Darla Nagel
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Lightening the Shadow

Progress for Patients in 2017: A Reflection

12/23/2017

2 Comments

 
2017 has been a year of progress for ME/CFS patients. We’ve done more to inform government officials and citizens about the severity and reality of ME. Research funding is still insufficient and a cure still elusive, but I’m encouraged by the following events this year:
  • The release of the award-winning documentary Unrest, featuring Jen Brea of #MEAction
  • The updated ME treatment information (i.e., not graded exercise therapy or cognitive behavioral therapy) on the CDC’s site
  • The accurate media coverage in the New York Times, Ms., Huffington Post, and other publications.
 
Merry Christmas, and may next year bring better health to everyone with a chronic illness or invisible disability!
Christmas
Photo: Kent Landerholm, Flickr Creative Commons

Darla Nagel is an editor and writing tutor who has an invisible chronic illness. She wants to help other patients and enlighten health care professionals about our experiences. If you’d like to be alerted whenever she writes a new post, sign up by e-mailing darla.nagel@gmail.com.
2 Comments
Linda Miller
1/10/2018 10:18:49 am

Encouraging. This represents steps in the right direction.

Reply
Darla Nagel link
1/10/2018 07:13:54 pm

Thank you for your comment, Linda! You're right, and I'm especially encouraged by the CDC's effort.

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    Author:
    ​Darla Nagel

    Darla copyedits biomedical research and writes natural health magazine articles while living with an invisible chronic illness. She has a big appetite for chocolate despite being a health nut.

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