Take Action for World MS Day

  • by  Teva's Lift MS® Team
  •   May 06, 2019

This month, we are celebrating the MS community and the achievements you’ve made. This World MS Day, we are thankful for your support and willingness to lend a helping hand. Together, our voices can unite us as we work toward raising awareness and educating others on the invisible symptoms of MS. Here are a few ways you can be part of the movement:

  • Join the cause. Raise your voice for those living with MS. Visit the MS International Federation and use the hashtag #WorldMSDay to share your story with friends and family.
  • Share knowledge. Provide information and resources to help others understand the invisible symptoms of MS.
  • Expand your toolkit. Explore these educational brochures and build your MS resources.
  • Get connected. Visit the Lift MS® Facebook page to chat with people who truly understand life with MS. Working with other people in the MS community can create an opportunity to build a strong support network. 

How are you celebrating World MS Day? We want to hear in the comments below.

COPAXONE® (glatiramer acetate injection) is a prescription medicine that is used to treat relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults.

Do not use COPAXONE® if you are allergic to glatiramer acetate or mannitol.

See Important Safety Information below and full Prescribing Information for Copaxone® (glatiramer acetate Injection).

COP-46133 August 2019
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7 Comment(s)
  • Tammy | June 22, 2016
    I resently learned of a close loved one being diagnosed with MS. I wanted that person to know I'm here for them. 29 years experience I felt would be of more help than anything. I offer whatever experience I've had, and always suggest a good professional specialist as well as prayer. I hope I can help many people with MS in my lifetime. I used to be a mentor. Hope to do more sometime.
    • Teva's Lift MS® Team | June 22, 2016
      It's great to hear you've found others who can relate to your experiences with MS. Support is so important! We hope you'll consider the Lift MS community a source of support as well.
  • Wendy | May 30, 2018
    I’ve. Had MS for 28
    Years n
    My
    Son
    Calls me a warrior I
    Always. Keep moving forward
    • Teva's Lift MS® Team | May 31, 2018
      We love your positive attitude, Wendy! Thanks for sharing it with the Lift MS community!
  • Myrna erickson  | May 10, 2019
    I have ms since 1974 and still
    Am here and doing well..I have done everything for myself with no help. I drive, still dance and never think of ms.









  • LaWsnde | May 13, 2019
    List symptoms again
  • M.S.Srinivasan | May 13, 2019
    Excellent job...!
    There are so many celebrities with the initial of M.S.
    I am happy to hear this group...!
    Congratulations !!!
  • Sherry | May 15, 2019
    Unable to participate at this time due to extinguishing circumstances. 😐
  • Sue Clements | May 20, 2019
    I have MS it doesn’t have me! On days that it does I That God cause I know what I have sucks but it is not fatal!