevention. Knowing if you carry a sickle cell trait SCT is important before and during puberty to prevent births to teen parents who are unaware which is common in many of the cultures listed with the SCT. You can proper test at link below or contact us for more details on flyer from the CDC in this section.
SCD Creative Outlets
Welcome SCD Alternative Medical and Outlet Programs with Game Saphe
At Sickle Cell Kidd Life Coaching Alternative and Medical Research and Development, we are passionate about finding solutions to the most pressing SCD medical challenges of our time. Our team of researchers is dedicated to advancing the field of awareness alternative combined medicine through innovative research and development and so we also understand we all need a way to. express ourselves and have positive distractions. A few of our outlets we use for living with sickle cell is art, gaming, photography, music and we also learned skills in the process.
We are using our mobile gaming equipment, virtual reality and services provided by our company we created as a family Game Saphe 360, LLC www.gamesaphe.com who will provide entertainment, gaming, and photography at all of our events for sickle cell awareness. this will bring creative fun to the sickle cell community and fun!!
Our events for the sickle cell community will be coming in Summer 2024 and we are committed to working with partners around the world to develop awareness, new treatments, preventative care with combined natural and medical care for sickle cell patients, their caregivers, educators, employers and the communities they live in.
Join Us
Help Our Cause
Your support and contributions will enable us to meet our goals and fund our mission for sickle cell awareness and life coaching. Donate blood to help sickle cell patients who has had a stroke. You can also see more about donating by pressing button below!