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| Name: | Brenna |
| E-mail address: | brenna@yahoo.ca |
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| Name: | Marilyn N |
| E-mail address: | mjnadulek@yahoo.com |
| Comments: | I am trying to figure this Fibromyalgia thing out. I've been told by a Chiropractor I've been going to that it is a "junk diagnosis for pain"! I have a herniated disk in my neck (car accident) I am not going back to him. I just set up an appointment with someone/a MD who is supposed to know about this but I will have to wait 3 months for my appointment.
Can SOMEONE help me understand this! |
| Name: | Christina |
| E-mail address: | dore@animal.ufl.edu |
| Comments: | After a bad accident in November 1993 wherein my L5 was hyerniated, L4, 5, & 6 bulging, C2, 3,& 4 buldging with years of chriopractic adjustments and massage therapy I can lead a semi-normal life. I have had several people tell me that I have fibromyalgia. But I have not ever been diagnoised. Who would I see to get a diagnosis? |
| Name: | Neo |
| E-mail address: | Neo@yahoo.com |
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| Name: | Sandy |
| E-mail address: | sboswell@ccrtc.com |
| Comments: | Have any of you tried the "Trigger Point Therapy Workbook" located at http://www.amazon.com/gp/product/1572243759/002-4549638-7434419?redirect=true&_encoding=UTF8&v=glance&n=283155
(Read some of the ***** reviews.) You have got to try this book! My daughter has been diagnosed with FMS. She said she felt like raw nerves were exposed on her feet and had felt that way for weeks. I bought this book for her. Within one or two hours after locating and massaging the trigger points for the muscles in her foot that were causing this pain, she was TREMENDOUSLY better. Her feet felt normal. She has located and massaged many other trigger points with outstanding results. She is beginning to have hope that this will help relieve much of her pain. |
| Name: | elizabeth |
| E-mail address: | elizabethkolling@yahoo.com |
| Comments: |
Thankyou for this wonderful website, i feel like i am no longer alone. I was diagnosed with FMS 1year ago , i battled for several years with pain before i was correctly diagnosed by a rhumetologist. I was very relieved to had finally had a name for what i was going through, any suggestions would be greatly appreciated, i will try anything at this point. the pain i have has already attacked just about every part of my body, i feel depressed three times a week, i have such hard times getting out of bed anymore, and can barely hold my eyes open at work, i am not ready to give in to this syndrome, i have 4 children and am only 40 years old with a wonderful husband. I am scared of becoming disabled , and dependant, and am afraid that if i dont find help through this soon, i may succomb. please e-mail me with any ideas. Thursday June 8, 2006 8:43pm |
| Name: | Cynthia |
| E-mail address: | rebecka0815@cox.net |
| Comments: | I am happy to see this cite. It was great to know that am not alone in this diease. I changed doctor recently because I the docotor that I had made me feel worst then I already was feeling, and the last straw for me was being told that it was in my head. I have been suffering with this for 4 years and I didn't understand why no one could help me with the pain. The first appointment with my new doctor and I was told what I had. This was a load lifted off of me. Now I can start to find the best medicine and pain management that will help me better deal with it. I have hope now that I will feel better. |
| Name: | ARLENE |
| E-mail address: | ene29@yahoo,com |
| Comments: | I HAVE BEEN SITTING READING THIS WEBSITE AND I FEEL SAD THAT SO MANY PEOPLE SUFFER FROM ALL THIS PAIN, INCLUDING MYSELF. ONE OF THE NEW MEDICATIONS THAT HELPED ME IS LYCRIA. MY DOCTOR JUST GAVE IT TO ME WITHIN THE LAST TWO MONTHS AND I CAN AND COULD TELL A DIFFERENCE WITHIN A WEEK OF TAKING IT. I TAKE 100 MG IN AM AND 100 MG AT NIGHT. IT HAS HELPED A LOT WITH THE PAIN. I HOPE THIS HELPS. |
| Name: | proudpapa |
| E-mail address: | proudpapa007@gmail.com |
| Comments: | I have had Fibromysia For some yrs now I just hate it when people tell me its all in my head and you just need to learn pain management I've tried that And it does not help.
I have accepted That I have a very painful disease and I will probably have it for the rest of my life. I am getting sick and tired of being sick and tired Sure the pain meds help somewhat then theres the side effects of those. I am a single dad and my life is at a standstill have no social life, friends when i manage to get a job i cant keep it because either im in so much pain or im too tired to do my job correctly. I think im finally going to have to give into this disease and go on a disability plan of some sort which i have been not wanting to do at the age of 29, This disease has taken over my life and my daughters as well i sure hope she does not get it. I found this website by mistake and im kinda glad I found. I can identify with everyone that signed this guest book. I also hope and pray everyday that they will find a cure to this disease. |
| Name: | Robin |
| E-mail address: | robinlaurice@cs.com |
| Comments: | Has anyone been taking mangosteen juice and experiencing a worsening of their symptoms with Fibromyalgia? I have been taking it for about 2-3 weeks now and I feel like I am going through withdrawl or something. I'm wondering if I should adjust my dosage? |
| Name: | blueangel |
| E-mail address: | blueangel4737@yahoo.com |
| Comments: | dear readers ihave been diagnosed fibromyaligia,degenerative disc disease.this pain is awful!
i fell at work,never had any back problems until i fell.doctors gave me the run around.this happened in 1999. my life today is terrible,i do not understand these diseases or how i got them from falling.i just know the pain is unbearable sometimes.is there any that can give me some information or know where i can get information. thank you for this web-site reading the other columns helped me alot. blueangel4737@yahoo.com |
| Name: | Royanne |
| E-mail address: | rsja@shaw.ca |
| Comments: | I have been diagnosed with fibromylsia and i think that this site is just awesome... I have been taking toradol for pain but it isn't working anymore..I was wondering if anyone has any more ideas on what pain meds work....
Ty Royanne |
| Name: | Anna Jennings |
| E-mail address: | ardore74@yahoo.com |
| Comments: | I have something I really want to share but please excuse me ahead of time for filling up a lot of space. I know in my heart that this can help some of us.
This is a letter that I wrote resently to a woman who had posted her fibro story on a website: Hi Jessie, You don't know me but I found your website through google. I am currently a graduate student getting my PhD in Nutritional Epidemiology at the University of North Carolina at Chapel Hill. I have had back problems on and off my whole life but I never had them seriously checked out until two years ago when the pain became so bad I couldn't get out of bed. I was diagnosed at that time with a herniated disc and what they suspected was fibromylsia. I tried to stay in school but the pain got so bad I had to take a year leave of absence. I came out to Colorado to live with my husband for a year and focus on my health. Since then the doctors have discovered (using MRIs) that I actually have 6 herniated discs, and they now feel that I am genetically predisposed and may have what they are calling degenerative disc disease. I am 29 years old and have spent the last year taking about 5 different kinds of muscle relaxers (cyclobenzabrene- flexeril, methocarbamol, tizanadine, valium and morphine), Ultram (a pain killer), and was recently prescribed an anti-epileptic medication called Zonegran. The doctors are recommending for me the- soon to be approved by the FDA- prosthetic disc surgery. From my academic background what I'm painfully aware of more than anything else is that the meds might be taking away the pain for now but they are destroying my liver and kidneys. A few weeks ago a friend of mine (knowing how much pain I am in and that my life has essentially come to a stand still) told me that he had been introduced to something that might help me. I was really skeptically at first but I checked out the scientific evidence that they were telling me about on the entrez pubmed scientific database (check out google to find it) and searched under garcinia mangostana (the scientific name), mangosteen, and xanthones(the antioxidant in abundance in the fruit) for evidence and surprisingly found over 30 years of scientific evidence. I was sold! I have been taking it for a couple of weeks and have been able to stop taking the muscle relaxers, the Zonegran and have halved my intake of the Ultram pain killer. I still have some pain but some doctors who have become big supporters of this juice say that it can take up to three months to see drastic effects). My energy is definitely increasing back to my norm. Anyway, I am really excited about what has been happening to me and wanted to share it with anyone who may be hurting like (or even worse than) me. I have paid a membership so that I can get the juice wholesale and have it delivered to my house so if you want to check it out or have any questions please feel free to email me. I would check out the websites mangosteenmd.com and wellspringsclinic.com (essentially a cancer clinic) to see what some of the doctors have to say and read some testimonials, and get some info about the juice (website xango.net). I found one testimonial on the website mangosteenmd.com that made me really hopeful that you all might be interested to read: I am a distributor for Xango and I have Fibromyalgia. I just wanted to tell you a few of the problems I have encountered with my Fibro and tell you about some of the successes I have had with the Xango Juice and my Fibro. I have had Fibro for over 8 years. I have been on many pain pills, muscle relaxers and anti-inflammatories. I took all of these before I was introduced to more natural and healthy ways a couple of years ago. I started seeing a chiropractor and he started me on different supplements. The Supplements and the adjustments helped but I was still having some issues. The issues I was having was.. I had a severe case of irritable bowl syndrome, acid reflux, chronic headaches, sore stomach, leg aches and leg cramping, abdominal cramping, sleep disorders and always being tired and never having enough energy. I also have an ovarian disease. Polycystic ovarian disease. I was having excessive bleeding and cramping and my cycle was very irregular. My O.B. Told me that this disease is linked to my insulin and my blood not being balanced. Being young and single you can imagine this puts a big damper on things. Dr. Lindberg my chiropractor introduced me to Xango close to two months ago. I was very skeptical. I have tried so many vitamin supplements and natural things. ,But having tried just about everything I figured why not. I started taking Xango and within a couple of days I noticed a difference. My stomach wasn't sore. I didn't have the burning acid come up my throat. My abdominal cramping and irritable bowls were almost gone. I continued to take it. My chronic headaches started disappearing. I wasn't having all the aches and pains and the leg cramping. Also my blood was being neutralized and my insulin was as well so My cycle became regular and not so heavy and I wasn't cramping as much. So I investigated the product. WOW.. I couldn't believe that it had Xanthones and Anti Oxidants. All the things that I needed to be healthy ,but especially the things I needed because I had Fibro. I went to a seminar to learn more about anti Oxidants and Xanthones. It is vital for everyone especially when you have Fibro. One thing with Fibro is that your body is to acidic. Xango helps neutralize the blood and helps your body to not be so acidic. Plus it is a natural anti Inflammatory, natural anti fungal, natural antibiotic, natural anti viral, natural anti bacterial, natural anti depressant, natural anti anxiety. This is only a few. The great thing about this product is It's natural, It's safe, It has medical and Scientific background and it works. I am so Thankful that I was told about this product. I have seen great success with my family and friends and many of the patients I come in contact with daily. It almost sounds to good to be true.. But once you research why we need antioxidants and xanthones it all makes sense as to why it has so many wonderful affects on people. Becky T., Orem, UT I hope this all helps, sincerely, Anna Jennings email: ardore74@yahoo.com |
| Name: | James O. Murray |
| E-mail address: | omurray@homexpressway.net |
| Comments: | Have F/M since 1985.Have tried everything in the book. Oxycontin help more than anything. Best wishes to all who suffer this terrible disease. |
| Name: | Shelley |
| E-mail address: | shelljon6@aol.com |
| Comments: | I have been suffering from Fibro for quite sometime, it is now the worst it has ever been, i am recently married in May and I do not think my husband quite gets it because I had been in pretty good shape for about a year, i told him i had this condition but I do not think he believed me. I am sick of feeling this way (PAIN) everywhere it is very hard for me to get out of the bed, my kids all say you are sick all the time mom, i can never do anything, that breaks my heart. they are teenage twins, i try to do it i force my self because I hate to disappoint them. also the other day my dr. told my that fibro is all psychological!! can you believe that! I cried, i know it does have psychological components but i am done with him. my mother has systemic lupus eurithmatosis that is the serious one that attacks the organs, her doctor wants to see me, and he is a UofM, the best doctors are there so i will go there. right now i am in physical therapy for 3 months 3times a week, it hurts just to get there. i have so many meds it makes me sick, now my doctor told me i need to quit my job. i need some support and you all seem like a wonderful people. and i know that all of you understand how i feel physically and mentally. thanks for listening :) |
| Name: | mugu |
| E-mail address: | mugu mugu@.com |
| Comments: | please i am here so keep off!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! |
| Name: | Ilse |
| E-mail address: | ilamb5@compuserve.com |
| Comments: | I was diagnosed with Fibromyalgia about 2 years ago. I had
terrible pain in my arms, shoulders, and hands. I got better for awhile, but now it is so painful to get out of bed in the morning. My ankles, knees, legs, and arms just ache. Having trouble sleeping at night. I am 56 years old and wonder what this will be like in the next 10-20 years. I am on an antidepressant but it does nothing for the pain. Can anyone give me some advice on what kind of treatment to get or any diet and exercise info. |
| Name: | eric |
| E-mail address: | new_dis@lycos.com |
| Homepage URL: | http://www.CasinoLasVegas-Online.com |
| Comments: | Great Site!Go On!!! |
| Name: | Jill |
| E-mail address: | STUNBALEANAHS @SALISBURY.NET |
| Name: | Jill |
| E-mail address: | STUNBALEANAHS @SALISBURY.NET |
| Name: | Jill |
| E-mail address: | STUNBALEANAHS @SALISBURY.NET |
| Name: | Ariza |
| E-mail address: | ariza@cuteandsingle.com |
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| Comments: | Phenomenal job on your site! |
| Name: | Steve Monson |
| E-mail address: | www.parttimemagic@yahoo.com |
| Homepage URL: | http://www.juiceplus.com/+sm03030 |
| Comments: | It's great to see other Whole Food Nutrition Websites out here.. We need to get the word out that correct diet and exercise can help many. Keep up the good work.
Steve |
| Name: | Peggy Richards |
| E-mail address: | happypiglet4@yahoo.com |
| Comments: | My 18 year old daughter was just told that she must have Fibromyalgia because her joint pain in her knees, ankles, wrists and elbows don't seem to be caused by anything. Feb, 2002 we went to Hawaii and she was bitten by something on her thigh. When we returned she got sick and lathargic, we though she had mono (her boyfriend got it while we were in Hawaii). Tested for Mono three times, always negative. Then since she still had no energy and her joints hurt, they started drawing blood for everything under the sun. Always came up normal. When she got back from her summer job (in considerable pain at times in her knees and ankles) had her tested for Lyme Disease. Negative. MRI's on her knee and ankle turned up nothing. More blood work was done, now her second Rheumotoligist says Oh, you must have Fibromylasia. Just get on with your life, see you in 3 mos. She is only 18, had to quit college because she couldn't continue to walk to classes, is currently taking an AT Home correspondence course, she can't work because standing kills her knees and ankles. They don't hurt all of the time, but when they do she sobs. She takes Vicadin when the pain is really bad. We are currently looking for a Naturalpath doctor. Does this sound like Fibromylasia to anyone else? The pamphlet we were given at the beginning ruled her out because she didn't have enough or the right symptoms. Are we crazy or continuing to search for help??
Waiting in Sumner, WA for anyone's ideas. PS. Your sight is great!! |
| Name: | Michelle Capolino |
| E-mail address: | LOUISENMICHELLE@wmconnect.com |
| Comments: | I have been diagnosed with FMS for nearly a year now and MVPS for just over 3 years, but believe that I've had both since I was a child. My support group is my family and friends, although some more than others. I lost my job on November 8, 2002, due to absence/leave early because of my conditions. Now I am considering filing for disability, but am still unsure about it. My body says go ahead, but my mind says I don't want to not work for the rest of my life. Has anyone else felt this way? I live in Gadsden, Alabama, and our access to adequete medical care is approximately 60 miles away. Plus the doctors are scared to prescribe pain medicine due to the uproar over oxycontin a few years ago. My mother also has fibromyalgia, but she says to suck it up and act like it doesn't exist. Every time she does this, I keep thinking about the proverb of walking in someone else's shoes. Anyway that is all for now. |
| Name: | Pat Goodwin |
| E-mail address: | pgoodwin51@aol.com |
| Comments: | I've been correctly diagnosed for 3 years now, but had Fibro/CFS for probably 15 yrs.I'm an Educational Consultant specializing in learning disabilities / stress reduction counselor. Sights like this are great sress reducers
We know we aren't alone or crazy. We can share tips for coping with our problems, Physical, Social and emotional. Together we will find a cure for this devastating disability. Things I've found that help , accupuncture, massage therapy,aromatherapy,Rainforest herbs, hot baths with epsom salts, water aerobics, gentle exercise,stretching, good counseling, a great doctor,prayer, meditation lots of rest on those bad daysa positive attitude ,laughter, hope and your sense of humor, understanding suportive friends and relatives. Don't associate with negative people that are ignorant dufusses, that say you look healthy etc. ad nauseum. Good luck my sisters and brothers!!. Current news flash,they may have found the cause and cure for our disorder---Mycoplasma fermentans,a nasty litttle bacteria that also causes Gulf War Syndrome,CFS, and possibly arthritis. Which is why I saw so many parallels between us and my Gulf War clients. The treatment is one year on doxycycline,minocycline and a few other antibiotics (which aren't mentioned in the article) but not penicillin because it can't penetrate the organisms' cell walls and kill the little bugger.Check out Dr.Nichol's research at www.immed.org. I'm taking printouts of the articles to my Dr. tomorrow. Let's keeep our fingers crossed!!! |
| Name: | Sandy |
| E-mail address: | healthandlogic@hotmail.com |
| Homepage URL: | http://www.ctds.info/ |
| Comments: | Congratulations on a well done fibromyalgia site from a fellow fibromyalgia sufferer. |
| Name: | Kathie |
| E-mail address: | farmgalkb@aol.com |
| Comments: | Just recently diagnosed with fibromyalgia after 7 years of excruciating pain and many doctors and many neurological tests and tons of blood taken. Enjoy reading comments and don't feel so alone. Thanks. |
| Name: | Big B |
| Homepage URL: | http://www.maintour.com/virginia/hrbhrb.htm |
| Comments: | Very Cool Site - Thank You.
I'm a guest so therefore I sign the guestbook. Now its time for a little vacation. |
| Name: | Christine Pedersen |
| E-mail address: | cmp@basicsofhealth.com |
| Homepage URL: | http://basicsofhealth.com |
| Comments: | Hello, I have contacted by email a few of your people in the Chat Room as I have worked with many people who are now experiencing relief from their symptoms through high quality whole food nutrition.
Are you interested in more information. Christine Pedersen |
| Name: | DONNA JEAN |
| E-mail address: | GOLDENGRL62@AOL.COM |
| Comments: | HI EVERYONE
I WAS JUST TOLD THAT I HAVE FIBROMYSIA FINNALY. I WAS SO TIRED OF BEING TOLD THAT THE PAIN WAS ALL IN MY HEAD I HAD BEEN GOING TO THE DR. FOR 3 MONTHS AND WE COULDNT FIND WHAT WAS WRONG WITH ME WE DID ALL THE BLOOD WORK AND EVERYTHING COMES UP FINE I'M GLAD TO FINALLY HAVE A CLUE TO WHAT I AM FIGHTING HERE I'M JUST TURNING 40 AND EXPECTING MY FIRST GRANDCHILD SO THIS IS SUPPOSE TO BE A HAPPY TIME AND INSTEAD IM SITTING HERE IN HORRIBLE PAIN ALL THE TIME IM TOOOOO BUSY TO BE IN THIS KIND OF PAIN I RUN 2 CLEANING COMPANIES HERE IN NJ IF ANYONE CAN GIVE ME MORE INFO ON THIS DISABILITY PLEASE EMAIL ME THANK YOU AND GOOD LUCK TO ALL, DONNA JEAN |
| Name: | Debbie |
| E-mail address: | Tita40@aol.com |
| Comments: | Hello. Iam waiting yet more) blood work results. My doctor believes I have fibromyalgia. He is trying to rule out everythin esle. I am soon to be 45 and have always been very healthy. Since 1999 I have been visting my doctor on several occasions complaining about arm pain, hip joint pain,adominal pain. All my test results have always come back negitive. The last few months my back is bad and I have visited the chiropractor 3 times a week for a few months. My back is better but my hip and hand are in constan pain. I get the feeling like people must think I bing a "baby".I finally visited my doctor last week in tears after a hip e ray was clear telling him that I have pain and stiffness everywhere. I am very active and busy. I contine to awake ech morning, get daughter off to school, keep a beautiful home, run business, etc.. but it is getting so difficult. I feel ike everyone around me has always expects me to keep going. I don't even want to tell anyone the pain I am in because I feel that they can't relate because I continue to go full speed ahead. It was good to find a place to vent to others who might uderstand
what it feels like to be in constat pain. Thank you for listening. God Bless |
| Name: | Jaide |
| E-mail address: | Jaide_19@hotmail.com |
| Comments: | I have had fibromyalgia since 1997 and even to today I still learn new things about it. I'm now disabled and tring to cope with that has been the hardest thing I have ever had to do. I would like to know more about this site if there is anything to join. I feel that the more I can learn from other people and support from others the more it helps me out. Thanks Jaide |
| Name: | Carol Jahns |
| E-mail address: | CarolJ_SteveB@msn.com |
| Comments: | I am trying to locate Stephen Plotnick, M.D., the Portsmouth Naval Hospital's Rheumologist, specializing in Fibromyalsia. I need his help. If you know his new phone number (I think his quit working at that hospital and started his own business in VA Beach), please either call him with my email address, or email me with a way to contact him, either address, phone number, or email address. I moved down here to Alabama, and ALL the doctors have their heads up their collective ass. I've been here 3 months, and still have not had either my primary doctors, a Rheumologist at UAB, 2 Pain clinics, a mental health doctor, or PT to differentiate the treatment he began with me back in March 02. I'm worse and no one wants or can help. Each doctor thinks the other should. HELP ME. |
| Name: | freda@yahoo.com |
| E-mail address: | freda_2002001 |
| Homepage URL: | http:// seeinthings |
| Comments: | Just came upon this site and decided to write.I'm 41 ,married ,2 kids and a home in Tenn. I"ve had fibro,osteo,and ra. for about 6 or 7 years. So there are days I feel like doing nothing. If anyone can relate e mail. Gotta go for now. |
| Name: | Barbra |
| E-mail address: | thisisbap@msn.com |
| Comments: | I have had Fibromyalgia, Lupus, Parkinsons, etc. for some 20 years. Last year my physician placed me on Nurontin (which is an anti-seziure medication) for my Parkinsons. It has done more to aleviate my Fibro pain than anything else has done so far. I also started accupuncture about the same time and my pain level is so much more tolerable now. My prayers and best wishes go out to all of the Fibromyalgia suffers in the world. |
| Name: | Martha Cassidy |
| E-mail address: | snunn@soltec.net |
| Comments: | My doctor diagnosed me with Fibromylasia 1 1/2 yrs ago. Along with the pain, I was deeply depressed. My doctor put me on Paxil, which has helped alot. I still have bad days and I have began having more "tender" spots. I am luckier than most though. Hopefully more info can be found to help with this disorder. |
| Name: | Kelowna |
| E-mail address: | kelowna@dealmaker.com |
| Homepage URL: | http://www.aboutkelowna.com/Kelowna-BC-Realtors.html |
| Comments: | Kelowna Real Estate, About Kelowna B.C. Realtors & Real estate: |
| Name: | JoAnn Medlock |
| E-mail address: | SXYEYESNVA@AOL.COM |
| Comments: | HI MY NAME IS JOANN, I LIVE IN HARRISONBURG VA, I WAS DIAGNOSED LITTLE OVER A YR AGO WITH FIBROMYALGIA, I AM HAVING A BAD TIME WITH MINE VERY PAINFUL,IT STARTED IN MY LEFT ARM, I THINK I HAVE HAD IT FOR A FEW YRS, BUT COULDN'T GET NO DOCTOR TO DIAGNOSE ME, IT HAS SINCE MOVED INTO MY RIGHT ARM NOW, IT IS GETTING TO A POINT NOW TO WHERE I CAN BARELY DRIVE ANYMORE, I HAVE TO DEPEND ON MEDS FOR THE PAIN, EVEN THEY ONLY HELP TO A CERTAIN EXTENT, I WAS CHECKING OUT YOUR SITE, I REALLY ENJOYED LOOKING AT IT, I SEE I AM NOT THE ONLY PERSON FEELING LIKE I DO, , THANKS JOANN |
| Name: | James Devlin |
| E-mail address: | jamesdev31@hotmail.com |
| Comments: | Diagnosed with FMS in January 2002,Culmination of twelve years (negative)testing for various other illnesses.
Now I have the diagnosis,I know what I am up against and I can start to fight back by trying different treatments until one works(or helps). Here in England,it has become almost impossible to claim disability benefits from New Labour Government with this illness.Why don't ALL doctor's recognise our pain? Best Wishes Jimmyd |
| Name: | Sindy |
| E-mail address: | Tea4me2@aol.com |
| Comments: | Am starting disablity application, I was diagnoised fibromylgia 3 yrs ago, and am no longer able to work 49 hrs a week, I have lost so much use of my hands, my staying power is about 10*15mins., before they go numb. That doesn't bode well for a florist.Am trying latest high protien and low carb diet.My doctors are very empathic but know admit they know very little about this. |
| Name: | Mercia |
| E-mail address: | mercia@american-eskimo-dogs.com |
| Homepage URL: | http://www.american-eskimo-dogs.com |
| Comments: | Your work on this site is very good! |
| Name: | -=\\DAYSTAR//=- |
| Comments: |  your site is GREAT! keep it up! and if you get the chance come by my site! 
cross the stars for a treat! |
| Name: | Rachel Brenner |
| Homepage URL: | http://216.122.180.47 |
| Comments: | Hello from Texas
|
| Name: | Diane |
| E-mail address: | advisor@alotek.com |
| Homepage URL: | http://www.alotek.com |
| Comments: | Please visit our www.alotek.com site! |
| Name: | masoud shirgholami |
| E-mail address: | masoudshir2001@yahoo.com |
| Name: | Tammy Williams |
| Homepage URL: | http://216.122.180.47 |
| Comments: | thanks |
| Name: | Sandy |
| E-mail address: | txtwister8@yahoo.com |
| Homepage URL: | http://don't have one |
| Comments: | worried about my mother. We have both been diagnosed with fibromylasia, although hers is alot worse than mine. |