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5 Effects of Stress on the Mind and Body & 10 Tips to Reduce Stress

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5 Effects of Stress on the Mind and Body + 10 Tips to Reduce Stress

5 Effects of Stress on the Mind and Body & 10 Tips to Reduce Stress

We all hear about stress these days and how bad it is for our health. Many people consider stress a part of modern life and learn to live with it, but stress is not normal and it can be overcome! You just need to learn how.

Originally Posted November 2016
Updated October 2019

Knowing the far-reaching effects of stress, not only on our psychological well-being, but also on our entire bodies, can help us remember to prioritize stress management and other self-care practices.

Stress, Cortisol, and Adrenals

You may have heard these terms used together, but are not sure how they are connected. Stress is any kind of outside factor that our body perceives as a threat to our safety or well-being. Many people think this only refers to emotional stress or trauma, but it also includes physiological stress on the body, such as infection, traumatic injury, or a poor diet. Stress can also include environmental factors like exposure to chemicals and other toxins.

Cortisol is one of the hormones that our body releases in response to stress. It is probably the one most commonly associated with stress, even though there are others involved.

The adrenals are two small glands located just above the kidneys that produce and release cortisol and other hormones into the bloodstream – learn everything you need to know about adrenals here. One of the bodily processes that occurs during acute stress is often referred to as “fight or flight.” It is the defense mechanism that kicks in when we are in danger – or think we are. In addition to the adrenals pumping out more hormones, bodily functions that are unnecessary in the moment (such as digestion), are put on hold to preserve energy for the “fight or flight.”

While this can be a very useful and sometimes life-saving response to a threat, problems can begin to occur if stress becomes frequent or chronic. As the adrenal glands become over-worked, they eventually can’t keep up with the body’s demands for the various hormones they’re responsible for.

How Stress Affects the Body

Here are a few of the major ways the mind and body are affected by chronic stress.

Mood

The adrenal glands produce more than just cortisol. They also produce neurotransmitters such as adrenaline (epinephrine), norepinephrine, and dopamine. Neurotransmitters are chemical messengers that help regulate things like mood, performance, weight, pain perception, and sleep. Depending on the degree to which the adrenals have been affected, the neurotransmitters become unbalanced in various ways.

Let’s take dopamine, for example. If dopamine is too high, someone may experience anxiety, hyperactivity, or paranoia. If someone has low dopamine, it can lead to addiction, cravings, or depression.

Hormones

In addition to neurotransmitters and cortisol, the adrenals also produce small amounts of the sex hormones, estrogen and testosterone (and their precursors). Along with balancing out hormones based on a person’s gender, sex hormones also help keep the negative effects of too much cortisol in check, acting as an antioxidant. But once the adrenals become chronically over-worked, more and more of the precursor materials (used to make sex hormones) get diverted to make cortisol, resulting in a decrease in sex hormones.

This results in lowered libido and other symptoms related to hormonal imbalances, such as premenstrual syndrome in women or erectile dysfunction in men.

Blood Sugar Regulation

When cortisol is released, the hormone glucagon is signaled and insulin is suppressed. Glucagon controls glucose storage in the liver so that glucose can be released into the blood. Insulin is the hormone that regulates the amount of glucose being taken from the bloodstream into the cells.

During chronic stress, the cells start to become resistant to insulin, leaving blood glucose levels elevated. This is why insulin resistance is the precursor to type II diabetes.

A few symptoms of insulin resistance include inability to lose weight, high cholesterol and triglycerides, cognitive dysfunction, and elevated blood glucose or insulin levels.

Learn more about insulin resistance here.

Thyroid

The adrenal glands are part of the hypothalamus-pituitary-adrenal-thyroid-axis (HPAT), sometimes just referred to as the HPA-axis. Here’s where the thyroid comes into play.

The adrenals are regulated by the hypothalamus and pituitary glands. When cortisol is released under stress, the hypothalamus and pituitary, which work in a feedback loop with cortisol, slow down their production of hormones. Unfortunately, this also slows down thyroid function since the hypothalamus and pituitary regulate thyroid hormones as well.

Stress can also negatively affect the enzyme that converts inactive thyroid hormone (T4) to active thyroid hormone (T3). There are a few other mechanisms involved in the stress/thyroid dysfunction connection as well. Hypothyroid symptoms such as cold extremities, dry skin, depression, and constipation often indicate sub-optimal adrenal function. Most likely, thyroid treatment will be less effective if the adrenals are not addressed as well.

Learn more about the adrenal-thyroid connection here.

Immunity

Stress triggers inflammation. Our body knows that chronic inflammation is damaging, so it compensates by slowing down the immune system in order to keep the inflammation in check. The immune system is also directly suppressed during stress since it is one of those “unnecessary” functions when we’re in “fight or flight” mode. This also affects thyroid health since a suppressed immune system can activate viruses capable of attacking and damaging the thyroid.

As you can see, so many functions in the body are interconnected and related back to adrenal function and the stress response.

10 Tips to Reduce Stress and Improve Your Health

This is only a brief overview of the effects of stress on the body. Chronic stress has also been linked to cardiovascular disease, Alzheimer’s disease, and cancer. It is estimated that as much of 80% of the population has weakened adrenal function.

Since there are different stages of adrenal dysfunction that require different treatments, it is a good idea to seek out a knowledgeable health care provider who can test your adrenal function and related hormones. Since many doctors only recognize adrenal disorders such as Cushing’s and Addison’s disease, you may need to search someone out who takes a more in-depth look at adrenal function using functional tests such as a salivary cortisol test.

There are some things you can do to help reduce stress which include:

Take Control of Your Thoughts

Many people have tons of negative thoughts in their head on a daily basis, without even being aware of it. This creates a stressful state and anxiety that keeps fueling your hormonal imbalances. A technique known as “thought‐stopping” can help you halt negative, obsessive thoughts.

The first step is to literally call a halt to this train of thought (like saying the word “Stop!” out loud or to yourself). Next, choose a positive thought on which you’ll focus instead. This way you’re swapping a negative, stress‐inducing thought for a positive one. To increase emotional comfort, it’s imperative to practice reassuring and realistic self‐talk (saying something along the lines of, “I am feeling anxious / irritable now, but I have the power to calm myself down.”).

Apply Self-Soothing Techniques

There are many physiological changes that are triggered, when we are faced with a stressful situation. Our breathing quickens, adrenaline is secreted, and our heart begins to race. This is called the fight or flight response – a natural survival mechanism intended to help us escape danger. However, when the threat is imagined, the fight/flight response is unnecessary and damaging to your health. Many people with chronic stress remain blocked in this state of alert, without being able to snap out of it.

Luckily, there are techniques you can learn to reduce your response to stress, like deep breathing techniques, muscle relaxation exercises and meditation. Deep breathing can help with a rapid heart beat. The most commonly utilized strategy is breathing by contracting the diaphragm, a horizontal muscle in the chest located just above the stomach cavity.

Using muscle relaxation exercises you can induce a relaxed state and physical comfort, by tightening and releasing muscles, beginning with the largest muscle group. Meditation is also a powerful way to bring back a peaceful state to your body and clearing up your mind from erratic and negative thoughts.

Check Your Diet

What does stress have to do with eating? A whole lot! What we eat and drink largely impacts our emotional state. Stimulating foods and drinks like coffee, sodas, chocolate, and alcohol can cause anxiety, trigger panic attacks, and increase feelings of nervousness and irritability, as well as trembling and shaking. Deciding to go “cold turkey” by abruptly eliminating caffeine is not always recommended since it can lead to withdrawal symptoms. You might experience headaches, restlessness, and irritability. So it’s better to decrease caffeine consumption gradually by replacing it with tea for example.

Regular alcohol consumption can also generate a lot of biochemical imbalances in your body, like blood sugar dysregulation, liver problems and dehydration, which add to the stress burden your body needs to handle.

Get Moving

By choosing your appropriate exercise routine you can reduce stress, improve mood, enhance self-esteem, and increase energy levels. Be careful not to over exercise, which can actually contribute to your stress level.

It’s a known fact that during exercise, the body releases chemicals called endorphins and norepinephrine, which interact with receptors in the brain. These chemicals determine euphoric feelings, reduction in physical pain and the ability to deal with stress more efficiently.

Get More Sleep

Losing just a few hours of sleep increases feelings of stress, anger, sadness, and exhaustion. It’s a vicious cycle since because of stress you might not be able to fall and stay asleep, but lack of sleep is also generating stress.

So try to get a solid seven to eight hours of sleep a night, and don’t feel bad about also adding a nap in the afternoon on days when you’re feeling especially drained. Go to sleep before 10 – 11 PM and don’t use the computer or watch TV before it, since these can interfere with your melatonin production and make it harder to fall and stay asleep.

Listen to Music

By choosing a type of relaxing music which you prefer, you can help the body and mind dissipate stress. Research has shown that classical music may help you unwind and improve your mood. You can also experience therapeutic CDs of “binaural beats,” which are meant to calm the mind and body and where different frequencies call forth different moods.

Begin and End the Day Right

In the morning, in order to make intelligent use of your energy for the day, take some time to reflect, meditate, read or better yet take a nature walk, away from computer and TV. You could do the same in the evening, or just simply delight in the rare pleasure of doing nothing. These can ease the stress of too much computer or office time, counteract overstimulation and boost your mood.

Doing Something Fun

Doing something fun always gets postponed due to the avalanche of responsibilities we have during the day. But without a balance in your life, frustration and so stress might arise. It’s been found that creating artwork, crafts or making time for a hobby helps to relax, can be very stress-reducing and takes your focus away from your own thoughts and worries.

Get a Massage

Massage is a great way to loosen the muscles that are habitually affected by stress. Think about all the frowning and scrunching of your face muscles and how relaxing it is to work on these! Essential oils can calm, center, and energize you by reducing the effects of stress and mental fatigue. You can give yourself a massage, while taking small breaks from your work, or you could have a professional massage to benefit your whole body.

Include Adaptogens

A class of herbs called adaptogens help your body to cope more effectively with the demands and stress of everyday life. They provide a sustained sense of calm, and while they increase energy, with the exception of Chinese ginseng, they are non-stimulating. Some of the most used adaptogens are: ashwagandha, rhodiola, holy basil, schisandra, shatavari, eleuthero.

Learn more about adaptogens here.

Lowering Stress and Improving Adrenal Function

Because of the great impact stress can have on overall health and well-being, it’s important to implement stress-reducing habits. Additionally, partnering with a knowledgeable physician to help address any underlying adrenal fatigue can prove very beneficial. Your mood, hormones, thyroid, blood sugar, and immune system (among other things) will be much healthier for it!

At Holtorf Medical Group, our physicians are trained to utilize cutting-edge testing innovative treatments to design a treatment protocol that is personalized to you. If you are experiencing symptoms of adrenal fatigue, give us a call at 877-508-1177 to see how we can help you!

References

1. NIH. “5 Things You Should Know About Stress.” National Institute of Mental Health.
2. Mayo Clinic Staff “Chronic stress puts your health at risk.” Mayo Clinic.
3. APA Staff. “Stress effects on the body.” American Psychological Association.
4. Dartmouth Undergraduate Journal of Science. “The Physiology of stress: Cortisol and the hypothalamic-pituitary-adrenal axis.”https://sites.dartmouth.edu/dujs/2011/02/03/the-physiology-of-stress-cortisol-and-the-hypothalamic-pituitary-adrenal-axis/
5. Harvard Health. “Understanding the stress response.” Harvard Health Publishing – Harvard Medical School.
6. Mayo Clinic Staff. “Stress symptoms: Effects on your body and behavior.” Mayo Clinic.
7. Josh Axe, DC, DMN, CNS. “7 Adaptogenic Herbs or Adaptogens that Help Reduce Stress.” Dr. Axe.

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**Comment**

This article is one of the best articles I’ve read on how stress affects the body and what you can do about it.

Lyme/MSIDS patients are in a war of epic proportions where nearly every single thing in their bodies is haywire. We need to do all within out power to reduce that stress.

  • The most important step is effective treatment for the infection(s), which is simply in a word antimicrobials. An example:  https://madisonarealymesupportgroup.com/2016/02/13/lyme-disease-treatment/
  • The next step is precisely what this article recommends – partnering with an experienced practitioner who will help you uncover your specific imbalances.  This looks differently on everyone but typically involves the thyroid and other hormone and mineral imbalances. I know of one patient who felt nearly well just by addressing the thyroid. People often don’t understand that the thyroid is the body’s thermostat and that if you have hypothyroidism (low amounts of thyroid hormone) your body’s temperature will be low allowing infections to proliferate. Address the thyroid and you’ve effectively made it tougher for pathogens to survive.
  • Taking appropriate supplements. Patients often complain about their Lyme literate doctor requiring them to take copious amounts of supplements. Unfortunately, they are usually right because of damage & imbalances caused by the infection(s).  The goal; however, is to only take what is required. 
  • Diet is key.  This too is very individual, with some only improving by eliminating gluten, dairy, and all sugars.  https://draxe.com/nutrition/elimination-diet/ This step often turns patients around entirely. Remember – food is medicine.
  • All the ideas in the article are very helpful and include listening to calming music.The first thing I do in the morning is turn on a relaxing music channel on Pandora. An example would be the George Winston channel.  For more on binaural beats: https://www.binauralbeatsmeditation.com/the-science/
  •  Binaural Beat demonstration. You need ear phones to listen.
  • If you prefer music: 
  • Regarding essential oil diffusinghttps://thetruthaboutcancer.com/diffusing-essential-oils/  After I turn Pandora on, I set up my essential oil diffuser with whatever blend I’m in the mood for. For a relaxing bedtime blend called “Counting Sheep”:  9 drops lavender, 4 chamomile, 2 frankincense, 2 bergamot. This would be for a large room. Divide in half for a small bedroom.  For a grounding smell try “Peace & Harmony”: 4 drops patchouli, 4 vanilla, 3 orange. 
  • Doing something fun seems frivolous to many patients but is so important. Unfortunately with Lyme/MSIDS, we tend to revolve around our illness.  Doing something to break away from this is so important for our mental health. Whether you enroll in an art class or just buy Play dough to mess around with at home – do it. I’ve found plants relax me. My house has turned into a literal green house through the years.  I love dirt!  Another thing you could simply incorporate into your habits is coloringhttps://www.psychologytoday.com/us/blog/modern-mentality/201803/are-adult-coloring-books-actually-helpful
  • Word of warning: It is often the case that when initially starting Lyme/MSIDS treatment patients are extremely sensitive to everything including light, sound, and smells. It’s always important you listen to YOUR body and although the suggestions in this article are good, they may not be good for you at the moment. If you are sensitive it’s a sure sign your body is seriously fighting a war and you need to assist it in anyway you can and often that means sunglasses even in the daytime, and eliminating ALL smells and sounds. The goal is to move past and heal from sensitivities so you can enjoy the suggestions listed here.
  • Final note and the best advice I was given: “Don’t be depressed about feeling depressed.”  I heard this from someone I contacted online who reached the other side of health who was willing to advise me in my desperation upon starting treatment and feeling so incredibly lousy. This advice helped me more than many things as there are some seriously dark days in treatment where you think dying would just be easier. Treating for this monster is unlike anything you’ve ever done before and will require serious dedication on your part. I encourage you to find a local support group for support and ideas on your journey.
Some of the best help through the years for me has come directly from patients.

 

 

 

 

 

 

 

 

 

 

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Online Practitioner Webinar on Saturday for Doctors Treating Lyme/MSIDS

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Wisconsinites – A Reminder to Please Write & Oppose Assembly Bill AB313 Today

As most of you are aware, there are numerous Lyme bills currently being voted on at the Wisconsin Capital:  https://madisonarealymesupportgroup.com/2019/11/01/update-on-wisconsin-lyme-bills-please-contact-your-representative-on-ab-313/

Many of these are quite good as they address things like putting signage at park locations warning about the risk of ticks and Lyme disease and making bug spray available; however, there is one bill – AB 313, which poses a serious threat to patients & to the doctors who dare treat them.

Exact wording of the bill: Assembly Bill 313

AB 313, previously LRBs 1652 and 3362Establishes a sixteen-member Tick-Borne Disease Study Committee to create a report for the legislature on consensus-based recommendations for policy changes on awareness, prevention, surveillance, diagnosis, reporting, and treatment of Lyme Disease.

This bill would allow Governor Evers to appoint a 16 member advisory panel to offer recommendations on how doctors diagnose and treat Lyme disease.

Many of us have explained to our representatives about the potential for that bill to go side-ways since nothing about Lyme/MSIDS is agreed upon in the medical community as well as the fact that appropriate Lyme guidelines already exist.

This bill is huge government overreach – telling doctors how to diagnose and treat patients.  All of the Lyme literate doctors I spoke with oppose this bill for numerous reasons – one of which is the fact this bill could seriously interfere with the way they currently treat patients as well as could increase scrutiny of their medical practice. They are already under severe scrutiny with many having to pay fines to the state medical board:  https://madisonarealymesupportgroup.com/2012/03/04/dr-hoffmann-updated/  My own doctor spent over 50K to protect his practice against such a witch hunt.

There are currently two different Lyme disease guidelines in play:
  1. Infectious Disease Society of America (IDSA) Guidelines:  https://www.idsociety.org/practiceguidelines#/name_na_str/ASC/0/+/  Under the IDSA’s tutelage, patients have been abused for decades and are told they have “medically unexplained symptoms” or MUS. Then they are sent to a psychiatrist and given anti-depressants. For an example for the typical handling of Lyme disease by mainstream medicine, see this graph:
  2. International Lyme and Associated Diseases Society (ILADS) Guidelines:  https://www.ilads.org/patient-care/ilads-treatment-guidelines/

Lyme literate doctors follow the ILADS guidelines as they take into account that people are often infected with numerous pathogens and that many of these pathogens are persistent, necessitating treatment to be overlapping in nature and often for an extended period of time. They also acknowledge that sexual and congenital transmission can occur.

The IDSA guidelines, followed by the majority of doctors, pretty much states that 21 days of doxycycline will cure this. They still deny the persistence of borrelia and other pathogens as sexual and congenital transfer.

The two guidelines couldn’t be more different yet we can not force doctors to follow one or the other. The old saying, “You can lead a horse to water but you can’t make them drink,” comes to mind. As much as we would love to force all doctors to follow the ILADS guidelines we shouldn’t. The practice of medicine is still, thankfully, up to the practitioner who underwent years of schooling to become a doctor. Doctors aren’t told how to treat cancer, diabetes, or a broken leg and they shouldn’t be told how to treat Lyme/MSIDS either.

Currently, patients need to see an experienced practitioner who is trained by ILADS.  This requires doctors to have continuing medical education specifically in the treatment of tick borne illness.  Mainstream medicine does not require this and most doctors are woefully educated; however, the choice to treat Lyme/MSIDS patients appropriately should be up to the practitioner.

Please write the following Representatives behind AB313 and let them know we oppose it:

Introduced by Representatives Mursau, Milroy, Anderson, Crowley, Edming, Gruszynski, Hesselbein, Kulp, B. Meyers, Ohnstad, Ott, Ramthun, Rodriguez, Sargent, Shankland, Sinicki, Snyder, Spreitzer, Tauchen, Thiesfeldt, Tusler and Rohrkaste; cosponsored by Senators Cowles, Miller, Hansen, Kapenga, Larson, Olsen, Petrowski, Ringhand, Smith and Tiffany

Please see the following letter written by Mike Nickel, current moderator for the online Wisconsin Lyme support group:

Letter regarding AB313

Dear Rep. Mursau

My name is Mike Nickel. I’m the past president of the Wisconsin Lyme Network {501 c3}, a statewide non-profit dedicated to the education of lyme disease and tick-borne illness to the general public and medical community of Wisconsin. We have liaison with medical professionals not only in Wisconsin, but nationwide as well as multiple Wisconsin support/patient groups as well as nationwide. The largest organization of MD’s in the country that deals exclusively with lyme disease and tick-borne illness is called ILADS. {International Lyme and Associated Disease Society of America}. www.ILADS.org

All of our organizations statewide and nationwide adamantly oppose AB313. It is our firm belief that the state legislature will greatly endanger lyme patient care and the practice of the state MD’s that provide that care by passing AB313. ILADS has already established lyme and tick-borne treatment guidelines which are utilized by ILADS trained practitioners nationwide.

We’re completely puzzled why the state of Wisconsin feels it should empanel a committee, made up largely of lay people to recommend any type of medical procedure much less something as complicated and severe as tick-borne illness.

Parts of the legislation are fine and some of the other Lyme bills are endorsed by us but AB313 recommending “guidelines’ can cause great harm to the patient community and even drive our lyme treating practitioners out of the state of WI.

Insurance companies and Medical boards can use any “recommendation of short-term antibiotics” as an excuse to sanction Doctor’s not treating to those specific guidelines. This would literally destroy effective treatment for the scores of lyme patients in this state and the 30,000 newly infected here annually. 

On behalf of the Wisconsin lyme community we ask that you please pull this bill. I would be more than happy to meet with you personally and discuss how we could proceed with a bill that would be fully supported by the community and be of great help to patients. I and other advocates look forward to working with the Assembly on effective legislation to benefit our patients. Please let me know a date that would work for you.

Thank you for your consideration,

Mike Nickel

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My letter to the Wisconsin Representatives:

Dear Wisconsin Representatives,
My name is Alicia Cashman, and I head up the Madison Lyme Support Group. Both my husband and I fought a ten year battle in treatment for Lyme/MSIDS and have finally achieved our health back. I can directly attribute this health to going to doctors trained by the International Lyme and Associated Diseases Society (ILADS). These doctors take on huge risk treating patients appropriately as they stand in direct opposition to the Infectious Disease Society of America (IDSA).
There is a very real probability that Assembly Bill 313 could put these ILADS trained Wisconsin doctors in jeopardy.
Thankfully in the United States medical practitioners are still allowed the freedom to diagnose and treat patients in the way they feel is best. I’m surprised that you would even consider telling doctors how to diagnose and treat patients. This is huge government overreach.
 
Every single ILADS trained Wisconsin doctor I spoke with is opposed to AB 313.
Why would you want to make things harder for our health professionals who already take on significant risk in treating us? Currently, patients from other states come to the state of Wisconsin where we have a handful of doctors who treat this appropriately. Passage of this bill could potentially make them want to take their practices elsewhere where they have a God-given freedom to diagnose and treat patients under the Hippocratic Oath free of government interference.
While I appreciate the intent, legislation has often worked directly against patients as well as doctors under the law of unintended consequences. I feel AB 313 would follow this path as it calls upon a panel that very well could be stacked against patients, not to mention the fact that nobody has the right to dictate how a practitioner treats patients.
Currently, there is activity at the federal level which is following this law of unintended consequence: https://madisonarealymesupportgroup.com/2019/05/20/petition-remove-eugene-shapiro-from-federal-tbd-working-group/.  The Federal Tick borne disease Working Group is now stacked with Infectious Disease doctors who deny the chronic/persistent nature of Lyme disease, that it can be sexually and congenitally transmitted, and that it takes far more than 21 days of doxycycline to affectively deal with this polymicrobial illness.
Also, back when Representatives Craig and Sargent wanted to put the nursing board in charge of “best practices” on how to treat Lyme disease, which would have effectively replaced one tyranny with another, a Wisconsin pediatrician showed up to the public hearing stating that Lyme testing used by ILADS treating physicians was “home brewed,” despite these labs being CLIA-certified, and passing the most stringent requirements for labs. This is just one example among a thousand how mainstream doctors continue to side with the Infectious Disease Society of America (IDSA) and its biased approach. I found his statement directly on the CDC website.
I’ve written this before but I include it again as it serves as a solid reminder that until things change at the federal level, state legislation will continue to be undermined by the CDC:  https://madisonarealymesupportgroup.com/2017/07/07/cdc-sabotages-state-laws-protecting-lyme-patients/.  This makes perfect sense when you understand the backstory:  https://madisonarealymesupportgroup.com/2019/02/22/why-mainstream-lyme-msids-research-remains-in-the-dark-ages/ and https://madisonarealymesupportgroup.com/2019/07/19/biological-warfare-experiment-on-american-citizens-results-in-spreading-pandemic/.
I seriously implore you to please remove AB 313.
Sincerely,
Alicia Cashman
Madison Lyme Support Group

Address

Phone number

 

 

 

Global Lyme Alliance Oversees Scientific Assessment of Lyme Disease Treatment Regimens Using Rigorous Evidence-based Approach

https://globallymealliance.org/press-releases/global-lyme-alliance-launches-its-first-observational-study-on-lyme-disease-treatment-protocol/

lyme disease treatment_clinical study_release

GLA OVERSEES SCIENTIFIC ASSESSMENT OF LYME DISEASE TREATMENT REGIMENS USING RIGOROUS EVIDENCE-BASED APPROACH

STAMFORD, CONN (November 4, 2019)—In an effort to move beyond anecdotal evidence to sound scientific validation in the Lyme treatment equation, Global Lyme Alliance (GLA) announced today that it is expanding its research efforts to include the first in a series of clinical studies to determine the effectiveness of non-validated, physician-developed Lyme treatment regimens.

At the request of a small group of motivated patients, GLA is taking the bold step towards validating community-based, physician-developed, Lyme disease treatment regimens by using the rigorous evidence-based clinical research process.

“There’s a high level of ambiguity surrounding the multitude of treatment options being offered to patients throughout the Lyme community; as such, GLA is committed to evaluating, through established scientific assessment, the efficacy of these patient care approaches,” said Timothy Sellati, Ph.D., GLA’s Chief Scientific Officer (CSO).

GLA’s first study will focus on the treatment regimen developed by Joseph Jemsek, M.D., the founder of the Jemsek Specialty Clinic of Washington D.C. Dr. Jemsek was chosen for his willingness to put his “Jemsek Protocol®” to the test following a thorough evaluation by GLA of several patients who experienced positive results from working with the physician.

“I am honored to be selected by GLA to be a part of their first study,” said Dr. Joseph Jemsek. “ I am confident in the treatment regimen I have developed to help patients suffering from this insidious disease and look forward to putting it through the extensive scientific assessment detailed in the clinical study.”

Through this initiative, a range of microbiological, immunological, genetic and metabolic assays will be conducted to distinguish patients who experience varying degrees of clinical improvement vs. those who do not along with a series of quality of life assessments. Within the patient population that responds favorably, changes in specific biomarkers may offer insights on why the Jemsek Protocol works.

“By collaborating with multiple prestigious academic partners, our hope is that at the end of this study we’ll identify biological-based indicators of treatment success that can be broadly used in evaluating other treatment options being pursued by Lyme patients suffering from persistent symptoms,” said Dr. Sellati.

To support this and GLA’s growing pipeline of studies GLA’s CSO has assembled a team of experts in clinical project development and management, regulatory compliance, biostatistics and Lyme disease nursing. These individuals as well as the GLA’s bio- and data-repositories will ensure the integrity of the clinical study process, the collected data and biospecimens.

Our ultimate goal is to shift the paradigm of treating Lyme disease from uncertainty, misunderstanding, and helplessness, to one of clarity. Our Lyme community has expressed frustration with the slow progress in Lyme research, lack of treatment options and specifically, the lack of scientific buy-in on community-based treatment regimens.  We listened to their concerns and are committed to supporting research that impacts the Lyme community today,” said Scott Santarella, GLA’s CEO. “We have to put all the science we can behind this disease, including the disparate treatments being offered to patients. The Lyme community deserves more.”

Lyme disease is the most common vector-borne illness in the U.S., and its incidence is growing rapidly. More than 427,000 people in the U.S. are newly diagnosed each year. Moreover, up to 20% of those who are diagnosed and treated early with standard-of-care antibiotics continue to suffer from a variety of symptoms. A recent GLA study estimated that more than two million patients could suffer from post-treatment Lyme disease by 2020. GLA is committed to better understanding treatment options to help patients.

For questions about GLA call 203-969-1333 or visit GLA.org. For questions regarding the clinical study contact 833-GLA-LYME (833-452-5963).

About Global Lyme Alliance
Global Lyme Alliance is the leading 501(c)(3) organization dedicated to conquering Lyme and other tick-borne diseases through research, education, awareness, and patient services. GLA has gained national prominence for funding some of the most urgent and promising research in the field, while expanding education and awareness programs for the general public and physicians. We support those around the globe in need of information about tick-borne diseases, finding a Lyme treating physician, and with the first Lyme-specific peer-to-peer mentor support program. Learn more at GLA.org.

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**Comment**

To which we all said, “AMEN and AMEN!”

For more on the study:  https://madisonarealymesupportgroup.com/2019/05/18/more-than-2-million-could-suffer-from-post-treatment-lyme-disease-syndrome-in-2010-study-says/

Two million is a lot of people; however, according to microbiologist Holly Ahern, that number is still low. The study uses the often quoted 10-20% who suffer with long term symptoms but Microbiologist Holly Ahern in this article:  https://madisonarealymesupportgroup.com/2019/02/25/medical-stalemate-what-causes-continuing-symptoms-after-lyme-treatment/ explains that the percentages don’t account for the 30-40% who are diagnosed and treated late. When you simply add the 10-20% with the 30-40% you get a whopping 60% that could potentially go on to have persistent symptoms. 

In this article I refute a Newsweek article that calls this an “Untreatable form of Lyme disease.” https://madisonarealymesupportgroup.com/2019/04/29/is-the-sky-truly-going-to-fall-for-patients-with-the-untreatable-form-of-lyme-disease/  This monster can be treated but not in the way it’s currently being treated in mainstream medicine. For an example see recipe below:

My husband and I are living proof that you can achieve your health back.

There are many more who have gotten back to the other side of health and you can too. If you are struggling with hope – let me give you some. Hang tight and learn all you can so you can partner with your health professional. Together you can beat this.

 

 

Yale “Dream Team” Lyme Disease Treatment Recipe

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Courtesy: Microbiologist Tom Grier

Yes, you are reading this correctly – the boneheads at Yale state that you shouldn’t get treatment even if you have the EM rash (which is indicative of Lyme disease), and test positive on tests, and that you should just wait around on your laurels to get worse.

There are still far too many noodle-headed doctors still following this antiquated and unscientific advice.
Please remember, some of the sickest patients NEVER test positive on tests which look for antibodies.

And while the EM rash is indicative of Lyme, many, many never get it. No one I work with gets the rash. The graph from Lyme Disease Organization shows those getting the rash range from 27-80% – hardly a sure thing. https://www.lymedisease.org/lymepolicywonk-how-many-of-those-with-lyme-disease-have-the-rash-estimates-range-from-27-80-2/

Don’t trust mainstream medicine with tick-borne illness. Get to an ILADS trained health professional.