What do you know about clinical trials?

[Jesmcd2]

~If you missed this the other night like I did, watch it now! It answers so many questions about clinical trials! And how important they are! This webinar gives you sites to look into besides our own mymsaa.org/ms-information/c...

It will also give you questions to ask when thinking about about a trial. Enjoy! I did! ~

BTW it answered my placebo question! ~

youtu.be/oWMcx1BLz7c(Not working as expected?)

Featuring Mitzi Joi Williams, MD

While multiple sclerosis affects all races and ethnicities, minority populations may bear an unequal burden from the disease, including a higher risk of aggressive disease and disability. However, minority populations are severely underrepresented in scientific research.

Presented by MSAA and Accelerated Cure Project (ACP), this archived webinar features expert neurologist Mitzi Joi Williams, MD addressing the role research plays in improving the health of people affected by MS, and the reasons why participation from minority populations is needed to develop treatments for all affected by the disease.

Jes🌠

[rjoneslaw]

thanks I'm doing 1 on fatigue. I look for the trail that don't involve drugs

[Jesmcd2 CommunityAmbassador in reply to rjoneslaw]

Makes sense! How did you find it? rjoneslaw ? 🤗💕🌠

[rjoneslaw in reply to Jesmcd2]

on the national ms society site

nationalmssociety.org/

[carolek572 CommunityAmbassador]

Good Post, Jesmcd2 Thank you for sharing. I am currently in a trial, and have been since my diagnosis. They collect my blood, at every visit, that is used and shared to hopefully find a cure.

[Jesmcd2 CommunityAmbassador in reply to carolek572]

Way to go 👏🎉 carolek572 🤗💕🌠

[carolek572 CommunityAmbassador in reply to Jesmcd2]

It was a no-brainer! Right up my alley, if you know what I mean (IYKWIM)