ME/CFS Awareness: What You Can Do

awareness-ribbon

Each year, May 12th is designated as International CFS Awareness Day and that date is quickly approaching.  Last year I wrote a post with a list of things that can be done to help raise awareness.  I wanted to republish that post since there were several good ideas we all can use. 

There are many other things that you or a CFS support group can do to help raise awareness, thanks to the CFIDS Association.  Their Grassroots Center has some ideas that I would like to share with you:

  • Support groups can designate one person for the Grassroots Action Center Listserv (GAC) program to receive the latest advocacy information on CFS and share it with other group members.
  • Either have your support group or several other people you know with CFS send an advocacy letter to your state’s two senators and Congress representative.
  • Don’t forget to include the CFIDS Fact Sheet.
  • Contact your local radio stations, newspapers, television stations, and magazines about CFS.
  • Try to educate at least three people about CFS and the impact it has on daily living.
  • Create a simple public service announcement (PSA) and send it to local publications and radio stations. You may be able to find a local graphic designer willing to creatively format your text at no charge.  The CFIDS Association can provide you with sample PSAs.
  • Distribute fact sheets or brochures on CFS to local libraries, pharmacies, grocery stores, churches, health food stores, and medical facilities.
  • Give presentations on CFS to local women’s groups, church groups, civic groups and schools.
  • Ask health care providers to display information about CFIDS. Don’t forget other health care professionals such as your dentist, optometrist and massage therapist.
  • Send your personal story to newspapers, radio stations – anyone who will be willing to interview you on your illness.

Please also check out the ME/CFS Awareness website – lots of great information on Awareness Day & Awareness Week events!

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Comments

  1. Hi Sandy

    It would be great to see you blogging for ME/CFS Awareness again in May 2010.

    Remember to sign up to the list at http://meaware.wordpress.com so we can collate a list of those who are blogging for ME/CFS Awareness this year.

    Thanks

    Rachel

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