This survey only has 96 responses so far.
Please fill this out. When you finish, you can see % results of experiences graphed out.
This was established by the PFS Foundation to collect data so if you can’t donate, you can at least participate.
Is there a way to see if I already did it? Can’t remember.
No, this is not true. I contacted the PFS Foundation about this survey and they have no record of it, nor any knowledge of it. Further, it has been in use since 2013.
Where did you get the link to this survey and who emailed it to you? If you don’t feel comfortable posting publicly, PM me.
This survey is in no way associated with the PFSF and I want to make sure this is not some dubious ploy by the drug company to collect info for legal purposes.
I think this is the one moonman started last year, Mew.
Ah yes, here is the original thread:
viewtopic.php?f=1&t=8058&p=72263&hilit=survey#p72263
Thanks for the reminder… carry on. 
Well, that was the best survey for every symptoms though.
CORRECTION: This is not from PFSF. My mistake.
Sorry about that. I made an incorrect assumption.
I suppose it could still be helpful for anyone who is interested in seeing how many other guys share the same side effects from PFS. I have no idea if the data is being used for any other purpose though.