• Sickle Cell Trait
  • Awareness
  • Who is Farron?
  • Donation Page
  • WDC Sports Camp
  • Risk Factors
  • Goals
  • About Us
  • Who is Deja?
  • Take the Survey here:
  • Contact Us
  • Community Outreach
  • WDC Radio! “Music & Talk”
  • More
    • Sickle Cell Trait
    • Awareness
    • Who is Farron?
    • Donation Page
    • WDC Sports Camp
    • Risk Factors
    • Goals
    • About Us
    • Who is Deja?
    • Take the Survey here:
    • Contact Us
    • Community Outreach
    • WDC Radio! “Music & Talk”
  • Sickle Cell Trait
  • Awareness
  • Who is Farron?
  • Donation Page
  • WDC Sports Camp
  • Risk Factors
  • Goals
  • About Us
  • Who is Deja?
  • Take the Survey here:
  • Contact Us
  • Community Outreach
  • WDC Radio! “Music & Talk”

WDC on SCT

WDC on SCTWDC on SCTWDC on SCT

¿WHATZ in your Genes?

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

September 2020

Contact me for an opportunity to share our Awareness

WDC Zoom 18 November 2020

One copy of the S gene. 

WDC Zoom 19 November 20

One copy of the gene Part2

Our Outreach

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WDC and DBC Speaking Tour

We travel to Churches and Outreach Events

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Help Fund Our Programs

Join us in the War on Sickle Cell Trait

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1st-12, and College Tour

Invite us to Speak on Sickle Cell Trait

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Support The WDC Radio Show

Help us reach the Masses

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Support Blood Drive Tour

Helping our Sickle Cell Community in need of Blood

Support our Projects

 Thank you for Supporting our Cause 

Pay with PayPal or a debit/credit card

Accomplished Benefits of Laughter: Fundraiser

iBeadForLife Campaign

Risk Factors

Soldiers, Athletes and people working out enjoying life and living their dream have collapsed and died from Exertional Sickling with Rhabdomyolysis.

Globally

*300 Million people Globally live with this gene and millions don’t know and are not aware of the risk factors and health complications associated with this inherited gene.

Children being born

*Babies are still being born with sickle cell disorder or sickle cell anemia and some parents had no idea they were carriers.

Bloodline not Skin Color

*Many think it’s just African American who carry this gene when really it’s a bloodline gene not a race only gene. Caucasians, Mediterranean, European, Asian and Hispanic to name a few all have this gene in their bloodline.

Red Blood Cells

*There are hundreds of other types of red blood cell conditions with out testing and a family planning process it’s possible to have a child with other types of blood disorders like Sickle Beta Thalassemia, Sickle Cell SC , Sickle Cell SD, SE and many more. 

Donate Blood

*Blood Transfusion and or Blood Exchanges are one of the few treatments for patients living with sickle cell which why it’s important for our Black and Brown  communities to donate blood. Find a American Red Cross near you. .

i Bead For Life

i Bead For Life

iB4L Campaign

Find your voice with us.
Awareness 

Education 

Prevevntion

Why i Bead For Life

Find your Voice with Us

i Bead For Life is an Awareness Campaign create by a young man in Canada who lost a friend to Sickle Cell Disease. He reached out to me to help him share his vision to the world.


We know this Campaign will help spread the message about Sickle Cell Awareness

i Beads Represent

-RED Bead represents if you carry one copy of any type of trait gene ie Sickle Cell Trait., Thalassemia Trait, C Trait, D Trait, E Trait and so one. 


-GREEN Bead represents if you battle with Sickle Cell Anemia or Disease 


-YELLOW Bead represents if you have lost a friend or loved one to Sickle Cell (our Fallen Soldiers)


-BLACK Bead represents if you have been educated through the #iB4L Campaign.


Awareness from Canada to California

Sherine A Benjermin: After her death her life inspired us to come together to speak out and share with the World that people Globally manage Sickle Cell Trait and Sickle Cell by the Millions. 

click link to order

Community Outreach Events

Sickle Cell Trait is a bloodline conversation not a race or color

Award Winners

Call To ACTION

DID YOU FIND YOUR VOICE TO HELP US or You have more questions?

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Awareness, Education & Prevention

Please send us a Message to let us know what areas you can help us spread Awareness about Sickle Cell Trait and Sickle Cell Disorder

WDC on Sickle Cell Trait

301 9th St, STE 100, Redlands, CA 92374, US

(323) 215-5384

Support us here

Military Tour

 School Tours

Radio Show 

Blood Drives

Stop, Sickle Sex 

Screening / Mobile Testing


Our Why’s

Awareness

We have to be able to reach the people!

Education

We deliver the basic fact.

People need to know the basic information on Sickle Cell Trait and not just S Trait carriers. You too could save a life. 

Prevention

There are Risk Factors with S Trait and many don’t know. 

Teaching Soldiers how to Manage Fatigue

Military Tour

Elementary thru High School Tour

Elementary thru High School Tour

We travel and speak on Military Bases all over the States and other Countries sharing my experiences with Sickle Cell Trait to bring Awareness and to possibly Prevent a Soldier from Collapsing and maybe even Sudden Death

Get More information from us

Elementary thru High School Tour

Elementary thru High School Tour

Elementary thru High School Tour

We help students connect with us on the conversation about Sickle Cell Trait as it relates to subjects they learn in school. Also for those who are Living with Sickle Cell we help create a relatedness so their peers are Aware of the Impacts around them.

Help us get into the Schools near you.

Blood Drive Tour

Elementary thru High School Tour

HBCU and College Tour

This is my family on my Father's side. My Cousin Nigel lives with Sickle Cell. This is my Aunt and her daughter and her grand children. Nigel is out to have the Community not only give blood but why it's important for our Black Families to Donate Blood. It's best to have a close match to your ethnic background. We know that blood donations saves lives.

Help with Blood Drives

HBCU and College Tour

Screening / Mobile Testing

HBCU and College Tour

We speak at the College level not only to make students aware of what's possible if the have a child with Sickle Cell and don't know they are gene carriers but also to educate the student athletes of the risk factors and can be caused by Sickle Cell Trait with Exertion due to exercising and Sports related deaths.

Connect Us with College Students

Stop, Sickle Sex

Screening / Mobile Testing

Screening / Mobile Testing

Is our Global Campaign to grab the attention of the reader to see what they know about the Global impact of Sickle Cell Trait and other Red Blood Cell conditions like Thalassemia Trait, C, D, E, Monroe, O Arab and many more. 300 Million Globally have SCT and in United States around 4 Million with Millions more not knowing.

Help Us Disappear The Ignorance

Screening / Mobile Testing

Screening / Mobile Testing

Screening / Mobile Testing

We have been able to provide Communities and Health Fairs with the Hemoglobin Electrophoresis Test. It's a Panel that will tell you if you have any inherited genes even other than sickle cell. New Born Screening started in California in 1990. So many have gone untested or got letters and forgot. We partnered with MediLab for 2yrs and plan on starting back up in 2020. This test is free to the Community help us keep it that way.

Find out more

Why we need not just funding but opportunities to speak.

Why we need not just funding but opportunities to speak.

Why we need not just funding but opportunities to speak.

Support us here

Listen here

Connect With Us


Military Athletes Parents Coaches Trainers Summit

301 9th St, STE 100, Redlands, CA 92374, US

(323) 215-5384

Copyright © 2013 WDC on Sickle Cell Trait  - All Rights Reserved. 

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