Jeffrey Lubell (EDS, ME/CFS, LongCOVID Research)
jefflubellc19.bsky.social
Jeffrey Lubell (EDS, ME/CFS, LongCOVID Research)
@jefflubellc19.bsky.social
I am researching treatments for my daughter, who has hEDS, ME/CFS and other conditions, with implications for #EDS, #MECFS and #LongCOVID. I am a researcher, but not an MD.
Ensuring a system like this works work well will be hard. But not nearly as hard as living with chronic illness for many additional years because we haven't figured out how to more effectively tap into patient and caregiver experience. 24/24
November 30, 2025 at 4:25 PM
It would also be useful to pair patients/caregivers with researchers that share interests. Funding will also be needed to pay for open-access fees and to ensure journals have the staff needed to handle the influx of additional articles they receive. 23/24
November 30, 2025 at 4:25 PM
Would patients and caregivers authors benefit from professional guidance? Yes, for sure. That's why, to really make this process work, journals should have open-minded medical professionals work with patients and caregivers to help them strengthen their hypotheses and articles. 22/24
November 30, 2025 at 4:25 PM
To make faster progress in addressing chronic illness, we should let the medical research field hear directly from patients and caregivers through publications in well-read medical journals. 21/24
November 30, 2025 at 4:25 PM
Some patients and caregivers have crossed over and published original research in conventional medical journals. I have as well. But we can’t expect all patients and caregivers to do this. 20/24 t.co/f1OTxiBbHt
https://bmjpublichealth.bmj.com/content/3/2/e002949
t.co
November 30, 2025 at 4:25 PM
They also have a wonderful journal of patient hypothesis to which I and others have contributed. But how will researchers find these hypotheses if they are not indexed in PubMed? 19/24 patientresearchcovid19.com/projects/pat...
Patient-Generated Research Hypotheses – Patient Led Research Collaborative
patientresearchcovid19.com
November 30, 2025 at 4:25 PM
The Patient-Led Research Collaborative @patientled.bsky.social has done a fantastic job organizing patient-led research that has led both to publications in established journals and to greater involvement of patients in research more broadly. 18/24
November 30, 2025 at 4:25 PM
This is just one small example of why more PubMed-indexed medical journals should accept case studies and hypothesis papers from patients and caregivers. Other patients & caregivers will have other ideas that the field needs to hear! 17/24
November 30, 2025 at 4:25 PM
I believe we urgently need more systematic research on this issue, starting with qualitative accounts and supplementing with medical records and test results. But how can I share this view with the medical research community if journals strongly discourage patient/caregiver submissions? 16/24
November 30, 2025 at 4:25 PM
But how can we know? Individual stories of patients and carefivers only tell you so much, but they can be analyzed systematically, both through retrospective and prospective qualitative studies and through social media and other content analysis. 15/24
November 30, 2025 at 4:25 PM
If a significant subset of #LongCOVID or #MECFS patients follow a relapse-recovery pattern, research is urgently needed on what causes the relapses and how to accelerate recovery. We will also need to segment treatment trials by place on longitudinal progression. 14/24
November 30, 2025 at 4:25 PM
Most research is cross-sectional, analyzing data from multiple patients at a single time. Cross-sectional research is important but is largely incapable of identifying longitudinal patterns. 13/24
November 30, 2025 at 4:25 PM
It is of critical importance to understand whether #MECFS & #LongCOVID are simple binary phenomena – you have them or you don't – or longitudinal disorders in which relapse events cause lasting damage that heals over time. (Or perhaps a combination, such as vascular damage + autoantibodies. ) 12/24
November 30, 2025 at 4:25 PM
A paper came out just the other day documenting the longitudinal experiences of COVID patients in the first 15 months after infection. Great to see a focus on longitudinal patterns, but the follow-up period is not nearly long enough. 11/24 t.co/b47on8dWJC
https://www.nature.com/articles/s41467-025-65239-4
t.co
November 30, 2025 at 4:25 PM
Unfortunately, more than 35 years after the “discovery” of #MECFS and more than five and a half years after the appearance of #LongCOVID we still don’t know how prevalent this pattern is in these illnesses. 10/24
November 30, 2025 at 4:25 PM
If you follow the accounts of people with #MECFS or #LongCOVID on social or print media, you’ll see this relapse-recovery pattern a lot. I cite some articles in the paper. Here’s a great example from Twitter. 8/24 x.com/jewstein3000...
Justine on X: "🧵 I think @jonfavs and others don't understand. THIS is how Long Covid happens in the vast majority of cases (including mine): 1. Someone has a relatively mild infection, is not hospitalized, feels "normal" in a couple of weeks, at most." / X
🧵 I think @jonfavs and others don't understand. THIS is how Long Covid happens in the vast majority of cases (including mine): 1. Someone has a relatively mild infection, is not hospitalized, feels "normal" in a couple of weeks, at most.
x.com
November 30, 2025 at 4:25 PM
Consider the experience of my daughter, who has #hEDS, #MECFS, #Craniocervical instability, #Chiari, and #POTS. Her illness has largely followed a relapse-recovery paradigm, with extremely slow recoveries following two major relapses. 7/24
November 30, 2025 at 4:25 PM
Why is this important? One reason is that patients and caregivers can report on the longitudinal progression of chronic illness, something that is difficult and expensive to study through conventional research. 6/24
November 30, 2025 at 4:25 PM
This is important, but not sufficient. It helps researchers refine their existing ideas, but doesn’t necessarily expose them to new ones. It also means other researchers are deprived of access to the first-hand experiences of patients and caregivers. 5/24
November 30, 2025 at 4:25 PM
There has been a lot of progress in recent years in developing mechanisms for patient input into research. But this mostly consists of providing researchers with feedback on the researchers’ own ideas and methods. 4/24
November 30, 2025 at 4:25 PM
In particular, I argue that more medical journals indexed in PubMed should accept hypotheses papers and case studies from patients and caregivers. This will help ensure their perspectives are readily available to medical researchers. 3/24
November 30, 2025 at 4:25 PM
My basic argument is that better and more direct mechanisms for patient and caregiver input would help the medical research field make faster progress in understanding and developing treatments for chronic illnesses like #LongCOVID, #MECFS and #hEDS. 2/24
November 30, 2025 at 4:25 PM