2013 Year In Review

National Fibromyalgia & Chronic Pain Association



  • Press release May 9, 2013:  National Fibromyalgia & Chronic Pain Association Launches National "CARE & Make Fibromyalgia Visible" Campaign, May 2013.  In the first 24 hours after its release, this notice had over 3,100 views and more than 300 clicks to the website.  It was the most successful press release ever launched by the CPR Strategic Marketing Communications Company.
  • Represented fibromyalgia and chronic pain conditions to the Food and Drug Administration and on national committees regarding prescription pain medication regulations as a voice representing concerns of people who are suffering and deserve the right to medications that help them.

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Call to Action on FDA Opioid Prescribing

Created by and for people with chronic pain, the NFMCPA believes our united voices:


  • educate policy makers and medical professionals;
  • generate supportive attitudes; and
  • change the way we receive health care. 
More than 100 million Americans live with chronic pain illnesses, including 10 million people affected by fibromyalgia.  It is important to our individual recoveries that we, as patients (and our families and loved ones), become empowered and proactive.

Through email alerts, the NFMCPA provides important information for calls to action.  When informed people unite, speak out, and get involved, current and future healthcare issues are resolved.

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Jan Chambers Speaks at NIH Workshop

NIH Workshop on Overlapping Conditions



Jan Chambers, president of the National Fibromyalgia & Chronic Pain Association, spoke on behalf of people with
 fibromyalgia and chronic pain at the standing-room only workshop August 13-14, 2012.  Eight overlapping conditions were discussed:  FM, TMD, VVD, IC, IBS, CFS, migraines, and endometriosis   She said:

"Thank you for this most valuable workshop.  Millions of people with fibromyalgia depend on our ability to communicate their needs for a better quality of life.  We appreciate the opportunity to have the patient voice in the discussion.  In answer to the question put to the leaders of the advocacy organizations, 'What would our patients want?' Jan responded:

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