Jenica Leah, a woman with dark skin and styled dreadlocks smiling and posing with her hand near her chin, wearing a red satin blouse and gold hoop earrings.

Biography

Jenica Leah has spent a lifetime building a life she was never supposed to live. She is a renowned speaker, author, and advocate with over two decades of experience in raising awareness about chronic illness and invisible disabilities, with a specific focus on sickle cell disease. Despite facing life-threatening complications from sickle cell, Jenica has transformed her challenges into opportunities, becoming an influential voice for patients worldwide. She is the founder of three non-profit organisations dedicated to sickle cell education and awareness, and the former President of the European Sickle Cell Federation.

From an early age, Jenica's life was defined by her condition. She experienced regular hospital admissions, excruciating pain from sickle cell crises, and the isolating effects of a largely misunderstood illness. Yet rather than let her condition define her, Jenica was determined to live a life filled with purpose. As a young adult, she pursued a career as a fashion model, working with top agencies such as Select Model Management, and gracing the pages of publications like Vogue Paris. However, health challenges continued to interfere with her professional life. In 2006, Jenica suffered a life-threatening complication, acute chest syndrome, which left her in critical care and required resuscitation. This near-death experience became a turning point, shaping her approach to life and how she navigated her condition.

After having undergone a series of surgeries, including hip replacements and gallbladder removal, as well as enduring severe health complications, Jenica began to advocate for better education around sickle cell and chronic illness, starting with her self-published children's book My Friend Jen. This book, written to educate young children about sickle cell disease, has since been recognised internationally and is widely used in schools and hospitals to raise awareness. Her advocacy continued to grow, and in 2019, Jenica became a founding member of the European Sickle Cell Federation (ESCF), a pan-European organisation focused on raising awareness, collaboration, and advocating for policy change on behalf of individuals living with sickle cell.

In 2020, Jenica made the bold decision to relocate from the UK to the Caribbean to live a healthier life, in pursuit of a new perspective on living with a chronic illness. This move, made during the COVID-19 pandemic, was a reflection of Jenica's commitment to embracing life beyond her illness. As someone who believes that a positive mindset can change everything, she has continued to overcome the challenges of her condition with an unrelenting focus on her health, personal growth, and advocacy work.

Jenica has consistently used her platform to educate and inspire others. She developed a YouTube series, Conversations with Jen, where she shares stories of individuals living with sickle cell. And, her podcast, Let's Talk About Sickle Cell, has become a critical resource for sickle cell education, featuring interviews with MPs, healthcare professionals, celebrities, and individuals affected by sickle cell. Through her online presence and her work with various NHS Trusts, Jenica has created a global community of support for individuals living with sickle cell and other chronic conditions. She is a passionate advocate for blood donation and has worked tirelessly to raise awareness about the urgent need for more black blood donors. As a result of her campaigns, Jenica has encouraged hundreds of people to donate blood, saving countless lives in the process.

Known for her warm, fun, and optimistic personality, Jenica connects with people from all walks of life. Knowing how unprecedented life can be, she lives by one belief: that no matter your circumstances, you always have the power to redefine what's possible.

Today, Jenica's impact is felt globally through her books, podcast, public speaking, and advocacy work. Her mission is simple: to empower people to build a life beyond their circumstances by redefining what's possible. Her tireless efforts to educate and empower others have touched the lives of hundreds of thousands, providing them with the tools to overcome challenges and live their best lives. Jenica Leah's story is proof that with resilience, purpose, and an unshakeable mindset, you can build a life you were never supposed to live.

TVJ SMILE JAMAICA – AUGUST 2023

Fighting an Uphill Battle with Grace

BLACK WALL ST. MEDIA – JUNE 2023

Gala Celebrating World Sickle Cell Day Shines a Spotlight on Progress and Awareness in the UK

BLACK DOCTOR.ORG – NOVEMBER 2022

Sickle Cell Warrior Writes The Children’s Book She Never Had Growing Up

ESSENCE – SEPTEMBER 2022

What It’s Like Balancing A 9 To 5 With 24/7 Sickle Cell Disease

ITV NEWS – AUGUST 2022

NHS urges LGBTQ+ ethnic minorities to donate blood following landmark rule change

THE VOICE ONLINE – JULY 2022

Code Red Switch-Up on Sickle – Jenica’s Story

THE BLACK PROJECT – JUNE 2022

In conversation with Jenica Leah

NOVO NORDISK DRIVING CHANGE – JUNE 2022

Novo Nordisk – Sickle Cell Disease

ITV CENTRAL – JUNE 2022

A new campaign to increase the number of black blood donors in the UK has been launched in Birmingham

BIRMINGHAM MAIL – JUNE 2022

Birmingham woman with sickle cell launches campaign to encourage black blood donors

OK! – MAY 2022

Black Pound Day: The best books for National Share-a-Story Month

ITV CENTRAL NEWS – OCTOBER 2021

‘It’s an everyday fight’: Author creates children’s books to highlight inherited blood condition

BBC SOUNDS PODCAST ‘If You Don’t Know’ – SEPTEMBER 2021

A Sickle Cell Crisis

BBC 1XTRA TALKS – JUNE 2021

Sickle Cell, Dating and Healthcare

CVM TV AT SUNRISE JAMAICA – FEBRUARY 2021

Book Donation Project with Jenica Leah | Sunrise | CVMTV

OK! – OCTOBER 2020

What is Black History Month and why is it important?A list of ways to support the achievements, cultures and contributions of black people in the UK

BLACK BALLAD – SEPTEMBER 2020

For Those With Sickle Cell Disease, Lockdown Continues

BBC THREE – AUGUST 2020

Young shielders: ‘Isolation felt like a parallel universe, but I’m scared to leave’

C HUB MAGAZINE – JUNE 2020

Jenica Leah’s Story Living With Sickle Cell and Her Book, My Friend Jen Series

FORBES – MAY 2020

36 Real Entrepreneurs Share Top Tips On How They Pivot Business During Lockdown

THE VOICE ONLINE – MARCH 2020

Award-winning young author has launch to celebrate World Book Day

BEYOUROWN PROJECT – FEBRUARY 2020

BYO Boss – Jenica Leah’s Story

SHE CAN 365 – JANUARY 2020

Specialising in publishing books written by young authors and that inspire young readers

CREATIVES IN FOCUS PODCAST – OCTOBER 2019

Writing for Impact

BOOKS & LIFE BLOG – SEPTEMBER 2019

Jenica’s Story & ‘My Friend Jen’

NHSBT – JUNE 2019

@givebloodnhs My Blood Story

i-NEWS – JUNE 2018

World Sickle Cell Day: Here’s what people with sickle cell want you to know

The Voice Online – DECEMBER 2017

First-Time Author Jenica Leah Wins Inspirational Award

TEDxBrum – OCTOBER 2017

Not All Disabilities Are Visible

BuzzFeed News – OCT 2017

These People Living With An Invisible Condition Are Doing Their Best To Raise Awareness About it

BBC NEWS ONLINE – AUGUST 2017

United Sicklers – Battling with sickle cell

AL JAZEERA – MARCH 2017

THE STREAM – Living with sickle cell anaemia

BBC WORLD SERVICE – MARCH 2017

World Have Your Say: A Future Cure For Sickle Cell

THE YOUNG EMPIRE – FEBRUARY 2017

First-time writer pens book to empower children with sickle cell after growing up embarrassed about her condition

THE POINT GAMBIA – DECEMBER 2016

UK philanthropist launches book on sickle cell in Gambia

NURSING TIMES – OCTOBER 2016

Navigating teenage years with a congenital disorder

MAD NEWS UK – SEPTEMBER 2016

Author Jenica Leah Creates Series Of Children’s Books Promoting Sickle Cell Awareness

XICKLE RBC – JULY 2016

Not Sure How to Teach Your Kids About Sickle Cell? Give This New Book a Try

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