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CFIDS & FMS FOGGY BLOGGERS + ADD YOUR SITE (15 members)
We are a chronic illness message board forum created by and for those with the disorders of CFIDS, FMS, CMPD, ME, ADDISON'S, CHRONIC MIGRAINE, and other chronic pain related "invisible" illnesses. We encompass many of them and offer friendship, support, HOPE, and help for those struggling daily with these things. We are a fun and genuinely loving group who is willing and able to reach beyond ourselves to give a bit of time to others suffecommunity. You are welcome to join if you offer much of the same. We are a G-rated community and ask that you meet the criterea for maintaining that G-rating. (no exceptions to this rule!). We prefer message board formats with a standard home page to refer to whenever possible. This encourages active participation in the community as a whole, and repeated visits. The Foggy Bloggers title refers to the days when the disorders take over our thought processes, and we get "fogged in" just trying to think through the day, and we need some friends to relate to that whole thing. We discuss our aches, pains, fog, family, friends, cats, dogs, spouses, frustrations, aggravations, etc... but... we also help support one another in ALL things. We encourage, uplift, offer kindness, help, hope and much valuable time for one another. If you wish to join our community, please plan to actively support not only your own site, but send those who come to visit you, to the other sites listed on the community. We exist to help and promote each other fully. Failure to support others on our list will result in removal from the community. Please keep your sites/forums current. If you do not have daily participation at your site, you will not be considered for this community. Update often. Participation can be nominal, but there must be daily visits by at least the site owner/administrator or moderator. If your site is an outstanding support group site that you wish to promote in our community, and you have good things to offer... We'd love to hear from you! MBA Boards, or restricted Boards will not be allowed in the Foggy Bloggers. You must have Boards, Blogs, Sites that are open to the general public and non-descriminatory in nature. We are now part of the larger interactive writing community called, "WRITER'S BLOCK". Our foggy bloggers portion of the community is called, "THE CFIDS/FMS & RELATED ILLNESS CHATTERBOX".

Blue Butterflies
Blue Butterflies is an open minded, cacommunity environment for sufferers of ME/CFS and FMS. We welcome friends and loved ones as well. We have 22 members, with our regulars being quite active. BB's has a range of activities from art to reading to discussion and research. We also have our own book shelf and blog for members, several eye friendly and pain free skins to choose from, fun emoticons and our own private chatroom with regular live chat sessions. Come and join the fun, we look forward to meeting you.

25% ME GROUP
The 25% M.E. Group is a unique nation-wide community based voluntary group. We have 2 members of staff paid for by the Community Fund and volunteers (most of whom are chronic ME sufferers). We provide a range of services to people affected by severe M.E. (Myalgic Encephalomyelitis), many of whom are virtually housebound and or bedbound.

CHATTER BOX - CFIDS/ME, FMS, & Related Chronic Invisible Illness Community
Formerly 'SafetyNet Friendship Board',we have moved to a new domain HERE: http://thecfidsandfmschatterbox.yuku.com/directory We are a community that pertains to the daily coping skills of those dealing with CFIDS, ME, FIBROMYALGIA, CMPD, MIGRAINE DISORDER, ADDISON’S, and other related chronic "invisible illnesses". If you suffer with any of these or other daily pain inducing illnesses, this is the place for you. You will find coping helps, loving friendship and support. You can come and vent, cry, gripe, moan, and groan if it’s what you need. We are friendly, and open and willing to lend a listening ear and helping hand. You are not alone in your struggle. We truly understand, so drop in and say “hi” and introduce yourself and share your struggle. A burden shared is a burden lightened. Feel free to share your personal experiences, faith, the things that are near & dear to your heart. We do not judge here. We offer only our friendly support, always. And you are always welcome. AND...if you have a site, blog, board, that offers information and support for the chronic illnesses mentioned, or any chronic pain inducing invisible illnesses that people must deal with in life...feel free to submit it to our Foggy Bloggers Community.

WRITER'S BLOCK
Writer's Block is an off-shoot of our original chronic illness support group, and the inspiration of it’s owner, linda carlson. It is a place of rest from a weary day. A place where writers may place their own special works to share with the world. It is relatively new and just getting a good start, and could use creative and talented writers to contribute and help build the community. It was started by linda, who has endured CFIDS, FMS, & CMPD for well over a quarter of a century. If you have a minute, please stop by and add your own creative flair and share part of your talent. Writing can be a very theraputic aid when trying to live with chronic illness. So oftentimes. daily pain, illness, suffecommunity, anxiety, can all spark great compassion and new insight into life's observations. Give us a try. PLEASE NOTE: We are in the process of moving Writer's Block HERE: http://wordsmiths.yuku.com/ YOU MAY VISIT THE ACTIVE LINK LISTED, TO VISIT OUR OLD COMMUNITY - BUT ALSO THE NEW URL LISTED ABOVE.

Fibrant Living
Fibrant Living is a blog and podcast for people with fibromyalgia or other chronic illnesses who want to live a vibrant, joyful life despite their diagnoses.

Jazzie\'S Studio
A collection of my art work including paintings, sculptures,crafts. A place for friends to share a poetry or two. My goal is to inspire and encourage those who are living with CFIDS/FMS and make their lives matter.

Abide| FMS & CFIDS
Abide is a place to gather links to a variety of resources, information, and support for people with fibromaygia and/or CFIDS, and their friends and families. I will also be posting personal reflections on life with fibromyalgia.

Hello My Memoirs
My blog is about me and my life with CFIDS and Fibromyalgia.

Look What the Cat Dragged In
My name is Stephanie. I was diagnosed with FMS in July 2002. My blog is an attempt to document the progession of my FMS and the emotional rollercoaster I have found myself on since my diagnosis.

Life in the Straightjacket
I live in the West Country of England and am determined that ME, Fibromyalgia, Rheumatoid Arthritis and now Lyme Disease will not rule my life. I am equally determined to help fight for proper recognition, bio-medical research and treatment for ME. Cats, cooking, gardening, Greece, writing, millinery, family history and my grandkids occupy me at other times. *** I do have a brain but it doesn't always work***

Texas Medical Freak
You name it, I have it or have a family member that does. Do you think that you should be on the TV show "House" and think, "hey, I need that doctor!" Well, this is the place for you.

L'ombre de mon ombre
An artist and maker living with M.E./CFS, two children, one old dog, 28 chickens, a rabbit and guinea pig

The Flower of Pain
This is a sort of scrapbook about living with FM & CFS/ME.. a diary and a research journal..

Cosmos
This blog is a stress journal. I've been diagnosed with fibromyalgia / Chronic fatigue syndrome (they mean either / or, or both), which I attribute to a lifetime of being bullied.

Chiari Malformation and Related Disorders Support
A support group for those who suffer from and or a family member or friend of Chiari Malformation and its related disorders. We offer support, education and awareness.