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Hello again friends!
I have a big announcement that I want to share. We have been working very hard on launching a new website, and it has finally arrived! It is for people who have 'invisible diseases' (CFS/ME, Fibro and Lyme Disease.) The site focuses on what connects us, rather than what divides us in our health. The symptoms of CFS/M.E., Fibro and Lyme are almost identical. The more that we bring our voices together, the more likely we are to be heard!
I am writing a column on it too, though we have just begun and the content needs to be expanded some. They are still working out some details and such, but I just couldn't wait to share some good news with everyone. Please visit the site at www.InvisibleDiseases.com
There is also a facebook group that was JUST started. Here is the link: http://www.facebook.com/home.php#/group.php?gid=67434616607
CALLING ARTISTS AND BLOGGERS!
We are also looking for people within the Invisible Diseases (ID) community who are artists, AND have established websites. We would like to help the community on an individual basis, and send patrons to your site, and hopefully help you out financially by purchasing some art items. InvisibleDiseases.com will not ask for a penny from you! The purpose really is simply to raise awareness and hopefully put a little more money into the pockets of "Invisible Diseases" artists!
We are also looking for links to active blogs about ID issues. We will help to generate traffic to your blogs. The only thing that we ask in return for posting your websites on our site is to mention InvisibleDiseases.com on your site. That also helps to insure that these artist / blogger websites are indeed within the ID community as well.
Please let me know if you have any other ideas or input about this. There really is strength in numbers. Again, the more that we bring our voices together, the more likely we are to be heard!
Wishing everyone happiness and continued health! Sending love...
Franky
AKA: Dr Dolan ;-)
I have a big announcement that I want to share. We have been working very hard on launching a new website, and it has finally arrived! It is for people who have 'invisible diseases' (CFS/ME, Fibro and Lyme Disease.) The site focuses on what connects us, rather than what divides us in our health. The symptoms of CFS/M.E., Fibro and Lyme are almost identical. The more that we bring our voices together, the more likely we are to be heard!
I am writing a column on it too, though we have just begun and the content needs to be expanded some. They are still working out some details and such, but I just couldn't wait to share some good news with everyone. Please visit the site at www.InvisibleDiseases.com
There is also a facebook group that was JUST started. Here is the link: http://www.facebook.com/home.php#/group.php?gid=67434616607
CALLING ARTISTS AND BLOGGERS!
We are also looking for people within the Invisible Diseases (ID) community who are artists, AND have established websites. We would like to help the community on an individual basis, and send patrons to your site, and hopefully help you out financially by purchasing some art items. InvisibleDiseases.com will not ask for a penny from you! The purpose really is simply to raise awareness and hopefully put a little more money into the pockets of "Invisible Diseases" artists!
We are also looking for links to active blogs about ID issues. We will help to generate traffic to your blogs. The only thing that we ask in return for posting your websites on our site is to mention InvisibleDiseases.com on your site. That also helps to insure that these artist / blogger websites are indeed within the ID community as well.
Please let me know if you have any other ideas or input about this. There really is strength in numbers. Again, the more that we bring our voices together, the more likely we are to be heard!
Wishing everyone happiness and continued health! Sending love...
Franky
AKA: Dr Dolan ;-)
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