Hjälp in i borreliavärlden

Har du svårt att hänga med på borreliasnacket? Eller vill du fördjupa dig? Här var ett jättebra dokument som ticktalkireland (http://ticktalkireland.wordpress.com/2013/08/01/help-for-newcomers/) la ut :) 

Help for newcomers.

Läkare med borrelia

För er som är borreliaintresserade så kommer här en samling kommentarer och berättelser och länkar från läkare som själva drabbats av borrelia. Borrelia drabbar alla! Men tyvärr är det först när man själv eller någon i ens närhet drabbas av långvarig borrelia som man inser vidden av sjukdomen och dess coinfektioner. 

Följande är rakt av kopierat från http://ticktalkireland.wordpress.com/lyme-links/doctors-with-lyme/

doctors with lyme

This is a selection of doctors who found themselves experiencing the same level of ignorance & despair that lyme patients suffer from when it comes to testing & treatment..

*Updated August 2013

Californian doctor relays his story ‘By spring 2006, I was unable to stand for the first several hours of the day without holding on to a walking stick. I’d become totally debilitated with back pain, and hadn’t a clue why. Several months into this misery, I happened upon an old colleague who—when I told him that “aging sucks”—suggested I had Lyme disease. I replied, “No way!” Not me.
But it was true. And now, 3½ years later, I still struggle with what became far worse than I could ever imagine.

The Lyme disease bacterium loves nerves and cardiac tissue. Brain, nerves, and blood vessels, muscle, and joints become home to this infection. But the symptoms any one person develops are a function of many factors including individual genetics and the role of co-infections.

Late stage Lyme disease can look like anything from nagging aches and pains to devastating brain and life-threatening heart syndromes. It’s not only a cause of massive suffering for those with the disease, it’s virtually impossible for most doctors to diagnose and treat. The reasons for this will be discussed in another article.

AUTHOR: Jon Sterngold is a Willits, CA, resident and physician.
- See more at:http://lymedisease.org/news/lyme_disease_views/220.html#sthash.2A1ySynE.dpuf

BMJ. 1999 September 4; 319(7210): 649. PMCID: PMC1116513
Personal views

My years with Lyme disease
Chris J F Wilson, surgeon lieutenant

I first became unwell in the wake of some students sadly succumbing to the meningococcus. I had non-specific symptoms—malaise, fatigue—but with the photophobia, headache, and difficulty on my feet they were serious enough to warrant admission to the neurology ward for investigation. The investigations were thorough, but no cause was found.

A label of “depression” was hung around my neck..


I was discharged back into the hands of a less than sympathetic university health service, and it was here that the mysterious spectrum of symptoms that graced my life earned me the title “malingerer,” chiselled deeply into my notes and even deeper into the clinical opinions of all those who saw me thereafter.



My aching joints were scrutinised by the rheumatologists. The neurologists put me under the inquisition again, trying to find some explanation for the interminable headache. Ultimately, as is often the case, I was directed to the psychiatrists. A label of “depression” was hung around my neck, and I spent several months at a loose end, my studies on ice, convinced that I was not psychiatrically unwell, yet being swayed increasingly to the point of view that I was somatising.

In the end it was easier to live with the symptoms rather than be ridiculed by those from whom I might seek advice. I learnt to accept the devastating effect that this malady was having on myself but most importantly on others. Constant pain, feeling permanently hung over, being unable to stand properly, and soaking erstwhile sleep partners, courtesy of night sweats, did not augur well for relationships.

For the full article go to: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1116513/

Outcomes in Cases of Chronic Disseminated Lyme Disease for Three Infected Physicians, Described in Their Own Essays, Published in Peer Reviewed Journals

by Virginia T. Sherr, MD
Hartford Marriott Farmington, CT 24–-26 March 2000

In 1972, a Swedish pediatric neurologist, 46 year old Dr. Ingrid Gamstorp, noticed generalized fatigue and paresthesias predominately in her left hand. Through the ensuing years, she developed serious balance problems, loss of fine sensation in both hands, multiple muscle pains, deep aches, weight loss, and painful feet. Colleagues dismissed her distress as being the Swedish equivalent of a “tender-foot.”” She began on a endless cycle of trips to doctors, each examining her and referring her on to another for new tests while suggesting stress as the likely cause. She became depressed and contemplated suicide. Comments had been: “You should know how it is for women of your age. You should just live with it!”

Sixteen years later, a friend noticed her blue hands and suggested Lyme disease, confirmed it with blood tests, started her on IV penicillin, then oral penicillin, then oral tetracycline and finally IV cephalosporin. These 9 weeks total of antibiotics stopped the progress of her symptoms and gave her tremendous relief from the burden of being underdiagnosed, non-treated and trivialized.


However, on-going neurological damage due to long-term, untreated and then partially treated infection left her disabled enough during her last 9 years of work that she was forced to retire early.


She said that while the infection was important to her, it “meant a lot to Swedish child neurology, which lost its only professorship at my retirement. Never pat women on the shoulder and say, ‘You know, women of your age..’”


Her article is Lyme Borreliosis from a Patient’s View-point in Scand J Infect Dis Suppl 1991; 77: 15-16.

Dr. Gamstorp was a pediatric neurologist, the first physician to recognize and describe what is now called Hyperkalemic Periodic Paralysis, aka “Gamstorp’s Disease”.

In 1987, the editor of the Finnish Medical Journal, Dr. Ilkka Vartiovaara, visited Canada and photographed a bug that bit him. Three weeks later, he had pain in his feet, knees and wrists, bone-deep chilliness, and pronounced losses of sensation, hearing, balance, energy and eyesight. He had dermal hyperesthesia and other severe bodily pains. He wrote in Living with Lyme, Lancet 1995; 345 June 3, his description of the illness that followed his trip: “Sixteen months later I could barely drive a car, type or work” and had to listen to: “Too much stress, Dr. Vartiovaara?” A year later, he received a diagnosis of Lyme disease with the help of an American colleague and began aggressive ceftriaxone IV treatments.


Unfortunately, the IV’s respite from his worst symptoms was too brief and too late to save his occupation. And rounds of oral doxycycline caused improvement but likewise did not last. After repeated on/off attempts at such treatment, Dr. Vartiovaara was forced to retire at age 45. A year later, his Lyme PCR turned positive. Despite new bouts of antibiotics, he wrote, “I am 49 years old, an invalid with a totally unknown prognosis.” He deplored “the label of chronic complainer which is put on Lyme victims.”


Download Dr Vartiovaara’s full story here..

In Jan.’00, I (Dr Virginia Sherr) wrote in The Physician as a Patient, Prac Gastroent 24; 1:28, of the acute onset in myself of chilliness, prostration, rampant cardiac arrhythmias, hyperesthesia of the skin, hyperacusis, excruciating muscle pains, painful facial and back muscle spasms, weakness, itching, sweats, tinnitus, and waves of malaria-like symptoms without the fever. Having had a ring-like rash, I called Dr. Joseph Burrascano who told me that to save my health and occupation, I would need to get immediate testing and then antibiotics. From that day 3 years ago to this, 2-22-2000, I have required IV or oral antibiotics. Of the three tick-infected doctors, I was the oldest at the time of onset of acute symptoms.


As a result of having received continuous antibiotic treatment, I am the only one of the three who is not yet so Lyme-disabled as to be forced into unwanted, premature retirement.



Dr Martz Lyme misdiagnosed as ALS

His story is riveting. After a lifetime of good health and a successful career as a physician practicing internal medicine-hematology-oncology for 30 years, in 2003, Martz suddenly started experiencing strange symptoms. First deep fatigue, then profound muscle aches and body-wide pain. Soon he was too weak to get out of bed. As his condition rapidly deteriorated, his physicians gave him a devastating diagnosis: ALS (aka Lou Gehrig’s Disease). They said nothing could stem his physical decline and he would likely be dead within two years.

But events went in a different direction. As his health spiraled downward, Martz connected with a Lyme specialist who prescribed hard-hitting, long-term antibiotics. The gamble paid off. By the end of 2004, Martz was a new man. In fact, the doctor who had diagnosed him so definitively with ALS, now pronounced that condition completely gone.

More information at: http://lymedisease.org/news/touchedbylyme/372.html

Dr. Harvey devised a lyme disease treatment plan to heal himself

“It was all pain, all brain fog,” he says. “I couldn’t think anymore. I had to quit my job. I went back to my house in San Antonio and figured that I had a fatal disease and nobody could figure out what it was.”

He says he recovered after giving himself massive doses of antibiotics.

Dr. Harvey believed he had chronic fatigue syndrome, a vaguely defined malady that many doctors didn’t believe was real. In 1999, he attended a medical conference on Lyme disease, which causes similar symptoms, although he says he was almost certain Lyme wasn’t his problem. At the conference, he learned of the use of oral antibiotics in treating Lyme disease and decided to treat himself with “high, high doses” of them to see whether they might help his condition, too.

“Little by little, I came out of the disease. Almost,” he says. He began taking antibiotics in even larger doses through a catheter and says he achieved complete recovery.

His wife, Pat, had experienced similar symptoms and had been “sick as a dog,” in bed for 12 years. She remains on antibiotics. “She’s mostly well and highly functional,” Dr. Harvey says.

More info follows at: http://www.lyme.ws/dr-harvey-devised-a-lyme-disease-treatment-plan-to-heal-himself/

Dr Ken Singleton – doctor & lyme sufferer writes book

Dr. Singleton is a Lyme-recovered physician who has been practicing Lyme medicine for over 10 years. He has a website & book called The Lyme Disease Solution (which is excellent by the way!) Looking at both traditional & supportive therapies, plus dietary changes needed to help with recovery, it’s a terrific resource for patients & doctors alike..http://lymedoctor.com/index.html

Dr Yost testifies at a hearing in Pennsylvania – it took him 5 years to get a diagnosis..


John Drulle, M.D. 1944-2003

If one could imagine a physician stepping out of a Norman Rockwell painting to spend all the quality time needed with you, with his attention focused totally on your symptoms, questions and fears, that physician would likely be the late John Drulle, M.D. Decades ago, when scholarly physicians were diligently discovering the Lyme bacteria and naming the disease, he was among the first handful of doctors on the frontlines of actually treating the condition. In the early days of Lyme disease, testing procedures and results were unreliable at best. That’s why John used the most sophisticated of devices available to diagnose and treat the condition – his ears. He would take all the time needed to hear a patient out, as there was a close relationship between close listening and appropriate diagnosis and treatment.


Because protocols were uncertain, he would never give a patient a medicine unless he tried it on himself first, because he himself was infected with Lyme as well as other tick-borne diseases.



To say his practice was patient-centered is an understatement – he would go so far as to pick up prescriptions and deliver them to a patient’s house when they were too sick to do so themselves. Even when he himself was battling chronic fatigue and pain, he kept a positive outlook and sense of humor. John Drulle was truly a blessing to all who knew him until he succumbed to Lyme disease and an untimely death in 2003.

John Drulle, M.D., was a pioneer in the fight against Lyme disease and other tick borne illnesses. He helped to initiate the New Jersey Governor’s Council on Lyme Disease. John worked toward educating the public about the need for prevention, treatment and research on tick-borne infections. He also worked toward educating the public about the special concerns regarding the effects of Lyme disease on pregnant women and the unborn.

He has a memorial fund to help continue the fight against lyme disease & has written some great articles including lyme in pregnancysteroids (avoidance of) in lyme diseaseseronegative lyme, persistence & pitfalls of testing. More at:http://www.johndrullelymefund.org/aboutjohndrulle.htm

The Physician as a Patient: Lyme Disease, Ehrlichiosis, and Babesiosis — A Recounting of a Personal Experience with Tick-Borne Diseases

Virginia T. Sherr, M.D.
Abstract reprinted permission from Practical Gastroenterology, 6:352-356
January 2000

There has been both too much and too little written about Lyme and other tick-borne diseases. On the one hand (at least in the U.S.), they are seen by some as the source of a hundred unexplained ills; on the other hand, there is a dearth of published authentic narrative description, especially in regard to the complex and fascinating neurological and neuropsychological effects of borreliosis.

If physicians contract such diseases, experiencing the impact for themselves, while at the same time maintaining their medical and scientific knowledge and detachment, a unique “double” narrative can result. This is Dr. Sherr’s situation: chance made her a victim of borreliosis, but her will and energy and intelligence have made her an expert on it too, and both voices—the voices of the patient and of the physician-investigator—are conjoined in this vivid and important personal narrative.

—Dr. Oliver W. Sacks

I stared at the strange red ring forming perfectly on the skin of my left leg, noting the tiny, glistening black spot in the ring’s red center. What is this thing? I reviewed my risks calmly—it’s too small to be a spider or tick, I thought. I had never seen anything like it. Perhaps a mite. Not likely to be dangerous or lethal. I’ll watch it and see what it does. When I checked it again in a few hours, the tiny black speck was not there. Going about my business, I felt pleased with my scientific brio.

Fortunate genes and Health techniques learned as a psychiatrist had gifted me with a strong immune system. I had almost never had any antibiotics in my entire life. I stayed healthy. There was no idea then, in the mid-1980′s, of what was to come a decade later.

The painless rash circle likely was a spider bite, one physician said; that was the first time I worried a little. In my experience as a physician and growing up around biologists and entomologists, this was not what I expected from the bite of the few local spiders that humans have to fear. And as a long-time gardener in a wooded area near my Pennsylvania home, I co-existed with multiple varieties of arachnids, all of which fled from my approach.

More follows at: http://www.ilads.org/lyme_research/lyme_publications22.html

Dr Virgina Sherr

From Wellsphere forum..http://www.wellsphere.com/exercise-article/raising-awareness-of-lyme-disease/363450

Today’s featured contributor is Dr. Virginia Sherr, who maintains the site The Human Side of Lyme.


Dr. Sherr is a psychiatrist who has experienced Lyme disease first hand over many years, and shares valuable information and resources to get the word out about this ongoing problem. She is particularly concerned about the incidence of undiagnosed CNS involvement, and points out that despite underreporting, more than 20,000 cases are reported annually, but “neuroborreliosis is still actually considered rare by a majority of physicians, most of whom are spirochetally naïve.”



She would like psychiatrists in particular to be aware of the possibility of Lyme as a cause of psychiatric complaints — see her brochure on What Psychiatrists Should Know About Lyme Disease.

Her website is a great resource of articles for people interested in the various manifestations of Lyme. For example, here is an article written by Dr. Sherr onBell’s Palsy of the Gut and Other GI Manifestations of Lyme and Associated Diseases.

Duke Doctor Beats the Odds and Survives to Help Others


Oncologist Neil Spector trained at top schools, cared for patients at leading medical centers and led a pharmaceutical industry team that developed breakthrough therapies for the treatment of breast cancer.

Still, he believes in his heart and in his soul that his greatest life lessons have come from his own experiences as a patient: a heart-transplant patient whose frustrating medical saga nearly took his life.

Dr. Spector, 54, received a new heart on July 20, 2009, after his own heart was permanently damaged by Lyme disease that had ravaged his body for years before finally being diagnosed in 1997…

..He was beyond physically fit, competing in marathons. He had no risk factors for heart disease, but quickly his body was beginning to betray him. Transient arthritis and transient cardiac arrhythmia came first, followed by a burning sensation in his heels. Then came the chest pains and rapid heart rates that made him a patient at every ER in South Florida. By his own admission, “It was weird and bizarre.”

Repeated blood tests came back inconclusive, but Neil Spector, the physician, began to suspect he might have Lyme disease. He had spent time running through the woods of the area surrounding Boston as well as on Cape Cod, and although he doesn’t remember being bitten by a tick, he must have been exposed.

He took a course of doxycycline—the antibiotic of choice for the treatment of Lyme disease—for a completely independent reason and his symptoms subsided, providing him with another clue that his hypothesis was correct. Yet, more blood tests were as nonspecific as all the others.


“My tests were interpreted at the top places that specialize in the diagnosis and treatment of Lyme disease, and we still had no confirmation that’s what it was,” he says. “I repeatedly described my symptoms and hypothesis, but the diagnosis was elusive because my numbers were not confirmatory by generally accepted medical criteria, or even by Centers for Disease Control criteria.”

Frustrated by the lack of a diagnosis, Dr. Spector was equally angered that it confirmed another suspicion about the changing profession that he had trained for and loved.


“Many doctors don’t have the time to actually listen to patients,” he says. “Instead they rely on tests and are locked into algorithms established by those who devise the standard tests. But patients are humans, and people don’t fit into nice, square boxes.”


More tests gave positive results that Dr. Spector’s heart had serious electrical problems, and he received a pacemaker/defibrillator as the standard of care in 1997.

By then he had lost 20 pounds, but he was still keeping a grueling pace caring for bone marrow transplant patients, even making house calls. It was work he loved because he felt he was making a difference, but he began to question how long he could continue. In addition, his area of research in academia had narrowed and he was enjoying it less. And on the personal side, the Spectors’ efforts to start a family had yielded multiple heartbreaking miscarriages.

A Living Nightmare

Although his heart was more resilient than any medical professional had believed—based on the numbers—that episode in June was the beginning of a steep slope to a heart transplant and the worst month in Dr. Spector’s life. The near-death experience in the hospital had taken its toll on his heart, which was already severely weakened. He began having 15 to 20 episodes of ventricular tachycardia a day.

“It was a living nightmare,” he remembers. “There was no telling when one of the episodes might kill me.”

On July 10, doctors tried to remove the pacemaker, and within minutes of going under general anesthesia, his blood pressure dropped to dangerous levels, and the procedure was immediately terminated. That was the last straw. Dr. Spector went into florid heart failure.

“I accumulated fluid in my abdomen so that I looked like I was six months pregnant,” he says. “I could not keep food down. I could not find a comfortable position to rest. My brain was not being adequately perfused with blood. I wasn’t able to think clearly at times.”

For the first time in the 12-year ordeal, he told Denise that he could no longer live like this.


“I had a great cardiac team at UNC, but they told me that my heart was barely pumping blood,” he says. “On Friday, July 17, I was told I had 72 hours to live. Without a transplant or a temporary mechanical pump, I would have been dead by Monday.



During a nine-hour surgery, Dr. Spector received a new heart. He distinctly remembers thinking there was a problem because of the feelings he was having internally, but he was assured the unusual sensations were the result of having a healthy heart as opposed to one working at only 10 percent.

Dr. Spector believes that the lessons he’s learned as a patient coupled with his knowledge as a physician will help him fulfill a lifelong mission: writing a book about his experiences.

The Spectors chronicled the heart transplant journey through a blog atwww.lotsahelpinghands.com. There, Dr. Spector acknowledges both that he is thrilled a new heart was found in time and that his body and psyche have taken a beating from the required post-transplant meds.

“It’s a constant adjustment to find the dose that keeps my heart happy and doesn’t cause too much havoc on the rest of me,” he writes. “The recovery from heart transplant is a journey. As someone once said, ‘It is not a sprint to the finish, but instead it’s a marathon.’ I’m in it for the long haul regardless of the situation.”

— Story byElizabeth Swaringen, a freelance writer and breast cancer survivor based in Pittsboro.

Doctor’s Dilemma, a paper

Edward L. McNeil, M.B., B.S., M.D.


This paper was originally presented to the Second National Lyme Convention held in Gettysburg PA on Saturday, July 27 and Sunday, July 28, 2002. Dr. McNeil himself suffers from tick-borne diseases.

..When Lyme disease was first recognized in Connecticut, the majority of the victims were infected by a single germ subsequently called Borrelia Burgdorferi, after Dr. Burgdorfer who identified it.

Unfortunately, most of those who have been bitten by a disease-carrying tick can now be infected with more than one disease from a single bite. One is Ehrlichia, another is Borrelia burgdorferi, and Babesia which is a malarial cousin and gives similar symptoms to malaria. The three mentioned organisms are not the only ones that can infect from the same bite, as these organisms depend on the geographical area from which they came. These diseases are not only prevalent in the USA but are found in every European country, Scandinavia, the Balkans and as far away as Australia.

Ticks are great travelers. They can catch a ride on a plane or a bird. They can be carried from one country or continent to another, attaching themselves to humans or their luggage. The disease they carry can be transmitted by blood transfusions and from mother to fetus, an infected fetus more likely to abort and, if born, to be diseased and die at an early age.


The doctors’ dilemma is they have been told early treatment with a short course of an antibiotic, usually Doxycycline, will cure Lyme disease. This may appear to be so but such treatment will not guarantee a recurrence will not occur, months or years later, without a further tick bite. This is especially so if more than one pathogen was in the bite.



That is not the only dilemma faced by the doctors because many of the blood tests to indicate Lyme disease are unreliable. A patient with negative results can be told they do not have Lyme disease when they indeed do. Treatment is then denied and the patients sentenced to an advancement of their disease(s) to a chronic form with increasing disability and death. Sadly, it is not unusual for patients to see 10 to 15 different doctors before a diagnosis is made. This is applicable to both the USA and the UK.

Diagnosis has to be made by taking a complete history of symptoms and physical signs elicited by a thorough examination, especially of the nervous system. For treatment to ameliorate some of the disabling symptoms, a prolonged course of antibiotics is necessary. Such treatments have shown success when prescribed by physicians specializing in the treatment of the tick-borne diseases and who have personally treated more than 5000 cases. Those who consider prolonged courses of antibiotics are harmful do not seem to apply the same judgement to other infectious diseases, such as Tuberculosis or AIDS, or to the use of prolonged courses of antibiotics for young people with acne.

A lot of expensive research is being done regarding what happens at the cellular level in the tick-borne diseases, but until repeatable, accurate tests are available to identify which pathogens are infecting a particular patient, research to show the effectiveness of particular treatments, is futile. Until that time, doctors are justified in diagnosing the tick-borne diseases clinically and ermpirically, treating with long-term antibiotics, judging the response over months rather than days. Long term exhibition of antibiotics is less likely to cause resistance to the antibiotics than short courses.

After penicillin with the advent of the antibiotic age, many considered we had conquered infectious diseases for good. How wrong they were. Emerging and changing infectious diseases now present an awesome challenge around the planet. In the fight against the harmful germs, we have not begun to win and great losses are to be expected. We may consider humans smart but the microbes have shown themselves to be even smarter in this present age.

Dr. Ted McNeil is an acadamician in the International Academy of Aviation and Space Medicine. He was a pioneer in International Medical Air Rescue and wrote the first text book on the subject. He also worked with NASA and designed the equipment for performing surgery in a weightless environment. Later, Dr McNeil worked as an emergency room physician in Connecticut. He is interested in all changing and emerging infectious diseases and gave a presentation on the subject to the Acadamy in Paris in September, 2001, in which he discussed tick-borne diseases among others.

The sad details of Dr Bleiweiss, physician & lyme patient who lost his life to Lyme..


He authored the excellent paper ‘When to Suspect Lyme Disease

Dr. Edward Stanley Arnold passed away in 2006

He attended Vanderbilt University, becoming a psychiatrist after eight years of studies. In June 2000, he contracted Lyme Disease. He hasn’t practiced medicine since 2000. His last treatment was at Vanderbilt University.




Dr. Jane Colfax passed away in 2005

After serving as an Army nurse during World War II, she attended Women’s Medical College of Pennsylvania and became an OB-GYN when she graduated in 1955. Albert Pineda, a doctor who worked with Colfax at St. Joseph’s, said she was the first female OB-GYN at the hospital.

During the late 1980s, Colfax contracted Lyme disease but it went undiagnosed for years, DeNike said.


“It was too late to cure it. With her it got worse and worse until she had to give up being a physician because she couldn’t use her hands at all,” he said.



Backer recalled Colfax’s last day at the office in 1992.

“She and I were the last to leave. We turned the key together. I kept telling myself I’m not going to cry, but sure enough I did,” she said.

Colfax and her husband retired to North Carolina, where her health continued to decline.


“She couldn’t walk very well. She was bedridden for practically 12 years until she passed away,” DeNike said.





Tips för ett bättre läkarbesök

Här kommer sex tips på hur läkarbesöket kan bli bättre, hur du kanske kan slippa bli förnedrad av läkaren och få den hjälp du förtjänar. 
1. Remind yourself that the doctors and the staff work for you, not vice versa.
2. Consider taking someone with you.
3. Bring a list to the appointment.
4. Let the doctor be the expert but don’t be afraid to ask questions.
5. Repeat back your understanding of the plan of action.
6. Don’t write off a good doctor because of one disappointing visit.
För att läsa hela http://www.psychologytoday.com/blog/turning-straw-gold/201307/don-t-be-intimidated-in-the-doctor-s-office-six-strategies 

Lyme disease awareness month

Nu var det längesedan jag skrev här. Det känns som om jag har väldigt mycket att uppdatera om. När det blir att man inte bloggar kan det bero på två saker, för mig i alla fall. Antingen att jag mår alldeles för dåligt och bara inte orkar alls, eller att jag mår såpass bra att jag varken har behovet eller tiden att blogga. Den senaste tiden har det varit det sistnämna! Jag har haft SÅ MYCKET ENERGI! Det är helt otroligt. Så mycket energi har jag inte haft sedan jag var frisk för över 4,5 år sedan. Efter den där IV-kuren jag fick i vintras så vände det - jag fick mitt liv tillbaka. En otrolig känsla. Jag skrattar högt på morgonen när jag cyklar till skolan, bara för att livet känns så lätt. Jag visste inte att livet kunde vara så enkelt att leva.

Jag är inte frisk än och har många symptom kvar, men mår så mycket bättre och för det är jag enormt tacksam. Och OJ vad fullt upp det har varit med allt möjligt den senaste tiden. Till exempel har Maj varit Lyme disease (= borrelia) awareness month över hela världen och jag har varit väldigt engagerad i detta. 

För er som vill veta mer om manifestationer osv som har skett under maj månad runtomkring i världen, och varför de skett: 
http://worldwidelymediseaseprotestus.blogspot.se/ (USAs sida)
http://borreliaupproret.wordpress.com/ (den svenska sidan)



I Sverige hölls manifestationer i Göteborg, Stockholm och Uppsala. TV4 pratade om borrelia på nyheterna hela veckan i samband med detta, GT och GP skrev om det i tidningen, Göteborgs närradio och Uppsalas radio tog upp det. Det blev väldigt lyckat och förhoppningsvis har många tack vare det här fått upp ögonen för att något står galet till med sjukvården vad gäller borrelia och vissa fått den informationen de behöver för att kunna få rätt hjälp och återfå sina liv! 

Sådana här flyers delades ut under uppropet i Göteborg (klicka på den för större bild):
Filmen Under our skin: http://topdocumentaryfilms.com/under-our-skin/
Om borreliauppropet: http://borreliaupproret.wordpress.com/
Svenska borreliaföreningens hemsida: http://www.borrelia-tbe.se/
Symptomlista: www.borrelia-tbe.se/media/dokument/symtomlista%20jrgens.pdf


Limegrönt är borreliafärgen, då sjukdomen på engelska heter Lyme disease. Över hela världen, i trettio länder, har det hållts upprop där folk klätt sig i limegrönt, haft plakat, hållt tal, delat ut flyers mm, och ett flertal kända byggnader har lyst grönt för oss borreliasjuka - och framför allt för att upplysa folk kring borreliaproblematiken!

Till exempel lyste niagarafallet grönt: 

Och i Göteborg lyste Lisebergshjulet grönt hela helgen 9-11 Maj (Foto: Maria Windt Wallenberg):
På Lisebergs officiella facebooksida skrev man såhär: 
"Ikväll lyser Lisebergshjulet grönt! Grönt är den färg som används över hela världen i kampen för att öka medvetandet om borrelia och dess följder. Liseberg stödjer Borreliauppropet, som är en internationell manifestation för att öka medvetenheten om borrelia. Runt om i världen genomförs manifestationer den 10–11 maj 2013. Bland annat kommer Niagarafallen, CN Tower i Toronto, Peace Bridge och Bell Tower i Australien att lysa i grönt. Och så vårt eget Liseberghjul då."
♥Tack Liseberg för stödet
Om ni vill komma i kontakt med andra borreliadrabbade eller har frågor kring hur man ska gå till väga ifall man misstänker att man har borrelia så kan ni gå med i den här facebookgruppen: https://www.facebook.com/groups/6509008833/10151672969383834/?notif_t=group_activity
(om inte länken fungerar så sök på Borrelia (Neuroborrelios) "kronisk borrelia" på facebook)

I år var första året de här manifestationerna hölls. TUSEN TACK till Charlotte Therese Björnström som var grundaren till detta och alla andra som engagerat sig - så många sjuka som släpat sig upp ur sina sängar för att vara med, inte för våran skull (för oss är det ju försent), men för att inte våra vänner och nära och kära, eller främlingen på gatan, ska tvingas gå igenom det vi gått igenom. Vi kommer inte ge oss förens det blir en förändring i diagnostiken och vården av borreliasjuka, för såhär får det bara inte fortsätta! Testerna måste bli säkrare, långvarig borrelia måste erkännas av sjukvården och drabbade måste ges rätt behandling. 
Alla ni som kämpar mot borrelian, sjukvården och folk runtomkring er som inte tror på er - ge inte upp, vi är många, och en förändring kommer att komma. Borrelia och dess coinfektioner drabbar alla, oavsätt ålder, religion, politisk åsikt eller yrke. Ju fler som drabbas, desto fler kommer få upp ögonen för vilket stort problem det här är och tillslut måste en förändring till. Jag bara önskar att förändringen ska komma INNAN alla dessa personer får sina liv förstörda 
"Never doubt that a small group of thoughtful, comitted people can change the world.
Indeed, it is the only thing that ever has". 

Yolanda Foster berättar om sin borrelia


Jag känner igen mig precis i det hon berättar! ...tex hur det är som att man sitter fast i en kropp som inte är ens egen. Hur man får massa läkemedel utskrivna för att lindra symptomen, men de hittar ingen orsak. Och hur frustrerande det är att bli skickad från läkare till läkare som tror att man är deprimerad - när man VET att man inte är det. Det är en lång, ensam och tung kamp, men wow vad det är värt det när man känner hur man långsamt får sitt liv tillbaka.

(för er som inte vet det har hon varit med i real housewifes i USA).


Vaccin mot borrelia

WHAT! Det finns vaccin mot borrelia - men det ges till hundar! 
Why? För att läkemedelsföretagen inte tjänar tillräckligt med pengar på det (nej såklart inte, eftersom massor med kroniska sjukdomar som de tjänar stora pengar på nästintill skulle försvinna om folk inte längre fick borrelia...). 


Det borde inte komma som en chock att läkemedelsföretagen mfl inte vill bota, utan tjäna pengar, ändå blir man lika besviken varje gång för man hoppas att människor ska inse att rädda någons liv betyder så mycket mer än lite extra pengar i fickan.

Bakom kulisserna, Lyme Disease


Ingen ska behöva gå igenom det här! Vilken otroligt stark tjej, och otroligt tålmodig och stark man - det är verkligen inte lätt att stå vid sidan om heller. 


Med den här videon vill jag säga att det oftast inte syns utanpå hur otroligt dåligt man mår... kollar man bara på alla fina bilder så skulle man tro att detta var ett superlyckligt nyförälskat par som åkte på härliga semestrar. 

Glöm aldrig att man inte ser hela sanningen... vi vet inte alltid ens vad våra närmaste vänner eller familjemedlemmar går igenom bakom kulisserna. 
Har man en kronisk sjukdom av något slag blir man duktig på att spela teater - för vem skulle orka vara med någon som alltid mådde dåligt, som aldrig log och skrattade? Men ibland är vi nog för duktiga på att dölja -sminka över, sätta på oss ett leende, låtsas att vi hänger med i samtal fastän hjärnan arbetar i slowmotion - så att folk inte förstår hur fruktansvärd den här sjukdomen är. När vi aldrig visar hur illa det faktiskt är så är det kanske heller inte så konstigt att till och med våra vänner och nära och kära tror att det "inte är så farligt". Det syns ju inte... Och tyvärr är det mycket lättare för folk att tro att en person hittar på och överdriver - "är för lat eller söker uppmärksamhet" - än att tro att det är fel på hela systemet. 

Varning, den är väldigt känslomässigt stark, förstår inte hur de har orkat, jag hade svårt att kolla igenom hela för att det var så smärtsamt att se:

Länk till videon på youtube:http://www.youtube.com/watch?v=So2K68r8pOY

PS. Lyme disease = borrelia.

På nyheterna, i USA

Man får lite hopp, om att det ska bli lättare att få hjälp för de som i framtiden kommer insjukna i borrelia!  Ju fler som får veta vilken otrolig kamp det är - inte bara mot sjukdomen, utan även om rätten att få vård, bli tagen på allvar och få rätt behandling - för oss som lider av "kronisk" borrelia, desto bättre. För såhär får det bara inte fortsätta! Och förändras synsättet på borrelia (lyme disease) i USA så kommer det även att förändras i Sverige, eftersom vi bygger våra sjukvårdsriktlinjer på amerikanska riktlinjer, vars riktlinjer styrs till mångt och mycket av försäkringsbolagen. Det där var mycket kortfattat hur det hänger ihop, men bara så att ni förstår varför jag blir glad över att det kanske börjar hända lite saker i USA: förr eller senare måste samhället inse att sk "kronisk borrelia" inte är en inbillningssjuka. Kanske krävs det att de som sitter på makten får det för att det skall tas på allvar... Usch, jag önskar ingen den här vidriga sjukdomen, oj vad den kan ställa till det!
Jag längtar tills jag har pluggat färdigt och kanske kan börja forska kring det, för det finns mycket intressant att forska på. Jaja, nog snackat, här är nyhetssändningen för de som är intresserade :)

Länk till youtubevideon

Dr Phil om kronisk borrelia

Borrelia kan även kallas för Lyme disease (det vanligaste namnet i USA) eller Lyme borreliosis. Här kommer Dr Phils program om kronisk borrelia. Oj vad jag är glad att det inte hann gå så långt för mig som för de här patienterna! Men det är lite intressant det en av tjejerna säger om att hon hade hjärtarytmier som slutade efter att hon började med antibiotika, precis som för mig.



Lite mer om reportern som drabbbats av Lyme och var med i Dr Phil:

En tittare som tackar Dr Phil och tar upp några andra viktiga aspekter på ämnet!

Jag undrar hur läget ser ut om tio år, är kronisk borrelia (dvs borrelia som inte botats av 14 dagars anitbiotika som de flesta läkarna säger slår ut borrelian helt) accepterat då? Har forskningen fört oss fram, eller ska läkarna fortsätta dividera hit och dit huruvida de patienter som sägs ha kronisk borrelia bara är uppmärksamhetsgalningar, deprimerade och fejkar? Det värsta är att samtidigt som debatten fortskrider så lider mängder av personer av det här utan att få någon hjälp.
Och min fråga till "andra sidan" är:  vad är det då, om det inte skulle vara kronisk borrelia? Borde man inte vara väldigt intresserad av att i alla fall komma på det så att man kan behandla det i så fall? Och om det skulle vara stress/utbrändhet/psykosomatiskt som "andra sidan" påstår, ja då har vi ju ett väldigt stort problem som är i akut behov av en lösning eftersom fler och fler drabbas av denna osynliga sjukdom. Svälj eran stolthet och hjälp oss!! Snälla, vi vill få tillbaka våra liv igen.

TACK Dr Phil för att du tog upp det här ämnet!


Eftersom jag själv tycker att det är intressant att läsa om andras erfarenheter och upplevelser, särskilt om någonting jag själv också går igenom, så tänkte jag dela med mig av de borreliabloggar som jag har hittat så att den borrelianyfikne som råkar trilla in här slipper ägna massa tid åt att söka runt massa på google efter fler bloggar som jag gjort haha:














Uppror mot borreliavården



Att vi är SÅ många som vi faktiskt är som inte får någon hjälp här i Sverige, fastän vi är rejält sjuka, är skandal. Vi blir hemskickade med att vi är stressade eller deprimerade, eller med en helt annan diagnos än borrelia - för att läkarna inte är pålästa eller vägrar öppna ögonen för hur stort problem borrelia (och dess koinfektioner) är.

Vi tvingas åka till Norge eller Tyskland för att få hjälp och för att ens få göra ett någorlunda pålitligt test (läkarna vet om att det test som i dagsläget finns i Sverige för borrelia är opålitligt men låtsas inte om det) och betala dyrt för det. Inte för att de lurar oss på pengar, utan för att det ÄR dyrt med vård om man ska betala det själv. 

Men behöver det verkligen vara såhär? Egentligen inte, det finns ju hjälp att få, och vettigare analysmetoder, tex att mäta CD-57 och göra ett LTT-test. Varför händer ingenting då med borreliavården här i Sverige, varför blundar de som har någon makt i frågan för vårt lidande?
Kanske lyssnar de om vi blir tillräckligt många som KRÄVER en förändring?

Har du, eller misstänker du att du har, borrelia men inte fått adekvat vård eller blivit tagen på allvar? Snälla skriv på det här borreliauppropet då: http://upprop.nu/KBJL
Här finns ytterligare ett borreliaupprop, skriv gärna på det också: http://namninsamling.se/index.php

De kan inte ignorera oss hur länge som helst, för det här är ett problem som bara växer och växer. Och förr eller senare drabbas de själva och vill ha den vård som de så länge vägrat borreliadrabbade, då kanske det händer något...


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