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
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
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
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
BOOKS & LIFE BLOG – SEPTEMBER 2019
Jenica’s Story & ‘My Friend Jen’
NHSBT – JUNE 2019
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
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