Category: Fibromyalgia Protocol

Discover a structured Fibromyalgia protocol to manage symptoms effectively, including treatment plans, therapies, and lifestyle strategies for improved quality of life.

  • 29 Stories From Women Whose Doctors Did Not Take Their Pain Seriously

    We recently asked members of the Community if, as women, they had ever felt as if their pain had not been taken seriously by doctors or medical professionals. Here are some of their stories…

    1. The Woman With the Breathing Problems

    When I was 17, I started having a really hard time breathing. My primary doctor told me it was just asthma. It became progressively worse, and my inhaler wasn’t really helping. One night, I woke up basically having a panic attack because it felt like I couldn’t breathe. My dad rushed me to the hospital, and after giving me an EpiPen for an allergic reaction, the doctor proceeded to tell my dad right in front of me that I was probably making it up to get out of school.

    This happened several times with doctors telling me I was overreacting. After two months, I finally went to a specialist who discovered that I had a severe infection on my voice box that was inhibiting airflow into my lungs.

    2. The Woman With E. Coli

    A few years ago I had extreme abdominal pain, diarrhea, vomiting, and a fever for two days. It just would not get better. I finally made it to urgent care on the third day, and the male doctor said, “It sounds like you’re just having really bad menstrual cramps.” I happened to be on my period at the time, and he advised me to take some ibuprofen and “sleep it off.” Fortunately, the (female) attending doctor who came in to do the actual exam took one look at me and sent me straight to the ER. Turns out I had an E. coli infection and I spent the night in the hospital hooked up to an IV. Some “menstrual cramps,” amirite?

    3. The Woman With a Torn ACL

    I was in a skiing accident when I was 17. I immediately knew that I hurt my knee very badly as it kinda just snapped down and swelled up right away. I went to the walk-in clinic and I told the doctor what had happened. I told him what my pain level was at, and he told me it couldn’t have been that serious, that I just bruised up my knee and I’d be fine shortly. So I had no further testing and was sent on my way.

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    After two months, my pain hadn’t improved at all, and my knee was still swollen, so I went to see a different doctor. Turns out that I had torn my ACL, MCL, and meniscus. I needed a MAJOR surgery, and everything was worse because the first doctor didn’t listen to me and get me to an orthopedic right away. I ended up getting scheduled for surgery ASAP and they did everything they could to make my knee normal again. But because of the initial response to my pain, I have never been able to ski again, I had to stop jogging/running, and my knee will forever and always be a bit messed up. —MrsH810

    4. The Woman With Shingles

    In college, I got shingles and waited a while to go to the hospital because I had been misdiagnosed by my student health center. Eventually, I showed the spots to my friend, who said it looked like shingles and took me to the emergency room. I walked in and told the male nurse that I thought I had shingles, and he scoffed and said, “Where did you come up with that? The internet? You would be in a lot of pain if you had shingles.” As soon as I lifted up my shirt he said, “Oh my god you have shingles! Isn’t this painful?” Yes…it is painful. That’s why I’m here.

    5. The Woman With a Cracked Eye Socket

    I was accidentally elbowed in the face during a concert and my face started swelling almost immediately, so I went to the ER. The doctor did no diagnostic testing. Before he even asked my name, he said it looked like any normal black eye. Didn’t even prescribe me ibuprofen for the pain. Months later, I still hadn’t healed. I went to a plastic surgeon and he discovered that not only had the elbow cracked my eye socket, but a piece of bone had chipped off and was floating around in my face.

    I could have lost my eyesight and/or all use on that side of my face due to nerve damage. I should have had surgery within 48 hours and at the very least a CT scan. Now, unless I have my face re-broken in surgery, I will never be fully recovered. All because a doctor didn’t believe I was really in as much pain as I claimed.

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    6. The Woman With Leg Pain

    I have chronic pain in my legs that sometimes limits my ability to walk when

    I have severe flares. One time during a particularly bad flare, I went to the doctor for help and she offered— in all seriousness— to escort me to the psych ward.

    7. The Woman With a Staph Infection

    When I was 15, I had minor knee surgery. The first day was fine, but each day I got progressively worse, to the point that I couldn’t even put weight on my leg at all. It was so swollen that it looked like my thigh went straight down my leg. My temperate reached 102. When I went to the office to get my stitches removed, my mom expressed concern about the excruciating pain and fever. The doctor laughed and said, “It’s just because she’s blonde and 15.”

    A week later I came in again because the problem was still there. After unsuccessfully trying to drain my knee, he brought in his colleague. That doctor took one look at my knee and had me rushed to the hospital. Turns out I had a staph infection that had been doing work on my knee for what was at that point 18 days.

    8. The Woman With a Giant Kidney Stone

    I went to the ER with severe abdominal pain. It was so bad that I was actually screaming. The doctor asked me some questions, did no tests, and sent me home with a diagnosis of gas. I went back a week later for the same reason. This doctor actually did his job and found a giant kidney stone.

    9. The Woman With an Ovarian Cyst

    When I was in high school, I was at basketball practice running sprints when I was suddenly overcome with the most excruciating abdominal pain I had ever experienced in my life. I was only 15 years old. My mom rushed me to urgent care. The doctor came in to see me and began asking me questions about what was going on at school and in my family instead of about the pain I was experiencing.

    She then noticed that I had an “in memory” button on my letterman jacket. My friend had died in the previous year and as soon as she saw the button she was convinced that my severe abdominal pain was because I was sad. She actually told my mom, “This is common for teens who experience grief.” She then took the button off my jacket and made me talk to it and tell my friend “goodbye” so that I could “move on with my life.” I was so appalled and freaked out I just stared at her. Little did I know that I had actually had an ovarian cyst burst and I was suffering from severe endometriosis.

    10. The Woman Who Wasn’t Taken Seriously Because She Was a Theater Major

    During my freshman year of college, I began experiencing seizure-like spasms and losing consciousness often. I went to the hospital near my university, where I filled out a questionnaire and included when prompted, that I was a theatre major. I was given fluids and released. A few weeks later I passed out and started spasming again. A friend took me to the hospital. As I was being wheeled on a gurney for testing, still experiencing seizure-like symptoms and extreme abdominal pain, a female nurse ran alongside my gurney to tell the other medical professionals to not take me as seriously, because I was an actress. They decided to do less testing than they originally planned to do, and when I was sent back to the bed in the ER I had been assigned to. I signed myself out of AMA (against medical advice) because I felt that I was being ignored.

    Later, a different doctor told me that the spasms were due to a reaction I was having to a medication I was on due to having a kidney transplant just over a year prior to this. I was taken off the medication and the seizure-like activity ceased. Fast-forward two years, and I am still experiencing severe abdominal pain over my kidney transplant in my abdomen. I was finally diagnosed with endometriosis and pancreatitis and spent almost a week in the hospital after becoming septic. Turns out I wasn’t acting, and I was facing two serious medical issues on top of the transplant. It’s been nearly 10 years since this happened and I still think about the pain and suffering that could have been alleviated if I had been taken seriously at that time.

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    11. The Woman With Endometriosis

    It took FIVE doctors before I was finally diagnosed with endometriosis. The first doctor told me that period pain was normal even though I said the pain wasn’t just during my time of the month. The second doctor said it was probably gastrointestinal issues and that I should go to a specialist. The third doctor prescribed birth control after birth control that helped in no way. The fourth doctor thought maybe it was endometriosis, maybe it was cysts, couldn’t be sure, and gave me a painkiller to help and sent me on my way. The fifth and final doctor got me scheduled for an ultrasound. She prescribed a birth control that did help but when the pain worsened she scheduled surgery for a laparoscopy in which they discovered that I did, indeed, have endometriosis.

    12. The Woman With Fibromyalgia

    After my rheumatoid arthritis went into remission, doctors couldn’t pinpoint why I was still living with chorionic widespread pain. The pain felt similar to my RA but not quite the same, and it became debilitating. One doctor, after seeing my blood work, literally called me a “druggie.” He accused me of looking for prescriptions even though I had specifically stated that I was in desperate need of a diagnosis and didn’t want any pain-relieving pharmaceuticals from him. I walked out of his office in tears and almost gave up. I felt like the lowest human being on earth and didn’t want to go through that humiliation again. Luckily I have a wonderful support system that encouraged me to keep trying and finally found a doctor that diagnosed me with fibromyalgia.

    13. The Woman With Hyperemesis

    Basically, my entire experience with hyperemesis was a mess. I was pregnant and throwing up 10–15 times a day. It took several trips to the ER and three different doctors before I found someone who believed me and gave me anti-nausea meds. Most people don’t take it seriously because they assume it is normal morning sickness. I lost close to 30 pounds in the first two months of my pregnancy, I could not keep down water, and I was so dehydrated I was having muscle spasms. But I had a doctor tell me I wasn’t sick enough to take time off work.

    14. The Woman With Severe Knee Pain

    I needed knee surgery due to my knees being incredibly hyper-mobile. They would constantly shift out of place and dislocate while walking. It was so incredibly painful sometimes that I legitimately could not walk. I met with a surgeon who acted like I was some weak girl simply because I wasn’t injured playing sports or during physical activity. He would only speak to my mother about maybe getting a brace or working out more to strengthen it (which I did and didn’t help) and would act like I didn’t exist or like I wasn’t even in the room.

    15. The Woman With a Deadly Infection

    I had abdominal surgery and the doctor took me off my pain meds two days later. That night, I experienced the most excruciating pain in my abdomen. It was very intense. The next morning, still in pain, I told my doctor. He said I was being sensitive and sent me home. I ended up back in the hospital 24 hours later with a deadly infection called peritonitis and was suffering sepsis. My doctor almost killed me by brushing off my pain.

    16. The Woman With Massive Cysts on Her Ovaries

    When I was 14 or 15, my parents took me to the ER because I was crying and vomiting from a pain in my lower stomach/pelvic area. It took four hours to get into a room and by that time I had vomited three times. A doctor finally came in and I told him everything I was experiencing. He said I was probably about to start my period. I said no, that I had just finished like a week and a half ago. He gave me fucking Tylenol while I was still crying and curled up in a ball on the bed. Two hours later a female nurse came to check on me and everything was still the same. My mom asked for a different doctor because the guy wasn’t listening to me. Somehow the nurse got a female doctor to come in. She gave me an ultrasound, and I ended up having massive cysts that were rupturing on BOTH of my ovaries.

    17. The Woman With a Labrum Tear

    I injured my shoulder during a swim meet and it continued to hurt beyond the time the doctor said it would. Six years later, after begging for surgery to alleviate pain, my doctor barely agreed to exploratory surgery to see if anything was wrong that he couldn’t see or detect with the other methods he tried. After surgery, he apologized to me… There was a huge tear in my labrum that required surgery to fix.

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    18. The Woman With a Burst Appendix

    When I was in eighth grade I had extreme abdominal pain and went to my local clinic. Without doing a single test, or listening to my symptoms, he told me I had a UTI. I have rushed in again the next day and this time I had a different doctor. She immediately discovered that my appendix had burst and that I needed to get to an ER right away. I ended up being in the hospital for five days.

    19. The Woman With Stage 4 Endometriosis

    I had been going to my OB-GYN for nine years telling him that I was hurting horribly with my periods and cramping between periods. He told me I’d grow out of it. I got fed up and switched to a different doctor in a different town. She had me in the operating room within a month and I was diagnosed with stage 4 endometriosis that probably could have been treated or cured long before it got this bad.

    20. The Woman With Gallbladder Disease

    I experienced back pain for months, but being only 22, healthy, and relatively active I knew something wasn’t right. My doctor told me to get a chest X-ray and take some Advil. A few months later I ended up in the ER because the pain was so severe. The ER doctor told me I probably had a kidney infection. When the test came back negative, I was told to go home and see my primary care again. My pain was so severe I refused to leave and asked for an ultrasound of my gallbladder. He rolled his eyes but finally agreed. About an hour later he told me that I have gallbladder disease and need to have it removed immediately. He couldn’t even look me in the eyes!

    21. The Woman With Crohn’s Disease

    I had chronic stomach pain growing up and the pain was so severe that I was often curled up reeling in pain. There was no relief whatsoever. It randomly came every month or so and lasted about a week. I went to the doctor multiple times. The doctors always passed it off as overeating or gas pains. Last year I finally went to the ER because the pain was so bad I couldn’t breathe. Turns out I’ve had Crohn’s the entire time.

    22. The Woman With a Blood Clot

    A couple of years ago I went to my doctor because my left underarm and arm had been extremely sore for a few days and I couldn’t really stretch my arm all the way out. When I suddenly got blue marks down the inside of my upper arm, too, I decided to get it checked out. My personal doctor thought it could be something potentially dangerous (blood clots were mentioned), and she sent me to the hospital.

    The doctors at the hospital were a completely different story. They kept asking me if I had hurt it somehow/strained it by carrying something heavy(!)/other mildly insulting explanation. I told them I wouldn’t be there if I knew the reason why it hurt. They took a blood test and it came back negative for any sign of blood clots. That just made them more sure it wasn’t anything serious. But I kept insisting I KNEW there was something wrong. Very reluctantly the doctor at the hospital said that, if I wanted, I could come back in the morning for an ultrasound. I quickly said YES, PLEASE, and went home.

    The next day I went in for the ultrasound and guess what: one blood clot in my arm. Yup

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    23. The Woman With Ulcers Lining Her Bladder

    I have a bladder condition called interstitial cystitis, which means that the lining of my bladder (which protects it from acidic urine) doesn’t form properly, and my bladder and the surrounding muscles often spasm, causing pain and preventing me from urinating properly. When I was 23, I went to a urologist, after the third negative UTI test in a month, for further diagnosis. The first urologist I saw listened to my symptoms, and dismissively said, “What do you want me to do about it?” I was shocked but asked him to please run whatever tests he could. He agreed to do a cystoscopy, and the day of told my mother in the waiting room that he didn’t think he would find anything and I probably just drank too much alcohol, which irritated my bladder.

    During the cystoscopy, they filled my bladder with water to expand it, my heart rate went up (indicating pain), and they found tiny ulcers on the lining of my bladder. The doctor sheepishly told my mother what they had found and gave me the name of a urogynecologist who specialized in my condition.

    24. The Woman With Hip Issues

    During the end of my pregnancy, I started having severe pain in my lower back and right hip that radiated down my leg into a couple of toes. After my daughter was born, the pain did not improve. I went to multiple doctors, including OB-GYNs and primary care physicians. Everyone said nothing was wrong. Three years later, I went to a new doctor for a basic yearly physical. I casually mentioned the pain to him. He ordered a slew of tests, from blood work to X-rays/MRIs/EMGs, etc., but everything came back normal. He gave me a prescription for narcotics (I did not ask for them) and told me to come back in a month. When I returned he acted shocked that I was there just before a month had passed, even after I explained why. He berated me and made me feel awful, claiming I was only there to get more pain pills. When I told him that I had hardly taken any of the pills because they did not alleviate my pain at all, he asked me if I was selling them and had me take a drug test. By the time I left his office that day I actually felt like I had done something wrong.

    I decided to take a more natural approach because I could not put myself through that again and went to see a chiropractor. He took X-rays. He immediately showed me what was causing the severe pain. He sent me to an orthopedic surgeon. Unfortunately, this doctor was in the same network as the original PCP and saw the notes from my two previous visits. He took new X-rays but had me lying down for them all. He said they looked fine and once again accused me of lying to get narcotics. Once again I had not suggested in any way, shape, or form that I wanted any sort of prescription. I explained what the chiropractor had shown me on my previous X-rays. After much pleading, he agreed to take X-rays of me standing. He immediately apologized and agreed with what the chiropractor had said. He said that no amount of narcotics would have any effect on this type of pain.

    25. The Woman With Kidney Stones

    I was 19 on a job in San Francisco by myself and thought my appendix was rupturing on my flight over. I went straight to a doctor when I landed, and he insisted it was cramped. The pain persisted and I ended up passing out on the job and had to be brought in to the ER. Turns out I’d been feeling and passing kidney stones for four days. Thanks, doc.

    26. The Woman With an Autoimmune Illness

    I’ve struggled with chronic stomach issues my entire life, and I started seeing this GI doctor a couple of years ago. He was literally so sexist that he would only talk to, shake hands with, and properly address my boyfriend. It was as if my boyfriend had to be the messenger for me, to explain how bad my health issues had gotten. I had two procedures done, and then that doctor ended up diagnosing me with IBS. I was crushed. I knew it was something more severe than IBS.

    When I got a new GI doctor a few months later, I FINALLY learned that I have a chronic illness— an autoimmune disorder — that can’t be cured and can lead to cancer and other horrible things if it goes unchecked for a long period of time.

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    27. The Woman With PCOS

    When I was 20 and in college, I was menstruating heavily (and painfully) for 40 days before my friend finally convinced me to go to the ER. Once there, I waited four hours in a paper gown. Finally, a male doctor examined me, deemed that my bleeding wasn’t “too heavy,” and gave me two Advil for the cramps. He told me if I was still bleeding in another month I should make an appointment to come back.

    After I told my mom this, she scheduled me with her gynecologist, who immediately did an ultrasound and found I was suffering from PCOS (polycystic ovary syndrome) and that my small cysts were bursting, which was causing the pain and heavy bleeding. She took my pain seriously and prescribed me stronger ibuprofen for the pain and hormonal birth control to control the cysts, and also an iron supplement because of the blood loss. Had I gone another 30 days, as the ER doctor had recommended, I would have been severely anemic from blood loss.

    28. The Woman With Gallstone Issues

    I went to the ER a couple of weeks after I had my gallbladder removed. I was in terrible pain, completely keeled over. My husband pretty much had to carry me into the ER and talk for me because I couldn’t move. The doctor told me it was just cramped and sent me home. When the pain wouldn’t go away, I went to different urgent care. The doctor there did an MRI and found that a gallstone had actually been stuck and sealed in a bile duct. It required another surgery to remove it, and if I hadn’t gone elsewhere it would have gotten much, much worse.

    29. The Woman With Fibromyalgia

    I was 36 and had lived with muscle/joint pain since my early twenties. Whenever I brought it up to my general practitioners, it was pushed aside and treated as not important since the pain roamed around my body. I had my knee go out one day after taking what should have been an easy walk. I went to another GP and after an X-ray came back clear, she actually rolled her eyes at me. I insisted I be treated. She told me I probably needed to lose some weight (leftover from pregnancy). I kept insisting something was wrong. She begrudgingly said, “I guess I can refer you to a rheumatologist.” Turns out I have fibromyalgia. And I have for about 15 years now. Don’t give up! Your health is too important!

    https://fibromyalgia-6.creator-spring.com/
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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Fibromyalgia аnd Sсаlр Pаіn: Whу Fіbrоmуаlgіа Can Cаuѕе Sсаlр Pаіn

    Fibromyalgia аnd Sсаlр Pаіn: Whу Fіbrоmуаlgіа Can Cаuѕе Sсаlр Pаіn

    Fibromyalgia is a complex соndіtіоn thаt is rеѕроnѕіblе for a lot of dіffеrеnt ѕуmрtоmѕ. Including wіdеѕрrеаd раіn mаnу ѕіtеѕ of thе body, system аrе affected. But yet, раіn іn thе ѕсаlр аnd hеаd is соmmоnlу experienced.

    Someone with fіbrоmуаlgіа also fееlѕ еxtrеmеlу tired, ѕuffеrѕ ѕlеер dіѕturbаnсеѕ, dерrеѕѕіоn аnd сhаngеѕ іn body habits – frequent urination and іrrіtаblе bowel symptoms – fоr example.

    The еxасt саuѕе of fіbrоmуаlgіа іѕ nоt rеаllу well undеrѕtооd but іt mау bе аn autoimmune соndіtіоn thаt аffесtѕ thе thуrоіd glаnd, causing іt tо become under асtіvе. This еxрlаіnѕ some оf thе ѕуmрtоmѕ but оthеrѕ mау bе duе to furthеr еffесtѕ оf thе autoimmune rеѕроnѕе.

    Having раіn or tеndеrnеѕѕ in the scalp іѕ different to hаvіng a hеаdасhе. Sсаlр раіn is fеlt аt thе surface оf the ѕkіn covering thе skull and tеndѕ tо bе ѕhаrр, ѕtаbbіng or рrісklу, with a tіnglіng sensation rаthеr thаn thе deep thrоbbіng раіn оf a hеаdасhе. It іѕ rarely аѕѕосіаtеd with оthеr hеаdасhе ѕуmрtоmѕ ѕuсh as nаuѕеа, vоmіtіng, or ѕеnѕіtіvіtу tо light оr ѕоund.

    Sсаlр раіn hаѕ several роѕѕіblе саuѕеѕ but is one of those health рrоblеmѕ that ѕоmеtіmеѕ рrоvеѕ іmроѕѕіblе tо dіаgnоѕе, ѕuggеѕtіng іt mау also hаvе a ѕtrеѕѕ соmроnеnt.

    Hair Lоѕѕ аnd Othеr Hair Prоblеmѕ іn Fіbrоmуаlgіа

    Adapting Your Hair Cаrе аnd Dеаlіng with Hаіr Prоblеmѕ in Fіbrоmуаlgіа
    Fіbrоmуаlgіа саn аffесt еvеrуthіng, including уоur hаіr. Sоmеtіmеѕ the illness іtѕеlf саuѕеѕ сhаngеѕ whіlе other tіmеѕ our ѕуmрtоmѕ аrе rеѕроnѕіblе.

    Thіѕ isn’t аn аrеа that’s been researched, whісh іѕ understandable – it’s nоt оnе of our wоrѕt symptoms bу any ѕtrеtсh, аnd іt also doesn’t арреаr tо be one of thе mоrе common оnеѕ. Othеr then that, thоugh, wе hаvе tо rеlу оn thе еxреrіеnсе оf оthеrѕ wіth thіѕ іllnеѕѕ to learn аbоut this раrtісulаr problem.

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    Hair Loss іn Fibromyalgia

    Hair lоѕѕ is оn thе symptoms lіѕt fоr fіbrоmуаlgіа. Thе gооd news іѕ that іt’ѕ tеmроrаrу: our hаіr falls out, аnd then іt grоwѕ bасk in. Thе bad news іѕ thаt wе has nо рrоvеn treatments fоr рrеvеntіng the fаll-оut.

    Mаnу people with fіbrоmуаlgіа rероrt that thеу lose hair durіng tіmеѕ оf high ѕtrеѕѕ оr durіng flаrеѕ. It’ѕ соmmоn tо hеаr about ѕоmеоnе wаѕhіng their hаіr only tо еnd up with their hаndѕ соvеrеd іn іt. Sоmеtіmеѕ оur ѕіgnіfісаnt others might notice an аbnоrmаl аmоunt of hаіr іn the bаthtub or оn a ріllоw.

    Whеnеvеr wе have so mаnу signs оr ѕуmрtоmѕ thаt can be dіѕаblіng аnd fоrсе significant changes uроn uѕ, іt mіght ѕееm ѕіllу оr frіvоlоuѕ to tаlk аbоut hair іѕѕuеѕ.

    However, thе wау and manner we look mау hаvе some a trеmеndоuѕ impact оn ѕеlf-еѕtееm, which саn оftеn tаkе a bеаtіng anyway whеn уоu lose аbіlіtіеѕ аnd іndереndеnсе to сhrоnіс dіѕеаѕе.

    Sсаlр Pаіn and Fіbrоmуаlgіа

    A less соmmоn соmрlаіnt thаn hair lоѕѕ іѕ ѕсаlр раіn. I’vе hеаrd from ѕоmе people that their ѕсаlр often fееlѕ lіkе it’s оn fіrе and thеу can’t еvеn bear tо wаѕh or bruѕh thеіr hair.

    Whіlе a burning ѕеnѕаtіоn thаt comes аnd goes certainly ѕееmѕ соnѕіѕtеnt wіth fibromyalgia раіn, wе dоn’t have аnу evidence that ѕсаlр раіn іѕ a fibromyalgia ѕуmрtоm.

    You ѕhоuld be sure to dіѕсuѕѕ оdd ѕуmрtоmѕ lіkе thіѕ wіth your dосtоr tо ѕее іf something еlѕе соuld bе gоіng оn.

    Hаіr-Cаuѕеd Pain

    One tуре оf fіbrоmуаlgіа pain іѕ allodynia, which іѕ раіn from something thаt don’t be раіnful, ѕuсh аѕ a loose waistband оr hair brushing аgаіnѕt thе skin.

    Eѕресіаllу big hair саn саuѕе pain as wеll, just from thе wеіght. These рrоblеmѕ make ѕоmе реорlе dесіdе tо cut thеіr hаіr ѕhоrt оr сhаngе thе ѕtуlе.

    Othеr реорlе report pain frоm hаvіng thеіr hаіr рullеd bасk іn a роnуtаіl оr bun whіlе hаіr сlірѕ аnd headbands mау bе too раіnful fоr ѕоmе of uѕ to wеаr.

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    Hаіr Styling Wіth Fibromyalgia

    Hаіr-ѕресіfіс symptoms can сhаngе thе wау wе approach оur hair, аnd so саn other ѕуmрtоmѕ such as раіn, fаtіguе, аnd excessive ѕwеаtіng.

    Thоѕе wіѕру lіttlе re-growing hairs саn dеtrасt from уоur hairstyle. Lоѕѕ саn noticeably thіn thе hаіr, and some people even rероrt bаld patches. Many of uѕ have changed or adapted оur hairstyles аѕ a rеѕult of thеѕе іѕѕuеѕ.

    Hоwеvеr, fоr a lоt оf us, styling оur hаіr аt аll іѕ dіffісult. Hоldіng thе arms uр tо bruѕh, braid, blow drу оr flаt іrоn саn lеаd tо аrm раіn thаt rаngеѕ frоm mіldlу annoying to ѕеrіоuѕlу debilitating.

    Whу Fіbrоmуаlgіа Can Cаuѕе Sсаlр Pаіn; Treatment

    Thе pain of fіbrоmуаlgіа іѕ bоdу-wіdе, ѕо іt shouldn’t be ѕurрrіѕіng that it еxtеndѕ tо thе ѕсаlр. Fіbrоmуаlgіа аnd сhrоnіс fаtіguе syndrome саn affect еvеrу аrеа of уоur lіfе, rіght down tо thе mоѕt оrdіnаrу tаѕkѕ оf daily life. Sоmеtіmеѕ, уоu mіght bе ѕurрrіѕеd bу how dіffісult “оrdіnаrу” thіngѕ have become for уоu.

    Sсаlр Pаіn Wіthоut a Cаuѕе

    If scalp pain, оr ѕеnѕаtіоnѕ in thе ѕсаlр ѕuсh аѕ tingling, fееlіngѕ of cold оr hеаt, оr a type of wrіgglіng feeling оссur without another ѕуmрtоmѕ, іt may bе thаt thіѕ is duе tо ѕtrеѕѕ or anxiety.

    It іѕ a symptom thаt іѕ reported by a lоt оf реорlе аnd іt сlеаrlу wоrrіеѕ them. Thinking that thе ѕеnѕаtіоnѕ іn thе scalp are duе tо ѕоmеthіng more ѕеrіоuѕ mаkеѕ thе рrоblеm worse.

    If the аbоvе соndіtіоnѕ аrе оbvіоuѕlу nоt рrеѕеnt, hоwеvеr, ѕсаlр pain аnd odd feelings in the ѕсаlр are unlikely tо be a ѕіgn that anything is seriously wrоng.

    It mау bе a gооd іdеа tо ѕреаk tо уоur doctor about it so that thеу саn set your mіnd аt rеѕt, аnd thеn аѕk аbоut ѕtrеѕѕ management ѕtrаtеgіеѕ оr relaxation thеrаріеѕ.

    The bе referred tо the tор of thе head frоm nесk muѕсlеѕ whеrе thеу attach tо thе ѕkull, hе соntіnuеѕ. In addition, аllоdуnіа іѕ аnоthеr kіnd оf раіn that mау bе рrеѕеnt іn fibromyalgia. Allo mеаnѕ оthеr and dуnіа mеаnѕ раіn.

    Allodynia rеfеrѕ tо whеn lіght tоuсh оn the ѕkіn is раіnful, It іѕ associated with increased activity оf a nеurоtrаnѕmіttеr called NMDA, and gеnеrаllу rеѕроndѕ tо overall treatment оf thе fіbrоmуаlgіа.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Convincingly Fibromyalgia Has Been considered As A Lifelong Crucial Apprehensive Sickness

    Fibromyalgia is the second most common rheumatic disorder behind osteoarthritis and, though still widely misunderstood, is now considered to be a lifelong central nervous system disorder, which is responsible for amplified pain that shoots through the body in those who suffer from it. Daniel Clauw, M.D., professor of anesthesiology, University of Michigan, analyzed the neurological basis for fibromyalgia in a plenary session addressed today at the American Pain Society Annual Scientific Meeting.

    Fibromyalgia can be thought of both as a discreet disease and also as a final common pathway of pain centralization and certification. Most people with this condition have lifelong histories of chronic pain throughout their bodies,” said Clauw. “The condition can be hard to diagnose if one isn’t familiar with classic symptoms because there isn’t a single cause and no outward signs.”

    Clauw explained that fibromyalgia pain comes more from the brain and spinal cord than from areas of the body in which someone may experience peripheral pain. The condition is believed to be associated with disturbances in how the brain processes pain and other sensory information. He said physicians should suspect fibromyalgia in patients with multifocal (mostly musculoskeletal) pain that is not fully explained by injury or inflammation.

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    “Because pain pathways throughout the body are amplified in fibromyalgia patients, pain can occur anywhere, so chronic headaches, visceral pain, and sensory hyper-responsiveness are common in people with this painful condition,” said Clauw.

    “This does not imply that peripheral nociceptive input does not contribute to pain experienced by fibromyalgia patients, but they do feel more pain than normally would be expected from the degree of peripheral input. Persons with fibromyalgia and other pain states characterized by sensitization will experience pain from what those without the condition would describe as touch,” Clauw added.

    Due to the central nervous system origins of fibromyalgia pain, Clauw said treatments with opioids or other narcotic analgesics usually are not effective because they do not reduce the activity of neurotransmitters in the brain. “These drugs have never been shown to be effective in fibromyalgia patients, and there is evidence that opioids might even worsen fibromyalgia and other centralized pain states,” he said.

    Clauw advises clinicians to integrate pharmacological treatments, such as gabapentinoids, trycyclics, and serotonin reuptake inhibitors, with nonpharmacological approaches like cognitive behavioral therapy, exercise and stress reduction.

    “Sometimes the magnitude of treatment response for simple and inexpensive non-drug therapies exceeds that for pharmaceuticals,” said Clauw. “The greatest benefit is improved function, which should be the main treatment goal for any chronic pain condition. The majority of patients with fibromyalgia can see improvement in their symptoms and lead normal lives with the right medications and extensive use of non-drug therapies.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Should I get a Service dog for my Fibromyalgia?

    “I have FMS, CFIDS, hypermobility, migraines, and a few other issues. My dog is already tremendously helpful to me. She can pick up things I drop and hand them to me, carry a pack so I don’t have the weight of a purse on my shoulders or waist, fetch things I ask her to get, carry messages or other things to my husband to save me trips up and down the stairs, and is learning to do things like turn lights on/off, pick up things and put them away, and even strip the dirty bedding off the beds and take them to the laundry room.”

    Just What Is a Service Dog Anyway?

    According to the Americans with Disabilities Act, a service animal is “any guide dog, signal dog, or another animal individually trained to provide assistance to an individual with a disability. If they meet this definition, animals are considered service animals under the ADA regardless of whether they have been licensed or certified by a state or local government.

    Service animals perform some of the functions and tasks that the individual with a disability cannot perform for him or herself. Guide dogs are one type of service animal, used by some individuals who are blind. This is the type of service animal with which most people are familiar. But there are service animals that assist persons with other kinds of disabilities in their day-to-day activities.”

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    For example, alerting persons with hearing impairments to sounds, pulling wheelchairs or carrying and picking up things for persons with mobility impairments, and assisting persons with mobility impairments with balance. However, “A service animal is not a pet.”

    What Does This Have to do with Fibromyalgia?

    Oh, let us count the ways! When your fibro has you in so much pain that you don’t want to get out of bed, that puppy still has to be fed and walked so you are forced to get up, if only for a bit. But that’s the “worst” part about a service dog to help with your fibromyalgia symptoms, and it’s not a bad thing either.

    Can you identify with the needs in this story? “Lily (57# Siberian mix) will jump off her bed from two rooms away and come to steady me when I wobble. It’s amazing how she knows. She also scans my body at nap and bedtime to see which area needs her warmth the most. I’ve seen her give Moira a look like, “Get over here and help me”, but Ri [Moira] is oblivious. On the other hand, this morning I couldn’t get out of bed because there was a pillow on the floor and I couldn’t step over it at that time of day. Moira accessed the situation and pulled the pillow out of the way.”

    Think through your symptoms, everything from fatigue and muscle pain to being foggy and depressed. Service dogs can help with all of these symptoms. In fact, “Anything from sitting on your lap, helping with orientation, finding calm spots, mobility support, retrieving meds or certain things you will need, even keeping eye contact is a task if it is necessary for you,” says the pros at Dogster.

    Service dogs can pull you up inclines or guide you downstairs to keep your balance. They provide body heat and contribute to overall well-being. As one happy fibro sufferer states, “I haven’t broken another bone since he has been trained to assist me, so I walk more in spite of the pain.” They can help you out of the tub and off the floor if you fall. Service dogs can also be trained to catch you just before your joints or back gives out and can even alert you before you overdo it or are about to crash.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Lady Gaga Fibromyalgia Announcement Gives Voice To Millions of Patients

    Logan, Utah. Statement from Sharon Waldrop, Vice President of the National Fibromyalgia & Chronic Pain Association on Lady Gaga’s recent announcement that she suffers from the illness:

    “We commend Lady Gaga for the incredibly brave act of revealing her fibromyalgia diagnosis. By sharing her story with the world, she is giving voice to the estimated five million Americans like me–overwhelmingly women–who suffer from the illness.

    Fibromyalgia is characterized by a long list of symptoms, including chronic pain and debilitating fatigue. The cause is still unknown, there is no cure and it lacks effective treatments and understanding. Better treatments and a cure can be found, if we raise awareness of the disease and the devastating challenges it presents daily to millions of American families.

    Fibromyalgia’s invisibility and the public’s misunderstanding of its effects often leave people afraid to reveal their diagnosis. When I was diagnosed with the disease I thought my life was over. My once-healthy body suddenly felt badly bruised and broken even though on the outside I looked completely fine.

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    I was even yelled at for using my disability parking pass because people didn’t believe it was mine. Those who suffer from fibromyalgia could be your friends, coworkers, neighbors, and family members, who have been suffering in silence with this disease for years. It is our hope that Lady Gaga’s courageous act to step forward into the light will inspire others to do the same.

    More answers are out there, but we need everyone’s help to advocate for increased resources toward finding them. We urge the public to contact their legislators and ask them to implement and fund the National Pain Strategy developed by the Department of Health & Human Services to address the burden of Chronic Pain in America.

    We look forward to continuing our work on finding a cure for fibromyalgia. With the support and participation of leaders like Lady Gaga, the government, advocates, and patients, no goal is unachievable.”

    The National Fibromyalgia & Chronic Pain Association is your partner in tackling fibromyalgia and chronic pain. Our goal is to end chronic pain conditions from derailing lives by promoting early diagnosis, driving scientific research for a cure, and advocating for appropriate, accessible, and affordable treatments.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • 10 Fast Fibro Facts to Help Spread Awareness

    10 Fast Fibro Facts to Help Spread Awareness

    Fibromyalgia Awareness Month may not be until May, but that doesn’t mean we shouldn’t make the most of every opportunity for people in the fibro community to share their stories and raise awareness of this often misunderstood illness.

    Sharing facts about fibromyalgia on social media platforms like Twitter and Facebook can help educate the public about what it’s like to live with the condition. To help you get started, we’ve put together some basic fibro facts, with help from chronic illness.

    • Fibromyalgia is considered a condition rather than a disease because there are no specific causes or recognizable symptoms. A syndrome is a collection of symptoms and medical issues that occur together but cannot be attributed to an identifiable cause.
    • There is no cure for fibromyalgia. Treatment is centered on managing the symptoms of the syndrome and making life more comfortable for those who live with fibro.
    • While men and children can develop fibromyalgia, 90 percent of sufferers are women.
    • Fibromyalgia affects all ethnic groups equally.
    • Diagnosis usually occurs in young women between the ages of 20 and 50, but as a person gets older they are more likely to develop fibromyalgia.
    • By the age of 80, around 8 percent of people meet the criteria of fibromyalgia from the American College of Rheumatology.
    • Widespread pain is the number one symptom of fibromyalgia. People living with the condition will have tender spots in various places on their body and will feel pain much more than those without the condition.
    • Chronic fatigue and psychological issues are also common symptoms associated with fibromyalgia.
    • The pain can be so debilitating it can interfere with everyday tasks and completely overtake patients’ lives.
    • Fibromyalgia often overlaps with other health conditions such as anxiety disorders, IBS, chronic fatigue syndrome, and depression.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Thetford woman fundraising to see specialist about her fibromyalgia hopes it could help to rebuild her life

    A woman who has spent the past eight years in constant pain is hoping the specialist treatment will help her to rebuild her life.

    In 2016 Emma Parslow Cope was diagnosed with the long-term condition fibromyalgia which causes an increased sensitivity to pain, exhaustion, headaches and problems with mental processes.

    The 27-year-old, who lives in Thetford, said the condition has had an enormous impact on her life. She has had to leave her job and it has put a strain on her relationships with family and friends.

    Miss Parslow Cope describes the pain throughout her body as like a “burning sensation” and she suffers from fatigue and has trouble sleeping.

    As a result of her condition she has developed anxiety and depression.

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    She is now hoping to raise £10,000 to cover the costs of seeing a specialist at the Fibro Clinic in London and any treatment, medication and accommodation needed.

    Miss Parslow Cope said: “I am desperate to get help so I can get myself in a state of managing so I can then do some volunteer work to build my life up.

    “The specialist should be able to put me on a programme and understand me as a person. I hope they should be able to give me treatment to help me get some sort of proactive life back.”

    A keen sportswoman, in 2010 Miss Parslow Cope hurt her hip during a college football match.

    She believes it was this injury which led to the fibromyalgia but she was not diagnosed for six years.

    On December 31 last year the former West Suffolk College student said she tried to take an overdose because of the condition.

    “I just did not want to be here anymore,” said Miss Parslow Cope who attends the Fibromyalgia Bury St Edmunds support group run by fellow fibromyalgia suffer Brett Robertson. “It just takes over your head.”

    She is now hoping to help raise awareness of the condition – which her twin sister Louise was also diagnosed with this year – which she says is misunderstood.

    She said: “I want people to be behind fibromyalgia suffers. I want people to understand and the more people who are aware of it and understand it the better.

    “I am tired of people saying it is not real because I am living with something which is severe and nasty 24 hours a day.”

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    Click Here to Visit the Store and find Much More….

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Good News: First License Granted to Treat Pain with Medicinal Cannabis

    License to treat pain with medicinal cannabis given the go-ahead.

    A license to treat chronic pain with medicinal cannabis has been granted here for the first time, it has emerged. A 3-month agreement was given the green light by the Department of Health to use Tetrahydrocannabinol (THC) people in constant agony.

    THC is the principal psychoactive constituent of cannabis. It is currently illegal to use medicinal cannabis here – but medical consultants can apply for the license on a case by case basis. A three-month license can be granted on foot of an application made directly to the Minister for Health under section 14 of the Misuse of Drugs Act.

    Under guidelines from Chronic Pain Ireland, the THC would NOT be consumed via smoking. A patient would ideally take it by vaping or in their tea. Under the strict terms, a medical professional would administer a starting dose, monitor the patient, and adjust the dose accordingly, they say. Patients will be placed under constant medical supervision.

    Last February, Health Minister Simon Harris announced that he would implement a Health Products Regulatory Authority recommendation that cannabisbased products be made available to some patients with multiple sclerosis and epilepsy, and those suffering nausea in chemotherapy.

    However, chronic pain was not included in Mr. Harris’ plan. It was on this basis that Chronic Pain Ireland applied to the minister for a license, for one of their members, along with their medical consultant.

    There were no formal application guidelines from the Department of Health, so Mr. McLoughlin created one from scratch. This is now available on Chronic Pain Ireland’s website.

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    The application included how THC would be administered, details of the patient’s medical consultant, and what dosage they would potentially start on.

    The patient can take the medicinal cannabis either through tea or by vaping.

    “Some people are desperate due to chronic pain,” said Mr. McLoughlin. “I personally know of people who use cannabis for chronic pain. Some say it works, some say it doesn’t. But you must always go to your doctor.”

    Professor of pharmacology and therapeutics David Finn, who is also the co-director of the Centre for Pain Research at NUI Galway, said the granting of the license was an “important development”.

    “This is a very interesting and important development which demonstrates a recognition by Irish medical professionals and the minister for health of the potential therapeutic value of medicinal cannabis for the treatment of chronic pain,” said Prof Finn.

    “Chronic pain is the most researched indication for cannabinoids, and the majority of clinical studies, meta-analyses, and systematic reviews conclude that cannabis or cannabinoids can be effective in alleviating certain types of chronic pain.

    “Approximately 20% of the Irish population suffers from chronic pain, and up to 40% of patients report that the management of their pain is inadequate, either due to the limited efficacy of existing treatments or unacceptably high levels of side-effects.”

    Solidarity-People Before Profit Alliance TD Gino Kelly has been a longtime campaigner for legalizing cannabis for medicinal purposes and brought forward an opposition bill towards this end.

    The Cannabis for Medicinal Use Regulation Bill 2016, is now entering its third stage of debate and will go before the Oireachtas health committee early next year. “The tide has now turned. It is a significant day for people with chronic pain in Ireland,” said Mr. Kelly.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • 9 Celebrities that came Forward to Promote Awareness of Fibromyalgia!

    It’s so important that celebrities with fibromyalgia come forward to help enlighten the public and promote awareness of the disease. They give a voice to fibromyalgia sufferers and promote awareness in ways that typical patients can’t.

    Here are just a few of the stars that have spoken out about fibromyalgia over the years:

    Michael James Hastings
    Also known as Captain Mike on the TV series The West Wing, Hastings was diagnosed with FMS around 30. Not only has he been able to raise awareness but he has helped raise millions of dollars for those organizations that are working towards finding more effective treatments and a cure.

    Sinead O’Connor
    The “controversial” Irish singer with a shaved head, Sinead O’Connor took three years off from music in 2003 to deal with her FMS and spend time with her kids.

    Jo Guest
    Jo Guest was a successful model in the 1990s and was very popular in England. She continues to stay optimistic even though FMS has taken its toll on her body. She says her husband is her support system and she’s hopeful not only that a cure would be found, but that she could resume her modeling career.

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    Morgan Freeman
    Known for his many roles in Hollywood blockbusters (including The Dark Knight Rises and Shawshank Redemption), Freeman has also been an outspoken spokesperson for fibromyalgia.

    Mary McDonough
    Also known as Erin Walton from the popular TV series The Waltons, it took 10 years before McDonough was diagnosed with lupus and fibromyalgia. In her book Lessons From the Mountain, she touches on her years of pain and her diagnoses.

    Florence Nightingale
    An English army nurse and Red Cross pioneer, Florence Nightingale’s best known for her role in modern nursing and hygiene practices. Although she displayed the symptoms of FMS and chronic fatigue, there was no name for it back in the late 1800s.

    Susan Flannery
    Flannery made the role of Stephanie Forrester on the soap opera The Bold and the Beautiful famous. She took a medical leave in 2007 to deal with her fibromyalgia. Even though she’s returned to the show, she still struggles with her symptoms, and like all patients, takes it day by day.

    Rosie Hamlin
    Hamlin was a singer with Rosie and the Originals; their most famous song was “Angel Baby.” She stopped performing in 2005 due to advanced fibromyalgia. She passed away on March 30 of this year at the age of 71.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Deficiencies quality of life and work life too often mysterious illness: Fibromyalgia

    Especially people busy with very common, most people “feel like beaten” a disease that has no sense to say that beyond sharing with you: Fibromyalgia. According to experts, “the era of the disease.”

    quite negatively affect the quality of life that permeates every aspect of our lives, even though it is very common with this disease, we will protect your mystery.

    Fibromyalgia is a chronic pain syndrome characterized by widespread pain and fatigue.

    Generalized muscle aches, headache, fatigue, exhaustion, fatigue, sleep disorders,

    Sometimes accompanied by a problem that we are also going to the toilet spastic colitis chronic disease.

    Fibromyalgia syndrome FMS briefly passing.

    The following symptoms occur when the person begins to manifest:

    • Knows himself, he begins to feel like the person I used to be
    • not enough for the body they want to do
    • since the former does not like to be touched
    • It is difficult to explain to those around him
    • Still in good condition, despite the fact that all these appearances

    The first data about the diagnosis, the person starts from a place of pain to be expressed that spread throughout the body.

    This pain; normally flammable, is described as sızlayıc. Sleep disorders; sleep a lot, sometimes insomnia: sleep is not supported with the mood of the person begins to deteriorate as a result. sometimes with burning pain, in addition to the above symptoms may be accompanied by a sense of imbalance.

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    Depression and anxiety are some of the symptoms used to diagnose.

    Fibromyalgia can cause depression and social isolation.
    This effect is caused by the tension of the FMS with great physical and psychological.
    This reduces the strain on our working hours can lead to loss of jobs and still our income.

    Fibromyalgia, despite the prevalence of rare cause disease is still not completely understood.

    However, it has been reported that seen in humans in the most sensitive and susceptible personality made.

    Moreover, today it is often misdiagnosed and misunderstood placed.

    Fibromyalgia, one of the most common diseases mixed with other disorders; because many other performances are very similar to the symptoms of the disease. There are also specific laboratory tests to diagnose the disease. At this point, people critical of the accuracy of these tests are performed in the complaints.

    In fact, fibromyalgia syndrome, symptoms of a type of community.

    (That’s why it is often confused with other diseases). When these symptoms occur at the same time, the likelihood of developing the disease or illness omen is too high.

    put people diagnosed with fibromyalgia; three months should follow the complaints and symptoms.

    At least 12 points (region of the head-neck neck, chest, shoulders, head, the outer side of the elbow, the inside of the shoulders, waisthip crossing point outside the outer side of the hip, knee, interior, etc.) be sensitive to pain, a basic requirement. The people complain when it comes to this, that the tests are done at this point is very important.

    Most women and observed in the group of young adults.

    Women changing hormonal systems (menstruation, menopause), stress, and anxiety that occurs, causing the power to deal with the situation. In this case, it is preparing the appropriate field in the recurrence of the disease and settlement. Women in menopause and highlighted the effectiveness of the stress hormone cortisol disease studies also support this.

    Menstrual periods of women, in addition to physiological factors such as changes in menopause and hormonal balance; The lack of habit of sports overload the body home, do excessive cleaning or frequently changing factors such as the location of the house is preparing the ground for fibromyalgia. In addition, environmental factors such as exposure to cold and heat differences can be counted among the causes of fibromyalgia.

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    Fibromyalgia affects many professions.

    Perfectionists work a holism and in an environment where they are not very suitable environmental factors Employees (architects, dentists, and even work office desk, brokers, journalists …) are considered in this group.

    the quality of work in person is reduced; Reduce attention skills and perception.

    Enjoy it affects a person’s life, motivation and reduces efficiency. The statistics of fibromyalgia in the United States, as it leads to job loss, then the cost of the highest-ranking in patients with heart disease who received second place. economy, ie business life and adversely affecting fibromyalgia ‘disease was’ daily life can also be said.

    So we see these kinds of symptoms in which we have to apply?

    First, we must apply the right direction for the diagnosis of fibromyalgia in rheumatology. However, because it is a complicated disease, your doctor may want the opinions of other experts.

    Or treatment?

    not a single expert treatment of fibromyalgia; multidisciplinary way. they need treatment to receive the support of many branches. especially in physical and rehabilitation, psychologists, therapists, and physiotherapists to get professional help therapy required. When queries are necessary to get support from other medical specialties.

    No one in all the symptoms can be very unlikely.

    There is a standard way to treat fibromyalgia. inform people, exercise, diet, there is a lot of psychological support for drug treatment stage.

    They can be summarized as follows;

    • Dress  according to weather conditions
    • Avoid the stifling atmosphere
      (Because it is not very likely to avoid stress),
    • learn ways to combat stress
    • obtain the necessary support to live in peace with our own psychologist
    • Good nutrition
    • To set the hours of work and rest
    • To regulate the working environment: ergonomic seats, a proper desk height, look at the computer monitor at
    • the elbow of the arm-shaped keyboard that prevents the fall.
    • Ourselves a good sport
    • One of yoga, swimming, thai-chi and tai-bo, can be very useful in activities that are physical and mental integrity.

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