Who would became Human guinea pig ?

In the far future, when some treatment will require humans for tests, i think everybody wants to take part at the project.

i guess lot of us is going to try any treatment in a blind way or at least supported by not well grounded theories.

I’m asking to myself if research group release some experimental drug (maybe tested only on rats) is better to advertise it ? or is better wait for a standard safety protocol ?

I think far future is very far.

i hope the contrary but i know is far

but in the case that some hi sperimental treatment is available, u would try it even if it’s risky?

however look it positive, also about our struggle to find solutions.

if there r stories like lorenzo’s oil, is possible that we obtain some result

There is no point in even thinking about this. There is a good chance that it will never happen. However, you will be glad to know that i would be more than willing to be propeciahelp’s official guinea pig.

in some way we are already guinea pigs lead by ourselves
If we r going to try everything before a target drug is synthetized, could be good organize our attempts

Now ther’s an antimicotic trend,
well, the experimenters have to take same dosage for the same time without other meds, and will see results

I really hate allot of the negativity on this forum sometimes.

Do you think the guys on here, especially the new guys who are close to “checking themselves out” need to here anymore negative stuff about how there will never be a cure so don’t even bother thinking about it.

I didn’t come to this site for 4 months for that same reason.

Have you looked at the research threads on this site? About the stuff that is going on right now? I sent my DNA to Italy along with a bunch of other guys and now they may be close to pinning down what is causing this, I have very little knowledge but from what Awor is said they have some pretty good evidence that points to a cause.

People are finally seeing some progress with this issue after years and years if anything now is the time to really turn up the heat on this and get some real action and funding going on. Its so simple to send emails, and make phone calls it amazes me that people complain on here endlessly but wont spend a few minutes writing an email to the FDA, a newspaper, magazine or their congressman or senator.

Of course I know a good portion of the people on this site have done this, however not all have. We need everyone who comes here, even if they don’t register but think there might be a slight chance they could have been hurt by this medication to write/email someone in the media/political/medical communities expressing their problems and letting the world know about them, and that something must be done.

people don’t give up, i know that some pfs studies are now travelling all around italy in different congress, so be patient