Fibromyalgia yahoo answers

Common Questions and Answers about Fibromyalgia yahoo answers


Avatar f tn I have been diagnosed with fibromyalgia. I have hundreds of lumps in the fat on my body. They are extremely painful and in all parts of my body. I started having them on my rib cage forty years ago and they have now spread over my whole body.They are in strands near my joints and the slightest pressure hurts. I need to know if other people who have fibromyalgia have these lumps. My rheumatologist says he has never seen a case of Dercum's and did not want to hear about it.
Avatar n tn I hope this bit of advice helps. I have researched many health issues over the past 1 1/2 years. I've even written over a hundred articles that have been published. My advice to you is NOT to get the surgery done. I know it is tough being overweight, but there are answers. I found lots of answers in a book written by Dr. Siegal, "Is Your Thyroid Making You Fat." Read his book and then follow his advice.
216278 tn?1308864682 Hi, I know that many women on this site are looking for alternative answers or therapies, as well as trying to take control of their own health/bodies! After my failed IVF, I needed other answers and through a series of occurences, I have found myself starting a protocol of low-dose naltrexone (4.5 mg at night)!
Avatar f tn Im 37 yo and have 3 kids and cant take being exhausted all the not functioning well at all. I just want answers..if anyone has any feedback or can suggest some tests i can ask for that would be appreciated. Thanks.
Avatar n tn Have you all checked with your physicians about Fibromyalgia? I have Fibromyalgia and Chemical Sensitivity and I was diagnosed in 1998 and they think I have had it longer then that yet. I also have burning sensations all over my body and have had this since I hurt my neck when I was a kid.
230948 tn?1235847929 Had problems with loss of hearing and tinnitus and now bouts of vertigo and pressure in the ear like a bubbling lie you get when you been on a plane, seeing ENT for 2nd time on Feb 2nd. Is there anything they can do for this. I also have fibromyalgia and MPS upset to have something else dx.
326149 tn?1203252341 I was wondering if this is odd or ordinary that my body is trying to fight 3 diseases APS, fibromyalgia and lupus anticoagulation? I have hunted every where to try and find an answer of whether or not anyone else suffers from this or am I the only one? HELP!
1464004 tn?1384139333 Hi Elli126 and welcome to the Fibromyalgia Community. Unfortunately conventional medicine cannot address fibromyalgia satisfactorily. And having no known cause-the new hype about excess palm sensory innervation being the cause of fibro, to my humble opinion,is just a sales pitch for SNRI drugs, according to a recent study (sponsored and paid by the 2 largest SNRI drug manufacturers)- this leaves the patients with very few viable options for treatment.
Avatar f tn I have seen two different doctors over the past fortnight, both of which have totally destroyed my confidence and belief in the NHS (I live in England). I was finally diagnosed with fibromyalgia last year after suffering for nearly ten years. I visited the GP recently as my symptoms were getting worse, particularly my chest pain.
573297 tn?1304712740 cause now getting heavier, my fibromyalgia has kicked in as well. I am just a mess right now....anything can set me off....sorry about the rambling but I have no counselor and I am trying to get one....someone to talk to because I am becoming too taxing on my friends....and my parents aren't supportive at all....I don't know what to do at all...I don't know what I want.....does anyone have anything?
Avatar f tn You could have the doctor in Cleveland call and talk to this guy, but then he'll probably be resentful. Any yahoo that thinks he can determine the outcome of a test without running it is a big baboon, especially when there are already indications something is wrong. When a doctor pawns you off with depression, anxiety, or fibromyalgia without doing any tests, it basically means he's in over his head and doesn't want to be bothered any more, so please go away.
182493 tn?1348056515 One of the books he gave me it The Fibromyalgia Handbook. so it looks like he feels that is what my symptoms compare to most. He gave me the tender point test but didn't tell me how many out of the 18 points I had. He made several comments about how tender I was. So I am assuming the test told him something. I need to fast for my blood work so I will have to do that another day since I had coffee before I went and a granola bar.
Avatar m tn com forums who have IBS and they never experienced loss of appetite or vomitting. People from yahoo answers saiad the same thing. My uncle who although is just a cardioligist, but obviously had to learn everything from medschool, said its unlikely to IBS, he siad he'd put his money on celiacs or h pylori. Ive also read on many websites the illnesses people have tend to get mistaken for ibs eg celiacs, h pylori, cancer etc.
Avatar m tn My ophthalmologist said for me to tell anyone who asks what I have to tell them MS. As for fibromyalgia, got that too. Fibromyalgia often piggybacks on other disorders.
Avatar f tn After going to the ER twice and being told it was vertigo and migraines, I decided I needed more answers. I found a primary who did some blood work, and told me she thought it could be fibro. The blood work showed up positive ana 1:160. then later negative, then agian positive 1:80. By this point, I was having pain in my legs and arms as well. So after a yr of trying to find a way to a rhuemy. I finally got into one. He took a five min look at me said it wasn't fibro and walked out.
Avatar n tn There is little downside in trying them and it may be worth a shot. I hope this answers your questions. Thanks for posting.
Avatar n tn where I hope those with costochondritis will come together and share what their experiences are, what they have learned, and support. Good luck to you.
410557 tn?1204860365 Adrenal dysfunction is now being recognized as contributing to Fibromyalgia and Chronic Fatigue, as well. I just learned this from my endo- who is a thyroid specialist. I found a reputable article on this subject and you can see if any of it applies to your situation. Find a doctor who is willing to work WITH you to find out the cause of your symptoms. Hopefully you can get adrenal tests done.
440728 tn?1234648902 The TSH is renowned for big swings. A woman on Yahoo Natural Thyroid Hormone site some years ago had TSH taken more than once on one day and got a result 3.0 points apart. When I was TSH 4.6 I was an absolute wreck. I also found that it was best to get blood tests done when I was feeling shabby. Don't worry too much, loads of people have difficulty with endos. You need to find a good doctor. This treatment is very very typical for hypothyroid people.
Avatar f tn not to mention the fatigue I am week 20 of 72 did not clear by 12th week but am sure I will be clear by 24 Not much encourageiment from Doc eather as his answers were no the rash is not gonna go away these are the side effects this time. I have a skin Doc and am seeing her.... Ya know I hate to write this cuz I sure do not want to discourage any let me say this my first TX peice of cake. Doc suggested think about it So here I am thinking and writing.
Avatar n tn Each time i went to the doctor she took a sample and looked at it under a microscope- she did not culture it. The first time she said she saw some yeast. The second time she said she did not see any yeast but saw some white blood cells which she said was indicative of an infection but I tested negative for everything else. I don't think I have any of the other problems that you mentioned.
Avatar f tn A piece of me is missing, in addition to all the flu like symptoms have not subsided. Feels like severe fibromyalgia. Achy mucles, sore joints. Tx def beat me up. I def shudve When am I gonna get better?
335728 tn?1331418012 Well I don't have Fibromyalgia...they said I have to have 11 points out of 15 or 16 to have Fibromyalgia and I have 6. So Fibro is out thank goodness! She said that my bursae on the outside of my thighs are very tender which could be a sign of bursitis but personally I doubt it because when I read up on bursitis the pain would be in a pain is in my WHOLE leg.
Avatar f tn He is sending me for an Ultra Sound of bladder and kidney's since I still can't pee right....Also a 48 hour holter monitor because my palpitations are just nasty. (yahoo, more tests!) I came right out and directly asked, "So, you still don't think I have MS?" and he said, "Nope".....
267243 tn?1189759435 Is it easier the quicker I do it (both from how long I have been using Suboxone and oc's full-time (3 months for each?) and how long should I taper? I don't expect direct answers because we are all different, I just would love to hear other peoples experiences (and help if I can.) Thanks for listening... good luck to anyone, let me know if I can help or at least be someone to truly listen.
Avatar n tn The only way to get answers, to a degree, is to go to Boston! Thank you so much for your input on this forum!
Avatar n tn Stiffness of joints, back, neck, tennis elbow 26. Muscle pain or cramps, (Fibromyalgia) * Respiratory and Circulatory Systems 27. Shortness of breath, can't get full/satisfying breath, cough 28. Chest pain or rib soreness 29. Night sweats or unexplained chills 30. Heart palpitations or extra beats 31. Endocarditis, Heart blockage * Neurologic System 32. Tremors or unexplained shaking 33. Burning or stabbing sensations in the body 34.
Avatar f tn I never got a formal diagnosis of anything other than fibromyalgia. I've always tested negative for the lupus antibodies, though have had ANA's as high as 1280 and as low as 40. I am on plaquenil and every now and then steroids to get me through some of the rough patches. I wondered if anyone gets bouts of feeling hot/inflammation all over when going through a flare? Not really a fever, per the thermometer, but just feeling like you have a fever?