Signatures 4690 total

Page: « ‹ 1, ... 42, 43, 44, 45, 46, 47, 48, ... 94 › »

1. 2201
   Name: Carol Libby on Jan 14, 2013

   Comments: Please make Ampligen available to those with ME/CFS, Thank You 34 years and counting, Carol Libby

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2. 2202
   Name: David Glaser on Jan 14, 2013

   Comments:

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3. 2203
   Name: Ken Liu on Jan 14, 2013

   Comments: Please sign this petition!

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4. 2204
   Name: Anonymous on Jan 14, 2013

   Comments:

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5. 2205
   Name: Ginny Judd on Jan 14, 2013

   Comments:

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6. 2206
   Name: Anonymous on Jan 14, 2013

   Comments:

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7. 2207
   Name: Anonymous on Jan 14, 2013

   Comments:

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8. 2208
   Name: Kyle Schafer on Jan 14, 2013

   Comments:

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9. 2209
   Name: Meg Robertson on Jan 14, 2013

   Comments: As a friend to 3 people affected by this illness, I urge you to allow access to this treatment option.

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10. 2210
    Name: Lena Afridi on Jan 14, 2013

    Comments:

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11. 2211
    Name: Sarah Lyons on Jan 14, 2013

    Comments:

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12. 2212
    Name: Eva Nagy on Jan 14, 2013

    Comments:

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13. 2213
    Name: P.van Zwol on Jan 14, 2013

    Comments:

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14. 2214
    Name: Mikela French on Jan 14, 2013

    Comments:

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15. 2215
    Name: Peter Yu on Jan 14, 2013

    Comments:

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16. 2216
    Name: Anonymous on Jan 14, 2013

    Comments:

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17. 2217
    Name: Jen Suh on Jan 14, 2013

    Comments:

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18. 2218
    Name: Jessica Choy on Jan 14, 2013

    Comments:

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19. 2219
    Name: Riddhi Mehta-Neugebauer on Jan 14, 2013

    Comments:

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20. 2220
    Name: Anonymous on Jan 14, 2013

    Comments:

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21. 2221
    Name: Nischit Hegde on Jan 14, 2013

    Comments:

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22. 2222
    Name: Nathan Kuerschner on Jan 14, 2013

    Comments:

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23. 2223
    Name: Anonymous on Jan 14, 2013

    Comments:

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24. 2224
    Name: Henry Tamarin on Jan 14, 2013

    Comments:

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25. 2225
    Name: M Martella on Jan 14, 2013

    Comments:

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26. 2226
    Name: Julia Wong on Jan 14, 2013

    Comments:

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27. 2227
    Name: Brigette Browning on Jan 14, 2013

    Comments:

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28. 2228
    Name: Willem on Jan 14, 2013

    Comments: Please give access to this drug and keep monitoring the developments. Too many people suffer without any hope!

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29. 2229
    Name: Maya Sherr on Jan 14, 2013

    Comments:

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30. 2230
    Name: Ivan Hou on Jan 14, 2013

    Comments: It is shameful that this potentially life changing drug that has been studied and tested for so many years remains unavailable to CFS patients. Please don't deny people who are suffering access to a medicine and treatment that can help them.

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31. 2231
    Name: Miranda Nelson on Jan 14, 2013

    Comments:

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32. 2232
    Name: Michael S. Allen, Ph.D. on Jan 14, 2013

    Comments: I am a clinical psychologist disabled for twenty years by what's variously called Chronic Fatigue Syndrome and Myalgic Encephalomyelitis. It has turned me into an invalid, taken away my ability to earn a living; it has isolated me and narrowed my ability to have a personal life. I've followed Ampligen since I fell ill in 1991. I know of patients who've done very very well on it. I had a doctor who assisted on the first ampligen trial in 1990 who told me that many patients did much better on it but that the drug company ran out of money. Ampligen is the only drug that's ever been up for FDA approval for CFS. Despite the fact that about one million people have been disabled by this horrible disease there are no other treatments available. From what I've followed, ampligen is likely to be effective for a subgroup of people with CFS not for everyone. But there are many drugs available for diseases that help only a subgroup of patients with any given diagnosis. We do need better ways to identify which subgroups will respond best to Ampligen but that's no reason not to approve it. The patient population -- myself included -- have long felt that are major institutions of medicine -- the NIH, CDC, FDA -- still think CFS is something minor and we have been profoundly let down to the point of despair by these institutions. Approval of ampligen as the first drug for CFS will help make the point that CFS is a profoundly real and devastating disease.

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33. 2233
    Name: Van Duong on Jan 14, 2013

    Comments:

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34. 2234
    Name: Anonymous on Jan 14, 2013

    Comments:

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35. 2235
    Name: Nina De Rooij on Jan 14, 2013

    Comments:

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36. 2236
    Name: Robert-Jan Kuijer on Jan 14, 2013

    Comments:

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37. 2237
    Name: Shelia Woodifn on Jan 14, 2013

    Comments:

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38. 2238
    Name: Sandra Bruce on Jan 14, 2013

    Comments:

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39. 2239
    Name: Donna Keyes on Jan 14, 2013

    Comments:

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40. 2240
    Name: Leigh Gowdy-king on Jan 14, 2013

    Comments:

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41. 2241
    Name: Roxie Herbekian on Jan 14, 2013

    Comments:

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42. 2242
    Name: Kathleenharper on Jan 15, 2013

    Comments:

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43. 2243
    Name: Susan Lau on Jan 15, 2013

    Comments: It is the only hope for so many for a long time to come

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44. 2244
    Name: Valerie M. Hendry on Jan 15, 2013

    Comments: Unless you, yourselves,have suffered through this,you have no way of knowing the effect this condition has on my life,my quality or lack thereof,of my life and those I love!Please reconsider your thoughts on the affect you play on our lives!Thank you!Sincerely,Valerie M.Hendry

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45. 2245
    Name: Valerie M. Hendry on Jan 15, 2013

    Comments: Unless you, yourselves,have suffered through this,you have no way of knowing the effect this condition has on my life,my quality or lack thereof,of my life and those I love!Please reconsider your thoughts on the affect you play on our lives!Thank you!Sincerely,Valerie M.Hendry

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46. 2246
    Name: Jonathan Lau on Jan 15, 2013

    Comments: This drug is what we need!

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47. 2247
    Name: Lisa Jaicks on Jan 15, 2013

    Comments:

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48. 2248
    Name: Cheryl Lafferty on Jan 15, 2013

    Comments: I have extreme ME/CFS and other physical disabilities that totally limit my life. This drug needs to be approved/licensed ASAP!!!

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49. 2249
    Name: Cheryl Lafferty on Jan 15, 2013

    Comments: I have extreme ME/CFS and other physical disabilities that totally limit my life. This drug needs to be approved/licensed ASAP!!!

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50. 2250
    Name: Cheryl Lafferty on Jan 15, 2013

    Comments: I have extreme ME/CFS and other physical disabilities that totally limit my life. This drug needs to be approved/licensed ASAP!!!

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