FDA should give CFS patients access to Ampligen!

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.

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ME/CFS Facts

Discussion

  • Albert Chang We are not asking for social security, or disability. We are asking for a treatment/drug that has shown to significantly help us -- people with conditions that is said to be preferred over having HIV from a variety of scientists/doctors from accredited institutions (Stanford, Harvard, etc.).

  • Barbara Bloom My son became ill at 16 after a viral infection that never went away.
    He has been sick for 10 years and he has not benefited from any treatment.
    Please don't deny him the possibility of benefiting from Ampligen.

  • Kerstin Händel Ich unterstütze das Anliegen !!! Lasst die Patienten selbst entscheiden, mit ME CFS kann man nur VERSUCHEN!!!!!

    Es ist eh kein Leben ansich - und schwerste ME Fälle , was bleibt uns denn übrig!?

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    Kim Graffagnino

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    Albert Chang

    3 weeks ago Comments: We are not asking for social security, or disability. We are asking for a treatment/drug that has shown to significantly help us -- people with conditions that is said to be preferred over having HIV from a variety of scientists/doctors from accredited institutions (Stanford, Harvard, etc.).
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    Riikka Rinne

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