DISCLAIMER
The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.compose your message
message sent
email sent successfully
Trusted Resources: Community Center
Online groups, photo galleries and blogs
Me Myself and Sickle Cell
Living her life with sickle cell anaemia, Jenica Leah has battled with the many complications that come with the disorder; but she has never let this stop her from achieving. From being a full-time model at the age of 14 to organizing and managing catwalks with an international events specialist by the age of 20, Jenica Leah refuses to let her condition hold her back.
In order to create and develop her award winning children’s book series ‘My Friend Jen’, Jenica Leah has done in depth research of the sickle cell condition to further her knowledge of what she already knows from living with it. Her vast understanding as well as her patient expertise has placed her second to none when it comes to discussing the topic of sickle cell education and raising awareness.

Related Content
-
education & researchCaregiver Stress: Don’t Forget Self-CareMaybe you take care of your spouse, who'...
-
videos & visualsReproductive Issues for Women With Sickle Cell Diseasehttps://www.youtube.com/watch?v=4vo_BPBn...
-
education & researchPerioperative considerations for patients with sickle cell disease: a narrative reviewPURPOSE: Approximately 200,000 individua...
-
Community CenterSickle Cell Mommies ClubThis is a place for moms with children w...
-
Community CenterThese people living with an invisible condition are doing their best to raise awareness about itIn 2013, an inquest found a failure to f...
-
Community CenterA Patient Advocate’s Take on Sickle Cell Disease: The Pain and the PromiseSeptember is National Sickle Cell Awaren...
-
news & eventsRare patients with sickle cell disease live nearly twice national averageWith a national median life expectancy o...
send a message
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.