Signatures 4670 total

Page: « ‹ 1, ... 44, 45, 46, 47, 48, 49, 50, ... 94 › »

1. 2301
   Name: Robin Bol on Jan 16, 2013

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2. 2302
   Name: Anonymous on Jan 16, 2013

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3. 2303
   Name: Peter on Jan 16, 2013

   Comments: Dear FDA, dont decide for another study, that means at least 2 years, maybe 3-5 years! Approve Ampligen now, every day earlier could help to reduce a lot of pain and not risk to destroy thousands years of lifetime! 1.000.000 - 4.000.000 in the USA! 20.000.000 worldwide! Your brother, your mother or your child could also be affected, think about that! Give hope to the world! We all pray for the right decision in the name of humanity! The patients from all over the world will thank you!

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4. 2304
   Name: Kirissa Moorer on Jan 17, 2013

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5. 2305
   Name: Jayden Moorer on Jan 17, 2013

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6. 2306
   Name: Olivia Moorer on Jan 17, 2013

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7. 2307
   Name: Sunset Blush on Jan 17, 2013

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8. 2308
   Name: Beate Clasen-Liebers on Jan 17, 2013

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9. 2309
   Name: Alex Shuman on Jan 17, 2013

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10. 2310
    Name: Donald Smith on Jan 17, 2013

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11. 2311
    Name: Karen Besanceney on Jan 17, 2013

    Comments: Please help my friend to a normal life!

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12. 2312
    Name: Matthew Stewart on Jan 17, 2013

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13. 2313
    Name: Kim Wirshing on Jan 17, 2013

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14. 2314
    Name: Jessica Inouye on Jan 17, 2013

    Comments: FDA: Please listen to the voices of patients suffering from this disorder and from their families as well.

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15. 2315
    Name: Anonymous on Jan 17, 2013

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16. 2316
    Name: Anthony Semasko on Jan 17, 2013

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17. 2317
    Name: Shirley Burke on Jan 17, 2013

    Comments: You need to release this medication for the people that are suffering from this and let them live a better life.

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18. 2318
    Name: Kevin O'Connor on Jan 17, 2013

    Comments: In this instance, please allow patients and parents to decide what is good for themselves and/or their children. Thank you.

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19. 2319
    Name: Lee Strieb on Jan 17, 2013

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20. 2320
    Name: Mr & Mrs Stanley & Dixie Semasko on Jan 17, 2013

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21. 2321
    Name: Rafael Leiva on Jan 17, 2013

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22. 2322
    Name: Ineke Markies on Jan 17, 2013

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23. 2323
    Name: Sherri Chiesa on Jan 17, 2013

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24. 2324
    Name: Diane on Jan 18, 2013

    Comments: My childhood friend has been dying slowly for 29 years. How can you ignore this?, I know I can't. Please help these people who did nothing to deserve such treatment or lack there of. I beg you!

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25. 2325
    Name: Mary Smith on Jan 18, 2013

    Comments: I pray every night that my sister will return to somewhat of a normal existence. She has so much to offer; it's such a shame!

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26. 2326
    Name: James on Jan 18, 2013

    Comments: People with CFS are too tired to fend for themselves, and yet are constantly having to jump through hoops! Give them some hope they so badly earn for. And, treatment they've been waiting on for over two decades = Ampligen. Thank you.

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27. 2327
    Name: Marty on Jan 18, 2013

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28. 2328
    Name: L Lewis on Jan 18, 2013

    Comments: Do the only right thing, and give ME/CFS patients this treatment right now.

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29. 2329
    Name: Mrs. R. Hill on Jan 18, 2013

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30. 2330
    Name: Rick B on Jan 18, 2013

    Comments: If you don't approve this drug?, you'll have blood on your hands!

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31. 2331
    Name: DONALD WILLIAMS on Jan 18, 2013

    Comments: I LOST MY WIFE TO THIS ILLNESS OVER TWO YEARS AGO. SHE WAS 45 WHEN SHE PASSED. PLEASE DON'T ALLOW THIS TO HAPPEN TO ANOTHER FAMILY.

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32. 2332
    Name: Erik Van Rossum on Jan 18, 2013

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33. 2333
    Name: Josephine Kammeraat on Jan 18, 2013

    Comments: We want to getter better. We are sick every day for many many years . You cannot ignore us. Please do not ignore us anymore.

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34. 2334
    Name: Cindy Little on Jan 18, 2013

    Comments: CFS = no friends, no comfort, no marriage, no kids, no career, no social life, no hope, no money & no relief in sight if you don't allow us the chance to receive Ampligen.

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35. 2335
    Name: Jeff Dean on Jan 18, 2013

    Comments: It's quite clear that our US government has placed their heads in the sand; allowing people with CFS to suffer year after year. Please stop this madness; it's so unfair. Thank you!

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36. 2336
    Name: Frank Freier on Jan 18, 2013

    Comments: HELP!!! Give Ampligen free, give us chance to come back out of hell!

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37. 2337
    Name: Thomas Duong on Jan 18, 2013

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38. 2338
    Name: R. Roig on Jan 18, 2013

    Comments: When you're suffering horribly in overwhelming fatigue and pain- while your life is passing you by, there is very little you will NOT try. Knowing there is something that could possibly grant you some or any degree of wellness if even for a few hours in a day, it is so worth trying. PLEASE, please give the suffering a choice to try this medication. Please give this mecdication the green light. R Roig

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39. 2339
    Name: Christine Howard on Jan 18, 2013

    Comments: Please approve this drug for CFS suffers! I believe that I am one of the lucky few who had a spontaneous remission. When I got sick, I just thought it was the flu but I was bed ridden for 12 weeks, no Doctor knew what I had, mild fever, flu like symtoms, constant exhaustion. After many doctor visits and blood tests it that showed elevated liver enzymes and they ordered tests on my gallbladder. That turned out fine and shortly after I went into remission and back to normal. I don't know if I had CFS or not, but I had thoughts of taking my own life as I had no interest to continue on if this was going to be my life. I salute those brave enough to continue on with this diease and the will power they must have. Please give those with CFS some hope

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40. 2340
    Name: Tom Jarrett on Jan 18, 2013

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41. 2341
    Name: Colin Roberts on Jan 18, 2013

    Comments: those that suffer deserve ampligen

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42. 2342
    Name: Jennifer Shane on Jan 18, 2013

    Comments: My life stopped when I was twenty-five years old because of Chronic Fatigue Syndrome and Fibromyalgia. I am not exaggerating. Every facet of my life changed within one year. Nothing was left untouched and it has never been the same. I am now thirty-eight years old. I am still too sick to work, return to school or even maintain any hint of a social life. I rarely leave my home because my body is completely overrun by the unceasing symptoms of these horrible diseases. Every single day I face this alone, without any hope of relief. In December I heard about Ampligen for the first time. If it can help any of the CFS population, it is a vital and necessary addition those members of the community must have access to. If not, the rest of us don't stand a chance.

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43. 2343
    Name: Robert Barker on Jan 18, 2013

    Comments: I cry every night because all I've lost because of this disease, please help us all and approbe this drug!

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44. 2344
    Name: Sabine Hillewaere on Jan 18, 2013

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45. 2345
    Name: Laura on Jan 18, 2013

    Comments: I know severely ill CFS patients who were able to function somewhat again while on Ampligen and there is no alternative to it. Please approve it so that we may have the option to use it.

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46. 2346
    Name: Anonymous on Jan 18, 2013

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47. 2347
    Name: Anonymous on Jan 18, 2013

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48. 2348
    Name: Hiemy on Jan 18, 2013

    Comments: Patients need drug, why FDA does not let them and doctors decide.

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49. 2349
    Name: Anonymous on Jan 18, 2013

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50. 2350
    Name: Katherine on Jan 18, 2013

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