Medical Homes in North Carolina
This page is designed to keep you informed about events and activities
happening in North Carolina that will help improve access to medical homes
for children with special health care needs (CSHCN).
Medical Home Initiatives
This section provides
information on state medical home initiatives/programs. States that are
a part of the mentorship network will have a "Promise to
the State" which outlines how they will achieve ensuring that all
children have a medical home by 2010. This is based on the Healthy
People 2010 goals which is a 10 year action plan to achieve and measure
success for all CSHCN.
North Carolina Medical Home Team Contact:
Name: Danielle Matula - Specialized Services Unit
Contact: Phone: 919-707-5674 | Email: Danielle.Matula@ncmail.net
North Carolina was selected to be part of the first National NICHQ
Medical Home Learning Collaborative - A fifteen-month collaborative
activity to improve care for the growing population of CSHCN. This initiative
focused on 3 practices in the state and assisted them in completing a
quality improvement process to provide medical homes to their patients
with special needs. NC worked with NICHQ staff to provide training regarding
Medical Homes for CSHCN. For more information go to: www.nichq.org/NICHQ/Programs/CollaborativeLearning/MHLC2005.htm.
North Carolina Statewide Medical Home Implementation Plan - Promise
to the State (www.medicalhomeinfo.org/states/downloads/NCpromise.doc)
2004 Update on Medical Home Activities: (www.medicalhomeinfo.org/states/state
/Downloads/North%20Carolina%20Initiative%20for%20MH%20%208-04.doc)

Related Grant Initiatives
This section provides information on current state
grants that are working on medical home initiatives. This includes the
grant abstract as well as key contacts for the grant.
Community Systems Building Champions Incentive
Grant
Goal: To create a Family Advisory Council which will
work with the North Carolina CYSHCN Unit to design data training modules
and implement data training with state and community shareholders. The
data training will provide an important resource for families and communities
to utilize as they work to design local initiatives that will improve
outcomes for families of CYSHCN.
For more information contact: Marlyn Wells, Family
Liaison Specialist, C&YB
Phone: 919-707-5675 | Email: marlyn.wells@ncmail.net
Early Childhood Comprehensive Systems Planning Grant
Purpose: The overall goal of this
planning project is to develop a comprehensive early
childhood service system that will allow multiple agencies
to work towards and document progress in achieving
school readiness for all children entering elementary
school in NC. The plan will serve to coordinate services
of a number of state agencies, and will incorporate
activities and priorities of other organizations to
create a plan that will guide and assist multiple stakeholders.
Name: Deborah Nelson, PhD., ECCS Grant Coordinator
Contact: 919-707-5677 | Fax: 919-870-4880
E-Mail: deborah.nelson@ncmail.net
Hemophilia Grant
Purpose: The 8 federally funded hemophilia treatment
centers from Region IV North in the states of Kentucky, North Carolina,
South Carolina, and Tennessee provide comprehensive care, including a
full complement of medical and psychosocial services, for all children
and adults with bleeding disorders. This regional network of comprehensive
prevention services is provided at the treatment centers by teams of physicians,
nurses, social workers, orthopedists, dentists, physical therapists, laboratory
technicians, and other appropriate personnel to over 1,700 individuals
with bleeding disorders.
Healthy Tomorrows Partnership for Children Grants 2005-2010
Connecting the Dots
University of North Carolina Chapel Hill, Chapel Hill, NC
Purpose: The goal of this project will be to establish
a hierarchy of services to prevent problem behaviors among children in
out-of-home childcare from becoming behavioral and psychosocial health
conditions. Child Care Health Consultants will offer consultation and
technical assistance to out-of-home childcare providers to improve their
response to challenging behaviors. Children needing medical services will
be screened and referred to their medical homes for primary health services,
and those with more serious needs will be referred on to pediatric mental
health services. www.medicalhomeinfo.org/states/state
/Downloads/NC
HealthyTom Grant.doc for more information on this project.
For more information on the Healthy Tomorrows Grant
Program go to: www.aap.org/commpeds/htpcp/index.html
For more information on this HTPCP project, please e-mail your name, address,
telephone, and fax numbers with your specific request to healthyt@aap.org
Partners in the State
This section provides information on who in the state (individuals
and agencies) are working together to create medical homes for children.
American Academy of Pediatrics (AAP) Chapter: NC Pediatric
Society (NCPS) www.ncpeds.org
The mission of the North Carolina Chapter of the
American Academy of Pediatrics and the North Carolina
Pediatric Society is to improve the health and well being
of children through the collective efforts of its membership
and to provide an organization for professional communication,
education, and fellowship. The NCPS Web site provides
information about membership and upcoming events, a calendar,
and related links.
American Academy of Family Physicians (AAFP) Chapter: www.ncafp.com
The North Carolina Academy of Family Physicians, founded in 1948, is a
professional association representing more than 2500 family physicians,
family medicine residents and medical students across NC. Affiliated with
the American Academy of Family Physicians, NCAFP's goal is to advance
the specialty of family medicine and advocate for the interests of family
physicians.
The North Carolina Title V and CSHCN Program are located
within the DHHS Division of Public Health’s Women’s and Children’s
Health Section.
Name: Dr. Kevin Ryan
Contact: 919-707-5512 | Fax: 919-870-4880
E-Mail: Kevin.Rayn@ncmail.net
Name: Carol Tant, Title V CSHCN Director
Contact: 919-707-5610 | Fax: 919-870-4880
E-Mail: Carol.Tant @ncmail.net
State Web Site: wch.dhhs.state.nc.us/cay.htm
Title V Block Grant to States
Title V of the Social Security Act is one of the largest Federal block
grant programs. It leads the nation in ensuring the health of all mothers,
infants, children, adolescents, and children with special health care
needs (CSHCN). Title V is administered by the Maternal and Child Health
Bureau (MCHB) as part of the Health Resources and Services Administration,
U.S. Department of Health and Human Services.
Title V and Children with Special Health Care Needs
MCHB Objective: Support development and implementation
of comprehensive, culturally competent, coordinated systems of care
for the estimated 18 million U.S. children who have or are at risk for
chronic physical, developmental, behavioral or emotional conditions
and who also require health and related services of a type or amount
beyond that required by children generally.
NC Commission on Children with Special Health Care Needs
The Commission on Children with Special Health Care Needs is appointed
by the Governor of NC and is legislatively charged to monitor and evaluate
the availability and provision of health services to children with special
health care needs in NC. In addition they are responsible for monitoring
and evaluating services provided to children with special health care
needs under the child health insurance program, NC Health Choice for Children.
The Commission meets every other month in Raleigh, NC.
Name: Danielle Matula
Contact: Phone: 919-707-5674 | Email: Danielle.Matula@ncmail.net
NC CSHCN Program and Specialized Services Unit
Programs and services focus on the special health care needs of infants,
children and adolescents with (or at risk for) chronic illnesses or developmental
disabilities. Families of children with special health care needs are
involved in policy development, planning and program implementation. Service
priorities include case management/care coordination, disability issues,
access to care, transition for children (for example, from early childhood
to school age and school age to adult); and linking children with medical
homes. The Child Service Coordination Program (CSCP), Children’s
Special Health Services (CSHS) Purchase of Medical Care Program, CSHS
health care and specialty clinics, Assistive Technology Programs for young
children and the NC Office on Disability and Health are located in this
unit.
Name: Carol Tant, Children and Youth Branch Head
Contact: 919-707-5610 | Fax: 919-870-4880
E-Mail: carol.tant@ncmail.net
Medicaid: www.dhhs.state.nc.us/dma/covgroups.htm
Medicaid is the largest publicly funded source of insurance for North Carolina
children from birth to 21 years of age. The program is administered by the
DMA at the state level, and locally by county Departments of Social Services.
North Carolina’s Medicaid program provides coverage for a comprehensive
array of primary and preventive services. The majority of children are eligible
under the Medicaid for Infants and Children (MIC) coverage category which
insures infants at or below 185% of federal poverty level; children ages
1 through 5 at or below 133% FPL; and children ages 6 through 18 at or below
poverty. Other children/adolescents are eligible through the following programs:
Medicaid for Families with Dependent Children; Medicaid for Pregnant Women;
Work First Family Assistance (TANF); SSI-Disabled Children; Special Assistance
to the Blind; or Children in Foster Care. Additional children are served
through the CAP Medicaid Waiver Programs.
Carolina Access
Carolina Access was introduced in 1991 as Medicaid’s primary care case
management program, linking Medicaid recipients with a primary care provider
(PCP). The PCP acts as a gatekeeper to provide and arrange for most of families’ health
care needs. Carolina Access is active in all 100 NC counties and has become
a national model for its strong support both among providers and recipients.
Currently, there are approximately 670,000 Medicaid recipients in the program
and 86,894 are children under six years of age. With the exception of the
one county with a Medicaid managed Health Maintenance Organization, Carolina
Access II/III serves as the primary vehicle for managing this population
in this state.
Carolina Access II & III or NC's Community
Care Plans
Carolina Access II/III was launched in 1998
under the leadership of a past Secretary of NC’s
Department of Health and Human Services. Access II/III
builds on Carolina Access by working with public
and private providers to form community-based systems
of care to better manage services to the Medicaid
population by devoting attention to issues of quality
and cost. Providers take responsibility for the enrolled
Medicaid population, to provide preventive services
and to develop processes by which at-risk patients
can be identified and their care managed. The following
features distinguish the plans:
- Bringing together local community representatives, consumers, and
providers to plan and develop comprehensive and integrated systems
of care
- Identifying at-risk enrollees through claims and assessment
- Implementing targeted case management;
- Developing and measuring budget, utilization, and quality targets;
- Developing ongoing commitment to community needs and values; and
- Strengthening the community “safety-net” for serving
the indigent population.
Each Access II/III network is expected to form a collaborative governance
structure. The network either forms a new not-for-profit organization
or uses an existing public or private non-profit organization. In both
cases, decision-making and responsibility are to rest with the community
partners. Each “not-for profit administrative entity” receives
a $2.50 per member per month (pm/pm) enhanced care management fee that
is budgeted and used to provide the resources to manage the Medicaid
population , such as hiring local care managers. Physician committees
carry out most of the clinical oversight work of the organization.
Each project sets up a Medical Management Committee to set the organization’s
direction relative to the project’s care and disease management
priorities.
Currently, there are approximately 470,000 Medicaid recipients in
the program and 146,485 are children under six years of age. The NC
legislature has mandated that Carolina Access II/III expand statewide
to include over 600,000 of the people eligible for Carolina Access
by June 2004. The NC Secretary of the Department of Health and Human
Services (DHHS) has identified this as a top priority.
NC Healthy Start Foundation: www.nchealthystart.org
Since 1993, the Division of Public Health as the state Title V Agency has utilized
the NC HSF for their coordination of maternal and child health public education/public
awareness campaigns and their materials development expertise. The NC HSF
utilizes cost-effective, and culturally/linguistically appropriate outreach
strategies and has produced Health Check/Health Choice campaign educational
and promotional materials in two languages; and has engaged both television
and radio. The Health Check/Health Choice Steering Committee’s realized
that while outreach efforts were successful in reaching eligible families
for enrollment and re-enrollment, many of these families were not accustomed
to having access to regular health care and were not using, to the best advantage,
their health check/Health Choice benefits. From that realization, a campaign
to encourage the development of the Medical Home began. Over the past year,
the NC HSF Health Check/Health Choice Campaign Coordinator has been interviewing
families, providers and outreach workers in order to determine effective
strategies, themes and messages for this new Medical Home Campaign.
Health Check: www.dhhs.state.nc.us/dma/healthcheck.htm
Health Check, started in 1993, was DMA’s enhanced replacement for the
Early Periodic Screening Diagnosis and Treatment Program (EPSDT) for children
birth through 20 years of age. Health Check facilitates regular preventive
medical care and the diagnosis and treatment of any health problem found during
a screening. The program has approximately 100 community-based Health Check
Coordinators throughout the state whose primary responsibility is to connect
families with information and resources. They have access to an Automated Information
and Notification System (AINS) to track enrollees’ use of the health
care system through claims. Currently, both the Health Check and Health Choice
programs allow 26 unmanaged outpatient mental health visits annually and a
non-specific diagnosis is allowed for the first six visits. (CSHCN can receive
additional outpatient visits with prior approval.)
Name: Jeffrey Simms, Assistant Director, DMA (Managed
Care and Health Check)
Contact: 919-647-8188
E-Mail: Jeffrey.Simms@ncmail.net
Name: Carolyn Sexton, Health Check/Health Choice Coordinator,
DPH
Contact: 919-707-5642
E-Mail: carolyn.sexton@ncmail.net
NC Health Choice for Children
Over 104,000 children age 18 and under are currently enrolled in NC’s
state child health insurance program (SCHIP). NC Health Choice for Children
covers uninsured children whose family incomes do not exceed 200% of the federal
poverty level. It is a non-entitlement program -- the number served is dependent
upon availability of funds. The benefits package is the same as that provided
through the state employees’ health plan (NC Teachers' and State Employees
Comprehensive Major Medical Plan), with the addition of both preventive and
maintenance dental coverage along with vision and hearing coverage. Benefits
for children with special needs are modeled on Medicaid guidelines, except
that services for long-term care are not covered, and respite care may be provided
under emergency circumstances. A provision for reimbursement for case management
for CSHCN as a cost containment and quality assurance measure is an approved
benefit. This provision has not been fully implemented. Families with incomes
150% of the federal poverty level must pay an annual enrollment fee of $50
per child or $100 maximum for two or more children. Children must be uninsured
on the date that NC Health Choice enrollment begins. Co-payments are required
for these families as follows: prescriptions - $1, $3 and $10 depending upon
whether the drug is generic or name brand; $5 for each
physician,
clinic, dental or optometry visit except that there are no co-payments for
preventive services;$5 for outpatient hospital visits; and $20 co-payment for
non-emergent care provided in the emergency room. copays recently changed.
They are now $1, $3 and $10 depending upon whether the drug is generic or
name brand.
Enrollees whose income has risen to 200%-225% FPL by re-enrollment may
buy-in for one year at full cost. The Medicaid and NC Health Choice application
and renewal processes utilize joint application/renewal forms; out-stationed
eligibility workers; mail-in option; multiple application sites; elimination
of assets tests; continuous eligibility for twelve months; and elimination
of child support enforcement as an eligibility condition. On-going outreach
campaigns help assure maximum enrollment.
Name: Cinnamon Narron, NC Health Choice Coordinator,
DMA
Contact: 919-855-4020
E-Mail: Cinnamon.Narron@ncmail.net
Web site: www.dhhs.state.nc.us/dma/cpcont.htm
North Carolina Office on Disability and Health (ODH): www.fpg.unc.edu/~ncodh
Since 1994, the NC Office on Disability and Health (NCODH) has been organized
as a partnership agreement between the Women’s and Children’s
Health Section and the FPG Institute at the University of North Carolina
at Chapel Hill.
The goals of the NCODH are to increase awareness and understanding of the health-related
needs of individuals with disabilities; improve access and inclusion; develop
health promotion programs and educational materials for consumers and professionals;
conduct and report on research and data collection; and affect disability policy
related to these areas. The ODH is sponsoring initiatives in four primary areas:
1) access to health care; 2) women’s health; 3) adolescents and young
adults in transition; and 4) physical fitness and recreation.
The NCODH supports the Division of Public Health and the NC DHHS with disability
and health leadership in building state capacity to effectively address and
eliminate health disparities. The goal of the Office, consistent with that
of the Division, is to improve access to health promotion and disease prevention
opportunities for people with disabilities through collaboration with state
and community public health programs and disability service networks.
Name: Karen Luken, NC ODH Program Director
Contact: 919-966-0868 Fax: 919-966-0862
E-Mail: kluken@email.unc.edu
Smart Start - Smart Start is a public-private initiative that
provides early education funding to all of the state's100 counties. Smart
Start funds are administered at the local level through local nonprofit
organizations called Local Partnerships. The North Carolina Partnership
for Children (NCPC) is the statewide nonprofit organization that provides
oversight and technical assistance for local partnerships. Services at
the local level vary depending on local needs. www.smartstart-nc.org/
Early Hearing Detection & Intervention (EHDI)
Contact(s):
State EHDI programs promote universal newborn hearing screening, develop effective
tracking and follow-up as a part of the public health system, promote appropriate
and timely diagnosis of the hearing loss, prompt enrollment in appropriate
Early Intervention, link newborns to a medical home and
strive to eliminate geographic and financial barriers to service access.
The newborn hearing and metabolic screening programs have been joined to create
the Genetics and Newborn Screening Unit. This unit focuses on consultation,
education, diagnostic testing, counseling and family support related to various
genetic conditions as well as identification, referral, diagnosis, amplification,
and intervention specific to hearing loss. Major service initiatives include
newborn screening and follow-up for both hearing and metabolic disorders, genetic
counseling, consultation to families and to private and public providers. Regional
genetic counselors, regional child health audiology and speech language consultants,
and program consultants focus on these initiatives.
Name: Joan Crissey, MA CCC-SLP Unit Manager Genetics
and Newborn Screening
Contact: Phone: 919-707-5630 | Fax: 919-733-2997
E-mail: joan.crissey@ncmail.net
Web site: www.ncnewbornhearing.org
Early Intervention/Part C Coordinator:
The NC Infant-Toddler Program is North Carolina’s interagency early intervention
program for children ages birth to three. The Division of Public Health (WCHS,
Early Intervention Branch) is the lead agency. Children with diagnosed developmental
delays, chronic illnesses, disabilities or other risk factors for developmental
delay are eligible for program services. The goal of program interventions
is to assure optimal physical, social, and emotional development for children
with special needs. Multidisciplinary program service providers and family
members jointly develop an Individualized Family Service Plan (IFSP) based
on professional assessments of child’s needs and other issues of concern
to the family. The IFSP is used to guide subsequent care decisions. The program
provides or arranges for assistance in obtaining all services that are required
to address issues contained in the ISFP. Program services are provided based
on the child’s needs and family interests. The 19 required early intervention
services are:
- Assistive Technology
- Audiological services
- Service coordination
- Early intervention
- Family counseling and/or therapy
- Health care services
- Medical care
- Multidisciplinary evaluations and assessments
- Nursing services
- Nutrition services
|
- Occupational Therapy
- Physical Therapy
- Psychological services
- Respite care
- Social Work services
- Special instruction
- Speech/Language Therapy
- Transportation
- Vision care and screening
|
Name: Deborah Carroll, EI Branch Head
Contact: Phone: (919) 715-7500 x251 | Fax: (919) 733-3075
Email: deborah.carroll@ncmail.net
Web site: www.ncei.org
Section 619/ Preschool Grants Program of the Individuals with Disabilities
Education Act (IDEA). This program provides free appropriate public
education (FAPE) for children, ages 3 through 5 years, with disabilities:
Name: Kathryn Baars, 619 Coordinator
Contact: Phone: (919) 807-3994 | Fax: (919) 807-3998
Email: kbaars@dpi.state.nc.us
Web site: www.ncpublicschools.org/ec/specialprograms/resources/
State Interagency Coordinating Council (ICC) Chairs:
The North Carolina ICC advises appropriate agencies on the unmet
needs in early childhood special education and early intervention programs
for children with disabilities, assists in the development and implementation
of policies that constitute a statewide system, and assists all appropriate
agencies in achieving full participation, coordination, and cooperation
for implementation of statewide system.
Name: Cheryl Mulloy, ICC Co-Chair
Contact: Phone:(704) 894-9885
Name: Azell Reeves, ICC Co-Chair
Contact: Phone: (336) 334-7665 | Fax: (336) 334-7580
Email: reevesi@ncat.edu
Web site: www.ncei.org/ei/ncicc.html
Resources/Documents
Official web site of the state of North Carolina and Governor
Mike Easley: www.ncgov.com
This Web site provides links to all NC state agencies and services.
State Waiver Information: www.cms.hhs.gov/MedicaidStWaivProgDemoPGI/08_WavMap.asp
Waivers are the result of a process that allows state Medicaid agencies to
apply for and receive permission from HCFA to provide services not otherwise
covered by Medicaid and/or to do so in ways not described by the Social Security
Act. Most Medicaid managed care programs require Waivers. The Waivers, which
can differ greatly, are known by their numbers (1115, 1119), or as home-and
community-based, or as Katie Beckett Waivers, CAP-C, CAP-D or CAP-MR/DD.
Educational Initiatives
This section provides information on training initiatives on the medical home.
Some states will discuss their outreach projects in relation to physicians,
families, and the community.
North Carolina will be developing an educational initiative for parents
and families of Children with Special Health Care Needs in conjunction with
the Family Support Network of NC over the next year.
Practical CME Day: Re-Tooling the Pediatric Medical Home
Saturday, March 6, 10am – 4pm
Andrews Conference Center
Wake Medical Center
Raleigh
Agenda
The AAP’s Medical Home Initiative
Re-Tooling the Pediatric Medical Home – One Practice’s Experience
Providing a Medical Home for NICU Graduates
The Culturally Competent Medical Home
Coding Issues for Children with Special Health Care Needs
The Healthy Family Program: Helping Overweight/Obese Adolescent Females in
the Office Setting
Quit Now NC! – A Statewide Collaborative and New Resources to Enhance
and Enable Smoking Cessation
There is a registration fee of $75
Check the website at www.ncpeds.org
for an official registration
Screening
Initiatives This section provides information on surveillance
and screening initiatives in the state.
State Newborn Screening & Genetics Programs:
genes-r-us.uthscsa.edu/resources.htm
- State Newborn Screening Program Links
- State Genetics Program Links
- Regional Genetics and Newborn Screening Collaborative Links
- Newborn Screening State Contact Fact Sheet
Assuring Better Health and Child Development (ABCD) Program:
http://12.109.133.213/_docdisp_page.cfm?LID=2A7898BB-5310-11D6-BCF000A0CC558925
The Assuring Better Child Health and Development (ABCD) Program is funded
by the Commonwealth Fund, administered by National Academy of State Health
Policy, and designed to assist states in improving the delivery of early
child development services for low-income children and their families.
NC was one of four states awarded a grant from the Commonwealth Fund
in 2001 for development and implementation of programs to enhance child
development services by improving service delivery and financing systems.
NC’s approach to this initiative has utilized the Access II/III
networks as its foundation. Partnership for Health Management (P4HM),
championed by Dr. Marian Earls, Developmental Pediatrician, led the development
of the model. In subsequent years, the model has been expanded to two
additional Access II/III networks and is slated for statewide expansion
across Access II/III in 2004. The program goals are to develop a comprehensive
community model to be used as a template for replication, and to form
a state advisory group to work in concert with tier-one activities. These
goals are being reached by:
- Development and implementation of a model program for children that
encompasses their health, social, and developmental needs;
- Securing local community involvement and buy-in on the delivery of
early childhood developmental services;
- Integration of services in order to assure maximally effective use
of current resources and to minimize duplication of service;
- Assisting parents to understand developmental milestones/behavior
and ways to facilitate healthy development;
- Identify and respond to provider concerns regarding developmental
screening
and surveillance in private practice;
- Identifying and responding to family concerns; and
- Monitoring and tracking the impact of the project’s effort by
implementing an
evaluative process.
The NC ABCD initiative has centered on interventions in private practices
to integrate developmental screening and surveillance into the practice
workflow, and to increase early and appropriate referral for children
with developmental delays (or risk factors for such delays).
Name: Sherry Hay, Office of Research, Demonstrations
and Rural Health Development
Contact: 919-715-1511
E-mail: sherry.hay@ncmail.net
Family Corner
State Programs and Services
Tender HealthCare at The Jordan Center: www.tenderhealthcare.com/index.html
Tender Health Care is a child care program
for children who are medically fragile. The program was developed as a
joint project between Pediatric Services of America and the Department
of Health and Human Services of the State of NC. Tender HealthCare provides
quality medical and developmental care in a warm and stimulating educational
environment. A nursing staff of experienced neonatal and pediatric professionals
provides the children’s overall care. Children receive continuous
assessment and frequent nursing interventions throughout their day. All
care is delivered under the supervision of the child’s primary physician.
Name: Joe
Harrelson, VP for Marketing, PSA
Contact: 1-800-950-1580
E-mail: jharrelson@psakids.com
Name: Danielle Matula - Specialized
Services Unit
E-Mail: Danielle.Matula@ncmail.net
Advocacy and Support Organizations
Family Voices: www.familyvoices.org/st/NC.htm
Partnering with professionals and families to advocate for health care
services that are family-centered, community-based, comprehensive, coordinated
and culturally competent.
The Exceptional Children's Assistance Center (ECAC) -
Since 1980, The Exceptional Children's Assistance Center
(ECAC) has grown from an all volunteer parent organization
to a full service Parent Training & Information
Center serving families in North Carolina with more
than 25 full and part-time staff and offices throughout
NC. All services are provided at no charge to parents
and families. ECAC also houses NC Family Voices. The
toll free parent information line is 1-800-962-6817. ecac-parentcenter.org/
NAMI of North Carolina (National Voice on Mental Health): www.naminc.org
Education, advocacy and support for persons with
brain disorders (mental illnesses) and their families.
NC Family Support Network (FSN): fsnnc.med.unc.edu
The Family Support Network of North Carolina FSN-NC, created in 1985, was one
of the first agencies in the state to establish formal parent matching programs
to link families of children with special health care needs for parent-to-parent
mentoring. It is composed of 16 affiliated, community-based family support
organizations housed in local settings that include: community hospitals, Children’s
Developmental Services Agencies (formerly Developmental Evaluation Centers),
and Family Resource Centers. All programs offer parent to parent matching;
other services include support groups, provision of information and referral,
and workshops for families with children who have special needs and those who
are at risk.
The Central Office of the Family Support Network of NC is a department
of the School of Medicine at UNC Chapel Hill. Staff of the Central Office
provides training, technical assistance, and consultation around program
development, data gathering, and program evaluation. The Central office
operates the Central Directory of Resources (CDR) for the state early
intervention program. Through this toll-free telephone line and the organization’s
web-site, family members, other caregivers, and service providers can
get information about specific disabilities, about disability related
issues and about resources and services for children with special needs
and their families.
All services are offered in English and in Spanish. Videotapes, books
and other instructional materials are available for loan from the Outreach
Library. The toll-free phone line is 1-800-852-0042.
Women’s and Children’s Section
Family Advisory Council
The purpose of the Family Advisory Council to the WCHS is to advise program
staff on the development of programs, policies and procedures that can best
help WCHS to carry out it’s function. The FAC is considered the link
between families and the WCHS and with other parent organizations, support
groups, service programs and advocacy groups.
Name: Marlyn Wells, Family
Liaison Specialist
Contact: 919-715-3811 Fax: 919-715-3187
E-mail: marlyn.wells@ncmail.net
Resources and Information
Early Hearing Detection & Intervention
(EHDI) Information for Parents:
Description of EHDI Program | Babies Referred from Screening
www.medicalhomeinfo.org/screening/State/north_carolina.html
Family Village: www.familyvillage.wisc.edu/index.htmlx
A global community that integrates information, resources, and communication
opportunities on the Internet for persons with cognitive and other disabilities,
for their families, and for those that provide them services and support.
This site offers informational resources on specific diagnoses, communication
connections, adaptive products and technology,adaptive recreational activities,
education, worship, health issues, disability-related media and literature,
and much, much more!
NC Family Health and Child Care Resource
Line( Toll free number is 1-800-367-2229.)
North Carolina’s Family Health and Child Care Resource Line combines
the services of the Title V-required MCH information and referral hotline
with those previously provided through the NC Child Care Health and Safety
Resource Center. This consolidation has increased access, increased breadth
of information, and streamlined services for NC families. This initiative
is supported through a combination of funding from: DPH; DMA; and the
Division of Child Development. The Resource Line is equipped to provide
technical assistance, information and referrals to a number of programs
for children and families, and advocacy on family health-related issues.
Services are available in English and Spanish and through a TTY service.
TelAbility http://www.telability.org/index.pl
An innovative, community oriented, interdisciplinary program
that uses telecommunications to improve the lives of children with disabilities.
Using real time video-conferencing and internet technologies, TelAbility
provides comprehensive, coordinated, family centered care to children
with disabilities across North Carolina and offers education, training,
and peer support for people who care for them.
The Special Needs Helpline (1-800-737-3028)
This is a toll free phone line that provides
information and referrals for children with special health care needs
across North Carolina. The Helpline operates from 7:00 am to 5:00pm Monday
to Friday. Individuals who call after hours can leave a message and
have
their call returned the next business day. Helpline staff answer questions
about programs serving children with special needs, provide advocacy
for
those having trouble accessing services, refer families to health care
providers in their community, identify resources, and more. The Helpline
is an excellent resource for families of children with special health
care needs.
The
Association for Retarded Citizen (Arc) Family Resource Guide http://www.thearc.org/familyguide/northcarolina.doc
This guide is written for families raising children with mental retardation
and related developmental disabilities. It tells families about benefits,
supports and services in their state that might help their child.
State Resources on the Internet:
www.medicalhomeinfo.org/states/index.html#res
Note: The information provided on the state pages was submitted by the
state medical home teams.As this is not an exhaustive list, please let
us know if you have additions for your state resource page. You can contact
us at: medical home@aap.org.
http://www.medicalhomeinfo.org/states/state
/north_carolina.html
Last Updated
May 1, 2007
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