I am just curious whether the foundation has a plan to hire more scientists who are dedicated to our problem. I think after more and more warning articles are written and with the expandation of our community and recognition of our condition all over the world there should be a lot more scientists interested at how to solve this disease and even governmental grants should be considered. With governmental help in addition to globalisation there is a realistic chance to fix or at least minimize our condition to the extend that we can function almost like pre Finasterid status
The studies underway are stepping stones to the next studies and on and on, as are our survey and 23&Me project. Everyone needs to take part.
More research will be conducted but at this stage we need to make sure everything builds on what has come before as funding is far from plentiful and getting government funding and assistance will be essential. We need to do the work to get to the point where we would be considered worthy of government funding which means coming and working together and presenting evidence that cannot be refuted
I hope that people are getting behind these ideas, I worry because there are more posts about eating broccoli than taking the 23&Me test.
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I’ve been looking into copies that can perform additional research on our condition, and haven’t found them, but did come across one company that performs tests against almost all known conditions.
I haven’t yet taken the tests, due to costs, but will do so. I do suspect if we reached out to them, they could change their testing a bit to help us, and did comment about this in the science category of the forum.
Their website is: https://aperiomics.com/
comment about this in the science category of the forum.
do you have link?