Conners Corner:
Conners Corner gives information on FMS and CFIDS. Good links. It tells how this has effected my life and how I cope with these conditions. Also included are my friends and pets as my page would not be complete without all of them.

Photo: Not Available.
URL: Conners Corner
E-mail: conners@rogers.wave.ca

Site Number 3:

This is the Home Page of the CFIDS/FMS Web Ring.


Photo: Not Available. URL: CFIDS/FMS Web Ring.
E-mail: Jagannatha@cheerful.com

Site Number 4:

Lindsey's CFIDS Page:
My personal story of my battle with CFIDS, along with a selection of links.

Photo: Not Available.
URL: Lindsey's CFIDS Page
E-mail: eponin19@idt.net

Site Number 5:

Nichole's Cave: CFS Tunnel:
I'm 20 years old, sick since I got mono when I was 15. I have a wonderful "net-hubby" -) named Bruno who lives in the Netherlands.
My site has info about CFS, info on CFS mailing lists and IRC channels, descriptions of CFS, and links to other sites. Other parts of my site has general homepage stuff, and stuff about the Netherlands.

Photo: Available
URL: Nichole's Cave
E-Mail: nichole@netnitco.net

Site Number 6:

MarilynK:
I am a Registered Nurse who retired due to the evolving, under-treated, and mainly undiagnosed CFIDS/FMS/MPS symptoms in 1994. I have had great success in bringing my FMS and MPS in remission in 1997, and continue to attempt to improve my quality of life by being a lab rat. My CFIDS/FMS Information Page: The CFIDS/FMS Info Page brings you frequently updated research, alternative and conventional treatments, surveys, and theories on cause.

Photo: Available
URL: MarilynK
E-mail MarilynK@email.msn.com

Site Number 7:

Anna's Bubble:
It's a Bubble full of stuff about me...to do with me....involving me....regarding me....it's basically just one big ego trip..

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URL: Anna's Bubble
E-mail: Ruddock@elk.softnet.co.uk

Site Number 8:

Robyn's CFIDS/NMH/FMS Pages:
My personal "life with CFIDS" web site, several CFIDS (and related illnesses) links, a comprehensive Neurally Mediated Hypotension (NMH) web site with several NMH and Tilt Table Test links, and the home of the CFS-20s Internet Mailing List

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URL: Robyn's CFIDS/NMH/FMS Pages
E-mail: tobyn@gate.net

Site Number 9:

Virtual Home Town CFIDS Center
CFIDS medical and personal links

Photo: Not Available.
URL: Virtual Home Town CFIDS Center
E-mail: deborah@virtualhometown.com

Site Number 10:

Joanne's CFS/ME web site:
Info about cfs, some personal details, links to other sites, how i live with it, things i've tried to help symptoms

Photo: Not Available.
URL: Joanne's CFS/ME web site
E-mail: joanne@idl.net.au

Site Number 11:

(W)Riting the Body in the Wild.
Hopelessly academic (but not hopeless) and narrative accounts of CFIDS and the "feminization" of disease. A scholar's home page with personal accounts of living with the wild body of CFIDS in a world where "normal" = "stable," "healthy" and "productive." Alternative realities proposed.

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URL: (W)Riting the Body in the Wild
E-mail: aporia@oursquare.com

Site Number 12:

Chronic Illness...Thief of Dreams...Vandal of Life
The day to day life of coping with an invisible chronic illness while living with the "healthy". The disappointments, pain, adjustments, and insults that contaminate and infect the entire family.

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URL: Thief of Dreams
E-mail: JUDI@CYBERENET.NET

Site Number 13:

Debbie Schofield
I am a mother of two children, Susie (7) and Joey (3) who recently and finally got a diagnosis. I am not thrilled with it but at least it finally has a name. I am still in the process of trying to learn all I can. So far it doesn't sound too promising. I go in spurts, as to how diligent I am in the search.. I have been seaking THE answer for over 4 years but from all the research I have already done, it appears I have had it much much longer.
We are now living in the Cincinnati area but have lived in Columbus Ohio, Charlotte and Lumberton N.C. and Fort Lauderdale and the Fort Myers areas in Florida.

Photo: Available
URL: fibro
E-mail: winman@one.net

Site Number 14:

Fibrom-L Mailing List Info, Fibromyalgia Books,
This page offers help for those subscribed to the Fibrom-L Mailing List who wish to learn how to make more effective use of it.

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URL: Fibrom-L Mailing List Info
E-mail: cdavis@webtk.com

Site Number 15:

Web Spinnings
Information on CFS, FMS, and NMH, with a bulletin board for posting and answering questions. This is the home of the CFS-20s webring, and Photo Gallery! Also information on myself and tarantulas.

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URL: Web Spinnings
E-mail: pfiefe@hotmail.com

WRITER'S HAVEN
I live with my real life hero of 26 years, our daughter, an Old English Sheepdog whose loyalty exceeds her intelligence, and a mouser who prefers lounging on lawn furniture to hunting.
My hobbies include: reading, travel, art, and music.
An artist by nature, a writer by trade, and a humanitarian by design, my cup is always half full. I led a very active life until fibromyagia invaded my life. Now I face the biggest challenge of my life.
If you'd like to know more about me, please visit my web site, WRITER'S HAVEN, a sanctuary for aspiring writers, where dreams become reality.
Cheers!
Terry:)))

Photo: Available
URL: WRITER'S HAVEN
E-mail: terryt@mail.uconect.net

Site Number 17:

Sheryl's Story
When I first got on line in 96, I had no idea there were so many people on the web that have Fibromyalgia. I was please to read their stories and it made me feel so much better to know that other's understood how I felt and knew the pain we live with on a daily basis. When it came time to "build" my own web site, the FM page was the most important to me, I was hoping that other's could read my page and find some comfort there for their own pain. It's expanded to several pages now, I have alot of quotes that I used to hand write in Calligraphy, something I can't do anymore. The quotes have always put a smile on someone's face and have had alot of meaning to others.
I invite you all to come with me "Somewhere Over the Rainbow" and have a little dream to help relieve the pain.

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URL: Sheryl's Story
E-mail: fannie@techline.com

Site Number 18:

Helen's Homepage
Learn about Fibromyalgia, a Tribute to Diana and also other links

Photo: Not Available.
URL: Helen's Homepage
E-mail: -hells-@geocities.com

Site Number 19:

Maureen Black:
After 26 years plus of working, I was involved in a motor vehicle accident in 1994 which triggered my present physical state, such as MPS (Myofascial Pain Syndrome), FMS (Fibromyalgia)and CFS (Chronic Fatigue sydrome, hypothyroidism, osteoporosis, plus other pleasantries uncalled for.
I’ve contributed to the CPRC which commenced last summer and all the visions and goals of the CPRC is also a forceful aim for myself. I live in an area where there is minimal help, but I’ve tried somewhat to induce our message to as many professionals as possible. My ambitions throughout has been to reach as many collective assemblys in order to end this battle of the CHRONIC PAIN PATIENT...and finally be heard not silently but loudly by those who have neglected us for too long. I recently was able to place my own web site on the Net as another means of trying to grasp people in all walks of life. I thank God I was given the added strength and ambition to do so. Let's Stop the Pain and Start the Humanity is Maureen Black's homepage

Photo: Available
URL: Stop the Pain and Start the Humanity
E-mail: mbblack@baynet.net
ICQ# 3152182

Site Number 20:

FYI - Info. on Different Chronic Illnesses
My site is dedicated to educating others about different chronic illnesses as well as providing a place for individuals to go to ease their pain or take their mind off of their discomfort.

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URL: FYI
E-mail: gloreb@cheerful.com

Site Number 21:

Still in queue


Photo: Not Available.
URL: FYI
E-mail:

Site Number 22:

Carol's CFS Realm on the Web
My CFS Site contains a lot of information, resources, and links to various CFS Sites on the Web. As well it offers links to Other pages of CFS Sufferers.

Photo: Available
URL: Carol's CFS Realm on the Web
E-mail: ladycare@webruler.com

Site Number 23:

Debra Richardson
Resources for Chronic Fatigue Syndrome and Fibromyalgia

Photo: Not Available.
URL: Healthwatch@ immunesupport.com
E-mail: info@immunesupport.com

Site Number 24:

Janet Weiner
I have links to many CFIDS and FMS sites as well as GWI and fun sites as well. I have included my medical history story on the site as well. I have to update some of the information soon!


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URL: Janet's CFIDS/FMS/ME Home Page
E-mail: jnw1220@aol.com

Site Number 25:

Snow White
friendly and fun, contains cool and Christian links, creater has CFIDS

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URL: Snow White's Home Page
E-mail: sarah-joy@usa.net

Site Number 26:

toonster
Hi all,
My name is Mike. I have had Fibromyalgia since a car accident in 1969. Of course the it was not too bad then because I had a young body. But I went to many different doctors and had hundreds of test and xrays done. No one could tell me what was wrong. In 1976 I went through a very bad spell but still no one could give me the answer as to what was wrong with me. Finally , in 1986 I was told I had Fibromyalgia and was told that it would burn it's self out in 6 years, HA HA HA! I was forced to retire in 1987 because I could no longer do my job. There is still not alot known about Fibromyalgia so we who suffer from this illness must keep putting the information out there for others.

Photo: Available

URL: FIBROMYALGIA
E-mail: toonster@inreach.com

Site Number 27:

Siobhan
On my site theres info about me (and a picture if the world is ready) and my family, plus links to my friends sites, and information about ME/CFS/CFIDS with links to useful pages in case you want more. Hope you like it!!

Photo: Not Available.
URL: Pritchard Page
E-mail: Siobhan@gurgle.globalnet.co.uk

Site Number 28:

Lady Freedom
Hello everyone! CFIDS/FM ... DSS has afflicted me over two decades now. Over the years it has been my fortunate gift to incorporate new-found freedoms to replace those stolen from me by chronic illness. This page is mainly to encourage, uplift, and comfort all people who suffer with illness. New information is consistently updated, and any new healing methods that have helped me will also be included.
(((featherhugs))) <>< Lady Freedom

Photo: Not Available.
URL: FMStory
E-mail: ladyfreedom1@geocities.com

Site Number 29:

Anna
In 1997, I was the "lucky" recipient of a diagnosis of FMS and CFIDS at age 38, after having occasional symptoms for 25 yrs. I had worked since I was 14. Married at 18. Had 2 daughters, a hysterectomy, and a divorce before age 28. I was the single mother who thought she had to be Super Woman and squeeze 30 hrs of work into a 24 hr day!
I found a wonderful man whom I married in June 95. Then, I got my wake up call on Oct 6, 1995, when I went down for the count and never got back up. Life isn't the same as it was before---thankfully!
I appreciate people and life so much more than ever. If I went into remission today, I wouldn't go back to that lifestyle! I am more at peace than ever inside, but my physical outside remains a challenge.
My favorite Sufi expression: "When the heart weeps for what it has lost, the Soul rejoices for what it has found."

Photo: Available
URL: Anna's Body, Mind & Spirit Home Page for the Chronically Ill
E-mail: oldworld@webzone.net

Site Number 30:

Still in queue


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URL:
E-mail:

Site Number 31:

Rachel
Nice colors, good information. It includes my story and information on several diseases. FMS, CFS, SAD,Depression and more.

Photo:Available
URL: Life Link
E-mail: MyRedRoseL@aol.com

Site Number 32:

Still in queue


Photo: Not Available.
URL:
E-mail:

Site Number 33:

Natalie Smith
A christian site and how God sustains through it all. Designs, music, adoption, living with illnesses, dealing with death.

Photo: Not Available.
URL: Crown of Glory
E-mail: sonshine@jps.net

Site Number 34:

K.A. "Thumper" Thompson
I started my web site last year soon after I was diagnosed with FMS. It began as a source for basic information on the disorder, and I have since added a personal story (the obligatory How-I-Came-To-Have-FMS tale) and a link to Danhjeun Breathing Exercises.
The breathing exercise page was added after discussion on the alt.med.fibromyalgia newsgroup about a need for nonmedicinal methods of pain control. A fellow martial artist helped with the site information, and my son modeled for numerous photographs to show breathing positions. We hope that at least some people will find these useful in pain and stress reduction.

Photo: Available
URL: Fibromyalgia
E-mail: MAWired@prodigy.net

Site Number 35:

Still in queue


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URL:
E-mail:

Site Number 36:

htbol - Happy to be on line
htbol has two great sites, one focuses on CFS and the other on FMS. For information on this member please see Entry #38 below.

Photo: Available
URL: Adventures with Autoimmune Diseases
E-mail: htbol@vol.com

Site Number 37:

Ruth
I am a 47 yr.old mother of 4. Married to a wonderful man, Aurele, for 26yrs. Have suffered with FM and osteoarthritis for the past 8 yrs. I am a crafter, sewer, artist and overall down to earth person. I love making new friends and am fairly new to the computer(since Oct./97) My homepage is a total reflection of me with my stories and information about topics that are affecting or have affected my life. Please come by and visit and maybe we too can be friends *G*

Photo: Not Available.
URL: Ruth's World
E-mail: rgallant@usa.net
ICQ: 3678199

Site Number 38:

htbol - Happy to be on line
Adventures with Autoimmue Diseases is written for those suffering and for those searching for help understanding and coping with Connective tissue diseases and Autoimmune diseases. Lupus, Fibromyalgia, Raynauds, Sjogren's Syndrome are some of the terms I had to learn and research after I was dx'ed in '96. My symptoms confused most doctors and rheum's to the point several gave up on me. I am still on my search for help and spreading the word about all these mysterious illnesses so that maybe someday a cure will be found. Adventures in My Life, is my story about my history and search for help continuing with updates to be added as I learn more and things change. Adventure was the best word to fit my site because I have taken what other have actually said, and posted their words for others to read. Realizing that your not alone is one of the biggest and most comforting things that can come to you if you suffer with one of these diseases. My life has been greatly blessed by the family I have met on the internet. It is my life line. Please stop by my site and read the words of these magnificent people who share their hearts openly with each other.

Photo: Available
URL: Adventures with Autoimmune Diseases
E-mail: htbol@vol.com

Site Number 39:

Cheryl
I have provided some tips & tricks for dealing with this disease as well as some "creative misdiagnoses" doctors have made on me for 45 years before a real diagnosis was made!

Photo: Not Available.
URL: Fibromyalgia - Your Pain May Have a Name
E-mail: cheryl@bnatural.com

Site Number 40:

Liz
a site by someone with fibro & several related illnesses, with lots of other stuff too.

Photo: Not Available.
URL: the fibro & related section at liz's humble abode
E-mail: artemis@serv.net

Site Number 41:

RAFT
RAFT - Responsible Adequate Fibromyalgia Treatment is dedicated to the adequate, responsible, accurate & expidited education diagnosis, treatment, research & services for those with fibromyalgia & those who live with them or treat them

Photo: Not Available.
URL: RAFT
E-mail: raft@dixie.ncplus.com

Friends of the CFIDS/FMS Ring

JAF Ministries