WPI WPI is dedicated to solving ME/CFS and other complex infection-associated chronic diseases.

A medical research center dedicated to the discovery of the mechanisms of disease, creating diagnostics, and promoting effective treatments for those who suffer from ME/CFS and other chronic post-infectious diseases.

This  , we celebrate the resilience, dedication, and strength that unite our community.At WPI, we honor those living wit...
09/01/2025

This , we celebrate the resilience, dedication, and strength that unite our community.

At WPI, we honor those living with ME/CFS and other post-infectious diseases — whose daily perseverance is a true labor of courage.

We also recognize the tireless researchers whose commitment brings us closer to answers, treatments, and hope.

Together, we’re working toward a future of health, healing, and breakthrough discoveries.

Earlier this week, we revisited a long-standing myth—“ME/CFS is Rare"For years, the estimated number of people affected ...
08/20/2025

Earlier this week, we revisited a long-standing myth—“ME/CFS is Rare"

For years, the estimated number of people affected by ME/CFS has hovered around 17–24 million globally, often cited as 1% of the population. But that math doesn’t add up.

1% of the global population is actually closer to 71.2 million—meaning over 40 million people have been overlooked in past estimates.

So here’s to the missing 41.2 million—welcome back into the conversation.

https://pmc.ncbi.nlm.nih.gov/articles/PMC11907965/?fbclid=IwY2xjawMS-5lleHRuA2FlbQIxMABicmlkETFWb3hYbm83MlhnV3F5STJxAR5Ildh2bD6tl4pgAYgG8wl5-jQRDZqJzw3y5z9fDd0VB85zRddGavB7pj8eCw_aem_nQaz4ihTCKvUJwq9gfe00w

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08/18/2025

It’s time to set the record straight on ME/CFS with a Myth busting Monday.

For more information on these topics check out the source articles below. If this information has helped you in any way, please like or share with your community.

Donations are appreciated to help the cause with research, education, and the navigation of this ever-present condition. Join the mission of awareness.

Myth 1:“ME/CFS is rare.”
Source: https://pmc.ncbi.nlm.nih.gov/articles/PMC11907965/
Myth 2: “Exercise will help people with ME/CFS feel better.
Source: https://www.omf.ngo/pem-in-mecfs/
Myth 3: “ME/CFS is all in your head.”
Source: https://med.stanford.edu/medicalgiving/news/biomarker-for-chronic-fatigue-syndrome-identified.html

Amazing watch! Validating, informative, and a reminder that serious research is happening even when it feels like no one...
08/13/2025

Amazing watch!

Validating, informative, and a reminder that serious research is happening even when it feels like no one is listening.

If you’re looking for answers, clarity, or even just a bit of hope — take the time to watch this.

Last week, we hosted Dr. Akiko Iwasaki to discuss her Catalyst Award-winning study, “Probing Functional Autoantibodies in Patients with ME/CFS,” and she shared how her work lays the groundwork for targeted treatment and advancing diagnostic tools. Watch here: https://youtu.be/9ar0xtGwmrQ?si=pHj8wS8nBXrd3Bbo

08/11/2025

CFS- Chronic Fatigue Syndrome, it’s not just being tired.
ME/CFS doesn’t steal your life all at once. It takes it in pieces — a walk you can’t take, a call you can’t return, a world that moves too fast for a body that can’t keep up. But you smile, so they think you're fine.
It’s a sum of invisible symptoms that make it hard to be present physically and mentally.

Post-Exertional Malaise (PEM)-A worsening of symptoms after even minor physical or mental exertion — delayed and lasting days or weeks.

Cognitive Dysfunction ("Brain Fog")-Difficulty concentrating, processing information, finding words, or multitasking.

Orthostatic Intolerance-Dizziness, lightheadedness, or fainting when standing up, due to poor blood flow regulation.

Unrefreshing Sleep-Sleep that does not restore energy, regardless of how long the person rests.

Chronic Pain-Muscle pain, joint pain, or nerve pain not visible externally.
Hypersensitivity-To light, sound, touch, chemicals, or even mild stimuli — causing pain or fatigue.

Flu-like Symptoms-Sore throat, swollen lymph nodes, chills, and more, despite no active infection.

Emotional/mental burden-Anxiety, depression, isolation — often due to disbelief, invalidation, or medical gaslighting.

Join us in the attempt to make the invisible visible. You can do that by interacting with this post, sharing it with people you know, or becoming involved with our organization and others like us who dedicate themselves to support this patient population, the research to understand it better, and educating to make a difference.

So many are living in isolation. It’s time to end this disease!
08/08/2025

So many are living in isolation. It’s time to end this disease!

In Home Medical Care 4 Severe ME. Invisible Lives, Visible Care

In the lead up to we invite you to listen to Chris Quill's podcast episode. In conversation Emerge Australia CEO, Anne Wilson Chris shares the challenges as he has transitioned from a fit, healthy family man, with a rich career giving back to others as a disability support expert to one living with after he contracted COVID.

Listen here: https://vist.ly/32ifd

One United voice for those with ME makes our voices heard!
08/08/2025

One United voice for those with ME makes our voices heard!

In honor of Day (Aug. 8), we’re joining forces to amplify the voices of those most often unheard.

Today, we launch , a shared hashtag to highlight stories, art, and education about Severe ME.

Together, as ME organizations and advocates, we’re committed to this community, not just today, but every day.

We invite you to join us. Use to share, support, and stand with people living with Severe ME.

Bateman Horne Center Open Medicine Foundation The Network

Today, we honor those living with severe ME/CFS — the most debilitating form of Myalgic Encephalomyelitis.While many wit...
08/08/2025

Today, we honor those living with severe ME/CFS — the most debilitating form of Myalgic Encephalomyelitis.

While many with ME/CFS face profound fatigue and limited function, those with severe ME are housebound or bedbound, often unable to speak, eat unaided, or tolerate light and sound.

They are missing from everyday life — not by choice, but because their illness leaves them with no choice.

August 8 is Severe ME Day.
Let’s make the invisible visible.
https://www.wpi.ngo/service

08/05/2025

Post-Exertional Malaise (PEM) is not just feeling tired.
It’s the worsening of all symptoms after even mild effort—like taking a shower or talking with a friend.
🪫 Imagine your body is a phone that never charges past 20%. That’s PEM.
It’s one of the most disabling aspects of ME/CFS, and one of the least understood. PEM can set in hours after exertion, and last for days or weeks. The only known treatment is rest and pacing.
Swipe to learn more.
Share this with someone who needs to understand ME/CFS better.

Sever ME Awareness Day is a week away!Emerge Australia Inc is Hosting a virtual symposium for Public awareness and educa...
07/30/2025

Sever ME Awareness Day is a week away!

Emerge Australia Inc is Hosting a virtual symposium for Public awareness and education. Whether you're a patient, caregiver, medical professional, or advocate, this is an opportunity to learn, listen, and stand in solidarity with those too sick to leave their beds.

Join the Conversation!

Welcome! You are invited to join a webinar: Emerge Australia Severe ME Day Symposium. After registering, you will receive a confirmation email about joining the webinar.

This patient study finds that individuals with ME/CFS and Long COVID share similar symptoms, which may temporarily impro...
07/08/2025

This patient study finds that individuals with ME/CFS and Long COVID share similar symptoms, which may temporarily improve depending on a symptomatic profile. Notably, antiviral therapy was excluded, possibly because it is not typically offered to most patients, despite its effectiveness in previous studies.

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and long COVID are persistent multisystem illnesses affecting many patients. With no kn...

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