Sasha
Senior Member (Voting Rights)
I haven't been following this - does the article (at the link) call for new actions and so deserve a new thread?
I don't really think it's a good idea to continue lobbying the NIH like this. Public agencies weren't meant to be lobbied. They aren't elected, and they have little motivation to respond to public will. It's a much better idea to lobby congress to take action or put on pressure.
It is a follow up letter after their meeting with NIH, so thought this thread was best suited.I haven't been following this - does the article (at the link) call for new actions and so deserve a new thread?
It is a follow up letter after their meeting with NIH, so thought this thread was best suited.
ah, I see what you mean. The twitter campaign was launched earlier, but don't know if it has its own thread here. Feel free to start oneI think it's good to have the follow-up letter here, but if they're announcing a new action, I think it would be good to have an additional, new thread so that people who are no longer following this thread realise that there's something that they should be doing. I'm not sure if people have been doing the action they call for all along, though!
@JaimeS, do you know?
Personally, I think the pace of progress with one percent funding is virtually zero.
Right now we need Dr. Collins to hear from you, the community, on how necessary it is for the NIH to take bold steps to urgently produce outcomes for people with ME. Dr. Collins needs to hear from every single person whose life has been affected by ME that we demand full throttle action now.
I wondered if it was a new action (in which case I think it should have a new thread) or an existing one that was having attention drawn to it again in a different context (in which case it probably shouldn't).There is an action attached to the tweet / article if that's what you mean, @Sasha ?