Voices 4 Cure For ME/CFS

Visit our website at http://www.blueribboncampaignforME.org

We now have a group on YouTube for you to join and post your ME/CFS awareness videos. http://www.youtube.com/group/BRC4ME
Please turn your sound up for this video. My voice is soft, and mic is not great.
This is my first video.
It is now captioned and possible to translate from English to your language.

A video about severe M.E./CFS and why we are asking you to use your moments to volunteer to help us out of our darkness. 28 million voices will be heard.

Category:

Nonprofits & Activism

Tags:

• Voices4Cure
• Chronic Fatigue Syndrome
• ME/CFS
• non-profit
• activism
• Myalgic
• Encephalomyelitis

[komodiakarma]

Bravo...It's so difficult for people to understand what this illness actually does do our lives. I am one of those who holds out hope for the day we will all be free... I have been far worse than I am at the moment...But it waxes and wanes. Somedays are far more challenging than others...Blue Ribbon..

FIRST PLACE..Like SEABISCUIT. We are all champions that just need a chance.

[killandra23]

Thanks...I like that 'We are all champions that just need a chance."

If you have any ME/CFS videos you'd like to share please add them to the BRC4ME group!! I'd like to collect a huge amount of them by next years campaign. Patients stories. Stories found from news explaining what has been holding us, back..all of it.

Trying to bring us under one banner!!

[ItStartsWithUs]

Andrea, you're doing such excellent work - I applaud you. Keep pushing, and keep making a difference. You're in my thoughts and prayers.

[killandra23]

|Thank you so much!! I will keep pushing! I want the world to know what ME/CFS and to wear and think blue to support it!! I and WE are so grateful for your support.

[1nerdse]

Nicely done. add my voice, fibro 23 yr, CFS 13 yr, worked until 9 mo. ago, demands of job too much, was going to make some terrible mistake from overwork, being sick, caregiving my mom when I could barely deal myself. I have finally realized I can no longer work full time the traditional way. It hurts. It feels like all I ever was is now gone, but I know that's not true. I am still mom, wife, RN, teacher, and most of all, Christian. I could not live like this without God's help.

[killandra23]

Thanks for adding your voice!! Do you have a webcam or a voice recorder? Can you video or tape your story and send me photos..I can put up your voice in video..let your story be heard.

I get by with the serenity prayer.

[pilomaya2012]

thanks so much brave soul! we are doing the best we can, but together we xcan get this cause heard. i am living in the dark. i such a strong person and have been through alot before this illness even. now i have it. i wish for a cure. my life is ruined in some ways.

[BondGirl070]

This is a great video. I had written more but for some reason it wouldn't accept it. Yes, we must be a voice and get the information out there.

Check out my video: It's All About M.E., Myalgic Encephalomyelitis... with more to follow.

[killandra23]

Thanks so much everyone!! I appreciate the support. So hard to be in front of the camera. I prefer being behind it. But if it helps..It's worth every moment.

[bodieangels]

5 STARS for The Whisper that WILL be HEARD !!!

You are lovely and your Courage and Strength shows thru the LCD screen.... *hugs* for all you do 4 ALL of us...

Please share Andrea's other videos ALSO with anyone you know that is a PWC's or has a family member or friend that

has ME/CFS,,,,,, "Voices 4 a Cure" Here we Come .....♥♥♥♥♥