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Brazil conference 2010 november

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  • 1. Nurture Grassroots Power:Engaging Your Members & Managing Your Growth
    Debbie Castro
    PHA Director of Volunteer Services
  • 2. Alex Flipse, Diagnosed 1998
    My Involvement
  • 3. Outline
    PHA
    Building a construct to change the history of an illness
    PH environment in the USA
    Elements of Success
    PHA and Volunteerism
    Medical Education Programs
    International Programs
  • 4. PHA: Founded on volunteer spirit around a kitchen table.
    Florida, USA, 1990
  • 5. 187 identified patients in the U.S.
    Patient survivability: 2.8 years for 50%
    NO disease-specific treatments
    Central organizing issue: ending isolation
    PH Environment in the United States in 1990
  • 6. PH Power of our Population
    20,000 to 30,000 patients are diagnosed with PH in the U.S.
    A huge growth from the 187 in 1985 and the 3,000 or so in 2001
    With a smaller population to fight back, each person is essential to the struggle
    The Power of One – you define the progress of this community
  • 7. All things are possible when building a constituency-driven organization with a clear sense of goals and a readiness to jump on opportunities
  • 8. Growth of the Association
    All Volunteer
    Handful of Programs
    Handful of key leaders
    Budget = <$100,000
    < 15 events a year
    < 80 Support Groups
    1 PH Treatment
    Staff grew, 2 to 40.
    Multiple Departments
    Structured Boards and Committees of leaders
    Budget = > $6,000,000
    60 events annually
    230 Support Groups
    9 Treatments
    1990 – 1999, First Ten Years
    2000 – 2010, Next Ten Years
  • 9. Elements for PHA’s Success
    Understanding the ongoing value of engaging and involving the grass roots
    • PHA believes that our members are our primary resource. Members of the PH community have the right to fight back. PHA has the obligation to create structures that make that possible.
  • Volunteer Management Systems
    Coordinated
    Intermittent
  • Patient-to-Patient Support Line
    What is the Support Line?
    Who are the volunteers?
    Staff administration
    Cheap and Effective
    www.PHAssociation.orgSupportLine
  • 20. Support Groups
    What do they do?
    How do they form?
    What do we offer?
    Impact in the community
    Impact in the PH Movement
    www.PHAssociation.org/SupportGroups
  • 21. Medical Education Fund
  • 22. 30 City Medical Education Program
    Description: Dinner programs presented at 30 second-tier cities throughout the U.S. and Puerto Rico. Second tier cities are defined as those that do not have a PH center or PH expert.
    Objectives: To present information on the diagnosis and management of pulmonary arterial hypertension (PAH) to physicians and other health professionals located in areas that lack recognized experts or centers for PAH.
    To create relationships with PAH experts so non-specialists will refer patients and will consult with experts on an ongoing basis when issues occur regarding patient management.
    Goal:20 attendees
    Format: Dinner, followed by 1.5 hour presentation given by a local PH expert on the classification, diagnosis, and management of PH; a brief case presentation; and a question and answer session.
     
    Venue: Hotels or restaurants in second tier cities without a local PAH center or expert
  • 23. Preceptorship Program
    Description: Full-day programs at renowned PH centers; content delivered by specialists from that center.
    Objectives: To facilitate direct education and training of medical professionals, particularly cardiologists, pulmonologists, rheumatologists, and possibly primary care physicians, by experienced pulmonary hypertension specialists in clinical settings. (Physician CME and nursing CEU credits will be available.)
    To increase the number of physicians in the United States who can suspect PH, refer these patients to a PH specialist, and work with the specialist to effectively manage the disease.
    Goal:25-30 attendees
    Format: Day-long didactic presentations given by PH specialist from the host center. At least two hours of the training is devoted to extensive case discussion and a question and answer session.
     
    Venue: Academic health centers recognized for their expertise in PAH
  • 24. PHA Online University
    Description: Centralized website for PAH-specific medical education for medical professionals including: CME courses for physicians and allied health professionals; online home of Advances in Pulmonary Hypertension; archived presentations from PHA’s medical meetings; and discussion boards
    Objectives: To sustain and expand a clear, focused website for medical education in pulmonary hypertension, segmented by levels of expertise and medical interest. (Physician CME and nursing CEU credits will be available.)
  • 25. PHA Online University
  • 26. PHA on the Road: PH Patient and Families Education Forum
    Description: One-day regional education events for patients and families, focusing on medical education and lifestyle issues, and with an enduring online component.
     
    Objective: To present information on the mechanisms, diagnosis and treatment of PAH and on coping and daily living with PAH to patients and family members in regional face-to-face settings, as well as adding content in a new online Virtual Patient Classroom and an awareness building component.
    Goal: 200 attendees
  • 27. PHA International Connections
    • 50 official Pulmonary Hypertension associations worldwide
    • 28. Email List
    • 29. Seed Grants
    Christine Dickler, Associate Director of International Services
  • 30. International Resources
    Building Effective PH Association Guide
    We began by doing all that was possible to help PH patients that wouldn’t cost anything or very little: give correct information; listen to their problems and if you have a solution that works, offer it … a million other things can be done with just a little money and lots of time and work.
    –AMIP Italy
    www.PHAssociation.org/IntlBuildingAssociationTips
  • 31. PHA has an obligation to involve anyone living with this illness as much or as little as they are able and willing to be involved.
    This volunteer spirit has been and remains PHA’s strength.
    Parting thoughts:
    Debbie Castro, PHA