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Triple Your Impact!

Help OMFCA

Accelerate Research Discover Treatments Find a Cure

Millions of men, women, and children suffer from ME/CFS, Long COVID, and related multi-system chronic complex diseases. They DESERVE access to proper treatments and quality healthcare. 

Every donation to Open Medicine Foundation Canada brings us one step closer toward finding diagnostic tests and treatments. Now is the time to triple your impact. 

All donations will be tripled up to $500,000!

What Is Triple Giving Tuesday?

Triple Giving Tuesday is our biggest fundraising event of the year. Thanks to generous matching donors, ALL gifts made to OMFCA will be tripled up to $500,000 until International Giving Tuesday on November 29, 2022.

Regardless of how, when, or where you donate, your gift will be tripled up to $500,000.
Every day of the week!

What do your donations fund?

Every donation brings us one step closer toward finding diagnostic tests, treatments, and a cure.

SEVEN
COLLABORATIVE CENTERS

OMF’s strategy focuses on collaboration so that precise diagnostic tools, life-changing treatments, and knowledgeable physicians can be available to people with chronic complex diseases as soon as possible.

WORLD CLASS
SCIENTIFIC ADVISORY BOARD

OMF’s Scientific Advisory Board is an alliance of world-renowned researchers, including two Nobel laureates. They dedicate their time, passion, and expertise to ending ME/CFS and related multi-system chronic complex diseases (msCCD).

GROUNDBREAKING
LONG COVID RESEARCH

OMF researchers have launched an international study on COVID-19’s potential conversion to ME/CFS (“Long COVID”). This research provides incredible insight into the disease process . OMF’s goal is to find treatments and prevention strategies at an accelerated pace.

MEDICAL EDUCATION
RESOURCE CENTER (MERC)

In partnership with Bateman Horne Center, The OMF Supported MERC will increase access to knowledgeable healthcare providers and improve patient care.

Help OmfCA support more research

Get Involved

There are many ways to join OMF’s mission.

Fundraise

You can make a difference. Kick off a digital fundraiser in 5 minutes or less.

Share your story

Raise Awareness. Inspire the community. Educate the world.

Spread the word​

Follow us on social media. Share our posts about Triple Giving Tuesday. Don’t forget to tag us!

Our Story

The OMF Difference

In 2006, OMF Founder & CEO Linda Tannenbaum’s 16-year-old daughter went from being a healthy teenager to severely ill overnight. She could not get out of bed, and all her energy had been drained. Her daughter had sudden onset ME/CFS. After visiting over 20 doctors, Linda quickly realized there was a huge gap in research – no treatments, diagnostics, or cure for ME/CFS exists.

In 2012, Linda set out to change this. She established OMF as a nonprofit organization with a mission to fundraise and facilitate large-scale research in search of diagnostic tools, treatments, and ultimately a cure. OMF’s board members, staff and volunteers that include patients and caregivers inspire, advise, and dedicate their time to this mission.

By 2014, Linda and renowned geneticist Ronald W. Davis, PhD, also a parent of a severely ill son, joined forces. Together they built OMF’s Scientific Advisory Board (SAB) of leading experts dedicated to our mission.

OMF has since raised over $40 million and leads the largest worldwide nonprofit effort to end ME/CFS and related msCCD. United by passion and scientific curiosity, our OMF Collaborative Research Network will not give up until answers are found. Your support ensures their success.

OMF's 10 year anniversary

TRIPLE GIVING TUESDAY

News & Articles

Ron Davis: New Neutrophil Study!

A new study from Ron Davis and Stanford colleagues aims to identify neutrophil abnormalities that are unique to ME/CFS patients.