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EPISODE NOTES    
Host Name: NFA
Show Name:

Lynne Matallana, President, National Fibromyalgia Association


Date / Length: - 1 hr
Description:
Tags:

Comments

Sher

Sher

Nice broadcast, good job for the first try. I'm sure it will get easier. Corin you have a lovely voice. It would be nice to have a picture of everyone who is speaking. To put a face with the voice. Thank you!

kim julson

kim julson

great info

MelFM

MelFM

I also want to add that I have a great support group online.Daily Strength it is the best online support group for fibromites that I have found..Thanks for doing this show today

MelFM

MelFM

I wish it had been on the full hour but it was good

GRENNY4031

GRENNY4031

WHAT I GOT TO HEAR OF THIS SHOW WAS GOOD AND INFORMATIVE BUT!!!! THERE WAS OVER 10 MINS LEFT WHEN THE SHOW WAS ENDED AND I NOTICED THAT COMMENTS WERE NOT ANSWERED IN SOME WAY. I RECOMMEND FMAWARE.ORG TO EVERYONE. IT IS THE MOST HELPFUL WEBSITE I HAVE FOUND ON FIBROMYALGIA. I HAVE A RHEUMATOLOGIST THAT IS PRETTY GOOD WITH TREATING FM. BUT I JUST THIS WEEK HAD TO GO TO A PSYCHIATRIST BECAUSE I NEEDED ON 2 DEPRESSION MEDS. IT IS A VISCIOUS CYCLE WE LIVE IN FM FEEDS DEPRESSION FEEDS FM FEEDS DE

Bob Anderson

Bob Anderson

Thanks for a such an informative broadcast.

GRENNY4031

GRENNY4031

PLEASE DO I CALL THE NUMBER ABOVE TO ASK A QUESTION OF LYNN?

GRENNY4031

GRENNY4031

WHAT NUMBER DO WE CALL TO ASK QUESTION?

GRENNY4031

GRENNY4031

DID I MISS THE SHOW I HAD TO LOGIN AND IT WAS N AND I CAME BACK AND NOTHING ON

Lizzie Lu

Lizzie Lu

Too short, not enough interaction with listeners or posts.

Lovinkeno

Lovinkeno

I loved listening to the podcast and look forward to more opportunities to receive hear from Lynne. Thank you for all that you do for all us fibromites. Lynne!

FOGGYDEE

FOGGYDEE

thank you for the info. though....lol

FOGGYDEE

FOGGYDEE

Boo!

FOGGYDEE

FOGGYDEE

started at 10am and only 1030am why is fibromyalgia awareness chat over already?

FOGGYDEE

FOGGYDEE

chat is suppose to be an hour? dont go...

gtrembley

gtrembley

I was just recently diagnosed with FM, but I believe I have had it for about 6 years. The first thing that happened to me was a lower back injury and then was stricken with Mono. I would like to get some sort of groups or recognition in the state of Kansas. We seem to be behind on the awareness here. I would love to find a FM group somewhere near or in Topeka, KS. I have two sisters that also have FM. One is disabled and has been for about 15 years, the other sister is about like me, she h

Dr. Lois

Dr. Lois

Do you have press releases available for May12 so I can help get word out locally?

Lovinkeno

Lovinkeno

I have FMS & would love to participate in the upcoming walk/run (so would my & husband & 17 year old daughter who also has FMS) but cannot afford the entrance fee, are there any waivers available?

FOGGYDEE

FOGGYDEE

Hi Lynn I've had fibromyalgia for over 20 yrs. and cannot work since 1995.

Hope1

Hope1

Watch NFA at 10am CA Time

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