Maine Family Voices
Maine Family Voices, the Maine chapter of the national Family Voices organization has an emphasis on access to health and health related services for children with special health care needs. The major program goal of Maine Family Voices is the creation of a statewide Parent to Parent program
Maine Parent Federation provides statewide coordination for Family Voices activities in Maine. In 1998, Maine Parent Federation was awarded a Robert Wood Johnson Foundation grant from National Family Voices to expand efforts in Maine to reach families of children with special health care needs. The Maine Family Voices project provides the opportunity for families of children with special health needs to become informed and active members of a network that will speak out on issues on behalf of children with health care issues.
Goals of the project
To create a network of well informed
family members.
Support families to be responsive to
health care issues at the state and national level.
To establish a family support component
to provide information and training
What's New
Maine Family Voices Has:
Hired a part-time staff person
Formed a Family Advisory Council
Outreach to families of children with
special health care needs and the professionals who work with
them
Fact sheets available on the Children's
Health Insurance Program and Managed Care
Developed a family health care survey
as a collaborative effort with Consumers for Affordable Health
Care (If you have not completed our survey, please call us at
1-800-870-7746 (Maine Only) for a copy.
These Are Our Children
Our children with special health care
needs are, above all, children who want to have a healthy, happy
childhood and grow up to be productive adults. Like all children,
they live with their families in the towns, cities, and rural
areas of the United States, attending school, going to church,
and enjoying community events.
However, unlike most children,
they also have challenging health conditions that usually make
their lives and their families' lives more complicated. Some of
our children have physical, mental, or emotional disabilities;
others live with a chronic illness; many present a brief but life-threatening
medical problem. Some of our children need only an accurate diagnosis
and routine treatment and monitoring; others will require life-sustaining
technology treatment, and medicines through out their lives.
Children
with special health needs tend to receive their health care from
a combination of private and public financing and delivery systems.
About 10 million children have a chronic health condition of some
kind; about four million children have a health condition that
limits their school and play activities.
Family Voices is a national, grassroots clearing house for information and education concerning the health care of children with special health needs. We stay on top of public and private sector health care changes that affect our children and families through the collective efforts of our families: a volunteer Coordinator in every state; 10 Regional Coordinators; and a small staff working in several locations around the country. Together, we share the expertise and experiences of families from around the country with state and national policy makers, the media, health professionals, and other families. We work in public and private hospitals, public health programs, in state capitals, in Washington, DC, serving on boards and task forces, working in partnership with health professionals and policymakers, bringing the family perspective to policy discussions and decisions. There are almost 7,000 Family Voices members - families of children with special health needs and friends and professionals who know and love our children.
The Principles of Family Voices Guide Our Activities
Above all, Family Voices believes that:
All children deserve quality health
care.
Families with children who have special
needs and professionals who work with them have an expert understanding
of what works and what doesn't work within current health care
systems.
Health systems built upon a set of
tested principles and practices that flow from this expertise
can improve the health status of all children and families.
Therefore, health systems serving children
with special health care needs must adhere to the following principles:
3. Flexibility
Quality health care means a coordinated system of comprehensive services - prevention, education, screening, diagnosis, primary and specialty care, hospitalization, medication and supplies, equipment and rehabilitation - all available as close to the family's home as possible.
5. Family-professional partnership
Outcomes improve when families and professionals make decisions jointly, respecting the expertise, talents and resources that each brings to the care of the child with special health needs.
6. Cost effectiveness
By focusing on outcomes, allowing family choice, and strengthening and supporting the role of families in health care systems, costs can be reduced. The elimination of duplicative procedures, unnecessary paperwork, and administrative overhead also reduces costs. As families, we practice cost containment every day!
7. Quality assurance
Working as partners and remembering these principles, families and health professionals must regularly review and provide feed-back on health care financing and delivery.
JOIN FAMILY VOICES
If you want to be part of a grassroots movement to make sure that children with special health care needs receive the health services they need and deserve or if you have a specific question or concern, give us your name, address, telephone number. You may either e-mail us at parentconnect@mpf.org, call us at 1-800-870-7746 (Maine only) or (207)623-2144 or write to us at:Maine Family Voices Maine Parent Federation PO Box 2067 Augusta, ME 04338
