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    • Home
    • Donation Page
    • Who is Farron?
    • Who is Deja?
    • Who is Dr Maisha?
    • Who is Jody?
    • About Us
    • Goals
    • Take the Survey here:
    • PSA
    • Contact Us
    • Who was Mr.Smith
    • Rhabdomyolysis
    • More Rhabdomyolysis
    • SCT Blog
    • Red Cells vs White Cells
    • Military and Genes
    • Hispanic Community
    • WDC Awareness Event
    • I AM WDC Award
    • Stop Sickle Sex Campaign
    • Community Outreach
    • Find Your Voice with Us
    • i Bead For Life
    • FarronD.com 2010-2019
    • WDC Radio! “Music & Talk”
    • Basketball Projects
    • Hey 19 (COVID-19)
WDC on SCT
  • Home
  • Donation Page
  • Who is Farron?
  • Who is Deja?
  • Who is Dr Maisha?
  • Who is Jody?
  • About Us
  • Goals
  • Take the Survey here:
  • PSA
  • Contact Us
  • Who was Mr.Smith
  • Rhabdomyolysis
  • More Rhabdomyolysis
  • SCT Blog
  • Red Cells vs White Cells
  • Military and Genes
  • Hispanic Community
  • WDC Awareness Event
  • I AM WDC Award
  • Stop Sickle Sex Campaign
  • Community Outreach
  • Find Your Voice with Us
  • i Bead For Life
  • FarronD.com 2010-2019
  • WDC Radio! “Music & Talk”
  • Basketball Projects
  • Hey 19 (COVID-19)

Inspirational Read

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Life of a 5yr old

This is the start of how I became this Advocate and the relationship with my Father from childhood til today. I inherited this gene from my Dad who passed away in 2019. I am so thankful we healed our relationship before he died.

Support the inspirational read

Coming to the City of Oxnard

Vision for our Awareness Platform 

Born To Talk Interview

Wrapping up 2020 with this Interview on Born To Talk

Health Fair Speaker

Sharing Sickle Cell Trait as a relatedness with people. Inherited Genes need to be shared in family dialogues.

Speaking with Nursing College and Community Members

 Awareness with Nurses will improve the relationship with our Sickle Cell Community 

Battle of the Genes Military Tour

Starting January 1, 2021 100% of the Donations go to WDConSCT.orgAbsorption Tour (Military)Donations We need 600 people to Donate $10.00 one time or once per year = $6,000 for the year to operate our Sickle Cell Trait Military Tour to speak to Soldiers. Covers Rental Car, Gas, Food, Hotel, and WDC Materials to pass out to Soldiers.12 trips to Camp Roberts. What would you need to make this happen? 

Help Our Cause

Your support and contributions will enable us to meet our goals and improve Awareness. Your generous donation will fund our mission.

Pay with PayPal or a debit/credit card

Who is Farron?

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Speaker: S Trait Experience

Internet TV & Radio Broadcaster

The Preventer : Facilitator

About Me
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The Preventer : Facilitator

Internet TV & Radio Broadcaster

The Preventer : Facilitator

My Story
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Internet TV & Radio Broadcaster

Internet TV & Radio Broadcaster

Internet TV & Radio Broadcaster

Watch Here

Depression / Anxiety

Mental Toughness

Sickle Cell and Mental Health
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Schedule A Conversation with Me

Awareness is important. Arming you with Questions I can.

Schedule Conversation Here

Connect With Us

  • Basketball Projects

WDC on Sickle Cell Trait

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

(323) 215-5384

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