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: News & Events
Latest announcements and gatherings
University of Illinois at Chicago awarded $4.6 million NIH grant for chronic pain research
The University of Illinois at Chicago has been awarded a $4.6 million grant from the National Heart, Lung, and Blood Institute to study the molecular neurobiology of chronic pain in patients with sickle cell disease and to develop potential new drug treatments.
While there have been many advances in managing the disease and acute pain crises, researchers still do not know much about how and why patients experience chronic pain.
The new funding will provide an opportunity for investigators to refine their tools and develop new therapeutic leads for treating chronic pain in sickle cell disease. They hope to identify various molecular mechanisms and explore ways to target one or more of these mechanisms for controlling pain in sickle cell disease.
Related Content
-
people & placesMichael Rutledge Debaun, MDMichael R. DeBaun is the professor of Pe...
-
education & researchPatient controlled analgesia for adults with sickle cell disease awaiting admission from the emergency departmentBackground: A treatment algorithm for s...
-
people & placesSimon Dyson, PhDSimon Dyson is Professor of Applied Soci...
-
Community CenterCMO Speaks: Making ED Care Better for SCD – Progress in 2023Welcome to CMO Speaks, a blog featuring ...
-
education & researchRisk Factors for 30-Day Readmission in Adults with Sickle Cell DiseaseBACKGROUND: Readmission to the hospital...
-
news & eventsStigmatizing language in medical records affects patient care, study showsPhysicians who use stigmatizing langua...
-
people & placesSickle Cell Anemia Foundation of OregonThe Sickle Cell Anemia Foundation of Ore...
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.
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.