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ADVOCACY PROFILE

Day on the Hill in Tennessee

                                       Deema Tarazi, staff writer

I n March, HFA attended the Tennessee Hemophilia and             to quality healthcare. Participants also discussed the history of
   Bleeding Disorders Foundation “Day on the Hill.” Twenty-      hemophilia, how therapies have changed in the last 10 years,
six community members attended the event, which included         and how vital treatment is in protecting an individual with
advocacy training and multiple meetings with legislators and     hemophilia from life- or joint-threatening bleeding.
their staff to discuss the importance of access to care for the
bleeding disorders community.                                    Access to appropriate therapies allows the community to lead
                                                                 healthy, productive lives. Additionally, a community member
The day started with an early morning training on how to         who has a personal relationship with his senator spoke one-
talk with legislators and an overview of the talking points. In  on-one with the senator about the challenges the community
addition to educating legislators about bleeding disorders,      would face with added working requirements to Medicaid.
community members advocated about the impact of adding           Legislators were engaged with participants during the
work requirements to TennCare, the Tennessee Medicaid            meetings and responded positively to the group’s messages.
program, for people with bleeding disorders and maintaining
the State Hemophilia Program budget, an important safety-net     HFA was thrilled to be a part of THBDF’s “Day on the Hill.”
program for many families in Tennessee.                          It was a great day for the Tennessee bleeding disorders
                                                                 community’s voice to be heard in Nashville. HFA encourages
Community members shared their personal stories about living     advocates to continue building relationships with their legisla-
with a bleeding disorder and the importance of having access     tors to ensure the community has a constant presence at the
                                                                 Capitol. Thanks to THBDF for allowing HFA to join you —

                                                                 we look forward to attending future events! S

 Access to appropriate therapies allows the
community to lead healthy, productive lives.

18	 Dateline Federation | Summer 2018
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