Google
Trusted Resources: Evidence & Education
Scientific literature and patient education texts
Cold temps and sickle cell: 4 tips on weathering winter
source: Children's Hospital of Georgia
year: 2018
authors: Abigail Roth, RN
summary/abstract:Many of us might not like cold winter weather. But for families of kids with sickle cell disease (SCD), winter is when they need to be really careful.
“While it’s entirely possible to control symptoms of sickle cell disease, times of stress—which can include extremes of weather, sickness and dehydration—can all cause symptoms to get worse,” said Dr. Nnenna Badamosi, a pediatric hematologist/oncologist and director of the sickle cell disease transition program at the Children’s Hospital of Georgia.
read more
+myBinderRelated Content
-
Patricia Kavanagh, MDPatricia Kavanagh, MD, is an Assistant P...
-
Clinical and haematological risk factors for cerebral macrovasculopathy in a sickle cell disease newborn cohort: a p...Children with sickle cell disease (SCD) ...
-
Kyriako Damavoletes Talks About the Stigma of Sickle Cell DiseaseKyriako Damavoletes has HbS beta thalass...
-
Association of Matched Sibling Donor Hematopoietic Stem Cell Transplantation With Transcranial Doppler Velocities in...Importance: In children with sickle cel...
-
Unheard Cries of DespairIt would be really unfair for me to comp...
-
Zebra Subway Car Runs Through Boston to Draw Attention to Rare DiseasesBostonians may be seeing stripes this mo...
-
Sudam L. Kate, MSc, PhDA true pioneer for sickle cell advocacy,...
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.
Powered by
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.