South Carolina General Assembly
117th Session, 2007-2008

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A398, R190, S775

STATUS INFORMATION

Joint Resolution
Sponsors: Senators Scott and Lourie
Document Path: l:\council\bills\nbd\11688ac07.doc
Companion/Similar bill(s): 4143

Introduced in the Senate on May 22, 2007
Introduced in the House on January 29, 2008
Passed by the General Assembly on February 7, 2008
Became law without Governor's signature, February 20, 2008

Summary: Multiple Sclerosis Healthcare Access Study Committee

HISTORY OF LEGISLATIVE ACTIONS

     Date      Body   Action Description with journal page number
-------------------------------------------------------------------------------
   5/22/2007  Senate  Introduced and read first time SJ-4
   5/22/2007  Senate  Referred to Committee on Medical Affairs SJ-4
   1/23/2008  Senate  Committee report: Favorable with amendment Medical 
                        Affairs SJ-15
   1/24/2008  Senate  Committee Amendment Adopted SJ-11
   1/24/2008  Senate  Read second time SJ-11
   1/24/2008  Senate  Unanimous consent for third reading on next legislative 
                        day SJ-11
   1/25/2008  Senate  Read third time and sent to House SJ-1
   1/25/2008          Scrivener's error corrected
   1/29/2008  House   Introduced and read first time HJ-37
   1/29/2008  House   Referred to Committee on Medical, Military, Public and 
                        Municipal Affairs HJ-37
    2/5/2008  House   Committee report: Favorable Medical, Military, Public 
                        and Municipal Affairs HJ-11
    2/6/2008  House   Read second time HJ-23
    2/7/2008  House   Read third time and enrolled HJ-27
   2/13/2008          Ratified R 190
   2/20/2008          Became law without Governor's signature
   2/21/2008          Copies available
   2/21/2008          Effective date 02/20/08
    8/6/2008          Act No. 398

View the latest legislative information at the LPITS web site

VERSIONS OF THIS BILL

5/22/2007
1/23/2008
1/24/2008
1/25/2008
2/5/2008


(Text matches printed bills. Document has been reformatted to meet World Wide Web specifications.)

(A398, R190, S775)

A JOINT RESOLUTION TO ESTABLISH THE MULTIPLE SCLEROSIS HEALTH CARE ACCESS STUDY COMMITTEE, TO PROVIDE FOR ITS MEMBERS, POWERS, AND DUTIES, AND TO DIRECT THE COMMITTEE TO STUDY THE AVAILABILITY OF HEALTH CARE SERVICES TO MULTIPLE SCLEROSIS PATIENTS IN THIS STATE AND REPORT ITS FINDINGS AND RECOMMENDATIONS TO THE GENERAL ASSEMBLY BY JANUARY 1, 2009, AT WHICH TIME THE STUDY COMMITTEE IS ABOLISHED.

Whereas, the identification and planning of systems to provide service delivery for persons with multiple sclerosis (MS) is vital; and

Whereas, multiple sclerosis is a chronic, unpredictable neurological disease that affects the central nervous system, is varied in frequency and severity of symptoms, and has no cure; and

Whereas, approximately 400,000 Americans acknowledge having MS, and every week about 200 people are diagnosed with the disease. In that there is currently no formal method of tracking the incidence of multiple sclerosis in South Carolina, it is estimated there are more than 3,800 South Carolinians living with MS; and

Whereas, though there is no cure for MS, early diagnosis and specialized treatment are critical to alleviating the symptoms and controlling the progression of MS and improving the function and quality of life of individuals with MS; and

Whereas, although there is a comprehensive MS center affiliated with the Medical University of South Carolina and the Charleston Veteran Affairs Medical Center, South Carolina currently does not have the manpower to meet the substantial needs of patients with MS in the State, and additional MS clinics or centers in other locations, or an expansion of the MUSC MS Center, are needed in order to more adequately meet the needs of individuals with MS; and

Whereas, the average waiting time for a patient to be seen by an MS specialist in South Carolina is six to nine months; and

Whereas, many South Carolina residents must travel great distances, often out of State, in order to obtain specialized health care for the treatment of MS. Now, therefore,

Be it enacted by the General Assembly of the State of South Carolina:

Multiple Sclerosis Health Care Access Study Committee created

SECTION    1.    (A)    There is created the Multiple Sclerosis Health Care Access Study Committee. This committee shall review the complex needs of persons with multiple sclerosis (MS) in South Carolina and the available resources to meet these needs and shall develop a statewide comprehensive plan for the delivery of coordinated services to persons with MS.

(B)    The committee is comprised of:

(1)    the director of the Department of Health and Human Services, or a designee, who shall serve as chairman;

(2)    the head of the Department of Neurology at the Medical University of South Carolina, or a designee;

(3)    the head of the Department of Neurology at the University of South Carolina School of Medicine, or a designee;

(4)    the chief executive officer of the South Carolina Medical Association, or a designee;

(5)    the president of the South Carolina Hospital Association, or a designee;

(6)    an MS nurse specialist upon recommendation by the South Carolina Nurses Association;

(7)    a representative of the Mid-Atlantic Chapter of the National Multiple Sclerosis Society;

(8)    four persons living with MS, including one from the Low Country, one from the Pee Dee Area, one from the Midlands, and one from the Upstate, upon recommendation of the National Multiple Sclerosis Society, Mid-Atlantic Chapter.

(C)    A vacancy on the committee must be filled in the same manner as the original appointment.

(D)    Members of the committee shall serve without mileage, per diem, and subsistence.

(E)    The Department of Health and Human Services shall provide and coordinate staffing for the study committee.

Plan to be developed for coordinated approach to service delivery

SECTION     2.    (A)     The committee shall study access to health care services for persons living with MS in this State and develop a specific plan for a coordinated approach to service delivery for persons with MS, using the resources of both the public and private sectors. The plan must include, but is not limited to, an evaluation of how the treatment needs of persons with MS can adequately be met in terms of the level of care and specialization available; the geographic location of services; and the availability of specialized services.

(B)    The committee shall seek consultation from other relevant service providers, including, but not limited to, social work, physical and occupational therapy, and speech and vocational rehabilitation.

(C)    In carrying out its responsibilities under this joint resolution, the chairman may appoint subcommittees as he or she considers appropriate. The committee and subcommittees may utilize the knowledge and expertise of any individual in another state agency, group, or association.

(D)    The committee shall submit a written report of its findings and recommendations to the General Assembly before January 1, 2009, at which time the committee is abolished.

Time effective

SECTION    3.    This joint resolution takes effect upon approval by the Governor.

Ratified the 13th day of February, 2008.

Became law without the signature of the Governor -- 2/20/08.

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This web page was last updated on Wednesday, December 2, 2009 at 3:32 P.M.