An informative article on primary-progressive multiple sclerosis (PPMS) appears in the summer 2011 issue of the International Journal of MS Care. “Meeting the Needs of People with Primary Progressive Multiple Sclerosis, Their Families, and the Health-Care Community” is part of a collaborative project between the Multiple Sclerosis Association of America (MSAA) and the National Multiple Sclerosis Society (NMSS) to recognize the needs of this specific population and to create programs to help answer these needs.

Cladribine Tablets were expected to be one of the next approved disease-modifying therapies to treat relapsing forms of multiple sclerosis (MS). Merck Serono announced on June 22, 2011 that they will no longer seek global approval for the drug.

My MS Manager is the Multiple Sclerosis Association of America’s new mobile phone application, provided free of charge to individuals with multiple sclerosis (MS) or their care partner to use on their iPhone, iPad or iPod touch. Developed in conjunction with Ringful Health, My MS Manager is available now for download in the Apple iTunes Store.

We are proud to announce the launch of the Multiple Sclerosis Emerging Therapies Collaborative. The Collaborative – which includes the members of the MS Coalition, the American Academy of Neurology, and the VA Multiple Sclerosis Centers of Excellence East and West – has as its mission: To develop and disseminate timely, evidence-based resources to persons affected by multiple sclerosis and health care professionals, in order to  promote optimal, individualized treatment of the disease by facilitating effective communication and medical decision-making.

EMD Serono, Inc., makers of Cladribine Tablets (an oral formulation of cladribine), announced today that they received a complete response letter (CRL) from the United States Food and Drug Administration (FDA). The FDA issues a CRL when it has completed the review of an application. However, in this situation, the FDA was not able to approve the application without additional information. The announcement was disappointing to members of the MS community, who were hoping to see another option added to the list of available disease-modifying therapies for the long-term treatment of MS.

Please join MSAA for a new program focusing on helping parents and children build a better understanding of MS, develop peer connections, and strengthen the family.

During MS Awareness Month, the Multiple Sclerosis Association of America (MSAA) invites the MS community to participate in a wide array of activities and events to help manage their MS.

MS can impact not only physical and cognitive abilities, but also a person’s emotional wellbeing. In cooperation with the research organization Infogroup/ORC and supported by an unrestricted educational grant from Avanir Pharmaceuticals, the Multiple Sclerosis Association of America (MSAA) conducted an independent, online survey of almost 20,000 of its members in the fall of 2010. The purpose of this survey was to better understand the extent and impact of a particularly challenging neurological condition known to occur among people living with MS: pseudobulbar affect (PBA).