November 2013

Cyclic Vomiting Syndrome

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Before I even wake up fully, my ears register the sound of my twelve year old daughter throwing up. It is such a familiar middle of the night sound for me that it has ceased to be alarming. She has been throwing up on a regular basis since she was 2 years old, in episodes that come and go, usually lasting one to two days. The vomiting that comes with these episodes is violent, frequent, and often accompanied by severe abdominal pain. Without medication, she will vomit every 10 to 15 minutes for hours; luckily, for the last few years, we’ve sometimes been able to successfully treat these episodes with medication.

Sometimes her episodes last longer, like one recent very bad episode where she was sick for 6 days on and off. At times during that episode the vomiting was controlled by medication, but not always. When her medication didn’t work, she would lie on the bathroom floor and moan, and say “Mommy, help me,” or worse, “Mommy, I can’t live.” We have been told that the medications we give her—prescription Zofran, over the counter dimenhydrinate (Dramamine), and Tylenol and Advil—are the only options, and that there’s nothing else we can do. But when I see her suffering, I have to believe that there must be something more that can be done, because nobody should suffer like that, especially not a child.

When she was younger, the episodes would come every month or two. She is my oldest child, and for a long time I assumed she was just very susceptible to getting stomach flu, and that she was severely affected every time she got a stomach virus. As my other two children got older, and I realized how unusual the severity of her vomiting was, and the frequency of her episodes increased, I started to suspect it was something bigger than just stomach flu. I mentioned my concerns to her doctor, and he agreed, and suggested it might be cyclic vomiting syndrome.

Cyclic vomiting syndrome, or CVS, is a poorly understood, and under recognized disorder. Although it was originally thought to be a pediatric disorder, it is now known that it can occur in all ages, and that it is more common than previously thought. It is characterized by episodes of severe nausea and vomiting that alternate with periods with no symptoms. Some patients with CVS have symptoms in addition to nausea and vomiting during episodes such as headache, dizziness, fever, sensitivity to light, and diarrhea. For each individual with CVS, the episodes are similar to each other: they generally start at the same time of day, include the same symptoms, and last the same length of time. For my daughter, she always started vomiting in the middle of the night or early in the morning, it lasted about a day, and occurred every month or two. As she gets older, everything about her episodes has become less predictable. They have sometimes lasted longer, or clustered in groups where she can have one episode per week for three weeks, then nothing for three months. CVS is thought to be a part of the migraine spectrum, and sometimes patients are able to identify things that trigger episodes such as certain foods, illnesses, cyclical hormone changes, stress, or fatigue.

Cyclic vomiting syndrome is difficult to diagnose, because there is no specific test for the disorder. Therefore, it must be diagnosed by excluding all other possible reasons for the vomiting and other symptoms. My daughter was referred to a gastroenterologist and an endocrinologist. In addition to her episodes of vomiting, she is very small for her age. After a workup by both doctors, they couldn’t find any reason for her vomiting or her small size. Her gastroenterologist was reluctant to offer any diagnosis at all, even when I asked about CVS.

Because there is no physiological defect that with CVS can be measured by the medical tests we have currently, many times patients are told that their problems must be “in their head,” or just caused by anxiety, depression, or other mental health problems. Similar attitudes are faced by patients with many other functional disorders, which are diseases where no specific defects can be observed by medical tests. Functional disorders include fibromyalgia, irritable bowel syndrome, migraines, chronic fatigue syndrome, complex regional pain syndrome, and restless legs syndrome. It is short-sighted and insulting to patients to conclude that their problems are not real just because current diagnostic tests can’t detect a defect, and in many cases disbelief or dismissal by medical professionals leads to long diagnostic delays, during which time the patient suffers needlessly without treatment.

My daughter was faced with a version of this attitude, when for a time her gastroenterologist seemed to question repeatedly whether she might have anorexia or bulimia. The concern is legitimate, and it is important to rule out the possibility; however, the issue seemed to come up over and over again for us despite our answers. My daughter was asked if she ever didn’t eat because she was worried about getting fat, and she looked very surprised, because she’s worried about the exact opposite—she would love to be bigger. Clearly she doesn’t have bulimia, when she is waking up in the middle of the night and vomiting in her bed, and writhing in pain on the bathroom floor. Sometimes it gets very frustrating when doctors don’t seem to listen to and hear the answers that they are being given, because they have other ideas that conflict with what you are saying.

We were lucky, because my daughter’s pediatrician mentioned CVS as a possibility very early on. Otherwise I don’t think we would have any idea what her diagnosis might be, because her gastroenterologist was content to just rule things out based on test results, and not offer any opinion on what the problem actually is. It has been beneficial for us to have what we think is a likely possibility for a diagnosis, because it has allowed us to figure out strategies for helping her, including trying to avoid her triggers. The medication that was prescribed by her pediatrician is very useful for helping to manage her episodes when they do happen, although it isn’t as much of a complete solution as I would like, and I am still searching for additional treatments that may help. However, her episodes are less debilitating than they used to be thanks to the medication, and overall she is thriving despite her illness: in between episodes she is a happy, healthy twelve year old who loves figure skating, soccer, Glee, and texting her friends.

 

Truth Seeker or Conspiracy Theorist? You Decide.

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I’ve always believed that the simplest answers to most problems are the ones that are closest to the truth. I don’t particularly like conspiracy theories. I generally find them to be offensive. So as not to offend the people who believe in conspiracies, I’ll refrain from giving an example, but I tend to think that what you see is what you get and that there aren’t any evil masterminds controlling the world. I don’t think that there is anyone smart enough to have evil plots that control the world. Rather, I believe that there are complex feedback loops that keep certain parties in power and others powerless. Of course, those in power work to protect their power, sometimes through greed, lies and cover-ups, but it’s not necessarily a conspiracy per se. It’s just people being people and trying to maintain the status quo because people generally don’t like change (and a million other complex psychological and sociological reasons why people like to keep those in power who are in power and those without power without power).

Then I got sick. I got sick because a prescription pharmaceutical, an antibiotic no less (Cipro), hurt me.  I was poisoned by a prescription drug that is considered to have an “enviable record of safe and efficacious use.” (1)  I started screaming about how it’s not okay to take away people’s ability to walk, sleep, work, etc. to treat their sinus or urinary tract infections.  I started screaming about how fluoroquinolone antibiotics (Cipro, Levaquin, Avelox, Floxin and a few other less commonly used drugs) are dangerous and over-prescribed. I started researching how fluoroquinolones work and was appalled to find that they dismantle and disrupt replication of DNA.  I began making connections between the side-effects the fluoroquinolones, and the various diseases that fluoroquinolone toxicity mimics.

Diseases of Fluoroquinolone Toxicity

Fluoroquinolones cause peripheral neuropathy (2), peripheral neuropathy could easily be mistaken for Fibromyalgia. Fluoroquinolones cause destruction of tendons (3) and cartilage (4), both of which are found in the joints, and thus fluroquinolone toxicity could be misdiagnosed as Rheumatoid Arthritis. Fluoroquinolones have many psychological side-effects including anxiety, depression and even psychosis (5), and thus they may be connected lead to psychiatric disorders. I found a study that connected topoisomerase interrupting drugs (6) (fluoroquinolones are topoisomerase interrupters (7), along with several chemotherapy drugs) with Autism. A conspiracy theorist was born.

Fluoroquinolone antibiotics can take an acute infection and convert it into a chronic illness (Fluoroquinolone Toxicity Syndrome). The new, chronic illness likely will be misdiagnosed and not recognized as a drug side effect, and the treatment of the misdiagnosed disease often leads to prescriptions for additional drugs. And, even though that line of thinking leads to more profits for Big Pharma, I don’t think that it’s a conspiracy. I don’t think that it’s intentional, even on the part of the companies that initiate and perpetuate it, Bayer and Johnson & Johnson (J&J). Though making people chronically ill through an antibiotic that is viewed as benign by almost everyone is convenient and profitable for them, I don’t think that it’s their intention. Perhaps I’m naive.

Somewhere between naively believing that Bayer and J&J have no idea what they’re doing, and pessimistically believing they are poisoning us all to turn us into lifelong customers, lies the truth.

The Truth about Fluoroquinolones

The truth, especially when dealing with something as complicated and multifaceted as biochemistry, cellular biology and genetics, is very difficult to comprehend. But the fact that it is too difficult for most of us to understand does not mean that there is no truth. The correct answers are probably not the easiest answers. They don’t fit into a box of good or evil. They aren’t linear. The truth about fluoroquinolones involves inconvenient things like delayed reactions, tolerance thresholds, system-wide cellular destruction that results in a wide array of disease states, enzyme depletion, etc. The truth about fluoroquinolones defies common sense because our common sense tells us that antibiotics are benign, that drug side-effects are rare, that when side-effects happen they’re treatable and transient, etc.  That “common sense” approach, unfortunately, is not the truth.

The truth is that fluoroquinolones disrupt and dismantle DNA.  This has been shown repeatedly.  Per a 1998 study entitled “The Mechanism of Inhibition of Topoisomerase IV by Quinolone Antibacterials,” Fluoroquinolones are “among the first antibacterial agents that efficiently inhibited DNA replication.”  (8).  The mechanism for action for Ciprofloxacin, as listed on the FDA warning label is, “The bactericidal action of ciprofloxacin results from inhibition of the enzymes topoisomerase II (DNA gyrase) and topoisomerase IV (both Type II topoisomerases), which are required for bacterial DNA replication, transcription, repair, and recombination.” (7) Disrupting the DNA replication process is how these drugs work (or at least part of how they work).  Denying that fluoroquinolone antibiotics damage DNA because it’s not a pleasant thing to acknowledge, is futile and it does not get us closer to the truth.

Very little is known about the consequences of disrupting DNA replication through pharmaceuticals. The truth that fluoroquinolones disrupt and dismantle DNA is only part of the puzzle; it is only part of the truth. As complicated and poorly understood as the effects of these drugs on DNA are, there are still multiple levels of questions regarding the effects of fluoroquinolones on the human body. Some of the questions, answers and truths likely lie in understanding the effects of these drugs on mitochondria. A thorough understanding of article “Mechanisms of Pathogenesis in Drug Hepatotoxicity Putting the Stress on Mitochondria” (9) and how it relates to fluoroquinolones will likely give you some answers about how these drugs do damage. There is evidence that fluoroquinolones cause cerebellar ataxia (10). The carboxylic acid molecule that is part of fluoroquinolone drugs likely leads to the formation of hazardous acyl glucuronoids (11). The interaction between broken mitochondrial DNA, acyl glucuronoids and cerebellar ataxia, combined with other ill understood and complex factors, is probably where the truth lies. It is hugely complex. It is impossible for the average person to comprehend and it is difficult for even the smartest person to understand. So, instead of seeking understanding and truth, the majority has chosen to ignore the fact that no one knows how these chemicals work in the human body and what their consequences are. We will take them because we know one small element of what they do – they kill bacteria – and believe that all other effects of these drugs are coincidental, accidental or rare.

Willful Ignorance about Fluoroquinolone Dangers

Willful ignorance has taken over, and faith-based assumptions about the good or evil that the medical system is have come to dominate the conversation. The established medical system is the entrenched party with the power, so those who support it are the majority; they are those with “common sense.” Those who rebel against the assumptions that the medical system is doing good are accused of being conspiracy theorists or worse. No one is really qualified to say that they have a position based on truth though, because there are too many unknown variables to know the truth (at this time). No one, not even the smartest researchers and scientists, fully know how fluoroquinolones, and probably many other drugs, affect every system in the human body. The human body is too complex and too little is known (at this time) about it, and how each of its systems interact, for anyone to truly know how everything works together. So little is known about the human body that ligaments, something that you can see with the naked eye, are still being discovered (12). If we don’t even know every ligament in the body, you can certainly bet that we don’t know every enzyme or neural pathway. Yet enzymes, neural pathways, mitochondrial DNA and other really important parts of human physiology are being disturbed by pharmaceuticals. And people are getting sick because of it.

Though the truth about how adverse drug reactions occur is difficult to ascertain, it should be sought. Questions should be asked. Experiments should be done. The effects of drugs on all bodily systems should be explored.  Perhaps answers to difficult questions about how drugs effect mitochondria, neurons, enzymes, etc. should be asked before drugs are released into the public.

Back in 1992, when fluoroquinolones were first gaining popularity, Scientists raised concerns about their use in an article published by the Proceedings of the National Academy of Sciences of the United States:

the interaction (of fluoroquinolones) with DNA is still of great concern because of the possible long-term genotoxicity of quinolone compounds, which are increasingly adopted as first-choice antibiotics for the treatment of many infections, and because it addresses the real mechanism of action of this class of molecules.” (13)

The question hasn’t been asked though.  People have been stuck on the faith-based assumption that fluoroquinolones have “enviable record of safe and efficacious use” because the only side-effects that they’re willing to see are allergic reactions. They have been intent on willful ignorance. Willful ignorance protects them. It keeps them from seeing that in frivolously over-prescribing dangerous and poorly understood drugs, we may have damaged our precious DNA, and that the consequences of doing so may be many of the “mysterious” systemic diseases that plague us.

There is a fine line between screaming about willful ignorance on the part of the majority and being a conspiracy theorist.  I’d like to think that I am reasonable; that my assertions are backed up by scientific findings, and that I’m right.  Of course, all conspiracy theorists also think that they’re right, so my conviction does very little to convince naysayers.  I hope that my screams are heard though. I hope that some people in power do something to stop the foolish over-use of these DNA damaging drugs.  I hope that it’s not too late to be prudent and cautious.

The real world is complicated. Sometimes human bodies work in ways that aren’t simple.  Sometimes problems are complex and difficult to understand. Sometimes pharmaceuticals work, or don’t work, in ways that are poorly understood. The power to do a massive amount of both good and harm is possible with modern medicine. Perhaps it is time that we start admitting that the harm that some drugs do is disproportionate to the good that they do. Perhaps it is time that we start recognizing that adverse drug reactions are not always immediate or easy to remedy. Perhaps it is time that we start insisting that the mechanisms of action for drugs be fully understood, at least by Scientists, before they are mass marketed to the public.

I don’t think that these suggestions and assertions make me a conspiracy theorist.  But if they do, so be it. The notion that the pharmaceutical/medical system is killing and sickening innocent people is a “conspiracy theory” that I know to be true.  So I will continue to fight to expose it, whatever the consequences may be.

Information about Fluoroquinolone Toxicity

Information about the author, and adverse reactions to fluoroquinolone antibiotics (Cipro/ciprofloxacin, Levaquin/levofloxacin, Avelox/moxifloxacin and Floxin/ofloxacin) can be found on Lisa Bloomquist’s site, www.floxiehope.com.

Participate in Research

Hormones MatterTM is conducting research on the side effects and adverse events associated with the fluoroquinolone antibiotics, Cipro, Levaquin, Avelox and others: The Fluoroquinolone Antibiotics Side Effects Study. The study is anonymous, takes 20-30 minutes to complete and is open to anyone who has used a fluoroquinolone antibiotic. Please complete the study and help us understand the scope of fluoroquinolone reactions.

Hormones MatterTM conducts other crowdsourced surveys on medication reactions. To take one of our other surveys, click here.

To sign up for our newsletter and receive weekly updates on the latest research news, click here.

What Else Can I Do To Help?

Hormones MatterTM is completely unfunded at this juncture and we rely entirely on crowdsourcing and volunteers to conduct the research and produce quality health education materials for the public. If you’d like help us improve healthcare with better data, get involved. Become an advocate, spread the word about our site, our research and our mission. Suggest a study. Share a study. Join our team. Write for us. Partner with us. Help us grow. For more information contact us at: info@hormonesmatter.com.

To support Hormones Matter and our research projects – Crowdfund Us.

References

  1. Expert Review of Anti-Infective Therapy. Levofloxacin: update and perspective on one of the original respiratory quinolones.
  2. FDA Drug Safety Communication: FDA requires label changes to warn of risk for possibly permanent nerve damage from antibacterial fluoroquinolone drugs taken by mouth or by injection.
  3. Quinolone Arthropathy in Animals Versus Children.
  4. Levofloxacin-induced acute anxiety and insomnia.
  5. Topoisomerases facilitate transcription of long genes linked to autism.
  6. FDA: Flouroquinolone warning label.
  7. The Mechanism of Inhibition of Topoisomerase IV by Quinolone Antibacterials*
  8. Mechanisms of Pathogenesis in Drug Hepatotoxicity Putting the Stress on Mitochondria.
  9. Current Drug Metabolism (v.12, #3).
  10. Surgeons discover new ligament in human knee.

Hello, Endo!

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There are some moments in your life that you will never forget as long as you live. November 7, 2012 is one example for me personally. After years of suffering with endometriosis, the seventh of November was the day that I was officially diagnosed with the horrible illness. I finally had answers behind numerous years of menstrual pain, painful sex, irregular bowel movements, and infertility.  I was relieved to have answers but crushed that I would have to learn to accept living with such a life-altering disease.

Two weeks later, at my post-op appointment, my gynecologist went over the laparoscopy and my endometriosis. He stated that the best way to fight endometriosis was to get pregnant. I remember hearing the brakes squealing in my mind. This was the same doctor who I had cried in front of just weeks before. I had begged him to perform a laparoscopic surgery while complaining of my pain and struggle to become pregnant. All signs pointed to endometriosis – I knew I was living with the disease. His response was that he had burned off all of the lesions that were covering my uterus, fallopian tubes, and ovaries and that I would not have any more issues while trying to conceive. I just needed to have intercourse every other day. No other treatment was offered to me.

Obviously, I left his office feeling disgusted. Five years of trying to conceive and he did not take that into account. As every woman who battles endometriosis knows, sex is painful. There was no possible way that I would be able to tolerate being intimate with my husband 3-4 times per week. I honestly did not know how I was going to come to terms with the fact that my own body was failing me. Although I do not remember the exact date of my postop appointment, it was another one of life’s moments that I will never forget.

Let’s fast forward to June 14, which is another night that will be instilled in my mind forever. I was very ill and after a night of pain and severe vomiting, my husband forced me to make an emergency room visit. After explaining all of my symptoms and medical history to the triage nurse and emergency room doctor, I was instructed to take a pregnancy test. I did not think anything of it, as I usually am given urine tests while in the emergency room. This moment would be different, I found out I was six weeks pregnant.

The night that I found out I was pregnant has been the greatest moment of my life. The only day that I know will be better is when I get to hold my daughter for the very first time. Although I continue to struggle with endometriosis despite my pregnancy, I am at an amazing point in my life. Through God’s good graces, Dr. Folkestad changed my life for the better and made it possible for me to have my miracle baby. I will always be grateful to Dr. Folkestad, for officially putting a name to my pain and taking me out of the darkness of infertility.

And now the worry begins.

As a woman with endometriosis who has experienced the darkest corners of the disease and infertility, I am feeling so blessed for being able to carry my child. I want nothing more than to have a healthy baby, so the gender of the baby honestly never mattered to me. However, my feelings changed when I found out that I was having a daughter. Do not misunderstand, because I love my baby girl more than anything in this entire world, but I am terrified that she will develop endometriosis.

I do not want my daughter to suffer an ounce of the physical or emotional pain that I have lived with and continue to live with despite being pregnant. Since endometriosis is thought to genetic, I cannot help but worry for my daughter. I know that I could never live with myself if she develops endometriosis. I will constantly live with this fear day in and day out until she begins menstruation and I can be certain that no signs of endometriosis are present.

On the bright side, I will be her biggest advocate. I will make sure that she has the best possible care at the first sign of any symptom. Although I know the emotions and recovery that come with surgery, I will never hesitate to consult an excision specialist. I have made it clear to my husband that I will monitor her periods and listen to hear if she has any complaints about how heavy or painful her cycle is. The moment I hear any symptom of endometriosis from her mouth, she will be given options for birth control and I will contact one of the top endometriosis specialists in the country.

Some may disagree with me that even considering birth control before she is sexually active is not good parenting or that she may view birth control options as an invitation to be sexually active. This is definitely something that has crossed my mind, but we will have that discussion as well. To those that feel that way, please understand that I will never do anything to jeopardize her health and well- being. As her mother, I am her biggest fan and biggest voice. There will never be a moment in her life that I will not advocate for her health. She is my pride and joy and I never want her to experience the dark path that endometriosis can take a woman down.

About the Author: Heather Pickens was diagnosed with three chronic illnesses and infertility at 25. She lives in the Southwest with her husband and two dogs. Her goal is to spread awareness while providing the utmost support to woman living with reproductive illnesses. You can also read about her journey at Hello, Endo! or follow her on twitter @helloendoblog.

 

Cerebellar Ataxia and the HPV Vaccine – Connection and Treatment

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Anecdotal evidence points to a connection between Gardasil and Cervarix, the HPV vaccines, and cerebellar injury. Here, from the journal Neuropediatrics comes the first published report linking the HPV vaccine to cerebellar ataxia: Association of Acute Cerebellar Ataxia and Human Papilloma Virus Vaccine: A Case Study.

I should note, from our research we’re also seeing cases of cerebellar ataxia post fluoroquinolone reaction and related to Hashimoto’s thyroiditis. The cerebellum appears to be particularly sensitive to insult from environmental toxins – to functional mitochondrial injuries, perhaps because it collects the millions of peripheral nerves coming from the body that control sensation and movement, as they pass to higher brain centers. As such, the cerebellum demands high levels of oxygen and nutrients.

For those of our readers new to neuroanatomy, the cerebellum is the cauliflower looking section at the base of the brain that controls motor coordination – the ability to perform coordinated tasks such as walking, focusing on a visual stimuli and reaching for objects in space. The walking and balance disturbances associated with cerebellar damage or degeneration have a very distinct look, a wide gait, with an inability to walk heal to toe – very much like a drunken sailor. Videos of cerebellar ataxia can be seen here.

The Case Details: Acute Cerebellar Ataxia Post HPV Vaccine

Approximately, two weeks after receiving the HPV vacccine, Cervarix, a previously healthy 12.5 year old girl developed nausea and dizziness with severe cerebellar ataxia, tremors and nystagmus. Initial tests came back normal and she was hospitalized on day 20 post HPV vaccine. Though she could sit on her own, she could not stand or walk unaided and the nystagmus prevented her from focusing on TV, reading or other activities. She had no fever. Heel-knee-shin and finger-nose tests indicated ataxia with terminal intention tremor and dysmetria (see videos: horizontal nystagmus or here for multiple types of nystagmus, heel-knee-shin test, finger-nose test).

All blood tests, cerebral spinal fluid tests and imaging tests were normal, with the exception of testing positive for IgG and varicella zoster virus – chicken pox and shingles – indicating earlier exposure. Tumors, paraneoplastic disease, cardiovascular disease, metabolic conditions and labyrinthitis (inner ear disturbance) were all ruled out. Her symptoms did not remit as was expected with acute cerebellar ataxia.

Treatment Options for Acute Cerebellar Ataxia

Beginning on day 25 post HPV vaccine, pulsed IV methylprednisone (1000mg/d) was administered for three days. Her symptoms persisted. On day 44 post HPV vaccine, IV immunoglobulin (IVIG) at 400mg/kg was initiated and run for 5 days. Her symptoms persisted.

At day 65 post vaccine, with no indication of improvement, immunoadsorption plasmapharesis was begun at a rate of seven times per month. The physicians report a gradual improvement of the nystagmus after two treatments with a full resolution of symptoms after 19 courses of treatment (day 134 post HPV vaccine). The improvement was short-lived, however, and beginning at day 220 post HPV vaccine, the symptoms began to return, gradually at first with nystagmus, and then completely. Immunoadsorption plasmapharesis was begun anew on day 332 post HPV vaccine. After five courses of treatment, the patient’s symptoms again remitted.

Immunoglobulin G (IgG) and Cerebellar Ataxia Symptoms

Of interest, symptom severity corresponded to IgG levels. Her initial IgG levels were not reported, but after 19 treatments, when symptoms disappeared completely for the first time, her IgG levels were 354 mg/dL (day 134). When the symptoms appeared again (day 332) her IgG levels were elevated at 899 mg/dL. Upon treatment, her IgG levels dropped to 503 mg/dL as the nystagmus abated and then to 354 mg/dL upon complete remission, for the second time, at day 332 post HPV vaccine.

HPV16L and Post HPV Vaccine Reactions and Death

The researchers from this study, speculate a connection between the IgG response, and an as of yet, undetermined antibody. Testing for a variety of known antibodies were negative. Since the HPV16L is molecularly  similar to certain cell adhesion molecules, enzymes, transcription factors and neural antigens, it is possible that the HPV16L particles triggered the response.

In separate studies, autopsies of girls who died suddenly post HPV vaccine have found non-degrading HPV16L particles linked to the deaths. In the first case, researchers performed secondary postmortem immunochemistry of two girls who died suddenly after receiving Gardasil. They found evidence of cerebral vasculitis linked to the HPV16L particles throughout the cerebral vasculature.

Similarly, a postmortem exam of another girl who died from the HPV vaccine, found HPV16L DNA particles in the blood and spleen.  The researcher reported that the DNA fragments were found in the macrophages, and protected from degradation because of the tight binding of the HPV16L gene fragments to the aluminum adjuvant. The fragments underwent a conformational change rendering them more ‘stable’ and resistant to degredation, perhaps explaining their presence in the blood and spleen six months post vaccine. This has been contended.

Methods in both of the above studies have been controversial and questioned and should be interpreted with caution. However, researchers from Italy compared HPV16 proteome in the vaccine to the human to proteome and found 84 identical proteins involved in cell differentiation and neurosensory regulation. According to these researchers, the homology between the vaccine and the human proteome, bound to aluminum adjuvant

“make the occurrence of side autoimmune cross-reactions in the human host following HPV16-based vaccination almost unavoidable”.

Whatever the exact culprit, in this case the cerebellar ataxia was acute and temporally related to the HPV vaccine. The favorable response to immunoadsorption and consequent reduction in IgG levels, indicates an auto-immune response.

Mitochondrial Injury, Thyroid, Thiamine and Cerebellar Ataxia

With a more slowly developing cerebellar ataxia and related symptoms, it is possible a medication induced mitochondrial injury, related to a depletion of thiamine is present. Thiamine is critical for mitochondrial function. Similarly, patients have reported cerebellar ataxias related to Hashimoto’s. Generally, when testing for both thiamine deficiency and Hashimoto’s is undertaken, both are confirmed.

Final Thoughts

This report represents one of the first clear linkages between the HPV vaccine and acute cerebellar ataxia. More importantly, it suggests a treatment opportunity when caught early. With so little data available, it is not clear whether immunoadsorption would work for more chronic cases. However, there is evidence of its success in Guillian Barre, Myasthenia Gravis and other autoimmune conditions. When combined with the early data pointing to Hashimoto’s and thiamine deficiency, paths forward post injury are emerging.

Participate in Research

Hormones MatterTM is conducting research on the side effects and adverse events associated with Gardasil and its counterpart Cervarix. If you or your daughter has had either HPV vaccine, please take this important survey. The Gardasil Cervarix HPV Vaccine Survey.

We are also conducting research adverse reactions associated with the fluoroquinolone antibiotics, Cipro, Levaquin and Avelox: The Fluoroquinolone Antibiotics Side Effects Study.

To take one of our other surveys, click here.

To sign up for our newsletter and receive weekly updates on the latest research news, click here.

What Else Can I Do To Help?

Hormones MatterTM is completely unfunded at this juncture and we rely entirely on crowdsourcing and volunteers to conduct the research and produce quality health education materials for the public. If you’d like help us improve healthcare with better data, get involved. Become an advocate, spread the word about our site, our research and our mission. Suggest a study. Share a study. Join our team. Write for us. Partner with us. Help us grow. For more information contact us at: info@hormonesmatter.com.

To support Hormones Matter and our research projects – Crowdfund Us.

 

 

 

Anti-Inflammatory Diet Friendly Organic Veggie and Grass-Fed Organic Beef Ragu

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The anti-inflammatory diet recipe I am sharing with you today is straight up comfort food during those dark, winter days. I’ve been struggling with infertility for over a year now, and was just diagnosed with two hormonal imbalances this week that have been a contributing factor, but which none of my previous reproductive endocrinologists would test for. By a simple blood draw (or five), my doctor is discovering the underlying factors of my infertility, and providing me with a plan to correct them. This will hopefully allow me to avoid the painful and expensive process of IVF, and any flares the fertility drugs might cause to my endometriosis. This cycle we tested my Estradiol (an estrogen) during ovulation, as well as seven days after ovulation, along with a slew of other hormones. Unfortunately for me, my Estradiol was not in balance. Bummer.

But when I am down, a good, hearty, stick-to-your-ribs meal goes a long way. And the great thing about the anti-inflammatory diet is that it works to lower excess environmental estrogens, something none of us really need. One way to do this is by choosing organic, grass-fed beef, which fights inflammation by increasing your Omega-3 fatty acids. It turns out that choosing organic, grass-fed beef can help to increase your Omega-3s in ways I hadn’t even thought about! And the best news…grass-fed beef tastes better!

This recipe came about from a long day, some vegetables that needed to be eaten, and my craving for (gluten-free!) pasta. The result is a sweet, savory, hearty meal that will become a regular in my house. I hope you enjoy it!

Anti-Inflammatory Diet Friendly Organic Veggie and Grass-Fed Organic Beef Ragu
(Isn’t that a mouthful!)

Ingredients for the Anti-Inflammatory Diet Friendly Organic Veggie and Grass-Fed Organic Beef Ragu

Ingredients (all organic when possible):
1 pound organic, grass-fed ground beef
1 onion, chopped
4 parsnips, peeled and chopped
3  carrots, peeled and chopped
1 red pepper, chopped
1 green pepper, chopped
2 tablespoons coconut oil
1/2 cup vegetable broth
1 teaspoon paprika
1 teaspoon Italian seasoning
1 teaspoon crushed garlic
salt and pepper to taste 

Directions:

Cooking the Anti-Inflammatory Diet Friendly Organic Veggie and Grass-Fed Organic Beef Ragu
In a deep frying pan, heat 1 tablespoon of coconut oil, and add all chopped vegetables, except the onion, and spices. Cover and sweat until slight color change is observed. Add 1/4 cup of vegetable broth, cover, and continue to cook over low-medium heat until vegetables are very soft and fragrant.

Cooking the Anti-Inflammatory Diet Friendly Organic Veggie and Grass-Fed Organic Beef Ragu

In another frying pan, combine remaining coconut oil and onion over medium heat. Saute for about 3 minutes, then add beef, seasoned with salt and pepper. Brown the beef, and add remaining vegetable broth. Continue to simmer until the broth is no longer visible. Drain excess oil, and add beef and onions to the vegetable mixture. Stir to distribute.

Cooking the Anti-Inflammatory Diet Friendly Organic Veggie and Grass-Fed Organic Beef Ragu

Serve over rice, quinoa, or gluten-free pasta. Smile, enjoy the sweet flavor, and think about the something warm and cozy. 😉

About the Author: Kelsey is an Early Childhood Educator and blogger from the Boston area. She chronicles her journey using sewing as a positive outlet while living with chronic pain and Stage IV Endometriosis. Diagnosed at 22, Kelsey has spent six years learning about her disease, and has recently become active in Endometriosis research and advocacy. She is a published poet who dreams of writing children’s books, and opening her own preschool that supports reading development. To read more about Kelsey’s daily dabblings in sewing, as well as recipes, preschool curriculum ideas, and information about endometriosis, visit her blog at www.silverrosewing.blogspot.com

The Fluoroquinolone Antibiotic Side Effects Survey

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Introducing the fifth in our series of crowdsourced health surveys and our first to include men and women: The Fluoroquinolone Antibiotic Side Effects Survey.

At Hormones MatterTM we have read the stories about the adverse reactions associated with the fluoroquinolone antibiotics, Cipro, Levaquin, Avelox and have been struck by the depth, breadth and life long nature of these symptoms. We are concerned by the lack non-industry sponsored data, and so, we created this survey, the first in a series of studies on this topic, to begin the process understanding fluoroquinolone side effects.

About the Fluoroquinolones

Individual reports abound about the dangers of the fluoroquinolone antibiotics. After over 30 years on the market, it is only recently that the FDA issued issued its black box warning about the risks of tendonopathies. We think this is too little too late and aim to determine the real breadth of reactions by going direct to you, the patient, the recipient of the fluoroquinolone antibiotics. Since the fluoroquinolones represent the most frequently prescribed antibiotics in the US, likely elsewhere too, and 39% of those prescriptions may be unnecessary, we think it is especially important to collect comprehensive and objective data about the risks and range of adverse reactions.

We need your help to gather these data. Please take this survey and share it with your friends, colleagues and anyone you know who has been given a fluoroquinolone antibiotic. Please post on your Facebook pages and share on Twitter, Linkedin, Reddit and other social media. We will need thousands respondents. That requires crowdsourcing. And since we are an unfunded venture, feel free to contribute to this research too, by clicking Crowdfund Us.

Purpose of the Fluoroquinolone Antibiotic Side Effects Survey

Patients and their physicians need more data about the side-effects of the fluoroquinolone antibiotics. There is a lack of data about who is at risk for adverse events and whether certain pre-existing conditions increase one’s risk for an adverse event. There is also a lack of data about the long term health effects of these antibiotics. The purpose of this survey is to fill that data void; to learn more about the risks for and nature of adverse events associated with each of the fluoroquinolone antibiotics, Cipro, Levaquin, Avelox and others. This will be the first of a series of studies on fluoroquinolone reactions.

Who Should Take the Fluoroquinolone Antibiotic Side Effects Survey

Anyone who have been given one of these medications, whether a reaction developed or not, and/or the parents or other family members of children too young or patients too incapacitated to take the survey for themselves.

How Long Does the Fluoroquinolone Antibiotic Side Effects Survey Take?

This is a long survey. We felt it was important to assess the full depth, breadth, onset and severity of adverse reactions in order to give patients and physicians the data they need to make informed medical decisions. This necessitated a longer than desired survey. We estimate it will take approximately 20-30 minutes to complete the survey.  We hope, given what is at risk, survey respondents will take the time to complete the entire survey.

Is the Survey Anonymous and Secure?

Yes. We do not collect personal identifying information and the survey is hosted with SSL encryption using a verisign certificate Version 3, 128 bit encryption.

How Will the Data be Used?

To inform future research and health decision-making.

Who is Conducting this Research?

Researchers from Lucine Health Sciences and Hormones MatterTM. For more information on Lucine Health Sciences, click here. For more information about Hormones MatterTM , click here.

Take the Fluoroquinolone Antibiotic Side Effects Survey Now!

What Else Can I Do To Help?

Our organization is completely unfunded at this juncture and we rely entirely on crowdsourcing and volunteers to conduct the research and produce quality health education materials for the public. This study, and many of our studies, are driven by patient requests and patient involvement.

If you’d like help us improve healthcare with better data, get involved. Become an advocate, spread the word about our site, our research and our mission. Suggest a study. Share a study. Join our team. Write for us. Partner with us. Help us grow. For more information contact us at: info@hormonesmatter.com.

To support this or other research projects – Crowdfund Us.

To take one of our other surveys, click here.

To sign up for our newsletter and receive weekly updates on the latest research news and opportunities, click here.

Thank you in advance for your help.

Crowdfund Hormones Matter – Buy an Unsubscription Now

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Hormones Matter is a labor of love, but an unfunded labor of love that needs your help. Hi, I am Chandler Marrs, PhD, founder, editor and chief trouble-maker at Hormones Matter. I want to continue our offerings and provide our community with as many resources as possible. This takes financial and human resources that I simply do not have. So I am offering you, our readers, community members, supporters, friends, family, and fellow health advocates, the opportunity to help crowdfund Hormones Matter.

Crowdfunding with a Twist – The Unsubscription

As with everything we do here at Hormones Matter, this crowdfunding campaign is a little bit different than others. Technically it’s not a crowdfunding campaign at all, because I am not going to offer you any kitschy certificates, t-shirts or other products you don’t need or want. Nope, I will not offer you any of the standard fair associated with traditional crowdfunding campaigns.

What I will offer is the continued health advocacy, science and medical reporting, and the research that you have come to trust, plus the much needed additions to the website that our community desperately needs. I will offer the opportunity to change healthcare dramatically, by giving voice to those with the invisible, difficult to diagnose and seemingly impossible to treat, diseases. And finally, I will offer the opportunity to contribute to a deeper understanding about medication safety and efficacy. If you believe in what we are doing here at Hormones Matter and want to be part of the healthcare solution, help us stay online and help me fund the next steps in our development.

Contribute Now by Purchasing a Hormones Matter Unsubscription

Yes, you read that correctly, an unsubscription. Why an unsubscription?  Well, I want our reporting, our research, everything we do, to be open to all. The unsubscription model, also called the pay-what-you-can model, allows those who can pay, to pay, and those who can’t afford to pay to still have access to all of the great health and science information we provide. I believe very strongly that one’s ability to access the latest health research should not be contingent on income, and hence, the unsubscription model.

If you have a few bucks and like what we do, send them over. If you have a few more and want to really see us grow, then buy a big unsubscription. If you’d prefer a one-time contribution, click the donate button.

Subscribe to an Unsubscription Now

$12.00 per year – $1.00 per month

$60.00 per year – $5.00 per month

$120.00 per year – $10.00 per month

$240.00 per year – $20.00 per month

Donation in any Amount

Is this a Donation?

Well, yes and no. Hormones Matter was formerly an arm of a  B-Corp (for benefit corporation), that I ran for many years as a service to the community. Without the resources to run this type of business endeavor any longer, and in an effort to keep Hormones Matter alive, I have closed the corporation and moved Hormones Matter over to a single entity LLC. What this means is that any money you contribute is not tax deductible, for that I would have to be a not-for-profit enterprise. So while the donation is a contribution to our on-going operations, it is not a donation to a non-profit.  Your financial contribution will help keep Hormones Matter online.

Understanding FDA’s Views on Opioid Painkillers: The PROP Petition

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For sufferers of chronic pain, the battle for appropriate medical pain relief has become more difficult in recent months. A controversial petition created by Physicians for Responsible Opioid Prescribing (PROP) called for changes to drug labels and prescribing practices for opioid based pain medications.

Briefly, the PROP petition called for three changes to the drug labels of opioid pain medications. For non-cancer pain, these medications are currently approved for “moderate to severe” pain, and the proposed changes would remove the word “moderate,” leaving the drugs indicated only for non-cancer pain that is severe. In addition, the petition calls for the addition of a daily limit of 100 mg of morphine or equivalent per day, and a maximum 90 day treatment period.

Just recently, the FDA responded to the PROP petition and has granted some of the requests in the petition and denied others. While some of the FDA response is good news for chronic pain patients, there is still significant cause for concern that labeling changes to opioid painkillers may affect the ability of patients with chronic pain to access these medications.

The FDA declined to add daily dose limits or maximum treatment periods to the labels of opioids, stating that the current scientific literature does not support such limitations. It is good that the FDA recognizes that there are no data to support arbitrary daily dose or treatment period limits. However, the FDA is recommending label changes for some types of opioid painkillers, in order to provide more information about the risks associated with use of these medications, and to better describe the population in whom these drugs should be used.

Label changes will be required for long-acting or extended-release opioid medications  (eg. MS Contin, Oxycontin, Fentanyl), rather than for immediate-release opioids (eg. Vicodin, Dilaudid, Percocet). The reason the FDA is targeting extended-release/long-acting (ER/LA)  products with the labeling changes is that FDA feels that the risk for abuse and misuse is greater with these products, and higher doses tend to be used, creating additional risk for a fatal overdose. The boxed warning section of the label is to be changed, to highlight the risk of misuse, abuse, neonatal opioid withdrawal syndrome, addiction, overdose, and death.

In terms of PROP’s request to limit the indication for these medications to “severe” pain only, the FDA requires the following new language in the drug label:

“[Tradename] is indicated for the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment options are inadequate.”

And, in the Limitations of Use section:

“Because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses, and because of the greater risks of overdose and death with extended-release opioid formulations, reserve [Tradename] for use in patients for whom alternative treatment options (eg. non-opioid analgesics or immediate-release opioids) are ineffective, not tolerated, or would be otherwise inadequate to provide sufficient management of pain.”

These changes are cause for some concern, particularly because a judgement call will be required as to what exactly constitutes pain severe enough to require daily, around-the-clock treatment. And although physicians can and often do prescribe medications off-label, in the case of opioids, with the current regulatory environment, physicians may worry that off-label prescribing of opioids may be considered inappropriate, dangerous, and not the standard of care.

Then the question will become, who has pain severe enough to require daily opioid treatment? Many times patients with chronic pain conditions, especially women’s health conditions such as endometriosis that are misunderstood and often mismanaged, feel that their concerns about pain are not heard or taken seriously by their physicians. As an endometriosis patient myself, at times when I’ve been asked to rate my pain on a scale of 0 to 10, after giving my answer, I’ve been told that I must be wrong, and I’m not experiencing pain at the level that I say I am. I am concerned that it will be easy for physicians to tell patients that their pain is not severe enough to require daily opioid treatment based on what they believe to be true about the patient’s pain, rather than asking detailed questions about the disruption of daily life, and duration, quality and severity of pain, then listening to and believing the answers.

Pain is a difficult symptom to manage, especially when the condition from which the pain emanates is not fully understood, or in some cases, is not even recognized as real. Perhaps rather than investing time and capital resources into labeling changes of pain medications, physicians and patients would be better served if the FDA and other governmental agencies were to invest in understanding and developing treatments for the conditions that elicit chronic, untenable, pain.