Panorama ME Investigation Campaign

Signatures 1890 total

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1. 1
   Name: E.John on Apr 15, 2010

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2. 2
   Name: Nicola Murray on Apr 15, 2010

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3. 3
   Name: Anonymous on Apr 15, 2010

   Comments: We have a silent disease, so we need to be extra loud to be heard!

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4. 4
   Name: J Kingman on Apr 15, 2010

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5. 5
   Name: DOROTHY MURRAY on Apr 15, 2010

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6. 6
   Name: Derek Benyon on Apr 15, 2010

   Comments: Make some NOISE for M.E!

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7. 7
   Name: Laura Whitby on Apr 15, 2010

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8. 8
   Name: Paul Kayes on Apr 15, 2010

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9. 9
   Name: MARIANNE HEMBROW on Apr 15, 2010

   Comments: make some noise for M.E and all the people who not only suffer from this disease but also the ignorance surrounding it! PLEASE!!

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10. 10
    Name: Sarah Watt on Apr 15, 2010

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11. 11
    Name: Gillian Kilcoyne on Apr 15, 2010

    Comments: i dont suffer from me,but i do suffer from fybromyalgia and agree with this petition for sufferers of me and also agree to shout about it until something is done for them,this is one of the invisable conditions that effect many people worldwide not just in this country but those people in other countries are treated a lot better than those in the uk,basically as far as the so called experts if it cannot be seen then its either in the head or it doesnt exsist,i would like to see them cope with the problems that me sufferes have to deal with on a day to day basis and for the rest of their lives and the impact this has on their families,so come on get into the real world where these things really do exsist.

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12. 12
    Name: Laura Dunks on Apr 15, 2010

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13. 13
    Name: Ian Henry on Apr 15, 2010

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14. 14
    Name: Marion Odger on Apr 15, 2010

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15. 15
    Name: Nicola Ann Henry on Apr 15, 2010

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16. 16
    Name: Sara Boreham on Apr 15, 2010

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17. 17
    Name: Janet Laverick on Apr 15, 2010

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18. 18
    Name: Duncan Laverick on Apr 15, 2010

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19. 19
    Name: Melanie Hilbourne on Apr 15, 2010

    Comments: It is time some serious money and effort is put into proper research and that all sufferers, irrespective of their age and their location, are given proper help and support especially from their GP's.

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20. 20
    Name: Pamela on Apr 15, 2010

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21. 21
    Name: Anonymous on Apr 15, 2010

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22. 22
    Name: H.Patten on Apr 15, 2010

    Comments: The way patients with the neurological illness M.E. are deliberately and cruelly denied biomedical testing and treatment in this country is a national scandal.

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23. 23
    Name: CJ Brennan on Apr 15, 2010

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24. 24
    Name: Puss Steinmann on Apr 15, 2010

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25. 25
    Name: Deborah Stapleton on Apr 15, 2010

    Comments: Please let there be more awareness!!

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26. 26
    Name: Lyndsey Mckinnon on Apr 15, 2010

    Comments: I've had M.E for 18 years and its getting worse, how many more people have to die before you act?

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27. 27
    Name: Sally Smith on Apr 15, 2010

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28. 28
    Name: Antoinette Christie on Apr 15, 2010

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29. 29
    Name: Susan Rothwell on Apr 15, 2010

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30. 30
    Name: Anonymous on Apr 15, 2010

    Comments: Good luck with this campaign, it is only when people join together and fight for justice that the truth can be found.

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31. 31
    Name: Daniel on Apr 15, 2010

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32. 32
    Name: Clair Hope on Apr 15, 2010

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33. 33
    Name: Andrew Isaac on Apr 15, 2010

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34. 34
    Name: Jane Maxwell on Apr 15, 2010

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35. 35
    Name: Tom Anderson on Apr 15, 2010

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36. 36
    Name: M Laverick on Apr 15, 2010

    Comments: This needs urgent action

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37. 37
    Name: John Walker on Apr 15, 2010

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38. 38
    Name: Anonymous on Apr 15, 2010

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39. 39
    Name: James Mcmanus on Apr 15, 2010

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40. 40
    Name: Anonymous on Apr 15, 2010

    Comments: Just a little investigation will uncover the truth ,its an absolute scannel whats being covered up !

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41. 41
    Name: Anita Lynch on Apr 15, 2010

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42. 42
    Name: Andy Salmon on Apr 15, 2010

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43. 43
    Name: Leah Lindsey on Apr 15, 2010

    Comments: its about time that the government and GP's started to recognize this illness and treat the sufferers with more respect and give more support its a big enough struggle living with it let alone having to fight every step of the way to get treatment or help!

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44. 44
    Name: Lucy Panasiuk on Apr 15, 2010

    Comments: We deserve recognition and proper treatment and respect. We do not choose to have this dreadful illness. ME/CFS should have a proper diagnosis route and treatment and/or management plan with defined investigations and medications and talking treatments, etc.. to be followed. Not each Health Authority doing its own thing. It is not a psychological illness and should not be classed or treated under psychiatric services. It is neurological and immunological/biochemical.

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45. 45
    Name: John Wells on Apr 15, 2010

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46. 46
    Name: Andrea Pring on Apr 15, 2010

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47. 47
    Name: Denise Longman MSc on Apr 15, 2010

    Comments: What have successive governments been covering up? It must be something so awful, to have allowed so many hundreds of thousands of people to suffer for so long. The truth will always come out in the end, and now is the time.

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48. 48
    Name: Aylwin Catchpole on Apr 15, 2010

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49. 49
    Name: Mrs Julie Jones on Apr 15, 2010

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50. 50
    Name: Debbie Anderson on Apr 15, 2010

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