Marvis' sickle cell campaign

Marvis' sickle cell campaign This is a platform owned by a young vibrant workaholic girl... Who believe everyone has a right to know and to live.

Creation of awareness for the younger minds and victims of Sickle Cells Disease.

24/10/2025
Sickle cell anemia is caused by a genetic mutation, not environmental factors—it's inherited, not "caught" like a diseas...
24/10/2025

Sickle cell anemia is caused by a genetic mutation, not environmental factors—it's inherited, not "caught" like a disease. Here's an elaborate breakdown of its causes:

1. Genetic Mutation (Primary Cause)
- At its root, sickle cell anemia stems from a single point mutation in the HBB gene on chromosome 11, which codes for the beta-globin subunit of hemoglobin (the protein in red blood cells that carries oxygen). This mutation swaps a single nucleotide: adenine (A) for thymine (T) at the 6th position of the beta-globin chain, resulting in glutamic acid being replaced by valine (Glu6Val). The abnormal hemoglobin is called hemoglobin S (HbS).
- Under normal conditions, red blood cells are flexible and disc-shaped, but HbS polymerizes (clumps) when deoxygenated, deforming cells into a rigid, sickle or crescent shape. This makes them sticky, prone to blocking small blood vessels (vaso-occlusion) and breaking down prematurely (hemolysis).

2. Inheritance Pattern (Autosomal Recessive)
- It's an autosomal recessive disorder, meaning a child must inherit two defective HbS genes—one from each parent—to develop the full disease (homozygous HbSS).
- If both parents have sickle cell trait (heterozygous AS, carrying one normal HbA and one HbS gene), there's a 25% chance per pregnancy the child will have sickle cell anemia (SS), 50% chance of trait (AS), and 25% chance of normal (AA). This is illustrated in a classic Punnett square.
- Carriers (trait) usually have no or mild symptoms because HbA dilutes HbS, but they can pass it on.
- No family history? It can still occur if ancestors carried the trait unknowingly—it's not always obvious across generations.

3. Evolutionary and Geographic Factors (Why It's Prevalent)
- The mutation likely originated in sub-Saharan Africa around 7,000–10,000 years ago as a survival adaptation. People with the sickle cell trait (AS) have partial resistance to malaria because HbS makes red blood cells less hospitable to the Plasmodium parasite. In malaria-hotspot regions like Nigeria (where ~25-30% of people carry the trait and 1-2% have the disease), this heterozygote advantage kept the gene in the population.
- It's also common in malaria-endemic areas like parts of India, the Middle East, Saudi Arabia, and the Mediterranean (e.g., Greece, Turkey). Global migration has spread it worldwide—about 300,000 babies are born with it annually, with 75% in Africa.
- In Nigeria specifically, it's the most common genetic disorder, affecting up to 150,000 newborns yearly, exacerbated by limited screening and high birth rates without genetic counseling.

4. Triggers That Worsen or "Cause" Symptoms (Not the Disease Itself)
- While the mutation is the root cause, symptoms don't appear until fetal hemoglobin (HbF, protective and dominant at birth) declines around 4-6 months of age. External triggers don't cause the disease but provoke crises in those who have it:
- Dehydration or low oxygen (e.g., high altitudes, asthma).
- Infections (bacteria/viruses exploit the weakened spleen).
- Extreme temperatures (cold causes vasoconstriction; heat leads to dehydration).
- Stress, surgery, or acidosis (buildup of acids in blood).
- In rare cases, compound heterozygotes (e.g., HbSC or HbS-beta thalassemia) have milder forms but similar causes.

Importantly, sickle cell anemia isn't caused by diet, lifestyle, or infections—it's purely genetic. Prevention focuses on genetic counseling, premarital screening (common in Nigeria via programs like those from the Ministry of Health), and prenatal testing (e.g., chorionic villus sampling). Newborn screening via heel-prick tests detects it early for better management. If you're in a high-risk area or planning a family, getting tested for the trait is a smart move—it's simple and can prevent heartbreak! Got questions on testing or inheritance risks? 🙂

Sickle cell anemia symptoms can vary in severity and frequency, often triggered by infections, dehydration, stress, or l...
23/10/2025

Sickle cell anemia symptoms can vary in severity and frequency, often triggered by infections, dehydration, stress, or low oxygen levels. They stem from the core issues: chronic anemia (from rapid red blood cell breakdown), vaso-occlusive crises (blocked blood flow), and increased infection risk due to spleen damage. Here's an elaborate breakdown:

1. Anemia-Related Symptoms
- Fatigue and Weakness: The hallmark of hemolytic anemia, where sickle cells die off after just 10-20 days (vs. 120 for normal cells). This leads to low hemoglobin, causing constant tiredness, dizziness, and shortness of breath during mild activities. Kids may seem pale and sluggish, while adults feel drained even after rest.
- Jaundice and Pallor: Bilirubin buildup from destroyed cells turns the skin, eyes, and mucous membranes yellow. Skin may appear unusually pale, especially in darker complexions where it's noticeable in the palms or conjunctiva.

2. Pain Crises (Vaso-Occlusive Episodes)
- Acute Pain Attacks: The most common and debilitating symptom, often called "sickle cell crises." These feel like intense, throbbing pain in the bones (especially back, chest, arms, or legs), abdomen, or joints, lasting hours to days. Triggers include cold weather, high altitudes, or illness; pain can be so severe it requires hospitalization and opioids for relief.
- Dactylitis (Hand-Foot Syndrome): In young children (under 5), swelling and pain in the hands and feet make them look puffy or tender, like "sausage fingers/toes." It's an early red flag.

3. Infection and Immune Issues
- Frequent Infections: The spleen, which filters blood and fights bacteria, gets scarred and dysfunctional early on (autosplenectomy by age 5). This raises risks for pneumonia, urinary tract infections, meningitis, and osteomyelitis (bone infections). Kids often get sick more than peers.
- Fever: Often accompanies infections, signaling a potential crisis.

4. Growth and Development Delays
- Delayed Growth in Children: Sickle cells impair nutrient and oxygen delivery, leading to slower height/weight gain, delayed puberty, and shorter stature. Teens might lag behind peers by years.
- Organ Enlargement: Early on, the spleen enlarges (splenomegaly) from trapped cells, causing abdominal fullness or pain.

5. Respiratory and Chest Symptoms
- Acute Chest Syndrome: A serious complication mimicking pneumonia, with chest pain, fever, cough, rapid breathing, and low oxygen. It can escalate to respiratory failure and is a leading cause of death.
- Shortness of Breath: From anemia or lung blockages, worsening with exertion.

6. Other Complications
- Vision Problems: Retinopathy from blocked retinal vessels can cause blurred vision or blindness if untreated.
- Leg Ulcers: Chronic poor circulation leads to non-healing sores on the lower legs, common in adults.
- Stroke Risk: In kids, blocked brain vessels can cause sudden weakness, seizures, or speech issues—silent strokes (no obvious signs) are sneaky and detectable only via MRI.
- Priapism in Males: Painful, prolonged erections (hours to days) due to trapped blood, which can damage pe**le tissue if not treated emergently.
- Gallstones: From excess bilirubin, causing abdominal pain.

Symptoms often start in infancy (around 4-6 months when fetal hemoglobin fades) and can flare unpredictably. Severity depends on genetics, environment, and care—some live near-normal lives with management, while others face frequent hospitalizations. In Nigeria, where it's highly prevalent (1 in 4 carry the trait), hot climates and infections exacerbate flares. Regular check-ups, hydration, and vaccines are lifesavers.

Common symptoms of sickle cell anemia include: - Pain crises (sudden, severe pain in bones, chest, or abdomen) - Fatigue...
23/10/2025

Common symptoms of sickle cell anemia include:
- Pain crises (sudden, severe pain in bones, chest, or abdomen)
- Fatigue and weakness from anemia
- Frequent infections
- Swelling in hands/feet (dactylitis)
- Jaundice (yellow skin/eyes)
- Shortness of breath
- Delayed growth in kids
- Vision problems.
These symptoms vary by individual, with severe cases requiring regular medical attention. Do you have further questions regarding treatment? 😊

Sickle cell anemia is a severe, inherited blood disorder classified as a type of hemoglobinopathy, where the body produc...
23/10/2025

Sickle cell anemia is a severe, inherited blood disorder classified as a type of hemoglobinopathy, where the body produces abnormal hemoglobin—specifically hemoglobin S (HbS)—due to a genetic mutation in the HBB gene on chromosome 11. This mutation causes red blood cells to adopt a rigid, sickle-shaped form under low-oxygen conditions, rather than their normal flexible, disc-like structure. As a result, these cells can clump together, obstructing small blood vessels and leading to reduced oxygen delivery to tissues and organs. The condition is autosomal recessive, meaning a person must inherit two copies of the mutated gene (one from each parent) to develop the full disease; those with one copy are carriers (sickle cell trait) and are usually asymptomatic. It's most prevalent in populations of sub-Saharan African descent, including Nigeria, where carrier rates can exceed 25%, as well as in parts of the Middle East, India, and the Mediterranean. Globally, it affects millions, with higher risks in malaria-endemic regions due to the trait's partial protective effect against the parasite. Physiologically, sickle cells have a shorter lifespan (10-20 days vs. normal 120 days), causing chronic hemolytic anemia. This triggers compensatory mechanisms like increased heart rate and spleen enlargement in early life, but repeated blockages (vaso-occlusive crises) can damage organs such as the spleen, kidneys, lungs, and brain, potentially leading to life-threatening complications like stroke, acute chest syndrome, or splenic sequestration. Diagnosis typically involves newborn screening via heel-prick blood tests for hemoglobin electrophoresis, while management focuses on symptom relief (e.g., pain meds, hydration), preventive care (vaccines, folic acid), and advanced therapies like hydroxyurea to boost fetal hemoglobin, blood transfusions, or bone marrow transplants for severe cases. Gene therapies like CRISPR-based editing are emerging but are not yet widely accessible. Early intervention is crucial to improve quality of life and reduce mortality, which has dropped significantly with modern care. If you're dealing with this personally, consulting a hematologist is key! 😊

23/10/2025

What is sickle cell anemia? Sickle cell anemia is a genetic blood disorder where red blood cells become sickle-shaped instead of round, causing them to block blood flow, leading to pain, infections, and organ damage. It's prevalent in individuals of African descent, such as in Nigeria, and inherited if both parents carry the trait. Management includes pain relief, hydration, and sometimes blood transfusions or medications like hydroxyurea. Early screening is crucial. Do you have questions regarding symptoms or prevention? 😊

Thank God for a successful completion of Sickle Cell Awareness Month.However, we continue to create awareness and advoca...
02/10/2024

Thank God for a successful completion of Sickle Cell Awareness Month.
However, we continue to create awareness and advocate for sickle cell disorder,
Till we achieve,
A WORLD WITHOUT ACHES AND PAINS,
A WORLD WITHOUT SICKLE CELL DISORDER.

02/10/2024

Big shout out to my newest top fans! James Israel

ADVOCATING FOR ANTIMICROBIAL STEWARDSHIP IN SICKLE CELL AWARENESS MONTH.I have observed that sickle cell disorder and/or...
19/09/2024

ADVOCATING FOR ANTIMICROBIAL STEWARDSHIP IN SICKLE CELL AWARENESS MONTH.

I have observed that sickle cell disorder and/or chronic fatigue syndrome causes irritable bowel syndrome (IBS).
I shared my experience with my haematologist and she confirmed that it could be both.
I am not surprised about this because I know that irritable bowel syndrome is associated with orishi rishi diseases as risk factors.
I am on medication for IBS and it is a long time treatment,
Only God knows when it will end.
I also observed that sometimes, IBS could occur with diarrhea or without diarrhea.
So, if as someone with sickle cell disorder and/or irritable bowel syndrome with symptoms of diarrhea,
Do not use antibiotics because the diarrhea is not due to an infection,
So, we do not abuse antibiotics,
And contribute to the global burden of antimicrobial resistance.

According to the WHO,
Antimicrobial resistance will put 27 million people into extreme poverty in 2030,
Antimicrobial resistance will cause 10 million human deaths and economic loss of US$100 trillion by 2050,
If the current trend of antimicrobial abuse or misuse are nor curbed.

@ September 2024.

Hello everyone! Here is an online research study to equip18-45 year olds with knowledge about navigating parenthood as a...
19/09/2024

Hello everyone! Here is an online research study to equip18-45 year olds with knowledge about navigating parenthood as a person living with Sickle Cell Disease or Sickle Cell Trait. Participants can earn $150 over duration of study!! The entirety of the study can be completed from the comfort of one's home.
Check Eligibility Here: https://qualifying4choices.ahc.ufl.edu/qualifying/

During a pain crisis,The normal function of the body can be altered.E.g. Urine can take a long time to come out when uri...
19/09/2024

During a pain crisis,
The normal function of the body can be altered.
E.g. Urine can take a long time to come out when urinating.

It is Sickle Cell Awareness Month - September.One of the most excruciating complaints that sickle cell warriors often pr...
19/09/2024

It is Sickle Cell Awareness Month - September.

One of the most excruciating complaints that sickle cell warriors often present at the emergency room (ER) of the hospital or a clinic is pain,
Often as a result of the pain crisis due to vaso-occlusion of the blood vessels.

Sometimes or most times,
Sickle cell warriors are not given urgent attention because some health workers do not believe or agree that the pain is excruciating and severe,
Especially because we do not scream like those in similar or lesser pain.

As a sickle cell warrior (HBSS) and medical doctor,
I can describe the pain crisis of sickle cell disorder as any of these:

1. The acute labour pain that a woman with term pregnancy experiences when the cervix is above 4 cm, having 4 contractions in 10 minutes, and each contraction lasting for 2 minutes.
2. The pain of multiple (not single) bone fractures.
3. The chest stiffness and tightness of an asthmatic patient in severe acute asthma when each breathe is strained by pain.

Please, let's stop the discrimination affecting the prompt and adequate care of sickle cell warriors.


Followers and Viewers
everyonefollowme

Address

Kaduna

Alerts

Be the first to know and let us send you an email when Marvis' sickle cell campaign posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to Marvis' sickle cell campaign:

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram