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Indicates Matter Stricken
Indicates New Matter
S. 821
STATUS INFORMATION
Senate Resolution
Sponsors: Senator Verdin
Document Path: l:\s-res\dbv\010we a.kmm.dbv.docx
Introduced in the Senate on May 2, 2019
Adopted by the Senate on May 7, 2019
Summary: Lissencephaly Awareness Day
HISTORY OF LEGISLATIVE ACTIONS
Date Body Action Description with journal page number
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5/2/2019 Senate Introduced (Senate Journal-page 9)
5/2/2019 Senate Referred to Committee on Medical Affairs
(Senate Journal-page 9)
5/7/2019 Senate Recalled from Committee on Medical Affairs
(Senate Journal-page 5)
5/7/2019 Senate Adopted (Senate Journal-page 5)
View the latest legislative information at the website
VERSIONS OF THIS BILL
TO RECOGNIZE SEPTEMBER 8, 2019 AS "LISSENCEPHALY AWARENESS DAY" IN SOUTH CAROLINA AND TO URGE ALL CITIZENS OF THIS STATE TO SUPPORT THE SEARCH FOR A CURE AND ASSIST THOSE INDIVIDUALS AND FAMILIES WHO DEAL WITH THE CONDITION ON A DAILY BASIS.
Whereas, rare medical conditions often receive inadequate attention from the medical community and society at large, regardless of their severity; and
Whereas, less than one thousand estimated individuals worldwide have been diagnosed with Lissencephaly, a condition that is characterized by agyria or pachygyria, which means the absence or incomplete development, respectively, of the brain gyri or convolution, causing the brain's surface to appear unusually smooth; and
Whereas, Lissencephaly is a chronic condition that may cause epilepsy, muscle spasms, partial or complete paralysis, low vision, and severe medical complications; and
Whereas, patients with this condition often live with endless therapies and medical expenses; and
Whereas, it may take years to receive a diagnosis of Lissencephaly, and medical professionals are often inadequately educated on the diagnosis and treatment of Lissencephaly; and
Whereas, an increased awareness and expanded knowledge of the realities of life with Lissencephaly will allow the community at large to better support people who struggle with the challenges of this condition; and
Whereas, We Are R.A.R.E. is a nonprofit charitable organization and initiative made up of parents of children who face these challenges and is aimed at providing research, awareness, and education for rare neurological disorders; and
Whereas, We Are R.A.R.E. and other groups around the country have joined together to promote Lissencephaly awareness and support, including improved education; and
Whereas, in order to promote awareness, the members of the South Carolina Senate and We Are R.A.R.E. urge Lissencephaly patients and their supporters, healthcare providers, and the general public to demonstrate their caring by sharing patients' journeys and facts about Lissencephaly, including the developing understanding of the etiology of the disorder and any potential treatments; and
Whereas, the community's focus on Lissencephaly and its impact on patients' lives will help guarantee hope for a better future for individuals with Lissencephaly. Now, therefore,
Be it resolved by the Senate:
That the members of the South Carolina Senate, by this resolution, recognize September 8, 2019 as "Lissencephaly Awareness Day" in South Carolina and urge all citizens of this State to support the search for a cure and assist those individuals and families who deal with the condition on a daily basis.
This web page was last updated on
May 8, 2019 at 9:44 AM