Signatures 4670 total

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1. 201
   Name: Audrey Dorfman on Dec 29, 2012

   Comments: Please give conditional approval to ampligen so I may be empowered to determine my own medical treatment and not those who have not walked in my shoes the past 29 years. Thank you

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2. 202
   Name: Michael A Quinonez, Jr. on Dec 29, 2012

   Comments:

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3. 203
   Name: Anonymous on Dec 29, 2012

   Comments:

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4. 204
   Name: Michael A Quinonez, Sr. on Dec 29, 2012

   Comments: Pass this drug, before my fiancee does.

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5. 205
   Name: Carol Olsen on Dec 29, 2012

   Comments:

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6. 206
   Name: Melanie Anderson on Dec 29, 2012

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7. 207
   Name: Carol Olsen on Dec 29, 2012

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8. 208
   Name: Sharon Shanklin on Dec 29, 2012

   Comments:

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9. 209
   Name: Peggy Munson on Dec 29, 2012

   Comments: I have lost 20 years of my life to ME/CFS, mostly bedbound. Give us Ampligen now -- give us a chance!

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10. 210
    Name: Astrea Fall on Dec 29, 2012

    Comments:

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11. 211
    Name: Michael Steiner on Dec 29, 2012

    Comments:

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12. 212
    Name: T Hasguga on Dec 29, 2012

    Comments: We need to start somewhere! If approval will help to get further study going to bring real help to those w/this crippling illness, it is inhumane for the FDA to keep this treatment from those it has helped, and could help.

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13. 213
    Name: Elizabeth Fall on Dec 29, 2012

    Comments:

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14. 214
    Name: Anonymous on Dec 29, 2012

    Comments:

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15. 215
    Name: WILLIAM SWIFT on Dec 29, 2012

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16. 216
    Name: Rik Carlson on Dec 29, 2012

    Comments: This is important.

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17. 217
    Name: Rik Carlson on Dec 29, 2012

    Comments:

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18. 218
    Name: Lee Lee Ingram on Dec 29, 2012

    Comments:

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19. 219
    Name: Glen Rich on Dec 29, 2012

    Comments:

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20. 220
    Name: Leela Play on Dec 29, 2012

    Comments:

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21. 221
    Name: L A Snow on Dec 29, 2012

    Comments:

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22. 222
    Name: Tiffany Buntin on Dec 29, 2012

    Comments: I am signing this petition to allow all CFS patients to have access to Ampligen.

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23. 223
    Name: Judy Day on Dec 29, 2012

    Comments: I have a family member suffering from CFS and I personally see how devastating this disease is so I encourage that they be allowed to take this drug.

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24. 224
    Name: Judy Day on Dec 29, 2012

    Comments: I have a family member suffering from CFS and I personally see how devastating this disease is so I encourage that they be allowed to take this drug.

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25. 225
    Name: Isabel Pitman on Dec 29, 2012

    Comments:

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26. 226
    Name: Steven Chilinski, MD on Dec 29, 2012

    Comments:

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27. 227
    Name: Caroline Koenig on Dec 29, 2012

    Comments: I support this!!

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28. 228
    Name: Amy Mandel on Dec 29, 2012

    Comments: A a severely affected ME/CFS patient, I know first hand the power of Ampligen. I am a responder and I have infused three different rounds since 2001. I always see improvement. In 2006/2007 after a year on the medication I went from a sedentary, homebound life to an almost three year remission. Please approve Ampligen so that more patients have the opportunities I've been so fortuate to have.

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29. 229
    Name: Janet Graham on Dec 29, 2012

    Comments: ME Patients need medical treatments. People are dying. Many, many clever people no longer able to work. Please help us!

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30. 230
    Name: Karen Willoughby on Dec 29, 2012

    Comments:

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31. 231
    Name: Anonymous on Dec 29, 2012

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32. 232
    Name: Wendy L Springs on Dec 29, 2012

    Comments:

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33. 233
    Name: Holly Hawthorne on Dec 29, 2012

    Comments:

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34. 234
    Name: Cheryl Gross on Dec 29, 2012

    Comments:

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35. 235
    Name: Lara W on Dec 29, 2012

    Comments:

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36. 236
    Name: Donna on Dec 29, 2012

    Comments: Give me hope. Let me make the choice.

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37. 237
    Name: Anja Olergard on Dec 29, 2012

    Comments:

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38. 238
    Name: Nina Burt on Dec 29, 2012

    Comments: There are no words to express how desperately we need this

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39. 239
    Name: Toby on Dec 29, 2012

    Comments: I've been waiting 17 years for this. If not now when? Please approve this now!

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40. 240
    Name: Matt Huber on Dec 29, 2012

    Comments: I am currently on Ampligen. The alternative is horrifying. Please approve it.

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41. 241
    Name: John Herd on Dec 29, 2012

    Comments: It is beyond cruel not to allow CFS patients to get Ampligen if it has a chance of helping them, especially given that there are no other specific treatments. Please leave that door open to them and let them decide if they wish to use it.

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42. 242
    Name: Anonymous on Dec 29, 2012

    Comments:

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43. 243
    Name: Amy Haskell on Dec 29, 2012

    Comments:

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44. 244
    Name: John_duncan on Dec 29, 2012

    Comments: Even if Ampligen is only very helpful for a subset of M.E. patients -- all evidence that has been compiled suggests that it is Very helpful for this subset. It's time for more research and more treatment, NOT less. Something shouldn't be disallowed just because it doesn't help everybody. Something shouldn't be disallowed because there isn't "perfect evidence." Something shouldn't be disallowed because No One is willing to fund research needed for "perfect evidence". Please help us break out of this cruel Catch 22!

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45. 245
    Name: Martina Stark on Dec 29, 2012

    Comments:

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46. 246
    Name: Otis Quila on Dec 29, 2012

    Comments:

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47. 247
    Name: Cheryl Benson on Dec 29, 2012

    Comments: 1991 survivor of myalgic encephalomyelitis, diagnosed by 2 infectious disease speacialists, the 2nd in 1994, Also diagnosed with Fibromyalgia 1991 by Rhumetologist. 1994 I was fortunate to have a good GP, who upon my request ordered kutapression for me, the earlier trials, 6 months worth. thou far from enought to return to work, it was more akin to living again abliet still with crashes not as long nor as severe. I couldn't stay on the shots and by mid 1996 the benefits were mostly gone. I recall reading about Mary Schweitzer in the 90's whos family had pulled together for funds for Ampligen and she was up and out of her wheelchair. Mary has to stay on it. others do not, some it doesn't work for like any medication. But since then and the similarlity between the 2 I wanted Amplegin but could not afford. Then the Canadian Emergency Health Dept allowed Ampleign in if you could pay for it and doctor/nurse infusing it, and cost recovery. That stopped many years ago. I am still alive thou the living dead and now damaged from prescribed medications because psychatrists thought it a psychatric problem or seritotion. We NEED THIS, there is a SUB SET of ME/CFS patients who will respond to this, some will not. The price to loose and it not work is too high, it would be beneficial that it not only was approved, but the price dropped. since dupont stopped investing, it has had a bad rap as hemipherix does not have the funds (nor to patients ill for years on disability) for the costly trials. One has to wonder WHY the FDA freqently approves drugs that KILL and known in trials, when amplegin does NOT. This has been kicked around as we have for 30 years, enough! If Big Phara was behind this and enough sales it would have been approved years ago and bringing the price down. We just don't die fast enough, and those of us that do, rarely make it to the media. However that IS CHANGING, SO IS THE MALTREATMENT by the CDC, FDA, HEALTH CANADA, AND OTHERS WORLD WIDE. PLEASE allow this to continue to be made, and hoepfully some agency/business will help hemipherix to have more trials, and before that, it is still given on compassionate care. signed near dead. Cheryl Benson

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48. 248
    Name: Debra Bradshaw on Dec 29, 2012

    Comments:

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49. 249
    Name: Ronda on Dec 29, 2012

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50. 250
    Name: Rio Henry on Dec 29, 2012

    Comments: Please! Any information that comes from this open-air study would be useful because of its scale and would contribute to dollar investments in this under-funded area.

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