03-09-2016, 02:13 PM
My baseline point is that having all of the T1s is a waterfall right now. Splicing the pathogen itself allows you to cultivate the holy grail very, very fast. My problem with the entire availability is that coupled with the pathogen stability analyzer and predictive subsystem, I could create at least one T5 within 10 minutes. While I understand that it is disappointing that you find out that none of the T5s are possible in your round, there has to be a better way to remedy this than providing a holy grail.
If you're suggesting that the reagent dropping system broke somewhere along the way, I can get behind that and check it out. Would fixing it alleviate these issues though or would it surface again in the manner of "it's unfair to expect people to drop reagents in there"? In the end, I don't believe that the microscopic examination of symptoms is critical to the pathologist's job. It is a really helpful thing for a traitor but once it's fixed I expect you to go the extra mile to find out which bit of the flavour text is OK.
As for flavour symptoms, I literally ran out of ideas halfway through. Ideas are welcome, patches containing reasonable symptoms are even more welcome.
If you're suggesting that the reagent dropping system broke somewhere along the way, I can get behind that and check it out. Would fixing it alleviate these issues though or would it surface again in the manner of "it's unfair to expect people to drop reagents in there"? In the end, I don't believe that the microscopic examination of symptoms is critical to the pathologist's job. It is a really helpful thing for a traitor but once it's fixed I expect you to go the extra mile to find out which bit of the flavour text is OK.
As for flavour symptoms, I literally ran out of ideas halfway through. Ideas are welcome, patches containing reasonable symptoms are even more welcome.