Covid-19 Resources for People with ME
Expand your activism repertoire with these great examples of advocacy from other groups and movements.
I am a very active person mentally always looking for new information online , in all areas of my conditions. My comment is they are using genetic testing for banks, for confirmation of desease.
Why don’t patients have the option to join genetic study’s But also with the option to be able to buy their genetic information. Instead of using 23&me. the low cost would fund a lot of grants once the word was out to the sick.
And world possible find some of our health answer at the same time. It just makes since to me. Same with biology labs if we could break down all patients information and find catergorys like high cortisol and you could send a low cost test to patient, and they would have confirmation of cortisol levels for doctors. I know it would be a lot of work in data entry but to be able to pull symptom or desease associative with ME subtypes and all People in date base with same listed in system . we could test a larger subject group faster
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