#TeachMETreatME: Celebrating An Impactful Campaign

We are THRILLED to share the rolling successes of our #TeachMETreatME campaign with you, as we report back on the amazing medical education events that have taken place so far – with many more to come in the upcoming months! (And don’t miss the global #MillionsMissing events later in the article!)

Over the past several months, clinicians and medical students across the U.S. have attended presentations, roundtables and conferences to learn about ME/CFS – and how to take the Mayo Clinic Proceedings Continuing Medical Education course on ME/CFSthanks to the incredible work of #MEAction advocates who dedicated so much to make this campaign a success! 

In the UK, #MEAction UK advocates pulled off a wonderful Postcard to Doctors Campaign encouraging medication professionals to take a CDP module on ME.

“It’s a cascade effect – imagine the number of future encounters now where the patient will be diagnosed instead of dismissed. It sounds cliché, but we’re changing the paradigm around ME/CFS in medicine.”

Stephanie L. Grach, M.D., M.S.
who presented at the #TeachMETreatME Mayo Clinic event

Roll Count, please!

#TeachMETreatME highlights so far: 

In the U.S.: 

University of North Carolina kicked off our campaign in April with a Grand Rounds, educating over 75 physicians about ME/CFS and Long Covid.

A few weeks later, 30 clinicians at the Mayo Clinic in Minnesota attended Dr. Stephanie Grach’s presentation on ME/CFS, where Rachael Carder spoke about her lived experience with ME and difficulty getting diagnosed.

Meanwhile, Dr Peter Rowe launched an ongoing four-part series on pediatric practices for children with ME/CFS thanks to #MEAction Maryland!

“This kind of dialogue in the medical community is vital to help ensure patients receive the best care possible.”

– Dr. John Baratta, MD, MBA,
head of the UNC Post-Covid Recovery Clinic

Medical students at Brown University learned about ME/CFS at its annual AMS Wellness conference, and Quinnipiac University held a seminar on ME/CFS for its medical students with #MEAction’s Scientific Director, Jaime Seltzer!  #MEAction Maryland held an awareness event at Georgetown University where they spoke with students and faculty about the global shortage of medical professionals trained in ME/CFS.

In Florida, #MEAction volunteers hosted a table at the INIM conference at Nova Southeastern, handing out fliers about ME/CFS and discussing the disease and how to take the Mayo CME. 

Meanwhile, we have many more #TeachMETreatME events approaching in the U.S. over the summer and fall at Emory School of Nursing in Georgia (with the CDC as co-presenters along with #MEAction Georgia!); Washington University in St. Louis; Northwestern University in Illinois; Sutter Health and Enloe Health in California; and at the One Medical conference in Chicago.

a black and white image of a map showing the US and the UK. There are red markings showing which cities hosted events.

In the U.K:

#MEAction UK created a Postcard to Doctors Campaign encouraging medication professionals to take a CDP module on ME. An advocate held an event at King’s Mill Hospital, Mansfield to encourage staff to enroll in the CPD accredited training. 

A general practitioners online study group, which features a group of general practitioners from different practices who come together as a group, have asked #MEAction UK to speak to them about ME. Plus, Medical English invited #MEAction UK to its weekly session to discuss ME.

And upcoming in the UK, is a webinar on ME and Long COVID at the Royal College of Physicians Edinburgh. This opportunity came to be as result of the #MEAction Scotland’s actions during last year’s #MillionsMissing. 

UK 1 (1)

#MillionsMissing 2024:

Across the globe, #MillionsMissing events took place to raise awareness and demand better treatment. These are only a sampling of the events across the world as there were definitely more!

#MillionsMissing Copenhagen 
A #MillionsMissing event at Fælledparken in Copenhagen, Denmark created an exhibit of shoes and passed out information leaflets about ME. Also, the group provided a quiz about ME for health personnel.

#Millions Missing Vancouver 2024
Organizers gathered outside Premier David Eby’s constituency office in Kits to demand that the B.C. government work with #MillionsMissing Vancouver to make a plan to improve patient care for people living with ME.

#MillionsMissing Brussels:
The Flemish Patient organization, 12ME, organized a #MillionsMissing event in Brussels. They displayed approximately 100 pairs of empty shoes to symbolize the millions of ME patients worldwide who have disappeared from daily life because of illness. With each pair of shoes they will place a testimonial from someone suffering from ME.

Brussles 1 (1)

MillionsMissing 2024 Bern Switzerland
The ME/CFS Association Switzerland, organized a shoe and deck-chair demonstration/presentation in front of the Government/Parliament House of Switzerland in the capital city, Bern. They had many speeches from patients, doctors, politicians, and the president’s of the Swiss ME and CFS association Sgme and Long Covid Switzerland association. Furthermore, they displayed art and testimonials about people with ME/ Plus, they distributed flyers and gadgets about ME.

#MillionsMissing Stockholm
A #MillionsMissing event at Sergels torg in Stockholm took place on Sunday, May 12th with an exhibit of shoes and stories from people with ME. 

You Showed Up From Home

How this community show up on social media during our #MillionsMissing campaigns never cease to amaze us! The power of #MillionsMissing is the strongest online and this year was no different!

We asked you to share the Mayo CME with your clinician (you can still do that using this language!), and we’ve already seen positive responses from the medical community!

“I appreciate this link! I have shared this link with our module colleagues as a starting point. The site looks like it has a lot of valuable information about this complicated and nuanced condition. I appreciate your sharing.”

Kaiser doctor
Northern California

You shared your stories and representations of what living with ME looks like:

You shared how long to being diagnosed, which combined to create these beautiful videos: 

Video description: Background of a black screen with name, years to diagnosis, and the country the person lives in show on the screen in white lettering. They change and get faster and faster as they go. They become more chaotic coming from different directions. At the end the text switches to what those years meant- years of waiting, being gaslit, etc.
This is a short video with some flashing words on the screen, so please be mindful when viewing.

You shared your artwork:

You shared while #TeachMETreatME means so much to you:

You shared the CME:

To everyone who shared something online this past week, we thank you so much for taking the time to raise awareness and add to the groundswell of support needed to advance the much needed care for those living with ME.

The #MEAction community is always impressive! Your tenacity, your determination, and your perseverance are all to be recognized and honored. #MillionsMissing does not exist without you, you are the reason we have an article filled with these many successes! THANK YOU!

In awe, 
All of us at #MEAction

Facebook
Twitter
WhatsApp
Email

Leave a Comment

Your email address will not be published. Required fields are marked *

Latest News

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 »
red rectangle with the #MEAction Scotland logo on the left hand side and the words Impact Statement 2022-2023 on the right.

#MEAction Scotland publishes impact statement

#MEAction Scotland is pleased to publish our impact statement, which covers March 2022 to May 23. It reports on our work to campaign for effective support, create stronger advocates and raise awareness. As a small group of volunteers, it’s unfortunately not always possible to continually update on our activities as they happen, so the statement

Read More »

#MillionsMissing Week is Here: #TeachMETreatME in Action!

We are excited to announce the kick-off of #MillionsMissing 2024 – our ongoing campaign to Teach ME and Treat ME by educating medical providers across our nation’s hospital systems and medical schools about myalgic encephalomyelitis (ME).  Throughout the spring, summer and fall, #MEAction teams are hosting 13 medical education events to encourage medical providers to

Read More »
Scroll to Top