Google
Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Sickle Cell Anemia Foundation of Oregon
4566 NE 87th AvePortland, Oregon, United States
Email Phone Web
The Sickle Cell Anemia Foundation of Oregon is a 501(c)(3) non-profit organization dedicated to educating vulnerable populations and to encourage testing for the presence of this painful and life-threatening, but treatable disease. The foundation helps patients with: Patient advocacy, Access to support groups, Parent education, Genetic counseling and referrals for free diagnostic testing, Ongoing education about SCD and about available treatments, Limited funds for home heating during winter months, and Moral support.
Our immediate objective is to identify all the patients and carriers of sickle cell disease living in Alaska, Idaho, Oregon, and Washington state. We are dedicated to assessing the health care needs of these patients and helping them by facilitating regular access to appropriate health care providers and services. Our Pacific Northwest outreach program aims to provide individuals with the information they need to be tested for the presence of sickle cell disease. Diagnosed patients are encouraged to sign up with the national “Get Connected” Sickle Cell Anemia registry.
+myBinderRelated Content
-
Let Your Light Shine: Sickle SocialPiedmont Health Services and Sickle Cell...
-
Patient controlled analgesia for adults with sickle cell disease awaiting admission from the emergency departmentBackground: A treatment algorithm for s...
-
Lori E. Crosby, PsyDDr. Crosby works in Cincinnati, Ohio and...
-
Pat Carroll, MDDr. Pat Carroll is the director of psych...
-
Southeast Alabama Sickle Cell AssociationThe Southeast Alabama Sickle Cell Associ...
-
Sickle Cell Carers Awareness NetworkSickle Cell Carers Awareness Network (SC...
-
The Affordable Care Act Improves Healthcare Access and Utilization Among Young Adults with Sickle Cell DiseaseIntroduction: The Dependent Coverage Pro...
