Signatures 4673 total

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1. 4401
   Name: Julie Crego on Feb 3, 2013

   Comments:

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2. 4402
   Name: Andrea Ralston on Feb 3, 2013

   Comments:

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3. 4403
   Name: Roberto Rivero on Feb 3, 2013

   Comments: Do any of the officials from the the FDA have CFS? That's probably why they don't approve it. The drug is safe to use and it has shown provement in patients with the illness, what else do they need?

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4. 4404
   Name: Anne Green on Feb 3, 2013

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5. 4405
   Name: Martin Del Vecchio on Feb 3, 2013

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6. 4406
   Name: Elizabeth Terczak on Feb 3, 2013

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7. 4407
   Name: Hannah Tsui on Feb 3, 2013

   Comments:

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8. 4408
   Name: Jamie Nelson on Feb 3, 2013

   Comments: Having CFS for nearly 9 years and without any treatment available, I urge you, please, to approve ampligen as a treatment for this disease.

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9. 4409
   Name: Jay Featherstone on Feb 3, 2013

   Comments:

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10. 4410
    Name: Phyllis Berry on Feb 3, 2013

    Comments:

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11. 4411
    Name: Raymond Berry on Feb 3, 2013

    Comments: Help my friend please!

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12. 4412
    Name: Anonymous on Feb 3, 2013

    Comments:

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13. 4413
    Name: Caitlin Featherstone on Feb 3, 2013

    Comments: This disease is so debilitating. We need more research into why this DOES work for some people. Keep this drug available for patients!

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14. 4414
    Name: Gina Bettor on Feb 3, 2013

    Comments: Kathryn Stephens listed!The exact reasons

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15. 4415
    Name: Gina Bettor on Feb 3, 2013

    Comments:

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16. 4416
    Name: Aneurin Canham-Clyne on Feb 3, 2013

    Comments: 95,000 doses is a lot of doses, and the improvement displayed by many patients such as Robert Miller are the best arguments anyone can make for the approval of ampligen.

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17. 4417
    Name: Alexis Rivera on Feb 3, 2013

    Comments:

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18. 4418
    Name: Amaranta Arcadia Castillo Gómez on Feb 3, 2013

    Comments: Once you approve Ampligen fot american patients, it will be a door open for Latin America patients.

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19. 4419
    Name: Anonymous on Feb 3, 2013

    Comments: Please approve this drug, I also suffer from immune disorders and know how painful and difficult life can be without treatment available.

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20. 4420
    Name: Amy Darling on Feb 3, 2013

    Comments:

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21. 4421
    Name: Emily Ross on Feb 3, 2013

    Comments:

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22. 4422
    Name: Kathleen M Lewis on Feb 3, 2013

    Comments: Please help get this approved asap...people's lives are at stake!

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23. 4423
    Name: Rebecca Thompson on Feb 3, 2013

    Comments:

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24. 4424
    Name: Jessica Whalen on Feb 3, 2013

    Comments: I have a friend who suffers from this disease and participated in the trial study. This drug has really helped her, why take it away from her now?

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25. 4425
    Name: Annette Baccari on Feb 3, 2013

    Comments: We need this drug approved for these individuals and the FDA should definitely do that for them.

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26. 4426
    Name: Andrea Parkes on Feb 3, 2013

    Comments:

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27. 4427
    Name: Adam Neugebauer on Feb 3, 2013

    Comments:

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28. 4428
    Name: Anonymous on Feb 3, 2013

    Comments: FDA must approve Ampligen Or be investigated for .....

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29. 4429
    Name: Anonymous on Feb 3, 2013

    Comments:

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30. 4430
    Name: Claudia Fuambi on Feb 3, 2013

    Comments:

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31. 4431
    Name: Diana Fessler on Feb 3, 2013

    Comments: dealing with any kind of cronic illness is hard. My prayers and support are with you.

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32. 4432
    Name: Liz Spencer on Feb 3, 2013

    Comments: 26 years,more than half my life, dying.To now watch my 12 year old daughter experiencing symptoms and being investigated seems cruel beyond belief.We deserve more than we have been afforded so far which is nothing.My childs situation has renewed my sense of injustice like nothing else could and I fully support the reasons for this petition.

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33. 4433
    Name: Ali Myles on Feb 3, 2013

    Comments: My son's Birthday! So finger's crossed for a good result!

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34. 4434
    Name: Dawn Piper, RN on Feb 3, 2013

    Comments: I am a Registered Nurse, and have never taken care of (or even known) a CFS sufferer. However, I can understand how devastating this disease is, and how it not only affects the patient, but how it impacts the entire family. I am at a loss to understand why this drug may not be approved. If a CFS patient desperately needs and wants this drug, is fully aware that it may, or may not, be effective for their particular condition, why not just give Ampligen a chance with provisional approval. The side effects appear to be minimal, and safety concerns appear not to be an issue. The only thing that these patients have left is hope. Don't take that away from them!

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35. 4435
    Name: Erin Jones on Feb 3, 2013

    Comments:

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36. 4436
    Name: Anonymous on Feb 3, 2013

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37. 4437
    Name: Linda Sullivan on Feb 3, 2013

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38. 4438
    Name: Bella Hoare on Feb 3, 2013

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39. 4439
    Name: Pam Pitillo on Feb 3, 2013

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40. 4440
    Name: Charlie Hoare on Feb 3, 2013

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41. 4441
    Name: Beverly Winfield on Feb 3, 2013

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42. 4442
    Name: Anonymous on Feb 3, 2013

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43. 4443
    Name: Jiří D. on Feb 3, 2013

    Comments:

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44. 4444
    Name: D Bowman on Feb 3, 2013

    Comments:

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45. 4445
    Name: D Bowman on Feb 3, 2013

    Comments:

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46. 4446
    Name: Whitney Carrico on Feb 3, 2013

    Comments: This is very important for all patients with ME who are suffering.

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47. 4447
    Name: Anonymous on Feb 3, 2013

    Comments: Why not if it helps some?

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48. 4448
    Name: GLORIA LARA on Feb 3, 2013

    Comments:

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49. 4449
    Name: Roberto Gonzalez on Feb 3, 2013

    Comments:

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50. 4450
    Name: Diane Wright on Feb 3, 2013

    Comments:

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