Very interesting. Fibromyalgia the "F" word of the medical world hahahaha!! Not to thrilled with the idea that my brain is small and sickly though.

I'm just happy to know that doctors are really looking at this and this doctor seemed to understand that not every fibro patient is the same so the same med's aren't going to work for everyone.

Narey,thanks a million for posting this link.It makes more sense than any other explanation, that I have heard.It is encouraging to know that there are those that are interested,in the research.Current available medications help,but they are not the answer to"HOW DO WE FIX THIS?".Thanks for sharing.........Cheryl

Extremely interesting! Thanks for posting this, it's greatly appreciated.

Hugs, Susan

Thanks for posting this-- The more we know the better!

I'm listening/ watching it now. (I did like that FIbro is the "F~word" of medicine. )

I have been telling folks that I have a Central Nervous System problem when I don't want to get into it, but do want them to realize I've got a problem. To explain the faltering gait, the inability to do certain things....

wow, AND... I had read up on psychological stuff and from what I read, I figured I needed some dopamine modulator. I take an antidepressant that works on both the serotonin AND the epinephrine but from what I've read, I could use some help in the dopamine area as well.... and that seems to be what he's saying!

hm, when I went to look for correct spelling, I came upon this page. It's got a LOT of info: https://www.neurorelief.com/index.php?option=com_content&task=view&id=149&Itemid=48

It was so nice to hear someone who an advocate for this so called F word disease. I wish I could be his patient. How nice that would be. I know he not a Rhuemy, but he seems to understand more than some of them I've talked to. Nice post. Thank you.
Blessings
Cathy

I'm thinking how wonderful it would be to have these studies done, and have a copy of all the charts made of myself.......then I could show people and say, "Hey, this is me, and yes, there really IS something wrong!" Thank you for this video clip. There were a few things I'm not sure I agree with completely, but it's very interesting and I want to listen to it again tomorrow......

This is awesome! I am so encouraged. Thanks for sharing this Narey. I'm going to pass it on to my family and my doctors.

Well damn it, gimmie some dopamine!

Great, my brain is shrinking...lol. Already knew it was broken when I was told I had Epilepsy 11 years ago. Now something else is assaulting it. Gonna be a vegetable in 20 years :-P

Fantastic post!! Watched every minute of it and can't wait for my husband to see it. He's hella smarter than I am and can process the info better.

Pam

Thanks, I am going to listen later, bit difficult at moment with my son playing playstation :)

What about the neck thing? How many here have neck issues?

I sure as Hell do.

OMG! I was just looking up intermittent cervical cord compression and I found this page.

http://www.nfra.net/nfra-2006-symp.htm

This lists all the studies discussed in this video, who authored them, etc... My dad's gonna love this.

I like the way he explained how all of us have similar symptoms but different causes. You just have to narrow down which symptoms mean what. This is where competent medical professionals would come in handy if only they would.

This is awesome, cutting edge information! I am forwarding it to my doctor! Thanks!

That is amazing! I am grateful that Dr. Wood is asking every question he can. I love that he is truly driven by research. I pray that he encourages others to seek answers for all of us that can not.

Thank you for sharing this.