Newly Diagnosed
It can be difficult to hear the words “you have MS” for the first time. When you are newly diagnosed, you will find that you have many questions about what this diagnosis means for you, and how it will impact your life and the lives of your loved ones. There are many challenges, but there are also many supportive options available to help you.
Resources, Support and Guidance at Your Fingertips
It can be difficult to hear the words “you have MS” for the first time. You will have many questions about what this diagnosis means for you, and how it will impact your life and the lives of your loved ones.
The National MS Society wants you to know that you are not alone. We are here to help answer your questions, provide resources and education, and connect you with supportive networks. We offer:
- Educational Materials
- Community Resources
- Support Groups
- Peer Support
- Teleconferences for the newly diagnosed
- Knowledge is Power
Call the Information Resource Center for more information at 1.800.344.4867.