'I Pinky Promise' founder wants more
awareness of children's disabilities
By Greg Miller
STAR STAFF
gmiller@starhq.com
Teena Bradley, founder of "I Pinky Promise," a support
group for families of children with developmental disabilities
and brain disorders, says she wants more public awareness
of children's disabilities.
Bradley says needs include more respite programs, more
participation in the school system, and additional recognition
of "I Pinky Promise" and similar support groups by other professional
agencies and organizations.
Bradley began "I Pinky Promise" about two years ago.
"Since then, the support group has ventured into many, many
other areas as far as advocacy, including being placed on
various councils, and one of many is the Region 1 Mental Health
Planning Council," she said.
"I am a voting parent member of this organization. You have
to be appointed by Gov. Phil Bredesen to be a part of this
committee. I would like to see more parent participation in
this particular council, especially the Children in Youth
Committee Council." Bradley was recommended by Jim Griffin,
coordinator of the Region 1 Council in the Tri-Cities.
"I Pinky Promise" is two or three different organizations
combined into one. Tennessee Voices for Children is the sponsor
of "I Pinky Promise". Project LINK (Leaders in Education Networking
for Kids), of which Bradley is chair, is an affiliate of the
Association of Retarded Children of Tennessee. Bradley said
she would like to see more Project LINK organizations formed
in the Tri-Cities area.
"My involvement is educating myself to be an advocate
to help other families of children with disabilities. We participate
in workshops. We travel to Nashville. We bring professionals
to speak on various disabilities pertaining to one of the
family members or to teach us on how to be advocates to help
other parents going through the same or some troubling issue
within the school system with their mental health.
"We're parents educating parents, and we share that information
with other individuals, other agencies. We want to learn how
to help ourselves and other families."
In June, Bradley attended an advocate training meeting in
Nashville, and, in March a "March on Nashville has been planned.
"We're hoping to get at least about 1,500 participants," Bradley
said. "This is for families with children with disabilities
and mental retardation."
The support group meetings are open to parents, professionals,
and representatives of various agencies. "We've got to work
together to change the system, not only for children with
disabilities, but for children without disabilities," she
said.
The support group meets at First Presbyterian Church, Elizabethton,
on the last Friday of each Monday from 6:30-8:30 p.m. A second
meeting place is being established at Girls, Inc., Johnson
City.
"We were able to get a grant to provide respite for parents
wanting to attend these meetings and workshops, so they can
bring their children, and daycare will be provided for them
at the meetings," Bradley said.
Local residents, business owners and representatives of local
civic organizations are invited to attend the support group
meetings. "Speak on what you offer to the community," remarked
Bradley, who said the support group can provide speakers to
local organizations.
For more information, call Mike or Ellie M. Hjemmet at 772-4146
or Bradley at 547-0517. You may also e-mail the Hjemmets at
hjemmet@wireco.net or Bradley at talishiabradley@earthlink.net.