The National MS Society advocates for those living with MS to move politicians and legislation forward in the areas that most affect the 400,000 impacted with the disease, including funding for MS research, health insurance, long-tern care and disability rights. In Maryland, advocacy efforts focus on local and state elected officials while the Society's Advocacy office in Washington D.C., focuses on national issues.
Thank you to everyone who participated in Advocacy Day in Annapolis during MS Awareness Week!
On March 14, we were able to meet with 130 legislators and tell them what issues are important to people with MS.
The issues we discussed with our representatives are:
• Stem Cell Research Funding
• Accessible transportation and other in-home supports
• Enforcing appropriate use of handicapped parking spaces
Take action on the advocacy issues that the Society is lobbying for in 2011 on both the state and federal level.
There are many ways to help us make a difference for those living with MS. Your voice can make a difference!
Do you know have all the resources you need to have your voice be heard? Check out our public policy resources to get the answers you need to advocate for those living with MS.