Triple Giving Tuesday is Coming Soon
We are thrilled to announce we will once again celebrate #GivingTuesday as Triple Giving Tuesday. Jack and Dilla Cosgrove and Family have generously pledged up to $100,000 to triple your support for research.
If you give $250, the Cosgrove family will match $750 and your gift will be worth $1,000. WOW!
We are tremendously grateful to the Cosgrove Family and encourage you to donate to our Triple Giving Tuesday campaign. The campaign will begin on Tuesday, October 17 and will continue through Tuesday, November 28. (Photo Jack Cosgrove, Dilla Cosgrove, Jill Von Ebers, Chris Quinn, Linda Tannenbaum)
International Giving Tuesday has become the single largest day of philanthropy around the world. OMF will once again celebrate this international movement as #TripleTuesdayOMF #GivingMEday #UnselfieME
OMF Strengthens Our International Ties
The End ME / CFS Worldwide Tour has built many new international alliances. We are thrilled to share that with the help of a team of over 30 volunteer translators, OMF will soon be sharing our news and newsletters in the following languages.
We have added a new translation section on our website to make these easy to find and share. We invite you to share them with your family and friends around the world.
End ME / CFS Worldwide Tour Continues with New Partnership
Linda Tannenbaum has been a strong supporter of Jennifer Brea since she began her extraordinary community building and advocacy efforts by founding #MEAction. We are pleased to announce that we have taken our partnership to a new level.
OMF is now an official partner of the Time for Unrest global impact campaign, which seeks to increase awareness, research, education and funding for ME. The campaign accompanies the award-winning documentary, Unrest, directed by Jennifer Brea. Since joining Jen for the film’s debut at the Sundance Film Festival, we have partnered with her at several screenings. We are delighted to include Unrest at some of our upcoming Worldwide Tour events. (*These events will screen Unrest.**Q&A with Dr. Ron Davis, Dr. Janet Dafoe and Ashley Haugen following Unrest screenings.)
|October 2** – Menlo Park, CA
October 2* – Santa Monica, CA (panel discussion with Jen Brea)
October 15* – Dana Point, CA
November 1 – New York, NY
November 4 – Boston, MA
November 11* – Fullerton, CA
February 11 – Los Angeles, CA
Thank you for participating in the Coins For A Cure campaign. We look forward to receiving your donations. Join Team OMF with your own creative fundraising events. We are thrilled to receive donations of any size. — Every donation helps accelerate research.
Back to School – Help Our Kids Succeed
New tools are available to help parents and children manage school related challenges. Make this back to school season a better one for children with ME / CFS. Thank you once again Faith Newton, PhD, Delaware State University, for creating such useful tools to help our children.
Parents: We encourage you to review these helpful materials, print them and share them with your local school.
Does Your Company Have An Employee Giving Campaign or Matching Gift Program?
We want to make giving to OMF easy for you. If your company has a matching gift program you can double your impact. Check with your HR department to see how you can make your gift go twice as far.
OMF is a proud charity partner of Community Health Charities (CHC). CHC is a nonprofit that raises awareness and resources for health and wellness by connecting the most trusted health charities, including OMF, across the United States with more than 17 million caring donors through workplace giving campaigns, causes, wellness programs, employee engagement, and strategic partnerships. If your employer is a partner of CHC (or any Employee Giving Campaign), please designate your gift to OMF and encourage your colleagues, family and friends too.
A Word from our CEO/President
A major focus at OMF is to keep patients informed and involved in research. Our recent Community Symposium was a perfect example of this. We brought together and educated thousands of people from around the world through the livestream and Youtube video. We will continue to use the Symposium model to keep you informed.
We know that working together as a united community we are stronger. We look forward to continuing to grow our research efforts with you as our partners.
With hope for all,
- To fast-track revolutionary research for ME / CFS and related chronic complex diseases.
- To support collaborative scientific research to discover molecular causes, find effective treatments, diagnostic markers, prevention approaches and cures.
- To communicate, engage and inform the patient community.
- To help drive & support global collaboration