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    • Sickle Cell Trait
    • Oxygen Deprivation & SCT
    • Support Here
      • Donation Page
      • Basketball Platform
    • Who is Farron?
    • Take the Survey here:
    • Contact Page
    • The Crew
      • Who is Deja?
      • Who was Mr.Smith
      • Who is Jody?
      • Who is Dr Maisha?
  • Sickle Cell Trait
  • Oxygen Deprivation & SCT
  • Support Here
    • Donation Page
    • Basketball Platform
  • Who is Farron?
  • Take the Survey here:
  • Contact Page
  • The Crew
    • Who is Deja?
    • Who was Mr.Smith
    • Who is Jody?
    • Who is Dr Maisha?
WDC on SCT

¿WHATZ in your Genes?

¿WHATZ in your Genes?¿WHATZ in your Genes?

Our WHY in the Community

Why This Matters

Individuals with Sickle Cell Trait (SCT) may appear healthy but are at risk for oxygen deprivation under certain conditions; especially during intense physical activity, heat exposure, high altitude, or dehydration. This can cause red blood cells to change shape ('sickle') and block oxygen flow to muscles, organs, and the brain; even without having full-blown Sickle Cell Disease.

What Happens in the Body?

When the body is deprived of oxygen (called hypoxia), especially during exertion:
- Red blood cells in SCT can sickle temporarily.
- These sickled cells can block small blood vessels.
- Oxygen can’t reach muscles and vital organs.
- This leads to sudden weakness, muscle breakdown (rhabdomyolysis), collapse, or even death.

Common Oxygen Deprivation Triggers:
- Heavy workouts or sports conditioning
- Dehydration or lack of rest
- High altitudes or flying
- Heatstroke or overheating
- Sickle Cell Trait + low oxygen = increased risk of collapse

The Role of Pulse Oximeters in SCT Safety

A pulse oximeter is a small, easy-to-use device that clips to your finger and measures:
- SpO₂ (blood oxygen level)
- Heart rate (BPM)
 

It helps detect dangerous drops in oxygen before symptoms become life-threatening;  making it an essential tool for SCT education and emergency response.

SCT Athlete Safety Zones

SpO₂ Reading | What It Means | What To Do
------------|----------------|-------------
95–100% | Normal | Continue with activity
90–94% | Caution Zone | Rest, hydrate, monitor
Below 90% | Danger Zone | Stop immediately, seek help

Prevention Tips for SCT Patients & Athletes

  

1. Stay well hydrated – before, during, and after activity
2. Rest every 15–20 minutes – especially in heat
3. Avoid all-out sprints or high-rep drills
4. Use a pulse oximeter during sports and high-risk situations
5. Recognize symptoms early:
 - Muscle cramps or weakness
 - Breathing difficulty
 - Chest pain
 - Dizziness or confusion
 - Blue lips or fingers

Get Involved to Learn More

Contact Us to Host a Workshop or Presentation 

At WDConSCT.org, we educate:
- Athletes, coaches, parents, schools, doctors, nurses and military personnel
- About the risks of SCT-related oxygen deprivation

Preventing Premature Complications

What SCT is: one gene for sickle hemoglobin, not a disease and not benign
 

  • Who it affects: 1 in 12 African Americans, also affects Hispanics, South Asians, and more
     
  • It can be passed on to children
     
  • SCT usually has no symptoms; but under extreme conditions, it can cause serious health risks
     
  • Diagram or infographic explaining inheritance (1 parent vs 2)

Risks & Health Complications of SCT

  • Rhabdomyolysis
     
  • Sudden death in athletes
     
  • Heat illness
     
  • Kidney issues
     
  • Blood in urine
     
  • High-altitude and flight risks
     
  • Exertional collapse (ECAST)

SCT with Military & Athletes

  • NCAA & military SCT screening policies
     
  • Real-life case studies or incidents
     
  • Prevention strategies
     
  • Coach/trainer education discussions
     
  • Contact the "Trait Doctor"
     
  • Testimonials and athlete stories

Farron Dozier show

Sunday Night 8p pt
 

  • Life with Athletes, Military and Community Outreach
     
  • Links to Spotify, YouTube, or KCAARadio.com

KCAARadio.com

the Farron Dozier show

Wednesday Evening 4p pt
 

  • Life around Military and First Responders
     
  • Links to Spotify, YouTube, or MBRadio.us

MB Radio.us

Purpose, Passions,& Gifts

2nd & 3rd Sunday's 


  • Listening to the Heart of Mankind with TNECC & M.O.R.
     
  • YouTube and Website

FarronD.com

Sickle Cell Trait and Rhabdo

Sickle Cell Trait Comes First — Rhabdomyolysis Is the Result

  

1. The Sickle Cell Trait Gene Mutation Comes First

• Sickle Cell Trait (SCT) is a genetic condition; something a person is born with.
• It occurs when a person inherits one sickle hemoglobin gene (HbS) from one parent and one normal gene (HbA) from the other.
• This gene mutation affects how red blood cells respond under stress but often causes no symptoms under normal conditions.

So from birth, the person’s red blood cells carry the potential to sickle, but usually don’t; unless triggered by stress like low oxygen or dehydration.

Read here

2. Rhabdomyolysis Comes Later — As a Result of Triggers

Rhabdomyolysis is not genetic — it’s an acute medical condition that happens later in life, often due to:
• Intense physical exertion
• Trauma or injury
• Dehydration
• Heatstroke
• Drug reactions
• Or in people with SCT; when their red blood cells sickle and block blood flow to muscles

In SCT, the sequence looks like this:

1. The person is born with the SCT gene (HbAS)
2. They participate in intense physical activity (e.g., military training, football practice)
3. This leads to low oxygen + high stress
4. Red blood cells sickle temporarily
5. Sickled cells block blood vessels in muscles
6. Muscle cells are starved of oxygen
7. Rhabdomyolysis begins — muscles break down
8. Toxic substances enter bloodstream → can cause kidney failure or death


SCT is the inherited condition. Rhabdomyolysis is the emergency that can happen when SCT is triggered.
 

Think of SCT as the match, and rhabdo as the fire that starts when the wrong conditions are present.

Here's how Rhabdomyolysis plays a role in Sickle Cell Trait (SCT) and oxygen deprivation:

What Is Rhabdomyolysis? 

 

Rhabdomyolysis (often called "rhabdo") is a serious and sometimes fatal condition where muscle tissue breaks down rapidly and releases toxic substances (especially a protein called myoglobin) into the bloodstream.

This can lead to:

  • Kidney failure
  • Heart problems
  • Sudden collapse or death


The Connection Between SCT, Oxygen Deprivation, and Rhabdomyolysis: 


1. Low Oxygen + SCT = Sickling

In people with Sickle Cell Trait, when oxygen levels drop (due to intense exercise, dehydration, heat, or altitude), red blood cells can sickle (change shape and become stiff).


2. Sickled Cells Block Blood Flow

Those sickled cells can block small blood vessels, especially in muscles that are working hard during physical activity.


3. Blocked Blood = Starved Muscle

  • When oxygen and nutrients can't reach the muscles:
  • Muscle cells begin to die.
  • The body starts to break down the muscle tissue.
  • That breakdown floods the bloodstream with toxic proteins and waste.


4. Toxic Proteins Damage Kidneys & Organs

The most dangerous byproduct is myoglobin, a muscle protein that:

  • Clogs the kidneys
  • Turns urine dark brown or cola-colored
  • Can shut down kidney function
  • Can lead to death if not treated quickly


Signs of Rhabdomyolysis:

  • Extreme muscle pain or cramping (often in the legs or lower back)
  • Dark, tea-colored urine
  • Swelling of muscles
  • Nausea or vomiting
  • Weakness, collapse, or confusion


In SCT Individuals, Rhabdo Often Happens After:

  • Football conditioning or all-out sprint drills
  • Long-distance military runs or hikes
  • Exercising in extreme heat or with dehydration
  • Being told to “push through” cramps or fatigue


Prevention in SCT Advocacy:

Monitoring oxygen levels (SpO₂) with a pulse oximeter, staying hydrated, and resting often are all key tools to prevent rhabdomyolysis in individuals with Sickle Cell Trait.


Bottom Line:

Sickle Cell Trait + Oxygen Deprivation → Blocked Blood Flow → Muscle Damage → Rhabdomyolysis → Organ Failure

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