After Unrest - (Low sensory version without music, link to original in description).

[@hopealways247]

Wow, Thank you for the no music version. Brilliant.

[@Mainysz]

*THANK YOU* (emphasis, not yelling) for having a version with no music. Sounds hurts me, so thank you for allowing me to focus on just words. Thank you!!

[@MECFSHEALTH]

You're very welcome :)

[@flaviac1096]

Thank you for sharing without music ❤

[@slovokia]

In the USA it is very hard to find doctors that know much about CFS/ME. Most of them are not very interested in learning more about it either. Overall the feeling I get is that the medical system wants little to do with us ME/CFS patients - they just want us to go away and not come back. Most medical schools do not teach their students about this illness either. I think in the long term we need to create a new kind of doctor that is trained and rewarded to care for people with complex chronic multisystem illnesses. The problem is that the existing medical system does not value that kind of care - it is optimized for acute illnesses that affect mostly healthy people. The quality of life of chronically ill people just doesn’t matter to the people in charge of the system.

[@rowanyth]

there's doctors kinda like that at cleveland clinic. not me/cfs-specific though should add, it's the center for functional medicine

[@yuhz1m1]

This was brilliant. And the patient resources that you shared...thank you so very much.

[@ginac7839]

Excellent Video! Thank you.

[@rerdb]

Thank your for that great video ❤️

[@kathleenkelley7701]

As you get more severe and less able to speak up for yourself, in my experience you have to confront more ignorance and judgementalusm even with a diagnosis in the past.