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  2. Sickle Cell Disease Association of America - Wikipedia

    en.wikipedia.org/wiki/Sickle_Cell_Disease...

    Representatives from 15 different community-based sickle cell organizations came together at Wingspread, a community center, as guest of the Johnson Foundation. There was a common belief that there was a need for national attention to sickle cell disease.

  3. The Sickle Cell Society - Wikipedia

    en.wikipedia.org/wiki/The_Sickle_Cell_Society

    The Sickle Cell Society , established as a registered charity in 1979, was founded by a group of people with sickle cell disease, their parents and their physicians, aims to improve understanding and management of the condition.

  4. Sickle cell disease - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell_disease

    Sickle cell disease (SCD), also simply called sickle cell, is a group of hemoglobin-related blood disorders that are typically inherited. [2] The most common type is known as sickle cell anemia. [2] Sickle cell anemia results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. [2]

  5. For people with sickle cell disease, ERs can mean life ... - AOL

    www.aol.com/news/people-sickle-cell-disease-ers...

    A study published in 2021 found that 50% of sickle cell patients reported having to wait at least two hours before their pain was treated, despite medical guidelines recommending such patients in ...

  6. List of ICD-9 codes 280–289: diseases of the blood and blood ...

    en.wikipedia.org/wiki/List_of_ICD-9_codes_280...

    280.9 Iron deficiency anemia, unspecified; 281 Other deficiency anemias. 281.0 pernicious anemia; 281.2 Anemia, folate deficiency; 281.3 Other specified megaloblastic anemias, not elsewhere classified; 282 Hereditary hemolytic anemias. 282.0 Hereditary spherocytosis; 282.2 G6PD; 282.5 Sickle-cell trait; 282.6 Sickle-cell anemia; 283 Acquired ...

  7. Congenital hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Congenital_hemolytic_anemia

    Congenital hemolytic anemia (CHA) is a diverse group of rare hereditary conditions marked by decreased life expectancy and premature removal of erythrocytes from blood flow. Defects in erythrocyte membrane proteins and red cell enzyme metabolism , as well as changes at the level of erythrocyte precursors, lead to impaired bone marrow ...

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