Julie Rehmeyer
@julierehmeyer
Author of Through the Shadowlands: A Science Writer's Odyssey into an Illness Science Doesn't Understand. NYT; WashPost; Discover; Slate; Stat News… She/her.
So half of a bone compressing my jugular is stuck in a nerve bundle and can’t be removed without major permanent nerve damage (half is out) Neurosurgeon: I will have nightmares about this! (jokes and steroids help, my bones ruining my life stays a joke) 🧵gofundme.com/f/help-emily-g…
I had the pleasure of helping the president of my alma mater, St. John’s College, write this important piece about the degradation of attention in our age and how education must be structured to help to reclaim it. latimes.com/opinion/story/…
I’m proud to be a matching donor for @Open_Notebook, which is an extraordinary organization improving the quality of science journalism by helping journalists improve their craft. Please, let me double your donation! theopennotebook.com/donate
I'm glad to see @BuzzFeed running educational content about tick- and vector-borne illness like #lyme, but I must disagree with Dr Shapiro, who is quoted in this article, that an infected tick *has* to be on for 24-36 hrs to transmit Lyme Disease. The 1/ buzzfeed.com/jillianwilson/…
This is a can't-miss for anyone interested in ME and Long Covid research.
We're hosting a Patient-Led Research Fund (PLRF) webinar on July 9, 1–4:30PM ET! Hear results from 10 PLRF-funded biomedical studies (on microclots, T cell exhaustion, trials, & more), all selected by a panel of patient-researchers. Register: us02web.zoom.us/webinar/regist… #LongCOVID
Last year, I spoke at the conference that led to this excellent roadmap for ME/CFS research. #MEAction has been advised to resubmit the proposal now. 10,000 signatures are needed to give it heft.
We are fighting for funding for the ME/CFS Research Roadmap. We have a letter urging Dr. Bhattacharya to allocate $50 million to fund the ME/CFS Research Roadmap. Sign our new letter now: bit.ly/MEcfsRoadmap #PwME #MECFS #NIH
Kira Stoops is KILLING it with her advice on how to live a fabulous disabled life. Her latest is on dating while diseased. Check it out! open.substack.com/pub/imperfectw…
This is fantastic and important research.
A new preprint confirms that generalized joint #hypermobility is a risk factor for #LongCOVID, while breaking new ground by examining risks of extreme hypermobility and whether hypermobility risk varies based on severity of initial COVID infection. 1/12 medrxiv.org/content/10.110…
A new preprint confirms that generalized joint #hypermobility is a risk factor for #LongCOVID, while breaking new ground by examining risks of extreme hypermobility and whether hypermobility risk varies based on severity of initial COVID infection. 1/12 medrxiv.org/content/10.110…
For those who deal with mold issues: The moldie communities that I know are super toxic places. Is there any way for a person new to the mold world to get decent peer support?
Exciting news this Giving Tuesday! We’re excited to announce that our nonprofit, Renegade Research, has been awarded a grant from @VitalikButerin’s Kanro Filantropic Fund to kickstart 8 innovative patient-led research projects focused on #MECFS & #LongCOVID. 1/8
Unless Congress acts in the next three weeks, Medicare will stop covering telehealth. For people like me, too sick to leave home for months, that would mean losing all access to healthcare. Please sign this petition prodding your representatives to act: actionnetwork.org/letters/preser…
Anyone know anything about sulodexide for treating endothelial dysfunction? It’s only available in Italy, where it’s over the counter.