The work we do in advocacy is divided into three areas on the government level: federal, state, and local. Although all levels reflect issues important to people living with MS, these policy priorities may change from year to year to reflect the political climate at the time. These priorities are showcased at our Public Policy Conference in Washington, D.C., the Cal-Neuroalliance in Sacramento, CA, as well as our coalition work in Nevada and local action alerts.
Federal
The Society’s Public Policy Office guides our federal advocacy efforts and works with MS activists to raise awareness nationwide. Annually, hundreds of MS activists unite in Washington, D.C. for our Public Policy Conference to visit their legislators on Capitol Hill and ask for their support on issues such as federal funding for MS research.
State
California
The Southern California & Nevada Chapter and MS activists are currently pursuing:
Health care reform
Improved community resources
Disability rights
Long-term care resources
Access to quality health care services
Increased funding for MS research
Accessible, affordable health insurance
State Issues
AB 369 Healthcare Coverage: Prescription Drugs
SB 419 Safe Needle Disposal: Drug Manufacturer Responsibility
AB 1800 Fair Out-of-Pocket Expenses
Nevada
We have worked with a couple of powerful coalitions in Nevada to make change happen for people living with MS, including but not limited to the Nevada Women's Lobby. We are tuned into all issues that are important to people living with MS in Nevada, but have identified these priorities for 2010-2011:
- Respite Care
- DME Coverage
- Health Care
We need your help! If you are passionate about advocating for people living with MS and what to find out how your talents can help, contact 310.479.4476.