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Survey for Ryan White Part A Planning Council Members

Thank you for taking our survey, all responses are anonymous.

Thank you for your time serving on a Ryan White Part A Planning Council.  The engagement of community, partners and allies like yourself since the early days of Ryan White programming has supported impactful planning, funding and strategy for nearly 30 years. We look forward to future collaboration and appreciate your time. 


This survey will ask you some questions about your time on the Planning council, what supported your meaningful engagement and when you might have felt frustrated or dis-empowered.  These surveys are 100% anonymous, we are not gathering any contact information. If you are interested in additional surveys or focus groups, you will use an alternative registration link. Please be as specific as possible when giving examples, your responses will be helpful as we provide feedback to HRSA and the US PLHIV Caucus MIPA on Planning Councils Working Group. There are no right or wrong answers and each question has space for an additional comment, please feel free to add any information you would like to share.


If you have participated on Planning Councils in several areas, please fill this survey out for each one. 


Thank you for your engagement

The US PLHIV Caucus
 
I do not serve on a Part A Planning Council but do serve on a Part B or other type of planning body and am interested in a follow up survey 

Link to Google Form
1.Planning Council Experience
2.What geographic area does your planning council represent?
3.How many years have you been involved in your Planning council?
4.How would you describe the experience?
5.Would you encourage your peers (people living with HIV, providers, HIV Service Organization (HSO) staff to join the Planning Council)?
6.Does your Planning Council hold effective meetings?
7.Does your Planning Council provide onboarding and continuing training to council members?
8.Are You familiar with your Council's by-laws?
9.When were your Council's by-laws last updated?
10.Does your Planning Council meet the required minimum, that at least 33%  of membership be people living with HIV who do or have received services and are not aligned with a funded agency (aka paid staff)?  To learn more, here is the Part A Planning Council Primer which detail the membership requirements on page 17 (add link)
11.Do the Council members living with HIV represent the demographics of people living with HIV in your area?
12.How are people in general recruited and more specifically people living with HIV recruited to join your Planning Council?
13.Are people living with HIV treated with respect and dignity?
14.Is their subject matter expertise valued?
15.Are you familiar with ways to express concern about your Planning Council including the HRSA grievance process?
16.What is your race/ethnicity?
17.What is your age?
18.What is  your gender identity?
19.What is your sexual orientation?
20.Are you a person living with HIV?
Current Progress,
0 of 37 answered