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FDA should give CFS patients access to Ampligen!

4,889 Signatures Goal: 8,000

An estimated 4 million US citizens and 20 million worldwide are suffering from Chronic Fatigue Syndrome or CFS/ME[CDC, CFIDS]. It's a life-threatening illness, as debilitating as MS[CDC]. There is no cure and no FDA-approved drug treatment.

Rintatolimod(Ampligen) has been undergoing FDA trials for over two decades and has benefited a great number of patients to no end and without ill effect.

An FDA Advisory Committee has recently seen fit to block marketing of Ampligen, even though they voted it safe for approval. Instead of encouraging drug companies to pinpoint the subset(s) of people who respond so well, theyexpect sponsors to attract millions of dollars without a return.Ampligen is safe and has been available in places like Canada and Brussels for 17 years.There is no alternative.

We urge the FDA toApprove Ampligen now.

Thanks to the efforts of people like patient/advocate Mr. Robert Miller, the FDA is inviting patients to attend its ME/CFS Stakeholder Workshopon April 25 and 26, 2013.

Find out how you can help herehttps://twitter.com/bobmiller42and show your support bysigning this petition. Share it with your friends and let the FDA know they too should hear us loud and clear: Let ME/CFS patients decide!

Enter your full name and email below and click on the blue "sign now" button. We're not looking for donations. The donation request some will see after signing is unrelated to this petition, but rather for/bythe site hosting it,ipetitions.com.

Sponsor

Fred. Neither patient, doctor, nor investor. I was touched by testimony.

Links

ME/CFS Facts

  • una Knight
    una Knight Ireland
    May 27, 2015
    May 27, 2015
    Please make the use of this drug available so sufferer's can get some help.
  • una Knight
    una Knight Ireland
    May 27, 2015
    May 27, 2015
    Please make the use of this drug available so sufferer's can get some help.
  • Layla Collins
    Layla Collins Germany, Lippstadt
    May 27, 2015
    May 27, 2015
    Hell yes !!
  • Naoise Keohane
    Naoise Keohane Ireland, Dublin
    May 27, 2015
    May 27, 2015
    it would mean the world to everyone with ME to have access to this drug.
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4151

Signatures

  • 14 hours ago
    una Knight Ireland
    14 hours ago
  • 14 hours ago
    una Knight Ireland
    14 hours ago
  • 20 hours ago
    Layla Collins Germany
    20 hours ago
  • 23 hours ago
    Naoise Keohane Ireland
    23 hours ago
  • 23 hours ago
    Barbara Kell United Kingdom
    23 hours ago
  • 23 hours ago
    Teresa Greenwood Spain
    23 hours ago
  • 1 week ago
    RUTH TITUS United States
    1 week ago
  • 2 weeks ago
    Kathleen Casassa
    2 weeks ago
  • 2 weeks ago
    Debra Knudson
    2 weeks ago
  • 2 weeks ago
    will smit
    2 weeks ago
  • 4 weeks ago
    M. Salzburg
    4 weeks ago
  • 1 month ago
    Lorelei Garrett
    1 month ago
  • 1 month ago
    Linda Stroecker
    1 month ago
  • 2 months ago
    Matt Kuiken
    2 months ago
  • 2 months ago
    Mike Muterspaw United States
    2 months ago
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