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Her Brain was on fire.

Her Brain Was On Fire: A Neuroinflammation Story By Cort Johnson on July 24, 2015 44 Comments 0 inShare 0 +100%- A Neuroinflammation Story Who knows how it started? Did those two mysterious red dots on a vein on her arm mean anything? Could that businessman who sneezed on her in the subway triggered her illness? Or did her biological stars just suddenly align in the strangest configuration ever? Susannah went from healthy to psychotic with terrifying speed Susannah went from healthy to psychotic with terrifying speed Nobody ever figured out what triggered Susannah’s “month of madness” and in the end it didn’t matter. What mattered was that a young New York Post reporter quickly got very ill and for quite a while nobody knew what to do about it. This is not a story about chronic fatigue syndrome or fibromyalgia but it could be. The subplots running through it – a woman with the mysterious illness, the predisposition to look for a psychological cause, the negative test results, the misdiagnoses, the strange “brain” symptoms – could be patched onto many ME/CFS and FM stories, and indeed other mysterious illness stories. Susannah’s story shows how bad neuroinflammation – a possible cause of chronic fatigue syndrome and/or fibromyalgia – can get, how much remains to be learned about the brain and at the same time how quickly the medical researchers are moving forward. Ultimately her story provides hope for people with mysterious central nervous systeme disorders. Susannah chronicled her story in a best-selling book called “Brain on Fire: My Month of Madness“. Her Brain on Fire Susannah Callahan was a young talkative, funny and dedicated New York Post reporter when her month of madness began. First came a unreasonable fear of bedbugs, then a flu-like episode, then a search through her boyfriend’s emails and letters. Even as she was appalled at the boundaries she was breaking she keep breaking them. She didn’t feel like herself; she was anxious, nauseous and unsettled. When her left hand went numb her gynecologist fixed her up with a neurologist described as “one of the best in the country”. Except for some swollen lymph nodes. though, all her tests were normal. Maybe, he said she had mono. Basically he told her she was OK and to relax. But she wasn’t. Over the next week she had trouble sleeping, was overwhelmed by the colors and bright lights in the city, and her erratic behavior increased. Her moods whipped from one extreme to the other. She thought she was having a nervous breakdown. When she had a seizure in the middle of the night her boyfriend called 911. overstimulation Crowded, visually stimulating environments began causing Susannah problems GET OUR FREE ME/CFS AND FIBROMYALGIA INFO New-postsLike the blog? Make sure you don’t miss the latest on ME/CFS and FM treatment and research news by registering for our free ME/CFS and Fibromyalgia blog here. Back to the neurologist she went. He proposed she was working and partying too hard and not sleeping. All she needed was rest and to get off the booze. A psychiatrist diagnosed her with a form of bi-polar disorder and put her on medication. Meanwhile her descent continued. Wild paranoid thoughts filled her mind. She accused her parents of kidnapping her. She tried to dart out of a moving car. Despite the seizure medication she had another one. Back again to the prominent neurologist she went – this time with her mother – who demanded more tests and better answers. After a normal EEG, however, the neurologist again diagnosed her with alcohol withdrawal. Despite her mother’s protests that her daughter had not had a drink in a week, the neurologist told Susannah to stop drinking and take her medication. (In his notes he reported she was drinking two bottles of wine a night). Psychosis Her mother would have none of it and Susannah was booked into 24 hour epilepsy EEG monitoring unit at the New York Langorne Medical Center. As she entered the hospital she had a massive seizure. Her delusions mounted. She asserted her parents were turning into other people. She felt people on TV were talking about her. She tried to escape. She declared she had multiple personalities. She became so unmanageable she was in danger of being admitted to a psychiatric hospital. Hints were made that that was a place she wanted to be. Five doctors were quickly on her case. Four days later four more including an infectious disease specialist joined on. As her psychoses began to recede leaving her in a zombie-like state at times a lumbar puncture was scheduled. options limited With her options running out Susannah was in danger of ending up in a psychiatric ward – perhaps permanently The slightly elevated levels of white blood cells found – the first abnormal test results yet – raised hopes she had an infection but further testing at the CDC and New York State Labs found no signs of infection (herpes, Lyme disease, tuberculosis or others) or autoimmunity. Her MRI and CT scans continued to be normal. When a top doctor abruptly quit her case her parents became distraught. With few positive test results and her options running out, Susannah was in danger of being diagnosed with a mental disorder and ending up, perhaps for the rest of her life, in a psychiatric hospital. Then one more doctor, Dr. Souhel Najjar joined the team. Najar’s ability to solve some mystery cases at the hospital had made him the go-to man for difficult cases. He discarded the psychosis diagnosis and despite the negative autoimmune test results he put her on five rounds of IVIG. Join Health Rising’s ME/CFS, FM and Chronic Pain Forums! ForumsShare your pain, make friends, find new treatment options, check out recovery stories and more in the Health Rising ME/CFS, FM and Chronic Pain Forums here Encephalitis Susannah, however, continued to worsen. She was diagnosed with catatonia and began making strange Frankenstein-like movements with her arms. Najar ordered another lumbar puncture. This time there was good news; a quadrupling of her white blood cell counts indicated central nervous system inflammation was present – lots of it. Her diagnosis was immediately switched from psychosis to encephalitis. brain inflammation It turned out that inflammation – eating away at key areas of her brain – was causing her problems. Najjar’s first examination of her proved to be groundbreaking. When asked to draw the numbers on a clock she fit all twelve hours into the right side of the clock leaving the left side blank. That clue suggested that the right hemisphere of her brain have been ravaged by inflammation – probably by an autoimmune process. Her brain, he said, was on fire. The probable next step was steroids, plasmaphoresis and/or more IVIG. First, though, Najjar wanted a brain biopsy. Reluctantly her family agreed. The biopsy showed massive numbers of microglial cells attacking her nerves. The biopsy indicated Susannah had an as yet undiagnosed autoimmune disorder. (She had been tested for only a few out of the hundred or more autoimmune disorders before). The treatment regimen was brutally simple: massive doses of steroids infused into her over three days to stop the immune attack in its tracks followed by lower doses to quell the remaining inflammation over time. Meanwhile her blood was sent to a Dr. Joseph Dalmu at the University of Pennsylvania. The results came back positive. A New Disease Four years earlier Dalmau had described four young women with psychiatric symptoms and encephalitis. Testing revealed NMDA-receptor antibodies were attacking the hippocampus – the center of memory and learning – and the frontal lobes – the center of higher functioning and personality. Two years later Dalmau published an account of twelve women with what he now called anti-NMDA receptor autoimmune encephalitis. A year later a hundred women had been identified. By the time Susannah because ill over 200 had been. When her results came back, Susannah Cahalan was the 217 woman to become diagnosed with the illness. In retrospect, the course of the disease had been very clear. The initial flu-like symptoms reflected the immune system starting it’s ramp up. The psychiatric symptoms occurred as the antibodies attacked the nerves in her hippocampus and frontal lobes. The catatonia was the result of progressive damage. Recovery The brain is radically resilient. Susannah Cahalan The steroids probably saved Susannah from entering a life-threatening stage of catatonia but her brain damage was severe. She was extremely cognitively challenged and had trouble speaking and smiling. Whether she would ever return to her former self was unclear. brain cells A new subspeciality – autoimmune neurology – has emerged. Najjar decided Susannah was too ill to try anything but the nuclear option. He would hit her overactive immune system as hard as he could and in as many ways as he could. Susannah would again get massive doses of steroids, but this time they would be followed by plasmaphoresis to purge her body of the antibodies, and then IVIG to further neutralize the antibodies. She would do this several times. Over the next six months or so she would get 12 IVIG infusions. Besides this she would be on five drugs: Atvian to prevent catatonia, Geodon for psychosis, Trileptal for seizures, Labetolol for high blood pressure and Colace for constipation and get speech and cognitive retraining. She began a slow recovery. A month later she wrote that her first real glimpses of recovery had occurred. Five months later she made her first tentative return to work in the New York Post newsroom. A couple of weeks later she dropped her anti-anxiety and anti-psychotic drugs. A year later she felt she’d returned to full health. Conclusions ..I realized now that my survival, my recovery – my ability to write this book – is the shocking part. ” Susannah Cahalan Susannah was one of the lucky ones. Without the seizures (not everyone has them) she would have ended up in the psych ward instead of the epilepsy ward. Perhaps she would have found another Najar there – a doctor on top of his game who was aware of a rare disease that had been recently discovered – but there’s no telling. However it happened she was lucky Najar. (Another case mentioned in the book describes a more typical story. A sophomore in college became paranoid, checked herself into a psych ward, was diagnosed with “psychosis, not otherwise specified”, sedated and released. A month or so later she was admitted to another psychiatric institution. The doctor there rejected the anti-NMDA receptor hypothesis because she wasn’t having seizures. She returned home and eventually became unable to add or do basic physical tasks. She returned to the hospital where her doctors, for the first time, informed her parents that her MRI test a year before indicated she had inflammation. As they prepared the IVIG a blood clot in her brain caused a massive seizure. During her seizure her father pushed Susannah’s article describing her illness into the neurologists hands. Her test for anti-NMDA receptor encephalitis was positive and she was air-evacuated to the University of Pennsylvania where Dr. Dalmau successfully treated her. She returned to complete health. (Despite proper treatment about 20% of patients are permanently disabled or die. Thanks to the work of Dalmau, Najjar, Susannah and her book those kinds of stories are disappearing. Since Susannah has diagnosed in 2009 over 2,000 women have been diagnosed with the disease. The New York Langone hospital also responded well. It put ten doctors on her case and her treatment costs were over $1,000, 000. There’s something comforting about the extent to which the medical system can go at times. Susannah’s story also revealed the limits of medical technology and how difficult making a diagnosis is the face of limited test findings. Susannah’s MRI’s and CAT scans were never abnormal. Even after she’d had seizures, psychotic episodes, sensory distortions and trouble writing and responding to people the wide blood cell counts in her lumbar puncture – indicating inflammation – were not particularly high. Her possible diagnoses at that point included hyperthyroidism, lymphoma, Devic’s disease and paraneoplastic syndrome. Only after she started drifting into catatonia were the markedly increased white blood cell counts indicative of severe inflammation present – and only after her antibody tests came back was her diagnosis ensured. Movement in the Medical Community Anti-NMDA-Receptor-Encephalitis has surely been around for many years. A search through the medical literature revealed some case reports dating back to the 1980’s but that was it until 2005. Once the disease had a name and a test progress was pretty rapid, however. At the time of Susannah’s diagnosis in 2009 Najjar believed that 90% of the cases went undiagnosed. Subsequent research suggests that was probably an underestimate. Dalmau’s found other receptor seeking autoimmune diseases since then. He believes by the time it’s all said and done more than twenty autoimmune diseases may be causing cases of”unidentified psychosis”, “encephalitis of unknown origin” and other idiopathic diagnoses. The understanding of the role anti-NMDA antibodies has broadened as well. They are now believed to play a role in at least some cases of autism, schizophrenia and dementia. Enough evidence has accumulated for a subspeciality called autoimmunity neurology to appear. It’s clearly a growth field. Susannah’s story is ultimately a hopeful one. The medical research community is responding. How many people with a now mostly treatable disease entered and remain in psychiatric wards is unknown, but since 2009 thousands of women have now been identified with the disorder. Susannah and others have created the Autoimmune Encephalitis Alliance to help spread the word. It’s not at all clear how, if at all, any of this applies to ME/CFS or FM. Autoimmune encephalopathies, after all, are still believed to be quite rare, but anything that helps explain central nervous system disorders that have defied comprehension is of obvious interest. That the medical community can move so quickly when it feels it’s onto something is encouraging as well. Next Up – Health Rising takes a deeper look at new world of autoimmune central nervous system disorders and Dr. Dalmau’s continuing work. Print Friendly Version of this pagePrint Get a PDF version of this webpagePDF Categories : Homepage Comments Pris Campbell says: July 24, 2015 at 4:12 pm Thank goodness one doctor finally had the knowledge to help her. This article illustrates all over again how so many doctors, when faced with symptoms they don’t understand, either call the person crazy or give stupid advice( stop drinking, when she wasn’t) . There’s a strong need for a computerized data system that doctors can use to plug in symptoms and have a variety of diagnoses to consider…if they would use it. Reply Cort Johnson says: July 24, 2015 at 8:42 pm Indeed, in the first neurologists defense a bit – Susannah later met a women in the epileptic ward suffering from seizures and other problems because of alcoholism – so it can happen. The neurologist clearly leapt to a conclusion – based on little evidence – and then stuck with it despite her continuing to get worse over time. Reply Greg says: July 24, 2015 at 11:00 pm If these cases offer an indication that neuro-inflammation may be a component of ME/CFS, does it explain how exercise/physical exertion directly causes a worsening of symptoms? And does it lead to any good guesses as to types of treatment that might lesson that effect? Anyone? Reply gloria says: July 24, 2015 at 4:39 pm why has my rhuematologist NOT referred me to a nuerologist for my “fibromyalgia” and chronic fatigue? it is hard for me to believe that there is nothing more to be found; this is a disorder that has very very hidden causes and i guess most of us aren’t worth the ‘cost;’ and so many of us just don’t have the energy anymore for dr appts or the costly co pays these tests cost; she-susannah had a support system and obviously good benefits and/or money Reply Linda says: July 24, 2015 at 5:09 pm All women sufferers? Odd. Reply Cort Johnson says: July 24, 2015 at 8:39 pm It’s another autoimmune disorder that primarily affects women. Reply David Fantle MD says: July 24, 2015 at 5:27 pm NMDA encephalitis does affect females much more often than males. We have diagnosed and treated a number of people with this disease over the past few years. The first one I recall was a young woman who, like the case you described, developed paranoid delusions and severe memory loss, and was admitted to the hospital psychiatric unit. While she had no clinical seizures, I read her EEG study and found frequent ‘silent’ seizure activity. This disease is often triggered by the immune system attacking a particular type of tumor, a teratoma of the ovary (which cross-reacts with brain tissue), which is what this patient ended up having. Removing the tumor often leads to recovery from the encephalitis. In neurology, we do often see psychiatric disorders that are masquerading as neurological ones, but also, like this, can find people with what appear to be primarily psychiatric symptoms, that are being caused by organic disorders that need to be discovered and treated. It makes for a challenging and fascinating relationship, and so rewarding when someone like this can be brought back to being them self again! Reply TAE PARK,M.D says: July 24, 2015 at 7:38 pm the basic pathology of me/cfs is neuroinflammation look at the study at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129915/figure/F2/ Reply EC says: July 25, 2015 at 7:12 am Does this suggest that some neuroinflammation starts in the sinus cavities? My first chronic problem was seasonal allergies 35 years ago. Then I developed fibromyalgia, then a few years later rheumatoid arthritis and a decade after that cfs. I’ve always thought they were connected. Reply TAE PARK,M.D says: July 26, 2015 at 12:18 am Trends Neurosci. 2009 September ; 32(9): 506–516. doi:10.1016/j.tins.2009.05.009 IF YOU LOOK AT THIS STUDY,CYTOKINE PRODUCED IN SIDE OF THE MICROVASCULAR SYSTEM:TNF-ALFA,IL-1BETA,IL-6–ALL LIKEY TO EXPLAIN YOUR RHEUMATOID ARTHRITIS,FIBROMYALGIA. Reply TAE PARK,M.D says: July 28, 2015 at 2:52 pm port of entry of pm.2.5 and UFP is nose and throat. it is so natural you will have sinus infections and allergy problem. then the pm2.5 travel through olfactory nerve–all the way to the brain frontal lobe and temporal lobe–which is the most common site of neuroinflammations of cfs/me Reply Cort Johnson says: July 24, 2015 at 9:15 pm The fact that she and others can make complete recoveries from such a debilitating and severe illness is one of the most astonishing things about the illness. Susannah was one of the patients who did not an ovarian tumor. Interestingly, it appears that patients with ovarian tumors are less likely to relapse. Because she had no tumor Susannah is more likely to have a relapse. Nobody knows why some people relapse at some point. Reply Alyson says: July 27, 2015 at 9:49 pm You likely have lyme disease. It is often misdiagnosed as ms or fibromyalgia. Tests for lyme are typically inaccurate. You will need to find a lyme literate doctor who will se d your blood to Immunosciences Lab in CA, and do a Western Blot test. It is the only test that is accurate. Best of luck! I have lyme… but was misdiagnosed for a whole year. Now imthe bacteria is riddled in my brain..causing lots of nerve and neurological symptoms. Reply Meg says: July 24, 2015 at 6:46 pm That is an amazing story Cort, and you write so well. Congratulations for bringing Susannah’s story to life. How wonderful that she herself has lived to tell the tale. One wonders how many other people with curable illnesses, as you say, die neglected in psychiatric institutions. I remember with deep regret a time when I should have ‘done something’ and didn’t, or couldn’t. I was a young physiotherapist doing a locum at a public hospital in the north of England. The hospital had been a poor house, and the stigma had persisted. Standards of care were low. I was called to clear the chest of a woman in a psychiatric ward who I was told had pneumonia. I soon realised the situation was far beyond my ability to make a difference. She was extremely ill, virtually unconscious and unable to cooperate. I was baffled that there was no line in for IV antibiotics, as I would have expected from her condition. I doubt she would have been capable of taking them orally. When I read her notes I was appalled. She was in her fifties and had been admitted a week previously after several days of personality changes and confusion. Why she was not shifted straight to a medical ward for proper diagnosis and treatment when her chest symptoms became apparent I have no idea, but I felt powerless (especially in the rigid hierarchical system of England at the time) to question the doctors. I thought of lying in wait for her family members and expressing my concerns to them, but in the end I didn’t do that either. Whether it would have made any difference if I had I will never know. I don’t know what became of her. I expect she died. There. Off topic or only tangentially related, but it has done me good to get that down. I haven’t written about it before and rarely talk about it, but I learned a lesson and am much more inclined to fight for those who can’t protect themselves now, and of course I have had to fight for myself as well. There is a lot of injustice in the medical system. Reply Ria Roegiers says: July 25, 2015 at 5:07 am It must have taken courage Meg to write this. I guess anyone of us working with people experience (if not denied) situations where we know we aren’t doing the utmost to help others … And the only thing we can do to put this ‘mistake’ right is by learning from it. Reply Chris Cantor says: July 24, 2015 at 7:54 pm Cort, your coverage of this is potentially misleading in a detrimental polarising way (either psychotic or not). You usually write brilliantly and I greatly appreciate your efforts but not this time. Some of the symptoms you described – e.g. delusions – effectively are diagnostic of a psychosis. From there doctors, even psychiatrists, take the next step of considering whether the psychosis could have an organic (disease or lesion) basis. [As a psychiatrist myself in psychotic patients I have diagnosed (often with the help of colleagues) encephalitis, brain tumours, epilepsy and more, sometimes with happy endings.] Once an organic basis has been excluded doctors only then settle on the “functional” psychoses e.g. schizophrenia, etc. If the illness is a newly discovered one that few doctors have ever heard of, is it surprising it could be missed? The issue of medical negligence and contempt for CFS patients is a very serious one that I am vaguely thinking of writing a paper on. However, if those of us concerned about the problem misrepresent it, doing so makes it all too easy for inept doctors to respond with more contempt suggesting that we don’t know what we are talking about. Reply Cort Johnson says: July 24, 2015 at 8:48 pm I agree that it’s not surprising that the diagnosis was missed. Actually it was surprising that it was found. I may not have brought that out clearly enough. One thing I wanted to show was how lucky she was to be in that hospital with that doctor. It appears I missed the boat on the dangers of being in the psych ward as well. It was strongly hinted in the book by the people running the epileptic section that she might be moved to the ‘psych ward” and that was a place she didn’t want to be because she wouldn’t get the kind of attention she was getting there. It appears that that is not necessarily true and I’ll amend the blog. Reply Greg says: July 24, 2015 at 10:15 pm I encourage you to write that paper, Chris. I personally can’t think of a group of severely ill people more unrecognized and mistreated/untreated in relation to the severity of disability than the ME/CFS crowd. And by the nature of this illness, most of us aren’t in much of a position to make much of a protest ourselves. Thanks. Reply marcie myers says: July 27, 2015 at 10:56 pm Dear Dr. Cantor, I was dx’d with CFS in 1994 and quit my nursing career in ’99. Since 2000, I’ve had 3 separate events that I can only call “psychotic breaks” but lasted less than 24 hours, one for only 4 hours and then, aside from the physical place that I found myself, e.g. the ER in 4-point restraints and then transferred to a locked psych unit for the weekend and then discharged with no medication or in an ICU being moved for the weekend to a locked psych unit and after a 15 minute session with a group of Medical College of GA psychiatrists during that time was quickly diagnosed Bipolar Type II. All of my labwork by the way was negative for any drugs or alcohol, including aspirin or ibuprofen so I mean negative when I say it. I have no idea what caused these extremely short-lived bouts of “psychosis” but I cannot deny that I was out of body and unaware of self during that period of time and have no memory whatsoever of the events during those short periods of time. I do feel that it’s somehow connected to the neuro inflammation of my CFS/ME but will never know what the bottom line is or if it will ever happen again. If nothing else, it was interesting and entertaining once the restraints were d/c’d and I was out on the locked floor entertaining myself with the other truly mentally ill patients and assisting them in my nursing and nurturing and good-natured fashion. Why these events would last for only a number of hours is truly the mysterious part of it to me; that without medical or psychiatric intervention I would become once again alert and oriented though no memory of the past event. Have you seen such before in your practice? And, guys, cut me a break on this story; it’s not one I repeat very often as it makes so little sense and I am fine thereafter except for having freaked my family and friends out. MM Reply Carollynn says: July 27, 2015 at 11:07 pm Thank you for your courageous and earnest comment, Marcie. Such horrific extremes of symptoms must reveal something about the other comparatively benign, though disabling, symptoms. Reply Becca says: July 24, 2015 at 8:10 pm There is much injustice in the disease management system. Most doctors do their best and want the best for their patients but are rarely trained in the courageously creative, out-of-the-box thinking displayed by Dr. Najar. Several years ago Dr. Mary Ackerley, a psychiatrist and the former Director of the Arizona State Homeopathy/Integrative Medicine Board (Summa Cum Laude from Johns Hopkins, mycotoxin certification by Dr. Rich Shoemaker) wrote a groundbreaking article “Brain on Fire” which became very well known. In it she succinctly described the severe behaviors from mycotoxin illness, which produces all kinds of brain and other inflammation symptoms mimicking numerous conditions, as undiagnosed syphilis does. Mold/Lyme and other pathogenic encephalopathies can be very complex and hit hard and fast depending on patient genetic strengths and environmental exposures. We are fortunate to to have Dr. Ackerley’s earlier, easy-to-access article as a complement to Calahan’s. Dr. Mary’s article was given to Nova U’s Dr. Klimas/NEID Clinic’s Dr. Irma Rey by a patient about the same time it was published, and she has run with it so enthusiastically that patients are now able to get treatment for mold/mycotoxin illness and perhaps related conditions. Brain, gut, microglial issues, the vagus pathway, methylation genetics: The links among these and environmental factors are becoming increasingly recognized as interdependent and will likely lead to much less suffering as patients assume more agency and educate their practitioners. Reply Cort Johnson says: July 24, 2015 at 8:50 pm I was quite encouraged that the hospital was willing to provide VERY expensive IVIG treatment based Najar’s recommendation which was based on a mildly abnormal spinal tap reading and no evidence of autoimmune disease. If he recommends it, apparently they’ll do it. That was really good to see! Reply Christine (Scotland) says: July 25, 2015 at 9:08 am I may have missed something obvious but if Dr Ackerley’s article is easily accessed, I can’t find it. Is there any chance of an easy to click link for the particularly cognitively challenged? Becca, Cort, anybody? Thanks – will reply separately with my strabge psychosis episodes aged 55 and 57. Thank you. Christine (languishing in a county without even an infectious diseases Consultant, where the resident Neurologist is so unpleasant, nobody ever asks to see him twice and the Rheumatologist refuses to see patients with CFS/ME/Fibro) Reply Becca says: July 27, 2015 at 7:23 pm Search the following sites: All link to her article. http://www.paradigmchange.me/wp/fire http://www.forums.phoenixrising.me/index.php?threads/brain-on-fire http://www.survivingmold.com/community I found many links to the article here in the US. It is easily accessed if enough search words are used on Google. Cognitive stuff though could make this more difficult. Search the sites when you get to them. Never give up. Do everything you can yoga-wise and otherwise to keep all inflammation down. Prolonged mold exposure can cause psychotic episodes or worse. Never eat inflammatory foods and see the best integrative practitioner you can, even if you have to consult by phone/Skype to do it. Australia and the US have practitioners that can at least consult on the inexpensive 23andme genetics test to get you started. If the orthodox systems have failed, abused or neglected you, go over their heads and have someone who knows these ropes guide you along the way. If a daily search is necessary, so be it. That is how others have fought their way through this former quagmire. You will find people to help and sort the helpful from the unhelpful if a positive fire is in your belly. Make it happen for a start, and I think you already have. Reply gloria says: July 24, 2015 at 11:28 pm it should be standard procedure to have an mri brain scan done and a lumbar fluid test done if a person has had fibro-pain and chronic fatigue for over several years- please write that paper Chris Cantor and thank you Cort for very informative articles Reply Danielle Bather says: July 25, 2015 at 6:47 am Only in the U.S.! If like me you have had years of chronic pain and fatigue and a rheumatologist diagnoses Fibromyalgia then that’s it, “live with it”is all you get in the UK. The NHS is a wonderful thing if you are critically ill, but if you are slowly dying like me forget it, sad but true. Reply Cort Johnson says: July 25, 2015 at 7:31 am I’m hoping that the new scanning techniques that can pick up neuroinflammation will find neuuroinflammation in FM and ME/CFS and they will become part of the standard testing protocols. Reply JulieG says: July 25, 2015 at 2:13 am Amazing. She expressed the same thoughts I had, as her TED Talk was ending, about all who had suffered in history because of misdiagnosis and no known treatment/cure. I had flashbacks of “Awakenings.” Wasn’t that the same disease, with patients who survived but left in permanent catatonic states? I haven’t read through the comments yet. Someone has probably already mentioned that. Reply Marline says: July 25, 2015 at 10:04 am I think that was Parkinson’s Disease in Awakenings. Reply David Fantle MD says: July 25, 2015 at 10:21 am No, it was a Parkinson-like condition caused by a pandemic of a viral encephalitis that happened around the turn of the century called ‘encephalitis lethargica’ that damaged the main waking center of the brainstem. It has never returned. Reply David Katcoff says: July 25, 2015 at 5:29 am If these protocols work for neuroinflammation of one kind, then they might work on another. I’d like to see the same successful steps tried on people with more garden variety illnesses like ME/CFS and Fibro. But maybe it takes more dramatic symptoms to summon up the more dramatic rescue techniques. Reply Becca says: July 27, 2015 at 7:47 pm Exactly. The least harmful protocols can sometimes be applied across the board. Just check the outstanding success of LDN 4.5, a cheap orphan drug that works wonders or partial wonders for many. All people are DNA-individualized, unique, and while many things work for a broad spectrum of people, not every approach fits everyone. People are running out of time, out of decades, to deal with this backwards-thinking, antiquated Western medical paradigm. Approaches that are more inclusive of the best of Western and Eastern work best in my experience. The best of Chinese and Ayurvedic medicine include the whole person as a unique being without the destructive and cost-prohibitive cookie-cutter approach of the dark side of Western medicine. The ancient/timeless traditions (not talking New Age here) do not punish the chronically misdiagnosed patient with possibly lifelong incarceration. Access to what produces results has often been denied, but it is not impossible. –Not even for M.E. folks. When in college I worked in a psych ward called the “hopeless” ward; many people had been discarded by their families for minor quirks. These broken hearts became truly insane from the horrible conditions there. All conditions were thrown together and all people were drugged together past sanity. (This happens everywhere.) Only steady human contact/compassion brought anyone out of it, and that was the purpose of our class — to give beyond labeling and, frankly, the medical brainwashing and neglect that stems from that. The first law of all healing (Hippocrates): First, do no harm. Has the old Western medical paradigm followed its prime directive? Reply Christine (Scotland) says: July 25, 2015 at 9:26 am This is so exciting Cort! I must get hold of Dr Ackerley’s paper and maybe the book. I apologise in advance for relating this blog to myself – as I usually do -but I’m totally on my own with CFS/ME. I’ve had CFS/ME since my early 30s but had so far isolated episodes of psychosis aged 55 and 57. To be fair to the psychiatrist, I was seen by, he arranged EEG and MRI of the brain. They were both ‘normal’ but as he isn’t a neurologist and told me he was looking for a brain tumor. He probably wouldn’t have recognised much. The first episode came during a long-standing neglected (not by me) UTI and I’ve considered that infection might have been a precipitating factor. Thank you for this post and everybody for the comments. I LOVE this blog! Reply Cort Johnson says: July 25, 2015 at 1:15 pm Thanks Christine, one of the things that impressed me about Susannah’s case are the many different symptoms neuroinflammation can cause. It’s extraordinary what can happen when the immune system targets a part of the brain! Reply Carollynn says: July 25, 2015 at 1:04 pm Is someone trying to recruit doctors Najjar and Dalmau into studying ME/CFS? We need more people like that–interested in and willing to look into something on the relative periphery of medicine–trying to help us. Who could that “someone” be to recruit them? Reply Cort Johnson says: July 25, 2015 at 1:19 pm It would be nice. I have a feeling though that both are fully immersed in this new field they’re helping to create. You never know though. ME/CFS and FM are MYSTERIOUS central nervous system disorders at least in part. I imagine that if the neuroinflammation studies work out – there will much more emphasis on looking for autoimmune basis for the inflammation. I can’t imagine that wouldn’t make sense to do that given the many similarities between autoimmune disorders and ME/CFS and FM. Reply John says: July 25, 2015 at 11:30 pm Hi Cort, Thanks for the immense service you are doing to the CFS/ME community keeping us apprised of the latest happenings from around the world. I was wondering if you have plans to interview Dr. Charles Shepherd and Dr. Abhijit Chaudhuri one of these days. With Neuroinflammation being the hot word in CFS/ME these days, I will definitely be interested in hearing more from them. Thanks. Reply TAE PARK,M.D says: July 27, 2015 at 10:34 am Air Pollution: Mechanisms of Neuroinflammation & CNS Disease Michelle L. Block1 and Lilian Calderón-Garcidueñas2,3 1 Department of Anatomy and Neurobiology, Virginia Commonwealth University Medical Campus, Richmond, VA 23298, USA 2 Department of Biomedical and Pharmaceutical Sciences, College of Health Professions and Biomedical Sciences, The University of Montana, Missoula, Montana, USA 3 Instituto Nacional de Pediatria, Mexico City, Mexico Abstract Emerging evidence implicates air pollution as a chronic source of neuroinflammation, reactive oxygen species (ROS), and neuropathology instigating central nervous system (CNS) disease. Stroke incidence, and Alzheimer’s and Parkinson’s disease pathology are linked to air pollution. Recent reports reveal that air pollution components reach the brain. Further, systemic effects known to impact lung and cardiovascular disease also impinge upon CNS health. While mechanisms driving air pollution-induced CNS pathology are poorly understood, new evidence suggests that activation of microglia and changes in the blood brain barrier may be key to this process. Here, we summarize recent findings detailing the mechanisms through which air pollution reaches the brain and activates the resident innate immune response to become a chronic source of pro-inflammatory factors and ROS culpable in CNS disease. Inflammation is increasingly recognized as a causal factor in the pathology and chronic nature of central nervous system (CNS) diseases 1. While diverse environmental factors have been implicated in neuroinflammation leading to CNS pathology, air pollution may rank as the most prevalent source of environmentally induced inflammation and oxidative stress 2. Traditionally associated with increased risk for pulmonary 3 and cardiovascular disease 4, air pollution is now also associated with diverse CNS diseases, including Alzheimer’s disease, Parkinson’s Disease, and stroke. Air pollution is a multifaceted environmental toxin capable of assaulting the CNS through diverse pathways. Until recently, the mechanisms responsible for air pollution-induced pathology in the brain were unknown. However, despite the variable chemical and physical characteristics of air pollution and the consequent activation of multiple pathways, inflammation and oxidative stress are identified as common and basic mechanisms through which air pollution causes damage 4, including CNS effects. Furthermore, while multiple cell types in the brain respond to exposure to air pollution, new reports indicate that microglia and brain capillaries may be critical actors responsible for cellular damage. In the following review, we describe the complex composition of air pollution, explain current views on the multifaceted mechanisms through which air pollution impacts the CNS, and discuss the new mechanistic findings implicating innate immunity and chronic neuroinflammation in CNS damage induced by air pollution. *Corresponding Author: Block, M.L. (MBlock@vcu.edu). NIH Public Access Author Manuscript Trends Neurosci. Author manuscript; available in PMC 2010 September 1. Published in final edited form as: Reply Lynda says: July 27, 2015 at 11:24 am Hi Cort, I read this book when it first came out. What struck me immediately was how different her support system was from most of us and how it really made it possible for her to be diagnosed, treated and obtain so much recovery. My general practitioner thought I was hyper anxious and put me on psychiatric drugs. My rheumatologist thought I had inflammation and FM, but treated me with standard drugs. My GYN removed an ovarian tumor. My neurologist told me I had progressive relapse/remitting MS. Scriptts told me I had hyper mobility and anemia. It wasn’t until Dr. Peterson did an LP that viral encephalitis, inflammation and white matter lesions were found. I was finally diagnosed with myalgic encephalitis, probably of several years duration and as a result I also have temporal lobe damage and several autoimmune diseases. This isn’t just my story, I’m sure it’s one many of us can tell. Meeting that one extremely essential doctor who does think out of the box is a luck of the draw for some of us. I believe that until ME/CFS is a required part of every med school’s criteria, all inflammatory illnesses will remain a mystery for most patients. I also consider myself very lucky. Reply Cort Johnson says: July 27, 2015 at 12:26 pm So interesting Lynda – thanks for sharing your story and as you say many peoples story – who find that right doctor. Reply TAE PARK,M.D says: July 27, 2015 at 4:09 pm READ THIS ARTICLE TELLING US MITOCHONDRIAL DAMAGE WHICH ESSENTIAL PART OF CFS/ME Ultrafine Particulate Pollutants Induce Oxidative Stress and Mitochondrial Damage Ning Li,1,2 Constantinos Sioutas,2,3 Arthur Cho,2,4 Debra Schmitz,2,4 Chandan Misra,2,3 Joan Sempf,5 Meiying Wang,1,2 Terry Oberley,5,6 John Froines,2,7 and Andre Nel1,2 1Department of Medicine, University of California, Los Angeles, California, USA; 2The Southern California Particle Center and Supersite, Los Angeles, California, USA; 3Department of Civil and Environmental Engineering, University of Southern California, Los Angeles, California, USA; 4Department of Molecular and Medical Pharmacology, University of California, Los Angeles, California, USA; 5Pathology Service, Veterans Administration Medical Center, Madison, Wisconsin, USA; 6Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison, Wisconsin, USA; 7Center for Occupational and Environmental Health, University of California, Los Angeles, California, USA Address correspondence to A. Nel, Department of Medicine, UCLA School of Medicine, 52–175 CHS, 10833 Le Conte Avenue, Los Angeles, CA 90095 USA. Telephone: (310) 825-6620. E-mail: anel@mednet.ucla.edu This study was supported by the National Institute of Environmental Health Sciences (grant RO1- ES10553) and the Southern California Particle Center and Supersite, funded by the U.S. Environmental Protection Agency (STAR award R82735201) and the California Air Resources Board (grant 98–316). This manuscript has not been subjected to the U.S. EPA peer and policy review. Received 18 September 2002; accepted 16 December 2002. The objectives of this study were to determine whether differences in the size and composition of coarse (2.5–10 μm), fine (< 2.5 μm), and ultrafine (< 0.1 μm) particulate matter (PM) are related to their uptake in macrophages and epithelial cells and their ability to induce oxidative stress. The premise for this study is the increasing awareness that various PM components induce pulmonary inflammation through the generation of oxidative stress. Coarse, fine, and ultrafine particles (UFPs) were collected by ambient particle concentrators in the Los Angeles basin in California and used to study their chemical composition in parallel with assays for generation of reactive oxygen species (ROS) and ability to induce oxidative stress in macrophages and epithelial cells. UFPs were most potent toward inducing cellular heme oxygenase-1 (HO-1) expression and depleting intracellular glutathione. HO-1 expression, a sensitive marker for oxidative stress, is directly correlated with the high organic carbon and polycyclic aromatic hydrocarbon (PAH) content of UFPs. The dithiothreitol (DTT) assay, a quantitative measure of in vitro ROS formation, was correlated with PAH content and HO-1 expression. UFPs also had the highest ROS activity in the DTT assay. Because the small size of UFPs allows better tissue penetration, we used electron microscopy to study subcellular localization. UFPs and, to a lesser extent, fine particles, localize in mitochondria, where they induce major structural damage. This may contribute to oxidative stress. Our studies demonstrate that the increased biological potency of UFPs is related to the content of redox cycling organic chemicals and their ability to damage mitochondria. Key words: concentrated ambient particles, dithiothreitol assay, heme oxygenase-1, mitochondrial damage, oxidative stress, polycyclic aromatic hydrocarbon, ultrafine particles. Environ Health Perspect 111:455–460 (2003). Reply Alyson says: July 27, 2015 at 10:42 pm For those of you with a diagnosis of fibromyalgia, ms, lupus, rheumatoid arthritis, and many other diseases, you likely have LYME DISEASE! MOST lyme positive patients go for long periods of time being misdiagnosed, and going without proper treatment! This has happened to EVERY Lyme positive person I know. I have been sick with Lyme Disease for 2 years. I was given other diagnoses such as migraine headaches and anxiety/pa ic attacks. They prescribed me meds for those supposed ailments.. which played no role in killing the “bacteria” that I was actually infected with. Lyme is an “infectious” disease. It is currently an epidemic, particularly in the East coast. Lyme is next to impossible to diagnose, as the traditional Lyme tests (Elisa) done by your pcp or hospital are extremely inaccurate!! My 3 tests came back with false negatives! Given the symptoms I was having, and knowing I was bitten by a deer tick, I KNEW I had Lyme Disease and wasn’t taking no for an answer. I was persistent.. and I seeked out a Lyme literate doctor (who are hard to find). He immediately started me on antibiotics, just according to my list of symptoms I brought to him. He said that he would do the traditional Lyme Disease test (Elisa)..but that it would likely come back negative because it is horribly inaccurate. He strongly urged me to have a special test done. It was called the “Western Blot”. This test was sent to the one lab that processes this test… “Immunosciences”. The Western Blot test ended up showing the levels of bacteria for not only Lyme Disease… but 4 other bacterial co-infections that I was simultaneously infected with. I happened to be bit by (and likely infected by) 2 ticks. Many people with Lyme Disease have no recollection or proof of a tick biting them. They never get the classic “bulls eye” rash.. so they are unaware of their lyme disease until it begins to show symptoms. then the fun really begins! I was one of the people who never got a bullseye rash. But..luckily, I was fully aware of my tick bites. Ok.. so this Western Blot test is not covered on your health insurance. It cost me $600 out of pocket.. and it was worth every damn penny…as I would likely be dead today if I did not get the test done. I have been on treatment for a year..but because it was caught late, and because I have multiple co-infections, I am still very sick. I am out of my “bed ridden” condition, and I am able to work a desk job. But my quality of life is horrible. The longer you are treated for your so-called fibromyalgia or other false diagnosis, and NOT treated with antibiotics for your Lyme Disease, the worse and worse you will get, and your neurological symptoms will reach catastrophic levels…and you will perhaps die. This is not to be taken lightly. People are dying from complications due to Lyme Disease. .such as a heart attack or stroke or pneumonia. Their cause of death then gets documented as one of those things.. but NOT as Lyme Disease. The statistics for deaths due to Lyme Disease are also horribly inaccurate because of this. And… the CDC does not want to recognize Lyme Disease as a chronic illness. Doctors are losing their medical licenses because they are breaki g the rules with treating their Lyme patients for longer than “allowed” with antibiotics. Most of these Lyme literate doctors are breaki g the rules to help their patients…because they also had/have Lyme Disease! It makes you an extremely compassionate person. We all know the suffering all too well. Anyway… here are a couple links… to read about lyme vs. Fibromyalgia diagnosis, and some info about the major red tape and politics behind Lyme Disease. https://www.psychologytoday.com/blog/why-can-t-i-get-better/201312/are-your-fibromyalgia-symptoms-due-lyme-disease http://www.healthline.com/health-news/you-do-not-have-chronic-lyme-disease-091514 Wishing you all good health, healing… and answers! ♡ Reply TAE PARK,M.D. says: July 28, 2015 at 8:18 pm http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743793/figure/F3/ if you look at this picture, all of the questions surrounding cfs/me is with air quality–pm 2.5, UFP. Reply Chimura says: August 4, 2015 at 7:05 am Off topic sort off Dead link in your post: Study Suggests Mold Exposure Can Cause Severe Effects in Chronic Fatigue Syndrome (ME/CFS) http://www.cortjohnson.org/blog/2013/04/13/study-suggests-mold-exposure-can-cause-severe-effect-chronic-fatigue-syndrome-finally-meet-mold-study-finds-high-rates-of-m/ Resources Check out Eric Johnson’s story here (not) Well at least something’s still to be found here: http://paradigmchange.me/erik/ Same surname, are you related? Nothing about Particulate Matter (PM) in general either, just saying. Like Tae mentions, I thought the same. Reply Leave a Reply Name (required) Mail (will not be published) (required) Website Notify me of follow-up comments by email. Our ME/CFS, FM and Chronic Pain Forums Are Open! Join Them Here! Get Our Free ME/CFS and FM Blog Name Email* Support Our Work! GIVE A ONE-TIME DONATION GIVE MONTHLY HEALTH RISING IS NOT A 501 (c) 3 NON-PROFIT The ME/CFS and FM Buzz P2P Report on Chronic Fatigue Syndrome Delayed After Irregularities Found Health Rising’s ME/CFS and FM Forum Plus Package is Open! Advocates Mostly Laud Committee’s Response to P2P Report Get the ME/CFS and FM Buzz! Your email: High quality vitamins, herbs, and supplements at ProHealth.com CATEGORIES Advocacy (67) FDA (10) Basics (1) Books (6) Community Reports (9) Conferences (11) Coping (10) Doctors (2) Dr. Peter Rowe (1) Events (2) Homepage (296) ME/CFS FM Buzz (27) Organizations (40) CDC (3) CFIDS Association of America (6) HealClick (1) Health Rising (13) NCNED (1) NSU (2) Open Medicine Institute / Open Medicine Foundation (7) Simmaron (4) Stanford (1) Workwell (1) WPI (1) recovery stories (1) Research (144) Autonomic Nervous System (24) Brain (22) Definition (6) Diagnosis (2) Exercise (7) Fibro (13) Gene expression (4) Gut (10) Immune (15) Pain (14) Pathogens (15) Small Fiber Neuropathy (6) Stories (29) The Last Best Cure (5) Tools (9) Treatment (128) Ask the Docs (1) Cognition (1) Diet (9) Drugs (19) Ampligen (1) Low Dose Naltrexone (2) Rituximab (2) Exercise (1) Gut (10) Heart (2) Herbal (1) Mind/body (10) Mindfulness (1) mold (2) orthostatic intolerance (4) Pain (6) Recovery Stories (1) Sleep (8) Supplements (7) Treatment Blogs (11) Dr. Cheney (1) Dr. Chia (3) Dr. Peterson (4) Uncategorized (9) Video’s (4) Our Sponsors Sponsor Health Rising FibroMapp for Health Rising Get it on Google Play Support Health Rising by Shopping on Amazon.com Shop in the U.S.

Read more: Her Brain Was On Fire: A Neuroinflammation Story http://www.cortjohnson.org/blog/2015/07/24/her-brain-was-on-fire-a-neuroinflammation-story/

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Everything you needed to know about Headaches by Dr Scopelliti

Headaches

Woman suffering with headaches

Headaches

So, You Suffer With Headaches…

Our office has very high success in treating headache patients.  Our success in headache treatment is accomplished drug free and without invasive surgery.  We have had a myriad of success treating patients with migraine headaches as well as tension headaches, and chronic daily headaches.  In fact, the vast majority of our patients have failed with multiple drug therapies prior to contacting us, typically as a last resort.  If this sounds like you or someone you love, you should consider calling our office for a no obligation FREE consultation.  You can find out about our migraine treatment and treatment for tension headaches before making any commitment to treatment.

For those of you wishing to know more regarding various causes of headaches, read on…

Tension headaches

Tension headaches represent one of the top three reasons patients consult their doctor, (with vertigo and back pain making up the other two).  It is one of the most costly diseases because of its very high prevalence. Tension headaches are the most common type of headaches. It has also attached the synonymous name of stress headaches.

The International Headache Society defines tension headaches more precisely and differentiates between episodic and chronic types. The following is a modified outline of the IHS diagnostic criteria:

Episodic Tension Headaches

  • At least 10 previous headaches fulfilling the following criteria; number of days with such headaches fewer than 15 per month
  • Headaches lasting from 30 minutes to 7 days
  • At least 2 of the following pain characteristics:  Pressing/tightening (nonpulsating) quality of headaches
  • Mild or moderate intensity (may inhibit but does not prohibit activities)
  • Bilateral location, (headache on both sides of head)
  • No aggravation of headache from climbing stairs or similar routine physical activity
  • Both of the following:  No nausea or vomiting associated with headaches
  • Sensitivity of light and sound is absent or only one is present with headaches
  • Secondary headache types not suggested or confirmed

Chronic tension-type headaches

  • Average headache frequency of more than 15 days per month for more than 6 months fulfilling the following criteria
  • At least 2 of the following pain characteristics:  Pressing/tightening (nonpulsating) quality of headaches
  • Mild or moderate intensity headaches, (may inhibit but does not prohibit activities)
  • Bilateral location, (headache on both sides of head)
  • No aggravation from climbing stairs or similar routine physical activity
  • Both of the following:  No vomiting associated with headaches
  • No more than one of the following: nausea with headaches, avoidance of light and sound with headaches
  • Secondary headache types not suggested or confirmed

Although formerly conceived as muscular contraction headaches, the more likely cause of these headaches is believed now to be abnormal neuronal sensitivity and pain facilitation, not abnormal muscle contraction.  Headaches are not related directly to muscle contraction, and possible hypersensitivity of neurons in the trigeminal nucleus caudalis has been suggested.

Frequency:

In the US: Tension headaches are the most common type of headaches, and women are more likely to be affected with headaches than men.

History: Tension headaches are characterized by pain that is usually mild or moderate in severity and bilateral in distribution. Unilateral head pain may be occasionally experienced as well, however. Headaches are commonly reported as a constant, tight, pressing, or band-like sensation in the head.

Common to Tension Headaches

  • The majority of these headaches last less than 24 hours.
  • Headache pain differs from the typical pulsating/throbbing quality of migraine headaches.
  • Prodrome and aura prior to headaches are absent.
  • The deep steady headaches differ from the typical throbbing quality of migraine headaches.
  • Occasionally, the headaches may be throbbing or unilateral, but most patients do not report sensitivity to light and sound, or nausea, which commonly are associated with migraine headaches.
  • Some patients may have neck, jaw, or temporomandibular joint, (TMJ), discomfort or dysfunction.

Migraine Headaches

  • Migraine pain may be localized to one side of the head, behind the eye, the back of the neck, or about the face. The pain is associated with nausea and sometimes vomiting. Patients become sensitive to light (photophobia), sounds, (phonophobia), and certain smells (osmophobia). Intermittent dizziness may occur. Some patients, called migraineurs, may develop an “aura,” that is, a feeling that comes on before the headaches begin. These auras may be associated with visual changes, such as spots, (scintillating scotomas),  tunnel vision, or wavy lines, (fortification spectra). The headaches may last up to three days and may occur several times per week or as infrequently as once or twice a year. Women are more prone to migraine headaches than men.

Cluster Headaches

Cluster headaches are given their name based on the fact that the attacks of headache pain occur in clusters that may last several weeks to months. The head pain is agonizing and usually affects one side of the face, involving severe pain behind one of the eyes with associated nasal congestion and runny nose. Oddly, men tend to get these types of headaches more frequently than women.

Where Do I Begin?

Before you seek any treatment approach to your headache pain, it would be wise to make sure that the underlying cause of your headaches is correctly diagnosed. Evaluations for your headaches typically involve your PCP, (Primary Care Provider), however, examination by an appropriately trained neurologist is wise. Our office specializes in extensive neurologic evaluation of each patient prior to undertaking any headache treatment regimen.  It is important that you have your condition(s) properly diagnosed so that you do not waste valuable time should the underlying cause of your headaches be serious and/or progressive, or, should such headache treatment be contraindicated for any reason.  Additionally, any headache treatment that you receive, be it from an allopathic, chiropractic, or other integrative approach, will likely not be as beneficial if it is not diagnosis directed.  The fundamental healing axiom of “first do no harm” must be a guiding principle whenever a medical provider encounters a patient. Patients seeking any form of manipulation should do their homework on the proposed providers and techniques used in order to find competent practitioners capable of performing such procedures as safely as possible. The risks and benefits must be clearly discussed. Just as one chooses their surgeon carefully, so too must a patient evaluate any practitioner who would attempt manipulation. So too should a patient scrutinize any proposed drug therapy headache treatment, or other drug treatment for that matter, without a logical accompanying diagnosis.

During the course of any headache treatment, it would be extremely wise to maintain a log of temporal course and severity of your headaches.  Rate your headaches from 1-10 on severity, and mark a calendar when you have a headache with the severity rating and also how long it lasted.  This will later prove invaluable when determining the benefits, if any, of your headache treatment, as you will have something to reflect back on to demonstrate reduction of severity or frequency of the headaches.

Free E-Consultation Right Now!

Because of the duration of examination and complexity of treatment that we offer, we are naturally limited to the number of prospective patients which we can take into our programs.  We therefore only accept patients whom we truly believe we can help.  If you would like to be considered for treatment, please start by filling out the Headache consult form, (the password is help), and submitting it by email to our office.  The doctor will review it, make a determination as to candidacy for headache care, and we will call or email and notify you as quickly as possible.  If we do not have immediate openings, you may be placed on a waiting list and we will call you when an opening occurs.  We appreciate your patience in this regard, but we give each patient individual and uncompromised attention which allows us to continue to maintain optimal outcomes.

If you would like to schedule a free in office consultation with the doctor to discuss your headaches, or just have questions, please contact us using the form on our Contact Page. Lastly, we recommend reading our Guest Book page to see what other patients have had to see regarding their treatment with Dr. Scopelliti.

References available upon request

Dr. Scopelliti is a Functional Neurologist in Monmouth County NJ.

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Patients Like Me.

 I had to add a second post regarding this site.  It is such important tool not only for you but to help others by your health information for research purposes.  You can communicate with others that have your same illness or use the history tool and health record to keep track of your own health records, then print it out to take to your Doctors appointment to share the information which is a win win on both parties, Helping your Doctor help you .  It’s a wonderful site.

We’re glad you’re here

Hi Kantheboyz,

Thanks for joining the PatientsLikeMe community! Thousands of people just like you are already tracking their condition and sharing their experiences. Over the next few weeks, we’ll send along some emails with tips and tricks to help you get the most out of PatientsLikeMe. Let’s start…

Video tour– Take a quick, 3-minute tour to learn the ins and outs of the site. See how to set up your health profile and start connecting to others in the forum.

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The PatientsLikeMe Team

P.S. – Don’t be shy if you have a question. We’re here for you anytime. Ask away.

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Ryan Adams and Meniere’s

Ryan Adams Discusses Prolific Career and Coping With Meniere’s Disease on ‘CBS This Morning’

Adams calls the affliction “an interesting thing to have and be me”

By: Rachel Brodsky // December 29, 2014

Ryan Adams recently turned up on CBS This Morning: Saturday to delve into his career, music, and even a “hearing illness” that made him feel like he “was losing [his] mind.” Speaking to Anthony Mason, the 2015 Grammy nominee described his latest period of prolificacy (“It’s cool. It feels like my soul is full and it’s overflowing and I’m taking just dictation from what I can get from it”) and coping with Ménière’s Disease, an inner-ear disorder that causes spontaneous episodes of vertigo (“[It’s] an interesting thing to have and be me”).

Watch his interview above.

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Jeffery Bowen and his journey with Meniere’s

Bowen is now winding down Starbooker, as his hearing loss and balance issues have become more acute. He is preparing for the eventual total loss of his hearing. Holly Bowen has taken over the remaining projects on the company’s calendar and will seek no future bookings or clients. Pollstar spoke with Bowen about his life and career, and about Meniere’s disease.

See the very end of this article for an open letter to the industry from Bowen.

Further information and resources regarding Meniere’s disease can be found here and here.

 Is Meniere’s disease treatable, or is total hearing loss inevitable?

It comes in varying degrees and attacks people in different ways. With me, it started 20-some years ago out of the blue. I was sitting at my desk and suddenly I got extremely dizzy and nauseous and I thought, “What in the hell is going on?” It took two years or so before I could even get a diagnosis.

At that point, I had it for a while and then it went away. But a few years later it came back, and came back like a freight train. I’ve been dealing with it ever since to the point where I am where I am and facing the facts. You’re never really cured, but some get to the point where it’s kind of in remission. Sometimes they say it’s as if the vertigo part of it and the tinnitus part of it get tired of fighting and kind of go away. But the hearing loss is what it is. There’ve been some pretty famous people who’ve had this from back in history to the present time. I did some poking around and there’s some famous people, including current entertainers, who have it that people don’t know about. Hearing loss is inevitable, especially when it goes bilateral, as mine has. I can be deaf one day and the next day my hearing will be back.

But when it comes back, it comes back a little weaker than before I had the attack. Generally, especially with bilateral patients, it’s almost an inevitable situation that you’re going to end up deaf. The bilateral type is much rarer than the single-sided Meniere’s. I’m not sure why that is, but it’s generally more prevalent to have it on one side than both. Usually it’s the left side, rather than the right side, and women tend to have it more than men.

There is associated dizziness and tinnitus. It could be ringing or whooshing or roaring like freight trains. Then there’s the inner ear pressure. It can be driven by the weather, allergies – the doctors don’t know. Some say if you’ve had a brain injury or even a blow to the head at some time, later on it can trigger Meniere’s. And when I was little kid, I did get hit in the head. Could this have been triggered when I was 13 years old? Did that cause it to happen? Everybody has a different reason. But some people have been able to abate it and come back. Alan Shepard, the astronaut, had it and was grounded but was able to control it with monitoring and medication back in the 1960s.

He got to the point where he was able to go back to the space program and take a second space flight as commander on Apollo 14. He had it, but he was able to control it. Ryan Adams has it, Marilyn Monroe had it. Vincent Van Gogh – you’ll laugh at this but one of the reasons people believe he cut off his ear was because he had Meniere’s on that side and was trying to get rid of the noise and the pressure. Peggy Lee, Emily Dickinson, Les Paul and Kristin Chenoweth have it. She was injured not too long ago because she fell, which is another side effect.

How did you go from acting into the concert business?

I went from theatre, to TV and films, and eventually into radio. From radio, I got into doing radio concerts and promoting. From that, got into booking. That’s how I got to where I eventually ended up. I kind of fell into it. I’d been promoting some concerts and marketing for various venues. I was working with shopping centers, promoting radio shows, worked with a production company in Winston-Salem, N.C., and had a partnership with Jim Brammer, who owns Special Event Services, still a very strong production company. I left that company and went on my own marketing things. Bucky Dame, who at that time was the director for the Lawrence Joel Veterans Memorial Coliseum complex in Winston-Salem, had an opening for booking director/associate director for the coliseum. He asked Jim Brammer if he knew anyone, and he said, “Talk to Bowen.”

You had a long run in Indianapolis before landing at the Sears Centre.

I was recruited by the Indiana Pacers. I moved to Indianapolis and worked for Pacers Sports and Entertainment for the next 10 years as VP of booking and production for them. We built Conseco Fieldhouse and closed down Market Square Arena. Then I was recruited by Ryan Cos. to go to Chicago and take over the Sears Centre. I stayed there until 2010, when it was taken over by the city and management went to Global Spectrum.

After that, you started Starbooker Presents?

At that time, I was contacted by Mike Crum of the Charlotte Regional Visitors Authority. He asked if I’d be interested in starting my own company and coming back to North Carolina. I could lead booking promotions and be an inhouse talent buyer for the CRVA in Charlotte to help them out in booking Bojangles Coliseum and Ovens Auditorium. The timing was perfect so I said yes. That’s how Starbooker Presents was born. My wife and I moved back to Greensboro where most of the family was. I’ve got two sons and our daughter moved back here. I’ve got five grandkids in Greensboro, too.

We were a very small organization, mainly me and my wife. We’d bring in outside contractors as needed depending on what the projects were. The primary focus was on talent buying but we also did consult. I did a lot of consulting for new business development and did a lot of mentoring for general management for venues and marketing. At the same time, we worked with other companies in bid processes. We helped other companies with requests for bids, everything from talent buying to staffing to general management to production, everything. We helped produce a lot of theater, festivals, and things of that nature so it was pretty all encompassing. We also did some artist management. We had musicians and actors, a couple of producers we worked with. Partnership-wise I have a couple I still work with.

Were you already considering retirement?

I never expected this to happen. I’d always told everybody that I’m never going to retire. They’ll find me passed out behind a road case on a tour somewhere and that will be the end of it. That was my story and I was going to just keep on keeping on and literally figured I’d die on stage or behind a case. But we won’t take on any new clients. I won’t be looking for new contracts or taking on any new spectacular projects.

Why have you decided to go public with your diagnosis?

I thought a lot about this in recent days. I looked at all the people I know or have heard about that have this same thing I’m wrestling with and I think it’s important for people, particularly in our industry, to understand what it is or what it does. I meet on Wednesday night with a group of people. We go to a coffee shop or a Panera Bread and we talk. It’s led by a young girl who is deaf and she teaches those of us who need refreshers on sign language and those of us who don’t know it. She can communicate in American Sign Language and Japanese Sign Language and other international languages. We sit around and talk with our hands.

Everybody gets excited and talks about what they like to do, what their hobbies are. A couple of weeks ago the main topic was “What is your favorite activity?” And when it came around to me the first thing I would normally have said was “listening to music.” And I had to stop myself because that won’t be my favorite thing to do before too long. So I went to my second favorite thing to do and signed it “cooking” because I don’t have to hear to cook. But it really stopped me in my tracks. Soon I’m going to be deaf. I know that it’s coming. It could be next week, next month or next year. I don’t know when. Music has been a part of my life for so long, and it’s been part of our lives for so long, and we don’t think about it until it’s not around sometimes. You play so much of your life into it. You can hear a song on the radio and immediately think of things you’ve done, places you’ve been and people you’ve been with. By almost every song you hear. How do you replace that? Even when I am experiencing those moments when I can’t hear anything, I still can hear those songs in my head. I can remember them. I hopefully can always have that memory.

Do you think industry professionals take the ability to hear for granted?

If there were some way that I can reach out to the industry and make them understand that importance, to get us to stop arguing over a deal or screwing each other over a dollar! Think a little while about the importance of these things. What can I do? Can I start a foundation? Can I start a movement? Can I start an awareness campaign? Can I start something now that I can’t do what I used to, to bring an awareness to people I worked with, in a different way that sheds light on this disease and this hardship, so that we think about the music, the entertainment, differently than we normally do? An actor can go onstage and use sign language and express themselves, because you are emoting with your body.

I don’t know how you do that with music because it’s inside. I have an invisible disease where, if you look at me you don’t know anything is wrong except maybe that I walk a little screwy sometimes. Until you talk to me, you don’t know that I’m any different than I ever was. What can I do to get others like me, the Ryan Adamses or the Kristin Chenoweths, who are in our business that feel the same way, to bring them together; people who have perfectly good hearing but who care?

There’s industry focus on protecting hearing from high decibel levels. Is Meniere’s related?

Meniere’s can happen to anybody and they don’t know that any one thing causes it because there’s so many different things. It can go through remission and exacerbation with so many different effects. It’s very episodic. I don’t know that being in loud music would trigger an attack.

If it can be unrelated, could people be ignoring Meniere’s symptoms mistakenly thinking its “just” ringing in the ears?

I know people in the business who have ringing in the ears all the time, and they say, “Oh, it’s because I never wore earplugs.” But it should be checked. Any time you have ringing in your ears it’s because your ears are in pain. People don’t understand that.

By talking about it publicly, you are certainly helping raise awareness of Meniere’s disease.

I can only do so much. My hearing is fluctuating quicker than it used to. I’m wearing a headset or I wouldn’t be able to hear you right now. I was out walking my dogs this morning and something just clicked and I couldn’t hear anything. In the 10 minutes, by the time I got home, it had gradually come back. I was just out walking the dog. We in this business have tended to rely, and we relied for so many years, on relationships.

That kind of changed over the years, more recently. Relationships don’t mean quite as much as they used to. We aren’t in control of our own destinies like we thought we were at one time. Maybe this was a way to wake up. Wake up to what, I don’t know. I just hope I can maybe make a difference, to get people to understand this disease and what it means.

An Open Letter From Jeffrey Bowen

Jeffrey Bowen emailed Pollstar in the days after the interview and asked us to include a note of thanks to his friends and colleagues. We’re happy to oblige:

These are friends in the “business” who have always been there to listen, guide, mentor, or just keep me straight when I needed to be. There are too many “building guys” to even begin to mention but a few do stand out such as Bob Klaus, Bucky Dame, Rick Fuson and Mike Crum who gave me tremendous opportunities in my career, and Steve Kirsner, John Mazzola, and Jim McCue who always knew the right things to say when times were tough.

I actually had some tremendous relationships with agents, no matter what some people think about them (that’s a joke by the way), guys like Kenny DiCamillo, Rob Light, Scott Pang, Steve Lassiter, Mitch Rose, James Yelich, have put up with my crazy offers and constant, neverending inquiries about their wonderful artists for many years.

I’ve come to love each of them, especially Rob Light’s annual Holiday card! And believe it or not I have a few artist managers that I can call friends too such as Irving Azoff and Howard Rose. They will probably never admit it but I am happy to. And foremost in that area is Harry Sandler. I’ve come to know, love and appreciate Harry’s creative soul over the past few years through his photography. Harry Sandler is a wonderful artist himself! Then there are the promoters.

Those with whom I competed against, partnered with, and sought to sell my soul to. And in doing so became great and steadfast friends: Ben Farrell, Paul Gongaware, John Meglen, Wilson Howard, Don King, Carlos Larraz, Louis Messina, Jerry Mickelson, Arny Granat, Steve Sybesma, and Dave Lucas.

Others such as Alex Hodges, Steve Moore and Mike McGee have been great mentors in my live. Producers/promoters such as Joe Thomas, Robin Mishik-Jett, and Neil Greenberg have been wonderful partners. I won’t start naming the artists that have touched my life; there are too many to name over the years. I’ll just place a bit of optimism here in honor of all of them as given to me by my dear departed friend, Red Skelton: “Never judge a day by its weather.”

Take it to heart my friends. The media has been kind to me all my life. I’ve never received a bad review, which isn’t to say I didn’t deserve my share from time to time, I’ve just been lucky. I haven’t received many honors and awards in my career, but the greatest reward I can walk away with is friendship.

Thank you to my wife, Holly, for putting up with those long hours without me around, and to my daughter, Savvy for having show business forced upon her. To my sons Christopher and Sean, I’m sorry I wasn’t there much when you were growing up. I love you all. I love almost everyone in the business. Thank you to everyone who made me what I was and ever could be. And thank you Pollstar. See you backstage sometime.

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Now I hear what you hear.

Now I hear what you hear

Learning to accept being hard of hearing is the hard part

Hamilton Spectator

I’ve got a secret. Just between you and me, I’ve been hard of hearing for many, many years. Procrastinating, postponing, delaying … that’s been me.

I’ve belonged to the Canadian Hard of Hearing Association for more than 20 years, but have never worn a hearing aid. Don’t get me wrong, I definitely have hearing loss. In fact, the hearing in my left ear is extremely poor. How did it happen? I’m not sure. As a child, I took a bad fall in an acrobatic class, maybe it was then. When I was 19 my family doctor discovered I had minimal hearing loss in my right ear. At that age, who cares? I was invincible or so I thought.

In my 20s I developed Meniere’s disease (inner ear dizzy spells), which I wouldn’t wish on my worst enemy. It would go in and out of remission and I survived, with the support of my family. Time marched on. One day I was on the phone at work and all of a sudden, I couldn’t hear out of my left ear. The hearing returned for a short while and then it was gone, never to return. It was then I learned Meniere’s could travel. I was now bilateral. And to keep life interesting, I’d also developed tinnitus (ringing in the ear), too.

Anyone with Meniere’s will understand my frustration. It was during this time I searched for a support group and found the Canadian Hard of Hearing Association. CHHA became my lifeline and sustenance. I became involved, gradually holding a number of positions, but what I found important was being able to help others with hearing loss, albeit in some small way.

More than a year ago my audiologist told me it was time for a hearing aid. These were busy times with many other things to do and I kept putting it off. This past year I began to require captioning while watching TV. One evening I was shocked while attending a local historical meeting. I could not hear or understand a single word spoken by the president or guest speaker. My astonishment was monumental! I was OK talking one-on-one, but totally confused in group conversations.

It was time to act. I went for my annual hearing test and had a mould made for an hearing aid. It takes some time to become accustomed to a hearing aid, but if others can do it, I certainly can, too. It will do me no good sitting in a drawer. Recently, I’ve learned by not wearing your hearing aids regularly (which I’ve been guilty of) the hearing nerve is not being continually stimulated and it will die. It is just like a muscle and will atrophy.

Wearing my brand new hearing aid I attended the CHHA national conference in Toronto this May. I realize it is selective perception, but couldn’t get over it that virtually everyone in attendance was wearing either a hearing aid or a cochlear implant.

What I find interesting, when I put my hearing aid on in the morning in the bedroom, I can hear the radio in the bathroom. I store it in the bedroom because washroom dampness and hair spray are definitely not good for a hearing aid.

I wear a behind the ear model basically because my ear canal is too small for in the ear styles. Initially, I thought everyone would see and notice I was wearing a hearing aid. Actually, it is not very noticeable unless you’re paying close attention and it’s a similar colour to my hair.

Recently we attended a function and I meant to put a new battery in my aid prior to leaving. Well, I was busy and didn’t get around to it. You guessed it, the battery died while we were out. Everyone around me sounded muted and muffled. I’ve learned my lesson. In future I will replace my battery at home or at least carry extras.

Life is full of future expectations. One event I’m really looking forward to is the Canadian Hard of Hearing Association’s meeting Dec. 3. It is called Deafened But Not Silent … Music & Hearing Loss. Speaker Peter Stelmacovich wears a hearing aid in one ear, a cochlear implant in the other, is an audiologist and plays guitar in a band. How cool is that?

So, my secret is out, I’m definitely enjoying (while not perfect, but) improved hearing.

Jacquie Reid lives in Hamilton. She is the newsletter editor for the Canadian Hard of Hearing Association (Hamilton branch) http://www.chha-hamilton.ca/chha-hamilton.

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Mind over Menier’s

A FREE Tool to Identify Your Meniere’s Disease Triggers

Managing Meniere’s disease can feel like an uphill battle.

It gets so complicated and confusing. Everyone is affected differently and what works for some people, may not work very well for you. I know how frustrating it can be.

But it’s important to figure out what’s triggering your symptoms, and journaling can help. It’s just hard to know what to keep track of…

Introducing the Mind over Meniere’s Symptom Trigger Tool!

When you have all the right information in front of you, it’s much easier to figure out exactly what is triggering your symptoms.

So I have created a simple and effective FREE tool that will help you:

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The Symptom Trigger Tool is a one page journal template PDF that will help you keep track of all of the important information you need to identify your Meniere’s disease triggers.

It can be filled out on the computer or printed, and filled out by hand.

The Symptom Trigger Tool Keeps Track of:

  • Daily Weather
  • Sleep
  • Diet
  • Exercise
  • Stress
  • Medications and Supplements
  • Vertigo Attacks
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Get your FREE copy of the Mind Over Meniere’s Symptom Trigger Tool!

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