Fibromyalgia research pdf

Common Questions and Answers about Fibromyalgia research pdf

fibromyalgia

358699 tn?1297650042 I have a theory that Fibromyalgia is caused by build up of Lactic Acid that somehow our body cannot break down properly or in adequate time it is produced when broken down by the liver. Perhaps an inborn metabolic error. I noticed that when I do any physical labor, and it need not be strenuous, the next day I can barely move. Something as simple as painting my bedroom kept me nearly bedridden with tight muscles and burning pain.
Avatar m tn • Seem to get sick from antibiotics I have been tested for a lot of things and am running out of things it could be. I spent some time at the mayo clinic seeing various specialists and was diagnosed with fibromyalgia basically because they just couldn’t find anything wrong with me so I struggle with accepting the diagnosis. All tests and bloodwork seem to come back normal except a moderately elevated anti-histone and slightly elevated liver enzymes.
975514 tn?1325001538 New Diagnostic Criteria for Fibromyalgia Saturday May 22, 2010 Tender-point exams are no longer the only way to diagnose fibromyalgia -- the American College of Rheumatology has provisionally accepted alternate criteria for diagnosing the condition and gauging the severity of symptoms. The diagnostic criteria doctors have been using were established in 1990. Once other possible causes of symptoms were eliminated, diagnosis was based purely upon pain.
181575 tn?1250202386 I am reposting articles / summaries on the treatment management of chronic HepB. "cajim" located these articles which are quite informative. I thought about putting them on a seaprate Health Page but didn't think it was appropriate since we didn't write them. Let's make this a sort of "Unofficial Research Thread" or "URT" for this type of information. Let's keep this URT free of comments.
143746 tn?1301278422 Satish Raj says "Patients with POTS demonstrate a heart rate increase of ≥30 bpm with prolonged standing (5-30 minutes)" ncbi.nlm.nih.gov/pmc/articles/PMC1501099/pdf/ipej060084-00.pdf I will feel dizzy when I stand up and have over 30 beats tachycardia for the first 2 minutes, but then it starts dropping below the 30 extra beats after that. Does this mean that I do not have POTS?
967168 tn?1477588089 //endometriosis.nichd.nih.gov/pdf/2715.pdf Per 100,000 Women Per 100,000 With Endometriosis U.S.
10947 tn?1281407852 Nicolson will also be answering questions on the role infections play and various treatments for ADD/ADHD, Autism, Alzheimer's Disease, ALS, Asperger's Syndrome, Crohn's Disease, Rheumatoid Arthritis, Multiple Sclerosis, Lupus, Inflammatory Bowel Diseases, Hashimoto's, Sjogren's Syndrome, Reiter's Syndrome, Graves Disease, Gulf War Syndrome, Chronic Fatigue Immune Dysfunction Syndrome, Fibromyalgia, Lyme Disease and cancer metastasis. Dr.
Avatar f tn , to educate the medical profession with appropriate guidelines to care for the patients, to fund research and provide treatmentsfor the disease, and critically to ban blood donations and stop the spread ofthis disease. It has failed its mission and goals, denying the epidemics, focusing wrongly on fatigue and psychosocial factors, pursuing meaningless research studies, and subjecting sufferers to uninformed medical neglect andhuman rights abuses.
Avatar f tn What treatment are you going through at the moment? I've had Fibromyalgia for more than 25 years now. There are things that I know help me eg. removal of all sugars and simple carbs, caffine etc. I am also convinced that there is some kind of auto immune difficulties associated with this because I have developed hay fever and also allergic asthma as well as food intolerances.
1505873 tn?1289727703 I was diagnosed with Endometriosis (surgically diagnosed), fibromyalgia, Chronic fatigue syndrome, Thoracic outlet syndrome, hypoglycemia, TMJ (surgically diagnosed) and complicated migraines. This is after 18yrs of going to see so many doctors and being treated like garbage. I was always left to believe that i was a hypochondriac and told I needed medication because I was depressed. What is funny is that I was depressed because I kept on getting disregarded as if I was faking it.
967168 tn?1477588089 //endometriosis.nichd.nih.gov/pdf/2715.pdf Per 100,000 Women Per 100,000 With Endometriosis U.S.
Avatar f tn Woo hoo ! Its nice to see that you've been keeping up to date on that. This is something that is VERY important and I hope other CFS'ers here know about what Dr. Reeves, and the CDC for that matter, have done to us. One of the CDC's embarrassing scandals was published in the Washington Post. The CDC tried to make up for it by having their Public Awareness Campaign, but they are now up to their old tricks again. Dr. William Reeves should be fired.
Avatar m tn I was given the diagnosis of Ebstein Barr over 20 years ago. I also have Fibromyalgia and Polymyalgia. EBV and Fibromyalgia are very real. I had to learn to live differently. I was always looking at what I could no longer do and felt useless and depressed. A therapist suggested instead to look at what I could do each day, even if it was to get dressed and out of bed at first. It sounded crazy, but slowly I stopped trying to be who I once was and learned to love who I am now.
Avatar n tn Andrew, Zithromax for a long time as discussed in the article below. Good Luck. Momfromtexas http://mmbr.asm.org/cgi/content/abstract/62/4/1094 to print the article go to the far right and select "full text pdf" In case you have trouble here is the citation... Microbiology and Molecular Biology Reviews, December 1998, p. 1094-1156, Vol. 62, No. 4 1092-2172/98/$04.00+0 Copyright © 1998, American Society for Microbiology. All rights reserved.
Avatar f tn Since this subject has been brought up here on the forum, I have to say that it has made me quite curious on the subject. I do intend to do some research, but like ess says, until the medical community comes up with a way to test the gray matter, I guess we can't have definite answers. I'll post if I find any facts that might enlighten us.
Avatar f tn //www.ncbi.nlm.nih.gov/pmc/articles/PMC2146789/pdf/canfamphys00077-0094.pdf Some article highlights: *Magnesium deficiency is more common than is believed. *His active lifestyle, which in itself decreases serum magnesium through sweat, combined with his eating habits, undoubtedly resulted in a negative magnesium balance and eventually a deficiency. (We understand that this condition is recognized in soldiers of the South African Armed Forces, such that Slo-Mg is prescribed prophylactically.
Avatar m tn 3 years post treatment Denise Wait, you disagree that her doctors could not attribute her issues to having taken the treatment, but then you describe your own problems, with a diagnosis of fibromyalgia. So, you're claiming that the treatment caused your fibromyalgia? And you're sympathetic that her problems are the result of her treatment? A couple of anecdotes do not data make.
2128874 tn?1335445782 To begin, I'm 5'4'' and 108 lbs (normal weight) and I have been diagnosed with Fibromyalgia. I currently take 10 mg of Elavil to treat this. I've had the majority of these symptoms for about 4 years, though the severity has increased with time.
Avatar f tn org/lyme_disease/B_guidelines_12_17_08.pdf You can also do some research online to learn more about it. It is controversial and most doctors are unaware of the inaccuracy of blood tests and the late stage symptoms. It took me 16 months of chronic worsening symptoms and 12 doctors before I got myself tested at IGeneX and went to an LLMD (Lyme Literate Medical Doctor) to get diagnosed and treated.
Avatar f tn diagnosed with Lyme Syndrome at 10, Fibromyalgia/Chronic Fatigue Syndrome/Epstein Barr at 18, Hypothroidism at 28, Chronic Lyme Disease at 30 (by a homeopathic doctor), and in between a history of GERD, hiatal hurnias, ulcers, anemia, hypoglycemia,random periods of vomiting and anxiety. Today, I found out I have quite a few food sensitivities - gluten/soy/dairy. I have already changed my diet and started a few supplements that my doctor gave me.
Avatar f tn These scandals were reported by the Washington Post and other respected news sources around the country. CDC officials diverted research funds away from CFS research and misled Congress about the matter, according to the Inspector-General's report. There is good news though... as a result of these scandals, the CDC did a public awareness campaign on Chronic Fatigue Syndrome and there were commercials and even ads in magazines about this disease. (it is a disease.. IMO).
662361 tn?1225338107 2008 guidelines on the ILADS web site. www.ilads.org/lyme_disease/B_guidelines_12_17_08.pdf Keep in mind that fibromyalgia is an acknowledged set of symptoms with an unknown cause. All of the symptoms are consistent with Lyme Disease, meaning that if a doctor ever suggests Fibromyalgia as a diagnosis, then Lyme Disease needs to be examined and ruled out.
220090 tn?1379170787 "The bad news now that I can see so well is that all my friends look so old! I never knew that cataract surgery could make all your friends age. " In that case, avoid mirrors.
Avatar m tn They're fun to look up and are great food for future research, but the money for the kind of research that would really reveal truth is never there, even for pharmaceutical products which are approved for sale before we know what harm they cause or even if they work on real people for any length of time, and are then reviewed after years of use to see if they pan out. Some do, most don't.
Avatar f tn What Part D plan is available to you is based on where you live. You should research what Part D plans are available and then get a copy of their latest formulary. Sovaldi + whatever other drugs to treat hep C are listed there To learn how to get Medicare drug coverage go to the Medicare web site. You will also need a Medicare Supplement.plan also known as a Medigap plan. If you are disabled and have high medical costs I would highly recommend a supplement with Plan F option.
Avatar f tn Honestly I think that has been the over all theme for many of our lives. I personally have spent the last 6 years researching this and am currently working on a research paper on this specific thing, it is 13 pages long with evidence, articles and explanation for the pain as well as treatment options that we at this point have found significantly helpful. Though the article is not done yet we do have some great health pages here on this site, top right on this page.
Avatar m tn //www.avaresearch.com/ava-main-website/files/20100401061256.pdf?page=files/20100401061256.pdf If I die from sepsis, which is a very real possibility given that I've been hospitalized twice already for bizarre infections that just spring up, my cause of death will be listed as "sepsis," not "complication of INF / RVN therapy," which would probably be the actual truth.
Avatar f tn http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1002404/pdf/westjmed00117-0052.pdf Here's a great article about false positive testing with some causes and references.
Avatar f tn I was told I needed to see an Infectious Disease Specialist but was unsuccessful in obtaining one so i went ahead and did extensive research and found other diseases that may make a Lyme result such as mine. I went to my OB/GYN and requested to be tested in the end of April, 2012 for Syphilis, HIV/AIDS, and Herpes as i also do annually.
Avatar n tn Do you know much about Fibromyalgia? Your symptoms sound alot like Fibro to me. Only a skilled Rheumatolagist can properly diagnose the 11 of 18 tender points, and I wouldn't go back to the individual you saw the first time as "he" may not be a believer in the condition. Best of luck to you! Just so you know, it usually takes a good 18 months to get the proper diagnosis and treatment, so don't give up but don't get too frustrated either.