Congressman Jack Bergman becomes Champion for ME!

Up with the Marines! We are so pleased that Congressman Jack Bergman (R, MI-1), a former Marine general, has become a champion for people with myalgic encephalomyelitis (ME).

Michigan advocates led by Lori Chapo-Kroger, RN, president of Pandora Org, and supported by the #MEAction Congressional team, did a video conference with Rep. Bergman several months ago. After listening to the advocates’ stories and being briefed on ME, Rep. Bergman said, “It sounds like life’s thrown all of you a curveball but you’re still swinging. I’ll be there swinging with you. Consider this a new chapter with me as your partner.” And, indeed, Rep. Bergman did what he said he’d do!

  • Rep. Bergman signed two letters that were circulated in March, one asking to add ME to the Department of Defense Peer-Reviewed Medical Research Program, and the other asking the Appropriations Subcommittee on Labor, Health and Human Services to appropriate $9.9 million for various Center for Disease Control ME projects.
  • Rep. Bergman gave passionate opening remarks at the Congressional Reception at the end of Lobby Day, 2019.
  • Rep. Bergman joined Reps. Zoe Lofgren, David Joyce, and Debbie Wasserman Schultz to co-sponsor the House resolution for International Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome (ME/CFS) Awareness Day.
  • Finally, Rep. Bergman asked to meet with Dr. Ron Davis and tour the Stanford Genome Technology Center. After hearing on the video conference that some people from Michigan had to travel to Stanford for medical care because of the lack of Michigan specialists and that Stanford was one of the leading research centers on ME, Congressman Bergman asked if he could tour Stanford to see what research they are doing! And so we arranged for a visit to happen. How wonderful is that – a Michigan Congressman cares enough about his constituents and had the curiosity to use his time on a House recess to learn about clinical care and research for ME!
Stanford researcher, Ron Davis, shows photos of his son to Congressman Jack Bergman.

During the visit, Dr. Davis explained how his son’s experience with extremely severe ME motivated him to spend all his time looking for the cause of ME and to recruit his colleagues to assist in the effort. He showed Rep. Bergman several labs, described the kinds of ME research he was pursuing, and also explained how the false belief that ME was psychosomatic had both slowed and discouraged research for years. Rep. Bergman asked many probing questions, seeking to understand the research Dr. Davis was doing and what role NIH was playing.

Send a thank-you note to Rep. Bergman

We are so grateful that Rep. Bergman recognizes that disease is not a partisan issue and that both parties must work together to end the scourge of ME. Let him know how much you appreciate his actions by emailing him at [email protected].

Congratulations to the Michigan team for their amazing success, many thanks to Rep. Bergman for his wonderful support, and much appreciation to Dr. Davis for briefing Rep. Bergman.

If you find work like this valuable, we hope you’ll consider making a donation to support #MEAction. We are now 35% of the way to our US$100,000 goal and 87% of the way to our £10,000 target! It’s very important that we meet our June crowdfunding goal. Thank you for your support!

Facebook
Twitter
WhatsApp
Email

2 thoughts on “Congressman Jack Bergman becomes Champion for ME!”

  1. I wrote a thank you email to the Rep. All support by doctors and government is deeply appreciated. A patient of ME/cfs at 72 now, I don’t want another generation to go without possibility of a cure.
    Thank you too always, #ME Action.

Comments are closed.

Latest News

a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.

Severe ME Artists Project 2024

Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by

Read More »
Light blue square with rainbows in the top left and bottom right corner. In the middle are the words, -Pride is Valid- No Matter How One Celebrates or Experiences It. #MEAction Board Member, Jennifer England, shares her views on Pride. The #MEAction logo in the top right corner.

Pride Is Valid No Matter How One Celebrates or Experiences It

In honor of Pride Month, #MEAction is sharing a heartfelt message from our board member, Jennifer England, about what Pride means to her and her wife who lives with severe ME. My wife and I have both been queer our whole lives, but in the 70s that was the quiet part you didn’t say out

Read More »

Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

Read More »
Scroll to Top