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PR Newswire reports Washington Post Ad!

Discussion in 'Media, Interviews, Blogs, Talks, Events about XMRV' started by pictureofhealth, Dec 6, 2010.

  1. pictureofhealth

    pictureofhealth XMRV - L'Agent du Jour

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  2. George

    George waitin' fer rabbits

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    A wonderful well written press release, by the patients for the public this is fantastic stuff!!!

    I'm sending out e-mails to my local news outlets with the link today!

    Chronic Fatigue Syndrome Patients Run First-ever Ad in The Washington Post


    Download image

    --Possible New HIV-like Retrovirus in Blood Supply--

    CORAL GABLES, Fla., Dec. 6, 2010 /PRNewswire-USNewswire/ -- In an unprecedented move, chronic fatigue syndrome (CFS) patients published a half-page ad in The Washington Post today. The ad brings attention to new, HIV-like retroviruses, including XMRV, which have been linked to CFS and aggressive prostate cancer, and have been detected in healthy blood donors. The ad was created through the ME/CFS Worldwide Patient Alliance (MCWPA), a grassroots patient collaboration formed in August 2010 with the support of P.A.N.D.O.R.A., Inc. From their beds and wheelchairs, patients spent decades watching researchers, scientists and physicians debate about the cause or nature of their illness. Now, they are adding their voice through a campaign that calls for biomedical research funding, fast-track treatment options and improved patient quality of life. CFS, also known as myalgic encephalomyelitis or ME/CFS, is a disabling, sometimes fatal NeuroEndocrineImmune disease that afflicts more than one million Americans and an estimated l7 million people worldwide.

    (Photo: http://photos.prnewswire.com/prnh/20101206/DC12334 )

    ME/CFS first gained national attention amidst the AIDS epidemic in the early 1980s. As early as 1991, a retroviral link to ME/CFS was discovered by Dr. Elaine DeFreitas of the Wistar Institute, but subsequent retroviral research was halted by the government. Although more than 4,000 peer-reviewed articles in medical journals have pointed to system-wide immune, neurological, endocrine, gastro-intestinal and cardiac abnormalities, a biologically-based diagnostic definition has eluded doctors. The result has been a catastrophic lack of care, ineffective (sometimes harmful) treatments and a shorter life span for those who are ill. The leading causes of death among patients are heart disease, cancer and suicide. The disease occurs in people of all ages, from children to seniors, and also has a higher incidence rate in families and has occurred in cluster outbreaks.

    "This can happen to anyone," said Sita G. Harrison, spokeswoman for the MCWPA. "ME/CFS is devastating and the lack of care has hurt us all. We ask the government and health care agencies that we put our trust in to help the millions of people who are suffering and to fund more research now."

    A major scientific breakthrough occurred in October 2009 when the Whittemore Peterson Institute (WPI) at the University of Nevada, Reno, working with the National Cancer Institute and Cleveland Clinic, published the results of a landmark study. The seminal study, published in the leading scientific journal, Science, discovered the third human retrovirus, XMRV, in the blood of 67% of ME/CFS patients and in 3.7% of healthy controls. This suggests that up to 10 million US citizens could already be infected. This finding was later confirmed by the FDA, NIH and Harvard Medical School in a study published in the Proceedings of the National Academy of Sciences. Their results linked a family of human gamma retroviruses (to which XMRV belongs) to ME/CFS at a rate of 86.5% and 6.8% in the healthy population, bringing the total of Americans who may be infected up to 20 million people.

    "The NIAID, the national institute responsible for infectious disease research, has yet to fund XMRV research in ME/CFS or any other disease," explains Annette Whittemore, President of WPI. "WPI has had its last six XMRV-related grant proposals turned down; despite the fact that our researchers have proven XMRV is transmissible and infectious."

    MCWPA is advocating for a budget that is in line with other NeuroEndocrineImmune diseases. Currently, only $5 million for ME/CFS research is in the NIH budget, far less than similar diseases such as multiple sclerosis ($l44 million) and lupus ($121 million). Patients also ask for antiretroviral and Ampligen clinical trials that have shown great promise in mitigating the effects of ME/CFS.

    For more information, to donate, or for more resources and spokespeople, including leading researchers, scientists, physicians, patients, and historians please visit http://mcwpa.org/ .

    About MCWPA: Our mission is to create an effective, cutting-edge advertising campaign addressing the poor quality of life of individuals with ME/CFS. By issuing a collective and unified statement, our community will no longer be silent and invisible. The MCWPA ad campaign is supported by P.A.N.D.O.R.A. Inc.™, Vermont CFIDS Association, Inc., R.E.S.C.I.N.D., Rocky Mountain CFS/ME and FM Association and the Wisconsin ME/CFS Association, Inc.

    CONTACT:
    Sita Harrison/Tina Tidmore
    561-313-1835
    205-680-6890
    Media@mcwpa.org
     
  3. parvofighter

    parvofighter Senior Member

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    Canada
  4. parvofighter

    parvofighter Senior Member

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    Spread the word - send the Press Release further!

    EASY ADVOCACY FOR AMERICANS: The CAA has a page here http://capwiz.com/cfids/home/ that enables you to search for media and elected officials by state, and that then connects you with their email addresses, a website and/or a direct messaging.

    FOR CANADIANS: If you would like to send a Letter to the Editor of any of our newspapers, ME/FM Action Network has a handy list of hotlinked emails/contacts here: http://fm-cfs.ca/editors.html

    Similarly, there is a list of links for Elected Officials, however that particular list is only current to 2007, so "buyer beware"! Here is that link: http://fm-cfs.ca/MPadoption.html

    Here again is the link to the Press Release: http://mcwpa.org/wp-content/uploads/2010/12/First-ME-CFS-Ad-in-Washington-Post.pdf
     
  5. Starlight

    Starlight Senior Member

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    Brilliant work. Well done all of you working so hard on behalf of all of us. It really helps so much.
     
  6. markmc20001

    markmc20001 Guest

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    Great Work!

    Somebody mentioned it would be a good idea if patients, who are up to it, emailed their congressman to alert them of the ad today.
     
  7. beaker

    beaker ME/cfs 1986

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  8. Nielk

    Nielk

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  9. muffin

    muffin Senior Member

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    Chronic Fatigue Syndrome Patients Run First-ever Ad in The Washington Post

    Chronic Fatigue Syndrome Patients Run First-ever Ad in The Washington Post
    --Possible New HIV-like Retrovirus in Blood Supply--
    http://www.prnewswire.com/news-releases/chronic-fatigue-syndrome-patients-run-first-ever-ad-in-the-washington-post-111363234.html


    CORAL GABLES, Fla., Dec. 6, 2010 /PRNewswire-USNewswire/ -- In an unprecedented move, chronic fatigue syndrome (CFS) patients published a half-page ad in The Washington Post today. The ad brings attention to new, HIV-like retroviruses, including XMRV, which have been linked to CFS and aggressive prostate cancer, and have been detected in healthy blood donors. The ad was created through the ME/CFS Worldwide Patient Alliance (MCWPA), a grassroots patient collaboration formed in August 2010 with the support of P.A.N.D.O.R.A., Inc. From their beds and wheelchairs, patients spent decades watching researchers, scientists and physicians debate about the cause or nature of their illness. Now, they are adding their voice through a campaign that calls for biomedical research funding, fast-track treatment options and improved patient quality of life. CFS, also known as myalgic encephalomyelitis or ME/CFS, is a disabling, sometimes fatal NeuroEndocrineImmune disease that afflicts more than one million Americans and an estimated l7 million people worldwide.

    (Photo: http://photos.prnewswire.com/prnh/20101206/DC12334 )

    ME/CFS first gained national attention amidst the AIDS epidemic in the early 1980s. As early as 1991, a retroviral link to ME/CFS was discovered by Dr. Elaine DeFreitas of the Wistar Institute, but subsequent retroviral research was halted by the government. Although more than 4,000 peer-reviewed articles in medical journals have pointed to system-wide immune, neurological, endocrine, gastro-intestinal and cardiac abnormalities, a biologically-based diagnostic definition has eluded doctors. The result has been a catastrophic lack of care, ineffective (sometimes harmful) treatments and a shorter life span for those who are ill. The leading causes of death among patients are heart disease, cancer and suicide. The disease occurs in people of all ages, from children to seniors, and also has a higher incidence rate in families and has occurred in cluster outbreaks.

    "This can happen to anyone," said Sita G. Harrison, spokeswoman for the MCWPA. "ME/CFS is devastating and the lack of care has hurt us all. We ask the government and health care agencies that we put our trust in to help the millions of people who are suffering and to fund more research now."

    A major scientific breakthrough occurred in October 2009 when the Whittemore Peterson Institute (WPI) at the University of Nevada, Reno, working with the National Cancer Institute and Cleveland Clinic, published the results of a landmark study. The seminal study, published in the leading scientific journal, Science, discovered the third human retrovirus, XMRV, in the blood of 67% of ME/CFS patients and in 3.7% of healthy controls. This suggests that up to 10 million US citizens could already be infected. This finding was later confirmed by the FDA, NIH and Harvard Medical School in a study published in the Proceedings of the National Academy of Sciences. Their results linked a family of human gamma retroviruses (to which XMRV belongs) to ME/CFS at a rate of 86.5% and 6.8% in the healthy population, bringing the total of Americans who may be infected up to 20 million people.

    "The NIAID, the national institute responsible for infectious disease research, has yet to fund XMRV research in ME/CFS or any other disease," explains Annette Whittemore, President of WPI. "WPI has had its last six XMRV-related grant proposals turned down; despite the fact that our researchers have proven XMRV is transmissible and infectious."

    MCWPA is advocating for a budget that is in line with other NeuroEndocrineImmune diseases. Currently, only $5 million for ME/CFS research is in the NIH budget, far less than similar diseases such as multiple sclerosis ($l44 million) and lupus ($121 million). Patients also ask for antiretroviral and Ampligen clinical trials that have shown great promise in mitigating the effects of ME/CFS.

    For more information, to donate, or for more resources and spokespeople, including leading researchers, scientists, physicians, patients, and historians please visit http://mcwpa.org/ .

    About MCWPA: Our mission is to create an effective, cutting-edge advertising campaign addressing the poor quality of life of individuals with ME/CFS. By issuing a collective and unified statement, our community will no longer be silent and invisible. The MCWPA ad campaign is supported by P.A.N.D.O.R.A. Inc., Vermont CFIDS Association, Inc., R.E.S.C.I.N.D., Rocky Mountain CFS/ME and FM Association and the Wisconsin ME/CFS Association, Inc.

    CONTACT:
    Sita Harrison/Tina Tidmore
    561-313-1835
    205-680-6890
    Media@mcwpa.org

    SOURCE MCWPA
    http://www.prnewswire.com/news-rele...ever-ad-in-the-washington-post-111363234.html
    PRNewswire-USNewswire Chronic Fatigue Syndrome Patients Run First-ever Ad in The Washington Post - December 6, 2010 - Section A-12


    http://mecfsposts.blogspot.com/2010/12/washington-post-mcwpa-ad-6-december.html
     
  10. muffin

    muffin Senior Member

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    parvofighter

    Thank you for tracking all the notices, posts, etc. Please continue to keep track of where you see this AD/PR and post here!!!!! Thanks so much!!!
     
  11. JohnnyD

    JohnnyD Senior Member

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    This is a very well written piece - fabulous! Fabulous Ad as well... congratulations on ramping up the awareness! The XMRV elephant is definitely the room!
     
  12. August59

    August59 Daughters High School Graduation

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    Upstate SC, USA
  13. Jemal

    Jemal Senior Member

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  14. acer2000

    acer2000 Senior Member

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    Interesting... USA today seems to have only picked up part of the press release. They left out the part where they quoted Annette Whittemore saying that the WPI has applied for 6 grants and been denied since their discovery in 2009, despite the fact that they were the ones that pioneered this research. Weird. At least all of the other outlets picked it up in its entirety.

    Very very well worded press release. Very well done indeed.
     
  15. serg1942

    serg1942 Senior Member

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    Hi guys,

    I am looking for the original article in the Washington Post, to post this news in some Spanish media, but I cannot find it....Any help?

    Sergio
     
  16. serg1942

    serg1942 Senior Member

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  17. alice1

    alice1 Senior Member

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    Fantastic.Thankyou to everyone involved.!!!!!!!!!!!!!!!
     
  18. lancelot

    lancelot Senior Member

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    Any of this good stuff making it over to the UK? Probably not! lol
     
  19. CateK

    CateK

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    I would like to link to the ad on my facebook page - does anyone have a link to the ad?
     
  20. pictureofhealth

    pictureofhealth XMRV - L'Agent du Jour

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    Haven't seen it yet Lancelot - even the ME Association haven't reported on it, let alone the UK press!
     

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