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Your help ensured the National ME/FM Action Network of Canada romped through to the Semi-Finals of the Aviva Community Fund competition. Now we need to vote again and see them through to the Finals and a chance at that all important $100,000! Vote online, each and every day from 02 - 11 December 2013!
You did it! Your online votes helped get the National ME/FM Action Network of Canada through to the Semi-Finals of the Aviva Community Fund competition.
Now it's time to vote again. You can make your vote each and every day, between 2nd and 11th December, and together we can try and get them through to the Finals and a real chance at that $100,000 jackpot!
Voting is so darned simple even I could do it!
Not voted before? Not a problem:
Go HERE and click on REGISTER in the top right corner.
You’ll be asked to enter your email address and a password. If you prefer, you can register using your Facebook account.
A message will inform you that an email has been sent to confirm your registration. Go to your email inbox, select the email and click the link provided to confirm your registration.
Now you can either use the competition search function to find our entry, “May 12th”, or click HERE. Then click on the VOTE button and you are done for the day.
If you have voted before:
If you have voted before then just go HERE, click VOTE and you are done - just don't forget to come back again on the following day!
You might need to SIGN-IN with your email address and password or if you can't remember your password, ask to change it and an email with a link will be sent to your in-box.
After voting, you might also like to leave a comment at the foot of the page, one that perhaps speaks of the importance of raising awareness for your disease in a world that remains largely ignorant of its existence not to mention the personal and societal impact.
To date the May 12th Fundraising Group has won over $10,000 for the National ME/FM Action Network of Canada and worldwide over $650,000 for charities. All has been made possible just by having the support of people like you to vote for our nominated causes in competitions like this one. Your votes can help make such a difference - so please vote every day.
Please consider sharing this article to your own Facebook page and help bring greater awareness to the competition:
You can use the share link (the green pop-out located on the left-hand side of the Phoenix Rising Home page version of this article), to 'like' on Facebook, to 'tweet' or to recommend the article on other applications.
Or, if viewing this article on the Phoenix Rising Facebook page, then simply 'share' and your friends and family might see it and perhaps they will be inclined to vote as well - especially if you add a message of encouragement.
Thank you all for your continued support.
The National ME/FM Action Network of Canada
The Action Network's contest statement is as follows:
“Our dream begins with awareness. May 12th Awareness Day is a chance for the 750,000 people living with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia (FM) to be seen and heard! These illnesses are real; the people are real; and they need help NOW!
ME/CFS and FM are chronic and severely disabling illnesses. They are as disabling as MS and are more prevalent in Canada than breast cancer, MS and AIDS combined! People are frequently bedridden and become isolated from friends and family – invisible in their own communities.
Dr Nancy Klimas, an expert in both ME/CFS and AIDS, was quoted as saying “A CFS patient feels the same or worse than congestive heart failure. The same or worse than late stage AIDS. If I had to choose between the two illnesses I would rather have H.I.V.”
These illnesses do not discriminate. All races, men and women, rich and poor, adults and children can be afflicted. It is devastating when a child is forced to cope with such a disabling illness.
We are on a mission to bring awareness in Canada for this community of people living with these illnesses and to set the stage for fundraising for research and more physician education. To date our volunteer efforts have been handcuffed as not only is our community very disabled, many are in financial distress. The illness limits our ability to raise the substantial amounts required to mount a large scale awareness event and to fund the desperately needed research. It is the dream of our community to erase stigma and finally be taken seriously by friends, family, researchers, government and those in our local communities.
This contest gives us a chance to fund a nation wide awareness campaign for 2014, the 22nd Anniversary of May 12th Awareness Day. It will also define Canada as a world leader in raising awareness as this day is also an international event. It will not only benefit 750,000 Canadians, but it will indirectly benefit the 20 million people that suffer worldwide.
We will use the funds to hold events in as many communities across Canada as possible which will lay the foundation for a strong network of organizations in Canada and future fund raising for education and research. We’ll connect with every MP and provincial/territorial representative in Canada and have May 12th proclaimed in cities nationwide. We’ll sport t-shirts, carry signs and have engaging speakers in as many communities as possible.
Each event will have its own venue but will share elements common to all. In order to unite the larger community across Canada we’ll also advertise in national and local papers, and, if funding permits, on TV and radio. As education is so critical, we will also target physicians, medical students and other health professionals with our letters and/or advertising. Brochures and a white board medicine video are planned.
We believe with awareness, will come action! Our community is desperately in need of treatment facilities and funding is required to support research and our scientists. A successful May 12th will bring many rewards for years to come. These activities will not only benefit us today, but they will be an investment in our future.
Aviva’s gift will help to unite our national and local communities and make a difference to the lives of many Canadians. It will give us credibility in our quest for treatment and a cure and hope for a better tomorrow.”
To quote Helen Keller – “Alone we can do so little; together we can do so much.”
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