This site is invaluable for sharing information. Unfortunatley, members want to talk about how we have candida or how stupid it is to think we have candida.
This site is so precious to us, it’s sad to see it not used to its full potential. When I first signed up here, my knowledge about our condition grew exponentially. But as my individual knowledge caught up with the collective knowledge, I came to a stand still. I grew frustrated, along with others. Bickering started over which theory was the stupidest.
I hope this vicious circle is coming to an end. And I believe it is. A few of us are rallying behind autoimmune theories and we are attempting to acquire the data needed to expand theories and come up with possible treatments. Imagine in a few months time when more and more members get immunoglobulin bloodwork done, and when awor presents his findings. Our knowledge will have grown exponentially.
Each member here has the possibilty to contribute the finding a cure to PFS. It could be something as small as getting bloodwork done and sharing your results. It could be just by donating money to awor’s team.
On the other hand, each member here has the possibility to set us back in finding a cure. And we’ve seen that before. Solon probably set us back a couple years with his nonsense and insanity. And as a result, xhorndog tapped out. We could’ve used his smarts, ambition and (seemlingly abundant) resources.