Welcome to Phoenix Rising!
Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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Thanks for posting this, Cort. I'm a patient at Dr. Bateman's clinic, and I can tell you that I've never seen a more dedicated group of people. They have considerable expertise in research, and it could benefit all of us with CFS much more if they had better tools and more funding.
CBS knows his databases - he worked on a similar project in Stanford that brought the department in alot of money via increased productivity. He can do the same here - he can help her to maximize her work and that will benefit us all. :victory::victory:
We can do this with little bits from each of us.
I donated my little bit. Thanks for putting this together CBS. What a great idea.
This project will make sure that patients who may not qualify for a study are stored in the database and on the short list even before the new criteria are entered.
Kati you're a doll. That's a real sacrifice! I hope we can get you back that subscription somehow.