Good Day / Bad Day Pictures of Children With ME/CFS – deadline 5/20th!

The federal government is looking for Good Day/Bad Day Pictures of Children with ME/CFS to mount on a parents’ ME/CFS information website. It is part of an Information and Resources site for children with various disabilities.

The Chronic Fatigue Syndrome Advisory Committee (CFSAC) Pediatric Working Group reviewed the revisions for the website.  It is looking pretty good, but could benefit from the graphic to make the point that these kids look perfectly “normal” on a good day and look absolutely lousy when sick.  Both parent and child must agree to the placement of the photos on an open-to-the-public website.

Photos are needed by Sunday night (May 20th.)  Send as attachment to: Kenneth.j.friedman@gmail.com

Thank you,
Kenneth J. Friedman, Ph.D.
CFSAC Pediatric Working Group

Millions Missing Event

Governor Declares May ME/CFS Awareness Month

2018 HS Scholarship Application * UPDATE – AWARD INCREASE!

2018 HS Scholarship Announcement-UPDATE March

AWARD INCREASE!

Who is eligible?

New Jersey high school senior or recent graduates, physician-diagnosed with ME/CFS.

The purpose of the NJME/CFSA Scholarship is to provide financial assistance to a deserving student who has ME/CFS and wishes to pursue his/her educational goals in college or technical school.

The NJME/CFSA Scholarship is a single scholarship in the amount of $2,000 to be applied toward the student’s tuition or educational related expense.

Leonard Jason announces an upcoming presentation

      Image may contain: one or more people and closeup   Leonard Jason

@CenterRes
Following Following @CenterRes
I was Invited to present on QuantiaMD about myths regarding
CFS. This will be used in educating medical professionals regarding this illness.
https://youtu.be/dguHdXZnrm4
A Q&A will occur
the week of May 7-12, 2018
@scra

 

ProHealth’s 2017 ME/CFS Advocate of the Year – Linda Tannenbaum

ProHealth is proud to name Linda Tannenbaum, founder of the Open Medicine Foundation, as ProHealth’s 2017 ME/CFS Advocate of the Year.

See full article  https://www.omf.ngo/2018/02/26/prohealth-angel-among-us/

Article Published Winter 2018

“Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: What Every Family Physician Needs to Know”

By Mary Dimmock, Susan Levine, MD, and Terri L. Wilder, MSW

New York State Academy of Family Physicians’ Winter 2018 “Family
Doctor” journal (p.23-25)

It ends:
“Most importantly, the family physician can validate the patient’s
experience and ensure that the patient is not harmed by inappropriate
treatment recommendations for exercise or talk therapy intended to
convince the patient they are not ill.”

https://tinyurl.com/ycb8mxzg
i.e.
http://www.nysafp.org/NYSAFP/media/PDFs/Family%20Doctor/Family-Physician-Winter-2018WEB.pdf

Unrest available on Netflix

https://www.netflix.com/title/80168300

HOW DISABLED PEOPLE CARE FOR EACH OTHER WHEN DOCTORS CAN’T

https://psmag.com/social-justice/how-disabled-people-care-for-each-other-when-doctors-cant

Info – UNREST on PBS

INFO – UNREST PBS showings and Bergen Mtg dates.
This was provided by the Bergen ME/CFS/FM Support Group
If you have a DVR you can set the program to record. Search “Independent Lens” for UNREST on PBS next week. I found the following dates and times:

Channel 13 – Jan 8 at 10pm 
Channel 13 – Jan 11 at 4:30 am
Channel 21 – Jan 9 at 12 am
Channel 21 – Jan 10 at 8:30 pm
Channel 11 – Jan 11 at 3:30 pm
Channel 21 – Jan 11 at 12 pm

Please search PBS online for tv schedules near you. I may have missed something. And it is likely that additional shows will be on in the future as well.