At-home educational program about MS

Looking to connect with other caregivers, family members, or people affected by MS? Self-help groups bring people together who share common life experiences for support, education and mutual aid.

Search for and connect with a trained peer support volunteer who can provide you with helpful tips, suggestions and emotional support for the challenges that MS throws at you. Connect via one-on-one ongoing telephone or email conversations.

MSFriends®connects you with a supportive, empathetic volunteer who understands life with MS and can say, “I've been there, too.” MSFriends meet for up to six months via phone, email or video calls based on your preference. Click here to learn more about MSFriends connection opportunity.

A list of pharmaceutical and non profit financial assistance programs to assist with the costs of MS medications.

This is a teleconference recording that aired on April 3, 2014. During this teleconference: Participants will be aware of normal bowel and bladder function without MS; participants will learn what dysfunction can occur related to MS; participants will be able to explore these issues with their health care provider for solutions that will lessen the impact on their overall quality of life.

Symptoms, disease patterns, diagnosis, prognosis, treatment, and research efforts.

Listen to audio from past teleconferences.

Learn more about The Wellness Center at the Historic General Hospital in Boyle Heights, CA.

Discusses some of the more difficult physical and emotional problems many families face. By Sarah Minden, MD, and Debra Frankel, MS, OTR.

Part 1- Thinking Proactively About Employment

This video is a resource for employers, featuring discussions about multiple sclerosis in the workplace.

Promising MS Research to Repair, Protect and Restore the Nervous System. Moderator Kate Milliken and panelists Dr. Ben Barres, Dr. Jonah Chan, Dr. Timothy Coetzee and Dr. Rhonda Voskuhl. December 5, 2013

The Spring 2013 issue of Momentum magazine, with a special bilingual feature on the Latino / Hispanic experience of living with MS.

The Winter 2012-13 issue of Momentum magazine. Features include "Not Your Friend's MS" and "The Pursuit of Happiness."

The Summer issue of Momentum, with features on disclosure and art therapy.

The Fall 2012 issue of Momentum, with a feature on families and MS.

There is a significant increase in requests for services from students with chronic diseases, like MS. This article explains how you can benefit from this change.

The surest indicator and best tool of an MS activist is information. We will arm you with what you need to fully understand activism and the issues. Here's a brochure about Federal Advocacy (please read and share it!).