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Now Is the Time for a National PR Campaign for ME/CFS!

  [ 6 votes ]   [ 5 Comments ]
By ME Advocacy.org • www.ProHealth.com • November 27, 2014


Now Is the Time for a National PR Campaign for ME/CFS!. Image courtesy pixabay
Image courtesy pixabay
To donate to the national PR campaign click HERE.

From ME Advocacy.org


"HHS, NIH, fasten your seat belts and return your tray table to the upright position because it's going to be a bumpy ride:)" Susan Maier (NIH)
 
I'm sure Ms. Maier didn't realize just how prophetic her statement would become.  ME patients are disgusted and disgruntled with the mistreatment perpetrated on this extraordinarily sick population by the NIH and CDC. We're mad as hell, and we're not going to take it anymore!
 
With FOIA access gained to internal documents from the IOM and P2P projects, the upcoming final P2P workshop, as well as upcoming IOM and CDC Multisite results, the time is now perfect for an all-out publicity campaign.
 
Let's Blow The Lid Off This Thing!

As great as our grassroots efforts have been, it's clear we need to apply even more pressure to achieve our goals.  First, we must demand that the three redefinition projects, the IOM, the P2P and the CDC Multisite Study, are stopped immediately. Their possible achievements are dubious at best and a waste of taxpayers’ money.  Secondly, we must demand that the Canadian Consensus Criteria (CCC) be adopted as the official definition of ME. Research using various definitions and cohorts renders the results uncertain. It’s imperative that a single clear definition, which includes the hallmark symptom of post exertional relapse, is used for diagnosis and research.
 
We're talking about turning up the heat 1000 degrees and blowing the lid off this thing. We’re talking about an all-out campaign which will make both the US public and our policy makers in Washington sit up and take notice. We're talking about demonstrations and having our spokespeople in the national media.
 
How can we possibly pull off such a thing?  Because all of us are incapacitated to some degree, this type of national campaign has never been done before.  The obvious answer, therefore, is to hire an innovative public relations firm to handle most of the work for us! 
 
As a community, we have raised $20,000 for the documentary, "The Forgotten Plague", and a whopping $213,000 for, "Canary In A Coalmine".  So we know that for the right project, big money can be raised.  We are asking for $26,400 which will finance a 6 month public relations campaign. The amount is not small, but we feel it's quite doable.  Are you fired up?  Are you ready to get this done once and for all?!  We think you are!
 
Are you fired up?  Ready to get this done once and for all?!  We think you are!
 
The Proposal

Here is the proposal from our intended PR firm, Crowds On Demand:
 
With a strong Public Relations campaign, the fight to stop the unjustified redefinition of ME is an issue that we believe will resonate well with the American public.
 
Complete lack of visibility is the major problem the movement is experiencing. Most Americans do not know about these changing definitions because the issue has not been covered by major media outlets or championed by any high profile policy maker. To be blunt, most Americans don’t know the reality of ME!
 
Hiring the innovative PR firm, Crowds on Demand, provides the opportunity to bring concerns about the NIH/CDC redefinitions to the public and get the issue the attention it deserves. The firm is known for an "outside the box" approach that has successfully assisted people and organizations in getting on the map. Unlike many firms, we do more than contact media outlets, we coordinate campaigns from the ground up involving lobbying, demonstrations and media relations.
 
Crowds on Demand will contact media, arrange for interviews on high profile shows (particularly morning shows), organize demonstrations and recruit policy makers to join the fight. Moreover, we will assist in the fundraising process by helping to make strategic partnerships with influential organizations and donors.
 
We have agreed to work for a heavily discounted rate of $4400 per month including all of these services because we believe in the cause (normally we would charge approximately $10,000 per month for such a campaign). Furthermore, we promise results within 6 months and promise a 50 percent refund if the organization is not satisfied.
 
A PR campaign with Crowds on Demand will get the cause on the radar and help the organization raise substantial funds from a donor network. We have excelled in the past working to bring attention to non-profits. For example, Crowds on Demand has worked with a relatively unknown charity in Los Angeles that worked on homeless mental health issues. It was originally unable to fundraise much or get attention. Through its campaign with us, they substantially increased fundraising and got attention in the media.
 
We want to bring our success to fighting the HHS’s ludicrous redefinition campaigns and getting the CCC universally adopted.
 
Adam R. Swart
 
Email: adam@swart.org
 
Cell:  650-353-0083

Click HERE to read the Full Proposal

For FAQs about the campaign, click HERE.



About ME Advocacy.org

ME Advocacy.org is a project of May12.org. As May12.org is a 501(c)(3) not-for-profit corporation, all donations are tax deductible.
 
Both sites are run by patient volunteers, with none of the waste on salaries, buildings, and overhead associated with the large patient organizations. We are not affiliated with any government agency, and operate independently to enhance and support the campaigns already put in place by our patient advocates.

For your convenience, donations can be spread over 6 monthly payments. If 440 people donated $10 per month for 6 months we would reach our goal. We feel this is an affordable amount for many people.
 
To spread your donation over several payments, select the full amount you wish to donate, and then select the number of payments to make on this amount.

Please donate today!



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Article Comments Post a Comment

Have Questions About This Initiative?
Posted by: caledonia
Nov 27, 2014
Hi fellow Prohealth members, I represent ME Advocacy.org, the group which is doing the fundraising for a National Public Relations Campaign for ME/CFS, mentioned in the article. I will be available over the next week to answer any questions you may have. Just leave a message in the comment section here, and I will get back with you.
Reply Reply

PR campaign
Posted by: AuntTammie
Dec 3, 2014
I think this is a great idea but this is the first I have seen any info about it, and I am online daily reading various ME sites. If this is to work, then it needs to be publicized as much as possible.
Reply Reply

 
Reply
Posted by: caledonia
Dec 6, 2014
We're on several large forums and blogs. I'm in the process of doing a social media push, so you should be seeing something there soon.

I still don't feel like I've identified all the best places for promotion though - where else do you think this campaign should be promoted?

 


Promotion
Posted by: caledonia
Dec 4, 2014
We're on several large forums and blogs. I'm in the process of doing a social media push, so you should be seeing something there soon.

I still don't feel like I've identified all the best places for promotion though - where else do you think this campaign should be promoted?

Reply Reply

 
Please Share
Posted by: caledonia
Dec 4, 2014
Also people on this forum can help by using the social media buttons at the top of this article to share with their networks.

 



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