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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"
DraftReport HERE
AND
Nov.2014- "Plague"-Published !!
VOA-PodcastAudioInterview HERE
Hardcover+Kindle+AudioBook
Amazon USA Link HERE









Showing posts with label DHHS. Show all posts
Showing posts with label DHHS. Show all posts

Tuesday, November 8, 2011

#122~ Restoring ME/CFS Research, Education, and Patient Care to New Jersey

Restoring ME/CFS Research, Education, and Patient Care to New Jersey
CFSAC Public Testimony, Nov. 8th, 2011
By Kenneth J .Friedman, Ph.D.


I wish to inform the Chronic Fatigue Syndrome Advisory Committee and other stakeholders in the ME/CFS Community that there is a window of opportunity to potentially restore ME/CFS research, education, and other, related, scholarly activities to one of this country’s most populated states: New Jersey. The Governor of New Jersey has formed a UMDNJ Advisory Committee the purpose of which is to advise him as to the future of the University of Medicine and Dentistry of New Jersey (UMDNJ). The options range from doing nothing and keeping UMDNJ, the largest, free-standing, academic healthcare University in the United States, as is, to completely dismantling the University and dividing its components and assets amongst other New Jersey academic institutions. The Committee is now willing to accept comments from the public.

The impetus for the establishment of the UMDNJ Advisory Committee may reside in the corroded image of UMDNJ, forever charred into this nation’s psyche, by its purposeful, $35 million dollar, double-billing of Medicare. However, of equal or perhaps greater concern to the ME/CFS Community is the February, 2010 decision of the University to ban ME/CFS research, education and related scholarly activities from the University using the pretext that such activity is not “professional” but rather “personal.” According to that policy, any and all scholarly activity related to ME/CFS may be performed performed by faculty only outside of regular, normal business hours. The policy further forbids use of the University’s portal to the internet for any ME/CFS-related research, and denies use of the University’s email client server for correspondence with anyone about anything related to ME/CFS.

The University’s policy to ban ME/CFS scholarly activity came after two, related New Jersey Medical School attempts to minimize the professional nature of ME/CFS related activities: (1) the New Jersey Medical School refused to consider the Consensus Manual for the Primary Care and Treatment of Chronic Fatigue Syndrome a peer reviewed publication despite its having been reviewed and approved for publication by the Senior Editor of Harvard University Medical Press, Dr. Anthony Kamoroff, and its translation into two foreign languages, and (2) the New Jersey Medical School maintains that five years of service on the CFSAC did not constitute professional, academic service at the national level since individuals without scientific background, such as Magic Johnson has served on Advisory Committees.

UMDNJ controls all three of the state’s medical schools, as well as the state’s only dental school, school of nursing, school of health related professions, school of public health, and graduate school of biomedical sciences. This ban of ME/CFS scholarly activity in the University is, therefore, impacts patient care in the greater New York metropolitan areas, as well as the advancement of ME/CFS research, and healthcare provider education and training throughout the United States. Equally important, however, is the precedent that this establishes for other medical schools and schools training healthcare professionals throughout the United States to establish similar policies.

UMDNJ’s actions are clearly an attack on academic freedom – the right of college and university faculty to pursue their academic interest – and should be opposed on that basis if for no other reason. If UMDNJ wishes to continue as a university, then it must behave as such and afford its faculty the rights afforded to University faculty elsewhere. For UMDNJ to continue as a healthcare university, it needs to comply with the principle of academic freedom.

Of particular concern to the ME/CFS community, is the failure of UMDNJ to honor the CDC’s ME/CFS policy as articulated by its Director in 2006, Dr. Julie Gerberding, who stated, “We are committed to improving the awareness that this [ME/CFS] is a real illness and that people need real medical care and they deserve the best possible help that we can provide.” Why does the Department of Health and Human Services’ continue to provide funding to UMDNJ when UMDNJ maintains that faculty who engage in scholarly activity related to ME/CFS are engaging in non-professional activity? The Department of Health and Human Services continues to give money to a University which knowingly and deliberately obstructs one of its agency’s mandates. Why?

Governor Chris Christie’s UMDNJ Advisory Committee has received testimony from UMDNJ employees expressing the belief that UMDNJ be retained in its current configuration. Current employees may have a vested interest in retaining UMDNJ in its current corpus. Stakeholders of the ME/CFS Community may have a different opinion, since dismantling UMDNJ would remove the ban and restore ME/CFS activities to New Jersey’s healthcare centers. The CFSAC may wish to make a recommendation to the U.S. Secretary of Health based upon the facts conveyed herein and, perhaps, after its own, further investigation.

According to what was published by UMDNJ, comments may be submitted via email to:

The window of opportunity for submitting comments is not specified.
I would not wait long.
Thank-you for your attention.

*************************
Thanks for your Testimony and for supplying the typed copy for the committee.
Send those emails.. Here's a Place WAITING to be Used Properly...
and if used for ME/CFS the Revenge would be OH SO Sweet !!

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Tuesday, October 18, 2011

#119~ Urgent: November CFSAC concerns:



Occupy the CFSAC via EMAILs ASAP ♥



Subject: Urgent November CFSAC concerns:

a) It has come to our attention and was confirmed that the CFSAC arrangements next month are concerning for a number of reasons, some of which seem to indicate that the government is once again marginalizing people with ME/CFS:

b) Thousands of us have UNITED over the past 2-3 years via watching the CFSAC meetings LIVE online and Sharing the info. Now they are Stating this
"LIVE-Streaming will NOT Occur at the November meeting"...

Please ASK as many of your friends as possible to Join Us and send an Email ASAP so that there will be
"NOT ONE WORD ABOUT US WITHOUT US" !!

This is violating their "accommodation for rehabilitation for people with Disabilities" and their past agreement to LIVE STREAM the Video AND the Audio. Many must listen, many can only watch IN SILENCE and read the text captions.
BOTH ARE VITAL !

This is an URGENT Vital Plea regarding Our knowing what OUR Federally Designated Committee and the attendees are saying about us LIVE !
Please Help PROTECT "OUR RIGHTS"~
"NOT ONE MORE WORD ABOUT US w/o US" !!

They ARE moving it to a Larger Room in another building so more than 50+ ppl can be accommodated, which IS a good thing.

If you have ME/CFS/FM/HGRV  or any NID, Please share this info with EVERYONE YOU KNOW and ask them to Help by sending an email, with the link to this blog.
Here is the Official Notice for the Next CFSAC meeting and they are violating our 508 Rehabilitaion Act  agreement to "stream it LIVE" so we can all SEE + Hear it LIVE !!

CFSAC Bylaws State:

"All materials posted on the CFSAC website shall be 508 Rehabilitation Act compliant to provide equal access to people with disabilities.

To the extent possible, meetings are broadcast over the Internet as real-time streaming video. Meetings "also" will be recorded and archived on the CFSAC website for viewers to watch at their convenience."

In MY book "also" means IN addition to....

The meeting will NOT be broadcasted live on-line like it has the last 2 years. Again, it is not clear why it will not be. Instead it sounds like audio will be available only with possibly video available later on. Certainly, this cannot be for lack of viewship -- Wanda Jones announced that several hundred people watched it live -- nearing 1000 at the May meeting. This is a huge increase as before the videocasts, had less than 100 people usually. CFSAC meetings are near impossible for the majority of ME/CFS patients to attend due to health or financial reasons. It should be noted that many, many NIH and DHHS meetings are videocasted live and probably with a lower number of people watching. The number of testimonies has also gone up over time and we believe this is partly due to patients better understanding what CFSAC is.




"NOT ONE MORE WORD ABOUT US w/o US" !!

© 2011 - John Herd
c)
People who have not presented at the meeting before will be given priority to present. Although this is done prima facie for fairness, it might also mean that people who are knowledgeable/ experienced about ME/CFS and the gov't's history of dealing with it might be shut out from testifying. Does this apply to reps from groups also ?

d)
Please FLOOD her/their inbox with emails
immediately using the layout below to:
Dr. Nancy Lee is the new designated
federal official and her e-mail is:

In the "TO" section:
"Dr. Nancy Lee"
"Dr. Nancy Lee"
and copy that name/address EXACTLY, Promise ?

Then in the "BCC" section: add

Howard Koh ,
Howard Koh ,
Kathleen Sebelius ,
Fancis Collins ,
Dennis Mangan ,
Wanda Jones ,


The last one in the BCC: section~ the one to bodieangels, so we can tabulate how many were actually sent, OK ? ♥ If you want, send a "BCC" to yourself so you can see what it looked like.

Be SURE to use the "quotes" then a Space and the to make the address Correct ♥ with a comma in between each one, OK ?


"NOT ONE MORE WORD ABOUT US w/o US" !!

and for:
"President Obama"

http://www.whitehouse.gov/contact     
(it's a form to prevent spamming)
 
I suggest you create your Letter in a plain text program FIRST ( NOT "Word" ) so you can simply Copy + Paste it into the email. It helps me when I do that.♥

--> Let's SEE if we can get 1,000 emails sent 

                                BY the End of this week, OK ?

d)
Please click "attending" if you Promise
to just even send one short email stating some of what we've written here requesting that they STAY Consistent and ask for "NOT ONE WORD ABOUT US WITHOUT US" and that they Accommodate the needs of the Disabled as in the past. Also, Please ASK as many friends as you can to just the same simple email. ♥

♥Hugs♥ and Thanks from Around the World !!
        ---->   WE CAN DO THIS !!!  <-----





e)
PS: For those submitting written Public Comment or doing the same LIVE in Person~


Finally, in terms of preparation for CFSAC, the CDC website is currently under review. I suggest that we encourage people to mention what negative impact the CDC website has had on their lives (e.g. how their docs took the information, how it might have skewed media perception of CFS, etc.) and how the website could be modified to make the situation better and educate GPs/MDs "properly" by providing Quality videos for them to watch for their CEUs to maintain their licenses.

Until they get THAT in line with the
2011 CCCriteria for ME, we will NEVER make any progress..IMHO.


Let us "Occupy the CFSAC via Email" this week, OK ? 
Luv ya all for helping OURselves and staying ProActive ♥

If you are having any problems creating a ltter there are a few samples in the comment section of the FB Event that you may use.
http://www.facebook.com/event.php?eid=233487310041319

PLEASE be sure to send one to Pres. Obama also..  SEE the notice BELOW !!

© 2011 ~ John Herd
 

UPDATE:
 


Dr. Lee clearly received a lot of complaints. The email many of us received is now on the CFSAC website.
I say we need to continue to write letters and apply pressure to let her know this "accommodation" is not acceptable.

KEEP SENDING THOSE LETTERS AND REPLY TO THEIR CANNED REPLIES ALSO, OK?

http://www.hhs.gov/advcomcfs/notices/n101811.html
FYI> RE: Section 508 ~

Office on Disability

Section 508 Update

Acknowledgement: Office of Equal Employment and Diversity Management, FDA

The goal of the Section 508 law (part of the Rehabilitation Act of 1973, amended in 1998) is to reduce electronic and information technology barriers experienced by people with disabilities. Under this law, the Federal Government is required to purchase and deploy new IT and other electronic products that are accessible or compatible with assistive technology used by people with disabilities.

In a memo to all HHS employees dated August 30, 2001, Secretary Thompson called this law an exciting opportunity to help close the digital divide for individuals with disabilities in America.

"Section 508 affects every employee within the Department, not just those who work with technology or procurement. Every HHS employee has a collective responsibility for compliance with Section 508's mandate to make our information accessible to individuals with disabilities. This means that HHS employees must take proactive actions to ensure that all electronic and information technology developed, procured, maintained, or used, and all new or revised information made available on the Internet and Intranet meet the new accessibility standards."

The accessibility standards provide technology access to members of the public and Federal employees who have disabilities. Lawsuits may be filed in federal court or administrative complaints may be filed with Agencies or the Department of Justice for non-compliance with the law. __  __  __

Successful implementation of Section 508 requires the support of every Federal employee who may be responsible for incorporating Section 508 into the design or development of IT systems requirements, or the development of web pages and their content. Any time there is a purchase request of any electronic or information technology, or at any stage in the procurement or IT development process, Section 508 accessibility requirements must be implemented.

For more information on Section 508, check out www.section508.gov, contact your agency Section 508 Official, or call the HHS Office on Disability.
******************************************************
THE WHITE HOUSE
Office of the Vice President
________________________
FOR IMMEDIATE RELEASE
February 12, 2009

VICE PRESIDENT JOE BIDEN ANNOUNCES KAREEM DALE AS SPECIAL ASSISTANT TO THE PRESIDENT FOR DISABILITY POLICY

First Time a President has had a Special Assistant Focused Exclusively on Disability Policy

BOISE, ID – Vice President Joe Biden today announced Kareem Dale as Special Assistant to the President for Disability Policy. The Vice President, who was leading a Presidential Delegation at the 2009 Special Olympics World Winter Games in Boise, Idaho, made the announcement during a stop at the Special Olympics’ Healthy Athletes Event, a worldwide program in which athletes receive a variety of health screenings and services.

"The commitment that the President and I have to Special Olympics and people with disabilities is deep and abiding. And we are backing up those words with real action at the White House," said Vice President Biden.  "This is our first step to ensure that we have a strong advocate for people with disabilities at the highest levels of our Administration."

Dale, who is partially blind, will have direct access to the President in this role and he will coordinate the Administration’s efforts to see that people with disabilities are on a level playing field with all Americans.
 >>>>Think DALE would want to HEAR the CFSAC meeting LIVE ?? <<<<
**************************
 ORIGINAL NOTICE:
http://www.federalregister.gov/articles/2011/10/05/2011-25739/meeting-of-the-chronic-fatigue-syndrome-advisory-committee


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Friday, June 10, 2011

#117~ "The FINAL Betrayal"


Posted with the permission of the author Danny Ze-dog.


I'm too sick at the moment to start my own blog, and even if I had one I wouldn't be able to say what I'd really like to the way I'd like to.  But in light of months of following the scientific (and anti-scientific) developments in the XMRV story, and given that it is XMRV Blog Week, I feel the need to say something.  So here it is.

I don't know for certain whether XMRV and any related MRVs cause ME/CFS, or are co-causes or co-factors, but neither does any other scientist.  I don't know what role it plays in ME/CFS, but neither does any other scientist.

I know this: I will not spend the rest of my life sick or die young because some researchers and research journals made a political decision to "close the door" on the MRV-CFS association before it was appropriately investigated.  
I want a true replication study NOW.

I want 'science' journals to stop publishing negative studies by authors who haven't used clinically validated assays to detect XMRV.  I want 'scientists' to stop claiming that non-replication studies ARE replication studies.  I want any researcher, journal editor, or 'science blogger'  who claims that true replication isn't necessary in science to be forced to seek alternative forms of employment.  I want an investigation by the Department of Health and Human Services into why the NIH's tiny CFS grant review panel has turned down a series of grant applications by the WPI.

I want at least one sliver of justice for millions of sick people who have had none.  If nothing else, we should have the benefit of supposedly dispassionate, objective science.  We were raised to believe that science is the backbone of modern civilization, and the last pure thing left in a world rife with politics.  If we cannot even get THAT without political interference, then even the highest court of appeal is corrupt.  

For well over two decades we have trusted that, at some point, the system that was ostensibly built for us will finally work in our favor.  At what point do we decide as a community that it clearly will not?  And at what point will we protest en masse that our rights as citizens and as human beings are being denied by medical, "healthcare", political, and scientific establishments?

The most blatant recent example, and the most immediately crucial issue, is the organized attempt to bury XMRV-CFS research.  With whatever energy we have, we need to fight to stop that from happening.  NOW.  We need to let those who would bury it, or let it be buried, know that we will not tolerate this.  We need to let 'advocacy' organizations know that they should either support us in this endeavor or stop posing as advocates and get the hell out of the way.  We need to strategize ways that we as patients and their carers can have a real impact on the scientific institutions and policy-makers that are normally walled off from us, and on the media that increasingly serves only as a mouthpiece for the 'official sources' with the best media connections.  If the high-profile discovery of a potentially pathogenic gammaretrovirus that may infect at least 4% of the population can be whitewashed from the memory of science and history, so can - and will - that of any other pathogen, be it HHV-6, Lyme, or anything else. 

This isn't just an issue for people who support the XMRV hypothesis - it is an issue for everyone who wants good science to be done on this disease, now or ever.    

*************************************


"Well said" Danny, and Thank YOU for letting me post your statement here.. There is MUCH Truth IN it ♥



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Monday, September 20, 2010

#80~ Dr Cheney "corrects" youtube Video !!! +more

VERY IMPORTANT CORRECTIONS TO READ FROM DR. PAUL CHENEY ON AN INACCURATE YOUTUBE VIDEO OF HIS XMRV POSTER PRESENTATION AT XMRV WORKSHOP - You many repost these comments as long as they are attributed to Dr. Paul Cheney (the video has now been removed).



‎"My biggest problem with this U-tube video was the emphasis on "heart failure" as opposed to heart dysfunction or "LV diastolic dysfunction" which predisposes to orthostatic intolerance rather than death by heart failure which is very rare... in my select cohort. My poster never said heart failure was associated with CFS. However, we do know that broadly defined diastolic heart failure does not typically occur until age 72 or later so what will happen to my patients when they get into their 70's is up in the air, assuming they are not treated with things like CSF's before then. There is also the semantic question of how heart failure is defined. If it is defined by organ failure and usually death within 5 years, I don't see this and is likely very rare in the age brackets I see with CFS with an average age of 49. If it is defined by organ dysfunction including heart, GI tract, exercise intolerance, heat intolerance and brain problems etc. produced by low cardiac output then you could use the term heart failure due to diastolic dysfunction in much of my practice. Death by such a functional definition is, however, rare compared to the heart failure patients admitted to hospitals with normal ejections fractions and deemed diastolic heart failure. Such a diagnosis is very lethal over the next five years with only a third alive after five years and virtually all are quite disabled and will remain so.

"Another problem is the "8 of 16 family members" positive for XMRV. The poster actually says 50% of healthy family controls or exposure controls (N=8) were positive. The U-tube video assumed that there were 8 positives when in fact 8 were tested and 4 were positive. 6 of 8 were healthy family members of CFS cases and 2 of 8 were CFS exposure controls and not family members. However, when we get the serology data back, I think the number of family members infected will be higher than 50% and the N value will climb well beyond 16 so this correction may soon be mute.

"I think the U-tube video misses the very important point that the cancer rate is much higher (47%) in the non-CFS, first order family members than in the CFS cases themselves. This will be the big story going forward as to how you answer the question of why this is so. Is CFS a compensatory response to reduce serious disease and early death? I will say that Dr. Jason's assertion (or perhaps it is only the U-tube's assertion) that death occurs 25 years before they should have died is a fallacy as that number is drawn from the average age of all those who actually "died" and not a large group of CFS cases. In addition, perhaps a third of deaths occur by suicide in the young CFS cases and that will skew that number of 25 years before their time.

"The U-tube's final assertion that XMRV is a killer is somewhat exaggerated, at least in CFS. It certainly can be a killer but the U-tube video paints the death rate as much higher than it really is in CFS. In their defense, XMRV is a killer but more-so in the non-CFS but infected cohort which I think will be much larger than CFS itself and drives many cancers to be very aggressive with much higher death rates than would otherwise occur (see Singh et al, PNAS, 2009). XMRV may also be driving the epidemic of diastolic heart failure now seen in those over 70 and most die quickly within five years once admitted to hospitals for heart failure (see Owan et al, NEJM, 2006). XMRV may well be a killer, but the paradox is that not as much a killer in CFS unless perhaps they reach age 72 or above but that is near our present human life expectancy. The most interesting question of all is how did they live that long with such a killer virus and with such severe disability comparable to heart failure?"

Paul Cheney, M.D.

***************************************************
The video in question was entitled 
Third positive MULV study: Cancer & heart failure in XMRV families with CFS" and the link can still be seen below on my wall but the video has been removed from Youtube.
***************************************************




This is all very interesting in the details...
esp. with the knowledge that Dr. Cheney himself
had a heart transplant and gave a talk about 5 years ago where he stated that people with LV diastolic dysfunction, IF they had stayed Vertical and were not Horizontal, like from CFS, that their heart would INDEED probably be dead in about 5 years because of the organ failure due to lack of oxygen because of the OI and POTS.
He stated at THAT time: that it was the Fact that we INDEED WERE Horizontal because of CFS that we STILL Alive....



I specifically remember hearing this because it made a HUGE impression on me personally....
because it was at THAT time I went to a Dr and he tested me for OI and I also started staying more Horizontal to  protect my heart from being damaged from the POTS... which I did experience when I was Vertical.. and as time has progressed each time I am more Vertical
my OI and POTS has become worse and and I am now having to do MORE to specifically prevent the POTS and keep the circulation flowing ... so I'm not sure if I buy TOTALLY his reply.. I think a LOT needs to be studied as to if the person is indeed XMRV +Positive or if they have CFS, but are XMRV -Negative, and what age  they had their Triggering Event .......


There seems to me to be quite a bit yet to be Clarified.. as Dr Cheney can ONLY speak for his current cohort, which does not include all of the 4 million with CFS in the USA, let alone the 17 million in the world.


I guess I will soon know which category I settle into.. As I had my Triggering event when I was 38, but "pushed myself between relapses" until I heard his talk about staying Horizontal to preserve the heart... As I am already 61, it will be interesting to see if I indeed only live to 72, or MY Family average which is closer to 90.
I definitely will NOT commit suicide and will go out kicking... I have already had too many friends die by suicide that had nothing to do  with CFS, and I have had Cancer on BOTH sides of my family...my mother by non-hodgekin's lymphoma, who had a mild form of RA, and my brother also has a variant of another immune system disease.


Either Way, these do not paint a pretty picture for "The Golden Years" even after working for 17 years in a hospital... Maybe if Dr Cheney could get a "Charitable Backer" he would make his Research info "more easily accessible" to the patients that have already been sick for 25+ years but "can not afford to go see him" and do all of his tests "let alone get Rx'd any Cell Signaling Factors" to help with their heart issues.. By not making his info MORE Publicly accessible to those that REALLY need it.. He is actually making things more confusing for us.
I would REALLY like to see him care MORE about the other millions of CFS patients out there that hang on his every word, but only give us dribs and drabs, cuz we can't afford to subscribe to this newsletter...
So, I think he is "fine-tuning" his wording now...

Mainly because~ here we go again...to the CDC's intentional poor choice of a name for this illness and their intentional covering-up of it's prevalence for the last 25 years... Since MOST Dr's did NOT know what we had, most of us could not get a Proper Diagnosis and thus we could not apply for Disability, and now that we have a Diagnosis, Soc Sec says we waited too long to apply... what? If I am disabled now, and I have my proper quarters in, I should be available to qualify for Disability~ Period.


So until we reach 65 we are stuck with NO medical insurance or income. This is another disgraceful situation and reality especially for those that live alone and tried to play by the rules all of these years.. Even without XMRV, again the CDC "Can't Detect Crap."...and leaves us stranded and uncared for now because we could not be diagnosed because they have been using the WRONG Definition..........
HOW MANY TIMES DO WE HAVE TO SAY THAT ??

I will not declare that I am depressed simply so I can get Disability because I am more "Ticked OFF" and VERY Disappointed in our Dept of Health and Human Services and the National Institute of Health and the CDC that were set up to "care for  the Health of their citizens" and they have Failed us in the extreme !!!

Adding "Insult to Injury" ......

 This is  Invisible Illness Awareness Week -- half of Americans live with a chronic health condition, and 96% of them are "invisible" -- even to our Government to whom we have paid taxes all the years we  WERE able to work... and what's with all of the "Job Fairs" ONLY for those that can stand in line for 5 hours... How about "caring" to HELP those of us that want to work~ but are bedridden... Our brains and laptops still work VERY well.. Where are the Job Fairs for us? Are we left to get scammed by a Craig's List job offer? How about some HELP for the Disabled that you have DENIED Disability to... so we can Happily pay some taxes and NOT end up living on the street....

The Devil is in the Details and everyone has ignored 17 million details.......LONG Enough !!!



Wednesday, April 28, 2010

#59~ CFSACmeeting~ 4/10/10 Public Comment ???

Would YOU wait bedridden for 6 months for a 3 min. public comment?

I was SO Shocked and Personally INSULTED when I saw this that I just HAD to post about it to all of you... Are you AWARE that not ONLY will this be a ONE DAY (instead of the usual 2 ) meeting BUT the Public Comments have been reduced 
to 3min each ( instead of the usual 5 minutes ) AND NOW I SEE that there will 
ONLY be 30 minute IN TOTAL allowed for Public Comment ??? 


That is a HUGE Slap in the FACE to the Constituents they ARE Being PAID to Represent and they won't even give us adequate time to comment ?  I HOPE all commentators have brought FAST SPEAKING Helpers or a prerecorded version 
that they can play in FastForward Mode "chipmunk voice" so that their entire statement  CAN be made.. Sheez.. 25 years of PTSD and now this ???


THANKFULLY, Annette Whittemore of WPi HAS been granted 3 minutes to speak. Hallelujah ~


If the QUALITY of this MEETING is NOT EXCELLENT enough to make up for the lack of time/days allowed... I think it is TIME for there to be a VERY Vocal 
Public Input... I won't say exactly WHAT and to WHOM yet we will be directing
all of our input, (obviously Elected Officials ) among MANY Other PLACES...


I'm talking a HUGE Patient UNITED Campaign... WAY MORE than the CFIDS Assoc has ever done.. as WE WILL BE HEARD THIS TIME .... IT IS TIME FOR THIS 
DISGRACE AND Lack of HELP to those of us that WANT to be WORKING AND PAYING TAXES AGAIN.. Hello ? Help this Economy ?? Do I need to add up for you the MILLION of Dollars/Sterling/Euros that the NEGLECT of the ME/CFS Community has COST not only the USA but the UK and other countries
around this world.. It might be truthfully enough to make a REAL dent 
in the deficit.


But FIRST, some folks NEED to Take the PLUGS OUT Of Their EARS
and "Get a CLUE"...


I *Thought*  we were having a World Recession...TOO BAD they decided NOT to help 28 million people that COULD be Working and Helping our countries... but NO.... We ARE Being ignored and falling thru the cracks and unless this meeting BLOWS the ROOF OFF the Building...because it is SO FANATASTIC.... then our plans WILL be put into action...
Enough is Enough...
We WILL Be Silent NO MORE. Period !!!



Please Be SURE to "Tune IN" on May10th or whatever DAY/Time it is based on your timezone ♥♥♥ 

For further contact:
Chronic Fatigue Syndrome Advisory Committee (CFSAC)
Office of Public Health and Science
U.S. Department of Health and Human Services
Hubert H. Humphrey Building, Room 712E
200 Independence Avenue SW.
Washington, DC 20201
(202) 690-7650 (Voice)
(202) 401-4005 (FAX)
cfsac@hhs.gov (Email)


                               Agenda
                                    May 10, 2010
                                


             9:00 am
Call to Order


Opening Remarks
Roll Call,

Housekeeping
Dr. Christopher Snell
Chair, CFSAC


Dr. Wanda Jones
Designated Federal Official
            9:15 amWelcome Statement from the Assistant Secretary for Health
New Members Statement on CFSAC Interests/Goals
Dr. Howard K. Koh

CFSAC New Members
          10:00amRemarks from Dr. Elizabeth UngerDr. Elizabeth Unger
          10:30amBlood Safety Update on XMRVDr. Jerry Holmberg
          11:00amReview/Update of past CFSAC recommendationsCommittee Members
          12:30pmSubcommittee LunchSubcommittee Members
            1:30pmPublic Comment
(on CFSAC charter)
Public
            2:00pmReview and Discussion of CFSAC Charter and ByLawsCommittee Members
            4:00pmAdjourn














Sunday, April 25, 2010

#56~ SCRAP the CRAP to CFSAC

Reprinted with Permission from the Author.....

Folks PLEASE get your Emails OUT to cfsac@hhs.gov -
Monday 5pm EDT-USA  DEADLINE

     Thanks and Blessings to you all 
*♥♥*(¯`'•.¸(¯`'•.¸*♥♥*¸.•'´¯)¸.•'´¯)*♥♥*

******************************************************************

TO: CFSAC, President Barack H. Obama, VP Joseph Biden , DHHS Sec. Kathleen Sebelius, ACLU (Washington, D.C.) Chair, House Energy and Commerce Committee, Chair, Senate Health, Education, Labor and Pensions (HELP) Committee

Welcome new Members! 

I thank you for your service to us, the patients without a voice.

Today the name of my Statement is SCRAP the CRAP, for some of us want to tear the Charter to pieces in front of the three major networks’ cameras, but heck, they too have abandoned us to the psychobabblers.

Dr. Jones, I honor you for your administration of these meetings. Thank you for the streaming video; however, could you get “audio only” added for the dial-up connections? I also ask for a return to 5-minute statements, and that these be added to the language of the Charter.

Now, regarding “scrap the crap”: I am so dismayed that at this vital time, when real science is finally showing the distinct possibility that a retrovirus may be either the cause or a serious contributor to the long-term effects of CFS (such as cancer and shorter lifespans), we are discussing the Charter. Didn’t the last two meeting of the CFSAC show where its priorities lie?

I therefore demand a return to the science and that the Charter be changed to reflect the true name of this disease, which is Myalgic Encephalomyelitis, or M.E., as the Canadians,and other enlightened nations have done, and which has been recognized by the WHO for over forty years. In addition, I demand the M.E. diagnostic code be reinstated in the U.S. at once.

The CFSAC Charter should be renamed the CFS/ME Advisory Committee in accordance with the above, in order to maintain their intertwined relationship in research and scientific studies.

My last request (demand, if you will) is that patient’s be given a stronger voice, by including language in the Charter that would allow the CFS/ME-AC to request a Congressional Inquiry into the lack of responsiveness from the DHHS to the Committee’s past recommendations; and further, investigation into the violation of patients’ human and civil medical rights from the lack of appropriate testing and treatment for a known disease process; if, after 60 days, the Committee’s recommendations have not been addressed by the DHHS, in writing, and with actionable intent, with Internet access to same.

The junk psychobabbling of the CDC (the crap) must go; science must be admitted and funded through the NIH, immediately, taking all the latest science into account in order to protect the world’s blood supplies, future generations from disability; and to prevent lack of future tax revenues.

Thank you for today, (which should have been two), on behalf of the three of us living together, (two blood related and one a significant other of 25 years): all with CFS/ME! P.S. thanks, Mary and Erik!

Kathryn Stephens
Mary “Fiba” Arispe
Kathy Lorentz