It is through KP Colorado, but a specific doctor is doing the research and has a limit of 300 people. If I glean info from the zooms this and next month, I will share it with the covid group here. My LC may have been easier for doctors to accept because the cardiovascular symptoms were blatant. There are a number of peer-reviewed (aka boring) medical papers on covid and LC in ResearchGate. Research is a slow process. LC is a difficult invisible disease and I hope you have a good support network. Pretty much we have to change our lives, how we exercise, diets, and manage the emotional and physical tolls of the disease.