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
Living Well With Sickle Cell: Andre Harris (Video)
My name is Andre Harris. We are in Houston, Texas. Well, my connection with sickle cell disease is first that I am a sickle cell patient and also I am an advocate for sickle cell disease. And so this is very important to me because I am a patient and a male so I identify with all of the areas that we’re talking about today. Yes, so black men, already dealing with a lot of stigmas, first being black and secondly being male.
I would say to doctors, nurses, health care providers within the emergency room setting that they need to learn their patients to as individuals and not as a statistic. And many providers treat their patients just to get them out of the door in the emergency room setting. But if they learned who they were and took the time to understand what brought them there that they’ll be able to provide them with the best quality care as possible.
+myBinderRelated Content
-
people & placesWHATZ DA COUNTWDC on SCT has dedicated his Organizatio...
-
news & eventsPfizer and the national newspaper publishers association collaborate to raise awareness of sickle cell disease and n...Pfizer Inc. and the National Newspaper P...
-
Community CenterToday’s Faces of Sickle Cell Disease: Linda Thomas WadeLinda Thomas is a health care educator, ...
-
education & researchThe psychosocial impact of leg ulcers in patients with sickle cell disease: I don’t want them to know my littl...BACKGROUND: Sickle cell disease (SCD) i...
-
Community CenterAn Almost-Love StoryI left after three hours, but after that...
-
education & researchUnderstanding patterns and correlates of daily pain using the Sickle cell disease Mobile Application to Record Sympt...Patients with sickle cell disease (SCD) ...
-
people & placesThe Sickle Cell Support Foundation of Jamaica (SCSFJ)In October 1992, sickle cell patients, C...
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.