USA: National Institutes of Health (NIH) intramural ME/CFS study

The ME community does not have a shortage of critics! But we do have a shortage of ME advocates who are public figures, and despite being ill, do their best to make positive changes!

I feel your posts are seeming more “off topic” to me, and deserve their own thread.

 

PACE was a trial of talk therapy and exercise.

The intramural NIH study is a deep biological investigation.

What's the comparison? Some people like to throw bombs with dumb hashtags and are still living in 1986. They also haven't spent time at NIH in the study. So, yes, a small faction of patients tried to derail the NIH study. Instead they're getting a deep biological investigation of PEM that was designed with input from patients. That's the last I'll say because I'm not interested in engaging with such a negative crowd in rehashing a debate that happened two years ago.

 

@B_V

Please don't shoot the messenger.
I'm only reminding you of what is out there. I am not writing about 1986 but 2015.
"Negative crowd?"( BV) I am alone in bringing this to your notice as a response to the question you posed.

 

@Binkie4
If you have any legitimate questions you can email Dr. Nath at: avindra.nath@nih.gov
I initially had questions that he graciously answered and in so doing availed any concerns I had about the study
and convinced me of his dedication to helping find us some answers. Were fortunate to have him heading this study up in my opinion.

Edit to add a thanks to those taking part in this study.

 

@Trish

"It does seem a pity that people are rehashing old worries which have beeneffectively shown to be incorrect"

(Apologies for not being in yellow)



Please do you have a link?

 

I am puzzled by why pwME who may have legitimate questions or even misgivings should be discouraged from expressing those. This is a forum, after all.

What if anyone individual espousing support for - and even participating in - an endeavor is wrong?

If he/she is right, good.

The discussion is part of the journey.

 

Great expression " the discussion is part of the journey". I thought that is what this forum is about. Thanks @duncan .

 

I think the study has some exciting elements, and other that might be interpreted as downright counter-intuitive, if not unnerving.

I have no reason to believe this observation is inclusively accurate, as much as I respect and admire @Trish.

Hopefully, just more informed. As advocates, I would think we should all agree on being more informed is better than less.

 

In 2015 and 2016, the group ME Advocacy expressed their misgivings by making a concerted effort to stop the NIH study before it began. They circulated a petition calling for its end and took other actions. Vicky Whittemore, who has nothing to do with the intramural study, took the brunt of a lot of the negativity. (She is involved exclusively with the extramural ME/CFS funding and the inter-institute ME/CFS working group and she is a very important ally for patients inside NIH.) The ME Advocacy people compared the study to PACE, which displays a distinct lack of critical thinking skills. They also spread misinformation on twitter and Phoenix Rising, claiming the study was about non-specific fatigue using Fukuda criteria. This effort was an extremely poor display of the worst side of the ME community. Fortunately, their misguided and poorly-informed attempts were unsuccessful and an important study is underway.

The NIH has made some missteps with the study, most of them in the realm of communications. But they've learned a lot and they explicitly involved patients in the design of the study (which is good). If people want to be suspicious of the brick walls of NIH because of the ugly history of neglect, then they are free to do so. If they decide to focus their anger on Brian Walitt for things he's said, then they are free to do that. But if people aren't willing to fully inform themselves by looking at the study protocol and the other information that is out there, then they should probably try to learn a little more.

I'd also encourage anyone who has had correspondence with Nath or Walitt to post those messages so everyone can benefit from the exchanges.

 

This is one history, certainly.

I am worried about its telling, not to mention bemused and unsure of its implications when taken in context with the early release of disease characterization.

The functional disorder control was only one issue.

Revisionist history can be a dicey thing.

After all these years, maybe we need to be careful.

 

I've heard NIH tales that aren't as sweet, although they are not directly related to ME/CFS.

Having said that, there are some tests I would embrace, some I would not, and if capable, some researchers I would decline, some I would prefer.

But I am only a patient who is unsure and who has questions.

 

Maybe they can do a group of longer patients later? If things are that much different, possibly treatments could be quite different.

I guess they didn’t want to pack everything into this one study to publish faster (or not so slowly anyway)?

 

That’s fascinating and encouraging, and thank you for sharing your reassuring thoughts.

I can’t apply as 1) sick too long 2) too ill to travel 3) too ill to recover from exercise test and 4) even too ill to have so much interaction over several days, but it does sound very hopeful that the results will be interesting.

 

I have emailed Dr. Nath and Brian Wallitt and both replied to my questions and were helpful. Dr. Nath didn't answer my most recent question about what the exact numbers are now in phase 2 but Brian has answered that here. I so wish the study wasn't so slow....my fear is not living to see the benefits but I have no doubt that they will uncover so much important info and answers. I think Dr.Nath is very approachable, down to earth and genuine.
As for the NIH, they are not investing enough in ME by a long shot. I am a severe patient myself but not entirely bed ridden. A sense of urgency is desperately needed but it ain't coming from the NIH as we all know. So I have no rose tinted specs on as my life is on the line.

 

For the research nerds, here's a shot of the amount of bloodwork they did post-exercise challenge. It was a lot but thankfully the same IV worked for most of it.

 

Damn, I'd be looking like a ghoul if they'd taken that much from me.

 

Whoa! Considering that some studies have shown low blood volume, how did you have any blood left in you after all that?

But seriously, thanks for sharing the photo!

 

I am hopeful the study will bring a greater understanding of the invisible elephant in the room.

We know there is an elephant in there, I think I saw his trunk move.