I am a patient at Cleveland Clinic Mellen Center. I received a letter from them that they wanted to use my MRI's, blood work, etc. as part of their new research study. Just wondered do you all allow your medical information to lots of studies? How do I know it is something I should do? Are there ever problems with having all your information out there? I want to do all I can to stop this disease but not sure what are good things to do like this?? Hope this makes sense. Here is a link I found that tells about MS PATHS https://consultqd.clevelandclinic.or...care-research/.
Thanks..,,
Thanks..,,
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