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CURRENT EVENTS:


Dec.2014 LauraHillenbrand FaceTheNation
ME+Unbroken Interview HERE -

AND
Dec 2014 ~ "NIH"P2P4ME"

NIH="InsufficientResearch"=DUH !
Treatment= more"SELF Management"
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Showing posts with label R.E.S.C.I.N.D.. Show all posts
Showing posts with label R.E.S.C.I.N.D.. Show all posts

Thursday, December 16, 2010

#99~ Please Thank Dr. Alter ~ He Speaks the TRUTH!



Dear Fellow ME/CFS patients, families and advocates~


Ten days ago, the American Red Cross announced a new plan to "actively deny" CFS patients from donating blood. The Red Cross controls about 50% of the US blood supply.


On December 6th we worked with the MCPWA.org to put an ad in the Washington Post about Dr. Alter and Dr. Lo's article that strongly backed up the SCIENCE paper from October, 2009 from the WPI.


Now, on the 14th of December, the FDA panel voted 9 to 4 to recommend banning any blood donations from any ME or CFS patients until XMRV is ruled in or out as a possible cause of disease.


Dr. Harvey Alter, after a long day of back and forth, where Drs. Mikovits, Hansen and Lo literally "wiped the floor" with naysayers like Dr. Coffin and Dr. Stoye, Dr. Alter came out with an unplanned statement which ended with:


“I'm not a CFS Dr, but have learned a lot in last 6 months.  Absolutely convinced when you define this by proper criteria, it's a very serious, medical disease.  Chars of a viral disease.  If it's NOT XMRV, we must continue the research to find out what is.” (thank you ValB626 for the transcription!)


It is our recommendation that you all write to THANK Dr. Alter at:

halter@dtm.cc.nih.gov

Please write him a clear, "concise and sincere" THANK YOU for his kind/wise comments.

XMRV might be the cause of ME and CFS and FMS and maybe even Autism, MS or Gulf War illnesses...not to forget Prostate Cancer, Lymphoma and possibly Breast Cancer. Whatever the cause, Dr. Alter has been convinced that M.E. and CFS are REAL! And they are SERIOUS!



THANK YOU DR. ALTER for being the ONE new SANE Voice in the Room to STAND UP and SPEAK the TRUTH LOUD and CLEAR.  




Thank you to ValB626 and XMRV Global Action for the following statement from Harvey Alter, M.D.


Dr. Alter:
"when a group finds a new agent, become biased it's real.  When it's not found by another group, they become even more biased it's unreal.

Our goal should be to find the truth.  The truth will out over the next year.  I concur we have no evidence for causality, esp when we're at the LoD and assay perf is so critical.

 But I still want to counter by saying that the current evidence for disease association is very strong that XMRV or MLV is strongly associated with CFS.

In those labs who do find the agent, it's very reproducible.  Year after year, same patients.

 Confirmed by sequencing, reproducible over time.

 Dr. Hanson has demonstrated how critical the assays are.  When tweaked assays, findings identical to Lo lab.

 Diversity of XMRV/MLV being confirmed in WPI lab, so not only agent being confirmed there.

 In 100s of negative controls in same lab, extremely negative, has done what Coffin recommended was also negative.  Always neg for contamination.  It isn't logical to suggest otherwise.

 Stoye used single-case anecdotal info to try to make a case.  Simply because it has happened in the past isn't valid to negate reproducible data from 4 different laboratories.

 I'm not a CFS Dr, but have learned a lot in last 6 months.  Absolutely convinced when you define this by proper criteria, it's a very serious, medical disease.  Chars of a viral disease.  If it's NOT XMRV, we must continue the research to find out what is."



********************************************************
Information taken from the National Institutes of Health Clinical Center


Senior Staff


Harvey Alter, MD
Distinguished NIH Investigator
Chief, Clinical Studies
Associate Director of Research
Department of Transfusion Medicine
Academic Degrees
B.A., University of Rochester
M.D., University of Rochester School of Medicine


Email: halter@dtm.cc.nih.gov


                                           Biosketch


Dr. Harvey Alter earned his medical degree at the University of Rochester Medical School, and trained in internal medicine at Strong Memorial Hospital and at the University Hospitals of Seattle. In 1961, he came to the National Institutes of Health as a clinical associate. He then spent several years with Georgetown University, returning to NIH in 1969 to join the Clinical Center's Department of Transfusion Medicine as a senior investigator becoming Chief of the Clinical Studies and Associate Director of Research in the Department of Transfusion Medicine at the NIH Clinical Center.


Dr. Alter is also a clinical professor at Georgetown University.


Dr. Alter co-discovered the Australia antigen, a key to detecting hepatitis B virus. Later, Dr. Alter spearheaded a project at the Clinical Center that created a storehouse of blood samples used to uncover the causes and reduce the risk of transfusion-associated hepatitis. He was principal investigator on studies that identified non-A, non-B hepatitis, now called hepatitis C. His work was instrumental in providing the scientific basis for instituting blood donor screening programs that have decreased the incidence of transfusion-transmitted hepatitis to near zero.


In 2000, Dr. Alter was awarded the prestigious Clinical Lasker Award and in 2002, he became the first Clinical Center scientist elected to the National Academy of Sciences (NAS) and in that same year was elected to the Institute of Medicine. Only a small number of scientists nationally are elected to both these scientific societies.


Selected Honors and Awards


Appointed as NIH Distinguished Investigator, 2008; Presidential Award, Society for Advancement of Blood Management, 2006; Recipient of the First International Award for Science, INSERM, Paris France, 2004; American College of Physicians Award for Outstanding Work in Science, 2004; Elected to National Academy of Sciences, 2002; Distinguished Scientist Award American Liver Foundation, 2002; Presidential Award, International Society of Blood Transfusion, 2002; Elected to the Institute of Medicine, 2002; Albert Lasker Clinical Research Award, 2000; James Blundell Prize, British Blood Transfusion Service, 1994; Karl Landsteiner Award, American Association of Blood Banks, 1992, Elected to the American Association of Physicians, 1992; PHS Distinguished Service Medal, 1977


Thank You R.E.S.C.I.N.D. for letting me rePost sections of this Info from your website.
************************************


Thank YOU to ALL of our Heroes~ Be they The WPI, Dr's, Parents, Friends, Advocates, Patients, we LOVE and Need ALL of you RIGHT NOW to help  MOVE This Cause FORWARD and Help us SAVE Our LIVES and Save those lives of the Innocent Public that has had this TRUTH Hidden from them also for 25 years.

Thank YOU WPI for adding Dr. Jamie Deckoff-Jones as the Chair to the Newly formed Clinical Advisory Board. What a PERFECT marriage !! Now you all Rock !!!


PS: Just this morning I received my XMRV test results and I am Positive.

As a 23 yr ME/CFS patient that TRULY Believes I got it while working in the hospital for 17 years before I had my Triggering Event,  I HONESTLY HOPE that we can get the PR and Public OUTCRY this Disease DESERVES. I already lived thru the days of HIV/AIDS and had to go to the SF Conferences for my hospital in the 80's and lost 5 of my closest friends to THAT illness... and have already been tested twice for HIV and was Negative. 

It's a CRIME to HUMANITY that the CDC has let THIS illness go on for 25 years and spread to the point where over 1 million and maybe 4 million of us in the USA already have XMRV XAND not to forget the 10s of millions of asymptomatic citizens walking around STILL donating Blood and they are NOT screening the Blood supply for that YET......   


HELP !

WHAT MUST WE DO TO MAKE THEM "WAKE UP" ?????




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Monday, December 6, 2010

#96~ CFS Patients Run 1st EVER Ad in Washinton Post

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

 
  --Possible New HIV-like Retrovirus in Blood Supply--
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/TinaTidmore 561-313-1835 205-680-6890 Media@mcwpa.org

SOURCE MCWPA


Read more: http://www.miamiherald.com/2010/12/06/1959341/chronic-fatigue-syndrome-patients.html#storylink=fbuser#ixzz17JpKWLPH

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