About MSAA

The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization and leading resource for the entire MS community, improving lives today through vital services and support. MSAA provides free programs and services, such as: a Helpline with trained specialists; award-winning publications, including, The Motivator; MSAA’s nationally recognized website, featuring educational videos, webinars, and research updates; a mobile phone app, My MS Manager™; safety and mobility equipment products; cooling accessories for heat-sensitive individuals; MRI funding; My MSAA Community, a peer-to-peer online support forum; MS Conversations blog; a clinical trial search tool; podcasts; and more. For additional information, please visit www.mymsaa.org or call (800) 532-7667.

MSAA’s Senior Director of Patient and Healthcare Relations Featured on K-LOVE Radio

Cindy Richman, MSAA’s Senior Director of Patient and Healthcare Relations, was recently featured on K-LOVE Radio as a part of the Closer Look segment that the station produces. If you missed Cindy’s interview you can hear it here:

https://soundcloud.com/emf-public-affairs-audio/closer-look-klove-wkvp-3-10-13

 

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MSAA’s Artist of the Month for April 2013

We have received many wonderful submissions from across the country and are delighted to share their work and their stories with you. Please visit our online gallery to view all of the submissions.

April 2013 Artist of the Month:  Susan C. Russo – Pearland, TX

 

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“I have been interested in art since I was a child. I love the creative process. I just close my eyes and let my thoughts come to life. I feel that my work is an expression of God’s love and His gift to me. It would be a great injustice not to share the talent He has given me.

Additionally, art is a beautiful expression of not letting my MS gets the best of me. On days when I don’t feel all that well, I just pick up a brush or pastel and express my feelings in my paintings and drawings…”
Read more from Susan…

Be inspired – please send an online card featuring artwork by MS artist Susan C. Russo and spread awareness of MS and MSAA.

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MSAA Partners with Modify Watches for MS Awareness

MSAA is excited to be teaming up with Modify watches as their Together Partner for the month of April.

Modify will be donating $20 to MSAA for EVERY Together Watch sold during April (even for members of our Mod of the Month Club who are receiving a 20% discount). If you would like to purchase a Together Watch to support MSAA visit Modify’s Non-Profit Collection.

Support  MSAA  today with themodify watch Modify Together watch!

 

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New MS Drug Approved

Tecfidera Approved for the Long-Term Treatment of MS

The United States Food and Drug Administration (FDA) announced that it has approved Tecfidera™ (dimethyl fumarate or DMF, formerly known as BG-12) for the treatment of relapsing forms of multiple sclerosis (MS). This is the 10th drug to be approved as a disease-modifying therapy (DMT) for the long-term treatment of multiple sclerosis (MS). Tecfidera is administered orally (by mouth) and is the third oral DMT approved for MS.

As with all of the approved DMTs for MS, Tecfidera is not a cure, but does slow MS disease activity. It reduces the number and severity of MS relapses (or symptom flare-ups) while reducing disease activity as seen on magnetic resonance imaging (MRI) scans — by reducing the number and size of brain lesions (areas of inflammation). Additionally, Tecfidera slowed the progression of sustained disability (in one of two large Phase III trials).

Please see MSAA’s online news article for more information!

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MSAA’s MS Research Update

MSAA's Research Update 2013MSAA’s MS Research Update is a comprehensive overview of research findings on the FDA-approved disease-modifying therapies, as well as many experimental treatments.

This 2013 edition of MSAA’s MS Research Update is the first to be printed as a stand-alone issue, reflecting the diversity and scope of research progress in MS. This information is based on a wide range of sources, including the extensive journal literature on MS and its management, a review of ongoing clinical trials, and papers presented at major national and international conferences.

Read MSAA’s latest MS Research Update.

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MSAA’s Senior Director of Patient and Healthcare Relations Featured on SecureACure4MS

On Monday, March 11, 2013, MSAA’s Senior Director of Patient and Healthcare Relations Cindy Richman was interviewed by SecureACure4MS. During the interview, Cindy discusses MSAA’s programs and services, as well as the ways you can support MSAA.

You can hear Cindy’s interview by visiting this link.

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Celebrate Scientists!

March is not only recognized as MS Awareness Month but is also celebrated as Women’s History Month. MSAA would like to thank and honor all of the women who have contributed to the advancement of medical and scientific research.

Female scientists, although sometimes lesser known, have contributed much in the past to initiate innovations in the medical field and advance research efforts. The following article (not published by the MSAA) celebrates female scientific innovators:   http://smithsonianscience.org/2013/03/five-pioneering-female-scientists-youve-probably-never-heard-of/.

MSAA would particularly like to honor all of those women who historically have worked and currently are working toward advancing research initiatives for MS.

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March is Multiple Sclerosis Awareness Month

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The Multiple Sclerosis Association of America (MSAA) recognizes March as MS Awareness Month. Throughout March, MSAA encourages individuals to expand their knowledge, understanding, and support of individuals whose lives are affected by multiple sclerosis (MS). MSAA offers the following ways to learn and support the MS community:

  • A new website, mymsaa.org, which features new sections and enhancements, providing easier access to more information, more resources, and vital tools for the entire MS community
  • My MS Manager™, MSAA’s mobile phone application to track disease activity, generate reports, and assist individuals with their treatment plan
  • My MS Resource Locator, an MS-specific, online database
  • S.E.A.R.C.H.™ program to assist individuals navigate through the ever-changing landscape of MS
  • MSAA’s educational events –  check out our calendar of events to see what is scheduled for your area

Interested in helping the MS community during MS Awareness Month?

  • Volunteer with MSAA! MSAA is also recruiting participants for our signature fundraising event – Swim for MS. Dive into action today to raise awareness of MS and you might be selected to receive one of two sets of park hopper passes from Walt Disney World! Register today at SwimForMS.org!
  • Help to spread MS awareness by using MSAA’s “March is MS Awareness Month” badge as your social media profile picture (right-click the image at the bottom of this blog post, save it to your computer, then use it on your Facebook, Twitter, or LinkedIn account profile pictures)
  • Become a part of MSAA’s online community: sign up to receive periodic email updates, become a fan of MSAA on Facebook; follow MSAA on Twitter; and view one of MSAA’s YouTube videos

 

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Is that Spring around the corner?

As we say goodbye to the shortest month of the year some parts of the country will begin to transition seasons. In particular parts of the country, it actually starts warming up to give milder spring like temperatures. While spring is considered a temperate and pleasant time by most, in some areas there may even be a few uncomfortably warm days.

This year, prepare early and get your cooling vest before those too warm (or in the summer, downright HOT) days arrive!  MSAA offers a program which provides free cooling vests and accessories to eligible individuals. Now is the perfect time to contact MSAA before the busy cooling season begins.You can learn more about how to apply for cooling at the following link: https://mymsaa.org/msaa-help/cooling/.

 

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February’s Artist of the Month

Presenting MSAA’s Artist of the Month for February 2013

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MSAA is very proud to present our Art Showcasecelebrating the work of artists affected by MS.

February Artist of the Month:
Mary E. Hetzel-Tingler – Hixson, TN

 “I was diagnosed with RRMS on Valentine’s Day 2006. I have been an artist nearly my entire life and this was quite a blow to be dealt, to not be able to create again. I started spending time daydreaming about the paintings I would do, and something magical happened. I started to visualize concepts, instead of just copying pictures or sitting outside and painting nature, or doing portraits like I did in the past. Even though I couldn’t paint them, I envisioned and captured the feelings and remembered them.

As I got more function back I did the first painting called ”Pitiful Joy” 2006. It was the first painting I did completely from my head, representing my loss of vision and speech, yet a mind alight with music, sculpture and art.”

Be inspired – please send an online card featuring artwork by MS artist Mary E. Hetzel-Tingler and spread awareness of MS and MSAA.

 

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