Hi - I appreciate what you're saying, but apparently your message did not reach the right people. Continuing to flood Mr. Pak with messages will be counterproductive - it's not his job to respond to individual constituents. His job is to meet with disease groups, so I'd encourage you to consider that.
MEadvocacy was targeting NIH funding. CDC funding is not nearly as important and was never at risk of erasure till now. See Jennie Spotila's blog -
http://www.occupycfs.com/2015/08/04/no-cdc-funding-for-cfs/
The CDC has done more damage than good when it comes to ME. Advocates have questioned whether it is a bad thing to loose CDC funding altogether.
MEadvocacy attended the NIH senate appropriations committee
meeting this past spring. They submitted
written testimony to both the senate and house appropriations committees.
MEadvocacy has a successful
demonstration at the Capitol. and have two ongoing "one click"
campaigns to reach every congressional representative.
So, to state that ME patients were not represented in Washington, DC, is a misstatement.