Are you using IRIS or Family Care (or neither) for SDS? Why?
Questions about Self-Directed Supports or Self-Determination
I'm a IRIS program participant I have been disabled with several medical conditions since really young. I have been on SSDI since 1999 and Medicare since 2000. I have had three strokes since 1996, a heart attack in 2003, diabetes Type 2, Fibromyalgia, and several other chronic medical conditions.
Since I became an IRIS participant in December 2010 I enjoy being in control of my own services and who provides those services for me. I am receiving only the services I really do need or want. I have several great caregivers and community service providers currently on my IRIS team. I like the fact I can talk with my IRIS consultant as needed and make changes to my plan as needed as my situation changes. Unlike the Family Care program I was involved in prior to becoming a IRIS program member. I came to the IRIS program after I could no longer make the Family Care program work for me under self-direction. It was decided with my family care case manager and team that I needed to switch to the IRIS program because my Self-Directed Supports could no longer help me reach my goals. I love the flexibility and support I get from the IRIS program. I'm in control of my life and what I want for my life. I have the right to control my own life and destiny. With the support of my family, friends and others who believe in these values, I can and will pursue my goals and be fully included in my community. I have achieved many of the goals I wanted too so far. If you want to know what I have achieved in the IRIS program ask me.