Jere

#Artist @IntegralArtist2 and one of the #MillionsMissing since 1984. #MyalgicEncephalomyelitis #Type1Diabetes #Addisons #Hashimoto

[Miriam E. Tucker @MiriamETucker]

If you believe “chronic fatigue syndrome” is trivial or psychological, you might change your mind after reading this.

[Steve Silberman @stevesilberman]

One of the most poignant stories I've read this year. Really heavy. A sculptor, passionately devoted to her art, realizes that her art is killing her. https://t.co/jjCSmnlBew

[Miriam E. Tucker @MiriamETucker]

Indeed. #type1diabetes has been "cured" over 400 times in mice. If you are a mouse and you still have #diabetes, you need to hire a better agent. https://t.co/DRofGMviSH

[Erik Johnson @erikmoldwarrior]

We don't have to speculate or wonder how many CFS researchers didn't look into this. For if any had, they would have found toxic mold in the teacher cluster, and told the world. So what is the number of CFS researchers who "responded" and told the world about toxic mold?
Zero!

[Miss Diagnoses @miss_diagnoses]

First Lyme Awareness Month 2018 post. 💚https://t.co/XrMauXHQNC @LymeChallenge @ProjectLyme @lymenews #LymeDiseaseChallenge #TakeABiteOutOfLyme #lymeawareness #LDC2018 #changemaker

[David Skidmore @Lymeloonies]

One thing I have learned is one can spread themselves out too much and it can muddy the waters.
If not for the Month of May, I may come out of my short lived retirement from #LymeDisease cartoons.
Maybe once a Month as apposed to 2-3 every week.
I'll try one. 💚

[Erik Johnson @erikmoldwarrior]

What do you do when medicine has no answers?

Try looking at the actual evidence.

[Erik Johnson @erikmoldwarrior]

You'd think on such an auspicious day for Unrest and advocacy for "ME/CFS" there would have been effort to get an original Royal Free survivor or Lake Tahoe survivor. But I don't see that any survivors of any outbreak at all were invited to talk about their experience.

[Independent Lens @IndependentLens]

When medicine has no answers for you, would you give up? Starting now on East Coast: Watch @unrestfilm on #IndieLensPBS @PBS https://t.co/rJJBF3mcfz

[Nasim Marie Jafry 🍉 @velogubbed]

UNREST movie has harnessed a global interest in myalgic encephalomyelitis (ME), the likes of which I haven't seen in my 35 years of illness. I am the author of The State of Me (2008) and my review of UNREST is here: https://t.co/zdkaQGVbl5 #UnrestPBS https://t.co/ec83aIqPcL

[Miriam E. Tucker @MiriamETucker]

Tonight PBS will air @JenBrea's extraordinary film about the serious illness known by the inappropriately benign-sounding name "chronic fatigue syndrome." Here's a 2016 Medscape story I wrote about some of the scientific research: https://t.co/LczxfqH21e #mecfs #pwme https://t.co/EJBuNobHZh

[Miriam E. Tucker @MiriamETucker]

Abbott's Freestyle Libre glucose monitoring system now covered under Medicare: https://t.co/7rvuAv8CEI #diabetes

[Miriam E. Tucker @MiriamETucker]

Great story by @sarahkaplan48: https://t.co/uqrUoCBUy2 I say as long as I don't see them and they don't bite me while I'm sleeping or destroy the building, live and let live.

[Erik Johnson @erikmoldwarrior]

Are "ME/CFS researchers" intending to CONTINUE to treat "mold at ground zero for CFS" with DISDAIN? Not a good idea https://t.co/zxKz7w23MH

[Miss Diagnoses @miss_diagnoses]

@integraljere Hi Jere! Thanks again for the retweet! 💚💚

[Miss Diagnoses @miss_diagnoses]

Anyone else do this regularly? "Fifty Shades of Brain Fog, Part Two." https://t.co/XftLjHX1PP #Lyme #spoonie #SpoonieProblems #Hashimoto's

[SleepyGirl FilmFest @MEepsMEepsMEeps]

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Please take a moment to watch and share Vicki's fantastic videos.

by @miss_diagnoses

https://t.co/Noj8hsWs5R

[Miss Diagnoses @miss_diagnoses]

@integraljere Thanks for retweeting!!! 💚💜❤️