Fibromyalgia symptoms youtube

Common Questions and Answers about Fibromyalgia symptoms youtube


Avatar f tn The one common thread with Lyme Disease is the number of systems affected (brain, central nervous system, autonomic nervous system, cardiovascular, digestive, respiratory, musco-skeletal, etc.) and sometimes the hourly/daily/weekly/monthly changing of symptoms. No one will have all symptoms but if many are present serious consideration must be given by any physician to Lyme as the possible culprit. Lyme is endemic in Canada period.
5682570 tn?1372290919 Hi sallyalewis and welcome to the forum. I have filed some notes and a couple replies to members on this- It just happens that I have a report relative to this for my Naturopathic studies, so it all came in handy. First some natural remedies you may want to look into: My daughter who's a holistic health practitioner and aromatherapist uses a few drops of Organic Peppermint Oil over the itchy areas. You may also try Aloe Vera gel, as this works well too.
5586759 tn?1370438872 I've had Fibromyalgia since I was a teenager and I have gone through one pregnancy already, but at the time I hadn't been diagnosed properly for the ailments that I have. It's now round two, I am pregnant again, and I'm wondering about good suggestions to help maintain lower levels of pain. Last time I was put on bed rest at 8 1/2 months and that was torture for my sciatica nerve. I'm trying to stay active and strong. I've been going through physical therapy and things of that nature.
Avatar f tn I have been treated for fibromyalgia for over a year now. The dr. never really stated I have fibro. I'm being treated for high cholesterol and trigylcerides. I'm taking welchol powder once a day and trilipex for this. I'm taking lyrica 150mg. bid and mirapex at bedtime. I went to get a lab slip yesterday for blood work and was informed i needed to be fasting for my cholesterol and trigy. levels.I have never been told this before. When I first started with this dr.
Avatar m tn Hello everyone! I would just like to thank you in advance for Reading my post. I am a 21 year old male who was once extremely active but my health has deteriorated over the past 5 years. I have been to over 25 doctor visits over the past 5 years but have been unable to find a direct cause for my symptoms. I can’t even count the amount of times I’ve had blood taken (>20 times).
1852058 tn?1320162300 Over the years, I kept increasing it which cured most of my symptoms. There is a new fibromyalgia med called Savella which I read praise after praise on another website. Also anti-depressants can serve as pain killers. I have severe migraines, which my headache specialist said to raise my current anti-depressant Effexor even more to treat the migraines. Due to one side effect from the Effexor, I said no. He then suggested Savella which I am going to switch to.
Avatar f tn why Medicine purposefully ignores the facts and brain wash people who suffer? Fibromyalgia and all these syndromes with "unknowed causes" untill we get cancer are caused by the toxins released by Candida colonies invasion. A mutant yeast, causing systemic invasion, opportunistic fungus which feed himself with our cells, sticking on our organs sucking glucose wherever he finds it. Our immune system is trying to get rid of it untill he gives up.
358304 tn?1409713092 I'm also a worry wart, and I worry about having fibromyalgia. Everything started about 1.5 years ago. August of 2014. After doing a lot of exercise and running, out of nowhere, I noticed one night, that when having intercourse with my wife, my erections would sometimes HURT. It was bizarre. I just thought maybe I strained something, and thought nothing of it. Then after about 2 weeks of erectile pain, I went to the Dr., and he was not concerned and said to give it time.
Avatar f tn Over the past two years I have had a decline in my sense of taste and smell. I have been diagnosed with chronic fatigue syndrome and fibromyalgia. I also have degenerative disc disease in my spine, have had lung surgery, and a stroke at 35. Could this in any way be a misdiagnoses? Upon reading everything about Mitochondria Disease I would like to be tested for it but don't know where I should go for the testing and a reliable doctor. I live in N.
1688444 tn?1305693229 He tested my ANA and all I know is that it was high and positive. He suspected Lupus. Sent me to a Rheumatologist. This dr said I had Fibromyalgia. This was 10 yrs ago. I have had complicated pregnancies, that being an understatement. Almost four yrs ago I gave birth to my last. My stomach issues started getting worse. When my baby was 9 months old I went to the ER with the worst migraine EVER. He used me as a pin cushion. Attmepted 6 times to do a spinal tap. Then the specailist did it.
Avatar n tn Cited: "It is thought that between 15% and 50% of those patients diagnosed with Lyme disease actually have fibromyalgia. It is important that you be tested for Lyme disease using a variety of different diagnostic tests, in order to rule out this disease. Long-term antibiotic treatment can result in serious side effects, and won't do anything for your fibromyalgia symptoms.
Avatar f tn I am on Domperidone which has been very effective in reducing the symptoms including acid reflux. I also have trouble emptying my bowel. I have the urge to go but do not seem to be able to completely empty it. This started in the last month. Finally, I have developed fasciculations all over my body the past month. I have them mainly on my eyes when closed, calves and forearms; however, they appear everywhere.
Avatar n tn If you have been suffering from chronic pain; CFS or Fibromyalgia please read this. You may have been infected with a tick borne illness, LYME DISEASE and co-infections of lyme disease. Testing for lyme disease is very unreliable, many have to resort to getting tested at a private lab, such as igneix. Many doctors and specialist do not want to talk about lyme disease. Please educate yourself on this.
5100586 tn?1363648354 I have a question regarding lyrica withdrawal symptoms ................ I am currently suffering with this and am on day 38 with no end in sight from these godawful symptoms ............... in fact, it has gotten worse in the last 48 hrs, which is so depressing, as I thought I would improve as I distanced myself from the drug ...
Avatar n tn Hello everyone, I have been browsing this site for a while now and its helped me during my attacks. Fisrt let me start out how this started, i am currently 17 years old, 5' 10" 175 lbs. about 4 years ago I had a panic attack out of no where, my first one, this included major chest pins and impending death. Ever since that day i wold have an attack at night, i was afraid of being alone at night for some reason.
1530171 tn?1448133193 National Fibromyalgia and Chronic Pain Association - NFCPA - google it and sign up for their magazine.
Avatar n tn Female, age 39 (really!)- neurological symptoms the past 6 months. Both PCP & Neurologist thought it was MS, had X-rays of back,MRI of cervical spine and brain- all tests came back fine. Never had blood tests. Now, they say "just wait, maybe your symptoms will just go away, and we will never know." Symptoms were: limbs falling asleep for hours at a time both sides of body. Shooting lightning type pains on face, arms, legs, hands & feet.
2010625 tn?1329375656 MY daughter was diagnosed with fibromyalgia...she had severe symptoms for many months....Eventually it was proved that her body was reacting to hidden mould in her loft at home....whilst she was poorly i took her on hol to spain...she made a "miraculous recovery within 48 hrs of being in the sun...when she returned home her health detiorated again...hence the investigation of poisonous mould in her house. she moved house and im glad to say that she has made a complete recovery.
591546 tn?1244640145 Fibromyalgia is just a group of symptoms, not a disease. It sounds like she thinks you may have a disease process causing the fibro. I hope not but it sounds like she will get to the bottom of it. As for your husband, I don't think they really ever understand. Maybe others will give you their experiences. I have found for me it's better to say as little about how I feel to him as possible. It stresses him out.
3065262 tn?1342126161 forget about Fibromyalgia. those are not the specific symptoms. moreover Fibro. is not really an established medical condition, it's only a name for a collection of similar symptoms therefore in practical terms to say someone has Fibro. means everything and nothing. what do you mean with knots? hard lumps? lymph nodes? where are they? (actually nodi is Italian for knots) is double vision vertical or horizontal? you see the objects overlapping left-right or top-bottom?
Avatar n tn The great difference being that all of these are treatable and, once treated, the symptoms will be relieved to a great degree (not to minimize the symptoms of any of these horrible conditions). With FMS/CFS or MS, there is little relief by standard methods of treatment. Take care and wishing you pain-free days in 2009.
Avatar f tn My daughter, 32 yrs. old has myasthenia gravis, celieac disease, fibromyalgia, and currently going to be tested for MS. SHe has had M. Gravis for 7 yrs., celiac for 4 yrs, and just recently fibromyalgia and the possiblilty of MS. I am at my wits end for her. I feel so bad for her. Actually the celiac is minor (she is on gluten-free diet). She is experiencing pain with walking and can't set for a long period of time. She is on medication for the M.G. and Fibro. But with all of the meds.
Avatar f tn * 0 = no symptoms 1 = few symptoms 2 = a moderate number of symptoms 3 = a great deal of symptoms The SS scale score is the sum of the severity of the 3 symptoms (fatigue, waking unrefreshed, cognitive symptoms) plus the extent (severity) of somatic symptoms in general. The final score is between 0 and 12.
Avatar f tn I've had the bed now for about 2 weeks and its just been in the last 2-3 days that I'm experiencing these symptoms. Could it be the bed or do you think there is something else going on? Thanks.
3195704 tn?1345125052 I have been diagnosed with Fibromyalgia about a year ago , now I am having bad fatigue and now bumps are coming up on my joints that hurt if they are hit accidently. Can anyone else tell me is this a sign of arthritis or is it Fibro too????? Have become very depressed not knowing what is going on with me and it is taking a toll on my house work and work....I just want to cry all the time, I am also on zoloft 100 mg and its not helping me at this time.
Avatar f tn Hypothyroidism causes a build up of mucin (means gluelike) so you will find it hard to pinch the skin. You can see the demo on youtube. Type into the youtube search bar: Hypothyroidism Type 2: Myxedema Symptoms. I would also mention magnesium as this is a recommended supplement for migranes (magnesium is found to be low in many migrane patients). Other symptoms of magnesium deficiency include fatigue (but also insomnia) chronic pain, nausea, vomiting, heart rhythm problems.
Avatar f tn LOL! Dear, i have the exact same symptoms... I don't mean to be rude and laugh at yours, it's that it was bittersweet finding out what that was about. During my last attack, my speech was so slurred, my mom thought i was trying to kill myself with sleeping pills or Xanax (she's the ultimate Yiddishe mama.. we're extremely dramatic) ..
Avatar n tn So far autoimmune thryoiditis, and some unspecified issues which may be starting of rheumatoid arthritis or sjogren's disease (elevated rheumatoid factor, bad dry eyes,and some other non specific joint pains, fevers and vague symptoms which my doctor does not feel related to Myeloma). I also have asthma that has flaired up this fall and I had to double my advair for a month to get it under control. Not really a clear question here, but anyone else dealing with multiple diagnosis?
Avatar f tn On my fathers side there is heaps a lupus and rhumatiod arthritis, as well as fibromyalgia, palindromic rheumatism and a few others similar! As I was growing up I always used to get reAllly bad 'growing pains' in my cales. Which Is normal, but now that I'm old I get them a fair bit at night, as well as what I can only describe as shin splints, which disable me from walking about once a month.
Avatar f tn Hi, I am at my wits end does this sound like fibromyalgia to anyone? I first noticed my tongue was sore three months ago, then my hands wee cold for no apparent reason and I had what I originally thought was a trigger finger. Soon my hands and fingers became really painful and would sometimes twitch and this horrible ache and burning nerve pain is now all over my body.