Trailer: VAXXED III

Watch the Trailer

“Children’s Health Defense embarked on a nine-month journey across America, gathering powerful testimonies from the people. Our interviews ranged from mothers and fathers to teenagers, families, medical professionals, whistleblowers, lawyers, and people from all walks of life.

What we discovered was nothing short of staggering. We listened to harrowing accounts of COVID hospital protocols that shook us to our very core. The consistency of these stories was alarming.

People also shared their experiences after taking the COVID-19 vaccine, revealing tragic outcomes of either death or serious injury. Now, fueled by these powerful firsthand testimonies, we are creating a documentary by the people, for the people.

Learn what we uncovered on the road. You can’t afford to miss it.”

Watch the Trailer

Not A Coincidence#android#iPad#retweet

As of November 2013 there have been 31,741 reported adverse reactions to the HPV vaccine, and the position of the Pharmaceutical companies which make the vaccine, as well as the Department of Health and Human Services which holds patents and profits on the vaccine, is that they are all a coincidence. .

Call your Congressman and tell them you want an investigation into the HPV vaccine and the damage it is causing to young men and women.

“Not a Coincidence” is a campaign started by The Canary Party to address the medical community’s repeated excuse that the symptoms, too many experience, after vaccination are just coincidental. Seizures, fainting, rashes, allergies, GI dysfunction, loss of speech, etc, etc all labeled a coincidence. It’s time to end the excuses and start to listen to the injured and the parents of the injured. They deserve a forum to be heard, they deserve a voice, respect, attention, hearings and answers. They need a medical discovery process that uses their symptoms and their progression of illness in the process of finding treatments. All injured are worthy of being treated individually instead of disregarding their many medical maladies because of a vaccination program that is not allowed to be questioned. It’s time for the government, the medical community and the media to start taking into account the too many that are affected. Please take the time to hear from these beautiful, well-spoken girls and Moms tell their stories of injury after Gardasil.

 

 

Gardasil: Don’t let your child become “One Less”#MTV#teen#Android

By Shannon Powers, Ohio

Our healthy active funny daughter became just that! I share our story hoping our experience will save another from becoming “one less” healthy child.

Gardasil and my new medical conditions

Our fifteen year old daughter, Leah is vaccine injured. It all began March 30th 2011. Leah was 11 years old, soon to be 12.  We had been referred to an Adolescent doctor so Leah could be placed on oral contraceptives to help prevent cysts from forming on her ovaries.

A month prior, February 20, 2011 Leah had an Oophorectomy losing her left ovary. We were told since we had just gone through this scary ordeal, in order to keep her healthy we needed to vaccinate with the Gardasil vaccine.

Trusting in doctors and believing what they recommend is best, I never questioned their belief that this was a “must” for Leah’s health. After all, Leah had received all her recommended vaccines prior to Gardasil.  What could we possibly have to worry about?

First, I have to tell you Leah has a very high tolerance for pain. The only way I knew I needed to take her to the hospital in February was because she was clammy and dry heaving. The surgeon who performed the Oophorectomy came and told us after, that she should have been in excruciating pain.

She laughed when telling Leah, “I tells my kids to quit complaining all the time, but YOU need to complain and let us know when something is wrong in your body. You know your body best and when something is off let mom and dad know!”

Recovery went smooth and we then were released and referred to the adolescent doctor for all of Leah’s follow-up care.

March 30, Leah received the first shot in the Gardasil series from Lot number #1437z. After we left the paediatrician’s office Leah said she felt sick to her stomach. I thought due to being only 4 weeks post-op she was going to feel a little ill from the car ride. But, by the time we got home she was nauseous and bloated.

I called the doctor and was told it all stemmed back to the surgery. They had removed her left ovary, so she probably was having effects from the anaesthesia that was used during the surgery. We didn’t question the response and left it at that.

The following four months she continued to have severe abdominal pain, bloating, nausea and feeling full after just a few bites of food. I called again during this time and was told because of the removal of the left ovary she was just feeling her body adjust to what her insides were adapting to with more room. They assured me it was normal and there was no cause for concern.

August 8, 2011, Leah received her second Gardasil shot from lot number 1271z. We didn’t mention anything about her new medical conditions during this visit because they had already given an explanation over the phone to why she was experiencing these symptoms.

For the next four months Leah’s symptoms did not improve. Every time she ate she felt sick. She was always nauseous and her stomach was extremely bloated. I start researching her symptoms and then became worried it might be ovarian cancer. All of her new symptoms pointed in that direction. Never once did I feel it was the vaccine. Doctors were all guiding me back to the Oophorectomy.

December 12, 2011, Leah receives the third and final dose of the HPV vaccine series from Lot# 1261AA. By this appointment I was very concerned with Leah’s health. She had continued to have the severe abdominal pain, bloating, nausea, feeling full, headaches came and went, and she was not sleeping well.

In order to appease me, doctors told me they would do a cat scan to make sure her right ovary was all right. I asked them to do a blood test, CA125. This would measure the protein in the blood, detecting early signs of ovarian cancer. I was told that it would come back positive because she had just had the Oophorectomy. So it would not be accurate to do the testing.

I will be honest, I hadn’t researched to see how long it would take from the time of the surgery for her to keep testing positive, if it would at all? I did keep questioning them. Again, I trusted them and thought they knew best. After all, they have the degree, I don’t…..right??

Cat scan came back normal. Everything looked fine. We were told to hydrate and make sure she was moving her bowels.  They changed the oral contraceptives thinking that would help relieve some of the symptoms.

All of 2012 Leah continued with the same symptoms. I kept telling her to push through because they said nothing was wrong. She is constantly coming to me with aches and pains, here and there…arms will hurt, legs hurt, feels funny. I ask my husband if we have made her a complainer since the surgery. I tell Leah she doesn’t have to tell me every time she hurts somewhere.

Looking back on this now, breaks my heart to think I ignored a lot of symptoms she was actually having. Like I said before, her pain tolerance is high, she wasn’t physically showing how bad the pain was or crying in pain, it was more of “matter of fact” so, I played it down instead of really listening.

The end of 2012 I take Leah to an actual OB/GYN. She had never stopped complaining with all of the symptoms from the last year. I was still scared and thinking it was Ovarian Cancer. This new doctor spoke with Leah and me and said she would order an MRI and double check that everything was okay. Leah to this date has never had an actual Pap screening concerning her cervix or uterus. MRI was normal and this doctor put her on yet another new contraceptive. Said a low oestrogen would help with the pain and the headaches.

During this whole time since her Oophorectomy, Leah has never had a normal cycle. She would bleed for maybe a day and it was always black blood. Of course they say this is normal and all due to the contraceptives; always assuring me that everything is fine.

The whole year of 2013 Leah continues to just push through the pain. The doctors say make sure she is hydrated, that her bowels move, it’s the contraceptives or normal teenage hormones. Her medication is changed several times trying to see if that would improve symptoms. It never did.

By the end of 2013 Leah is complaining about her vision. She does wear prescription glasses/contacts so I made an appointment to have her eyes checked out.

Before I tell the rest, I have forgotten to tell you about who Leah truly is… Leah is an honor roll student. She loves to read and write stories. She will finish a book in just under a day. She was active in 4H and loved taking animals to our county fair. She has taken pigs, rabbits and goats as well as creative writing. Excels in her studies and plays various sports.

You will laugh in her presence when you don’t feel like it because she will do or say something silly to change your mood. She is very outgoing and always makes friends wherever she goes. She is always laughing and singing 80’s music.

The year of 2011/12 she was playing with the local YMCA club volleyball, basketball and softball for her middle school along with travel softball in the summer. She continued with the softball for the school and the travel ball throughout the next two and half years. Softball is her favourite!!

She was excited for the summer of 2014. It was to be a great summer before becoming a sophomore in high school. Players were starting to write to different colleges that they would be interested in attending and possibly to play softball for. They would write to the head coaches and explain they were interested in playing for them while attending their college. Asking for them to come and watch them play for their travel ball teams, in hope of gaining their respect by wanting them to represent their school. Hoping they would keep in touch during the rest of their high school years.

When your academic scores are high and you play ball well enough, colleges are pleased to offer scholarships. Leah was taking this very seriously. One of the colleges Leah wrote to, Rhodes in TN, came to Ohio and watched her play. She was ecstatic and that just made her want to strive harder. She pushed through last summer playing in more pain than before, but worth the pain for the sheer joy of a sport she loves and was wanting to continue playing through college.

We are now in the beginning of 2014. It is January and her vision had changed so we order new contacts and glasses.  The Optometrist never questioned anything out of the norm when examining Leah. Wrote a new script and we were on our way.

Leah’s headaches were increasing and not leaving her at all. She is still suffering from the severe abdominal pain, bloating, feeling full, and nausea. She was now having blurred vision even with her new script.  Doctors were saying the contraceptives will cause eye issues. Nothing they could do.

She starts having bladder spasms and feels like she always has a bladder infection. When doctors sample her urine we are told just traces of white blood count and that she doesn’t have an infection.

Sharp shooting pains down through her groin. Her right hip is always hurting. We are told over and over to make sure she hydrates!

It is February and she is conditioning for softball. She is having difficulty keeping up. Feeling as though she wants to pass out. Not able to keep her breaths regulated. Of course we are told she needs to hydrate and she had taken the winter off so she was out of shape.

This continues the rest of the school year. She keeps pushing through just so she can play ball.  School is over end of May. Travel ball conditioning starts up. Her headaches are more severe along with all the other symptoms. She is experiencing all over pain that won’t go away. She sleeps the day away until it is almost time to go to ball practice. She practices two to three times a week and plays all day on the weekends.

I have noticed that she sits more when not playing. She will come and sit with me, not wanting to join in with the others. Not just at ball but when we are out as well, she will not leave my side. She starts acting like she is afraid to do anything by herself.

Headaches get so severe we go to the ER. Right away they see that her optic nerves are swollen. They call in an Ophthalmologist and he confirms what they see. They do a CT on her head, it shows normal so they ask us to come into the office the next day for more abrasive testing. Next day all tests come back fine.

They tell us to give it a month and come back for recheck. If they are still swollen but no change in tests then it is a birth defect.

THIS is when I finally wake up! How can it be a birth defect if the eye doctor didn’t see it back in the beginning of the year? Or when we were at the doctors for bladder pain?? Doctors always check your eyes, wouldn’t they had seen it then?

I was ignored and asked to schedule for a month out. Meanwhile, we were referred to a Headache clinic.

This Clinic acknowledged what other doctors saw and said her headaches were more than likely genetic headaches. Take some pain reliever and rest, along with drink more water!!

Even with Leah’s pain she still pushed through. She wouldn’t take any type of pain reliever. Said it didn’t help, so why take it? She hides the pain well, so I would just try and make sure she was staying hydrated.

Did Gardasil cause my new medical conditions?

Ball season comes to an end…School will be starting in a week. She is sleeping more. Emotions are all over. She acts like she is still afraid of everything. She won’t even walk by herself from the car to a friend’s front door. Wants me to walk with her??? Wherever I am she wants to be. Not wanting me to leave her side. She is becoming anxious, having lucid dreams. Trouble sleeping, pain is all over her body. She is waking up drenched in sweat. Cold and hot throughout the day. She feels as though her body cannot support her own weight. Tremors in her arms legs and face. Her hands and feet keep going numb. She was having low grade fevers and all the symptoms she has had for the last three years have increased.

She is changing from once a healthy girl to one that can’t even get out of bed. It is August 2014, her sophomore year starts and she is excited. She is planning on getting her temps in October, attending homecoming and playing fall travel ball.

Leah comes home from school exhausted. She falls asleep right away and wakes up in more pain than before. She says she is hurting so bad at school she has a hard time concentrating and understanding what the teachers are saying. She’s having a hard time hiding the pain from her friends. As she walks to each class she says she feels as though she is going to pass out. She’s still having severe back pain and new pains going down into legs. Lights hurt her eyes while inside and when she steps outside the pain shoots through her head making it difficult to see. Lights are too bright all over. The sun is torture. Her legs are having more spasms and her heart keeps racing even when sitting still. She started to just stare off into space and writing words over and over in her school work like she is stuttering, not realizing this until she reads her work.

Research came to my attention about the Gardasil vaccine and adverse reactions. When Leah came home from school one day I asked her to please write everything down, all her pains and odd things that was happening with her body. I told her I believed it was all happening because of this shot.

I made an appointment with her pediatrician and started to research. The more I researched I was certain this was what was happening.

When we saw the doctor she didn’t think that was the case. I told her there was a lot of research out there and how was it that Leah’s symptoms were the same as what was happening to all the other children claiming it was the vaccine as well??? The only common factor was the GARDASIL.

She listened and because of all of Leah’s symptoms she referred us on to several specialists. She ordered what blood work she was able to do. Said she would look into it and would be in touch.

I requested the lot numbers from her adolescent doctor and checked them from a study I found on SaneVax. Dr. Lee had done a study back in 2012 and found several lots to be contaminated with a non B conformation DNA attached to the aluminium adjuvant.

I wasn’t sure what all that meant, but reading through all the information I could find, I started seeing that this shot was sheer poison. When I checked Leah’s lots against what Dr Lee had tested I started to cry. There in black and white was the very first lot number that Dr Lee had tested-the same lot Leah had been injected with!

I was sick. I was mad. Then I realized I had Proof!

As I continued my search for the truth about this vaccine, I was discovering that thousands among thousands all over the world were injured the same as my daughter. Some far worse than her. None that I had found had one of the lot numbers in the study. That told me that EVERY LOT of this senseless vaccine could have the same contaminates as the one in the study!

We have been to eleven different specialists. Most of the tests all come back normal. A few have discovered some type of medical disorder. I have to say that I guess I wanted to rule out any major diagnosis. Doctors are quick to get you out of their office once you mention the possibility of vaccine injury. We are left feeling our only hope is a Bio Medical doctor that does not treat from a pharmaceutical manual. I have lost all trust and respect for any doctor that treats and diagnoses their patients from those manuals.

We were not treated with respect and care. We were told there was no way the Gardasil vaccine could be the reason for all of Leah’s new symptoms. Some even questioned why we would even consider a biomedical doctor. Most found it hard to believe Leah was having all of these symptoms at the same time. Several referred us to a psychiatrist!

I had a phone conversation with one of the psychologists, let’s just say once I started describing what was happening to my daughter and how I had PROOF, they were NOT going to diagnose her with Conversion disorder!

Our conversation ended with, “I am so sorry you and your daughter are going through all of this. My services are not needed at this time. If you feel like you would need for Leah to ever talk to someone, please let us know!”

WOW!!! Thanks doctor for the wonderful concern!

My daughter IS VACCINE INJURED from the HPV vaccine GARDASIL. She has been diagnosed with Lyme disease, metabolic disorder, immune deficiency, and encephalopathy, chronic gastritis with pre-cancerous cells throughout her stomach and colon, and ovarian failure.

She has several ACTIVE viruses within her system which include; Bartonella, babesia, coxsackie B, francisella tularensis, and HPV-6. The HPV-6 was a strain that this senseless vaccine was to fight against!!!

She is heavily toxin with heavy metals that do not want to leave her body.  We are receiving treatment and trying to detox her body. Hopefully one day soon Leah will be her Healthy, Active, Funny self.

I urge you if you have not yet received the vaccine, DONT!!! DON’T LET YOUR CHILD Become “ONE LESS” HEALTHY ACTIVE TEENAGER!

Research for yourself and look at the prescribing information that comes with each vaccine. I promise you, if you do you will never vaccinate your loved ones again, with any vaccine!

If you are injured as well from this horrific vaccine, I am truly sorry!  You have found HOPE by finding this site.

I promise to ALL of you that are injured, I WILL NOT STOP FIGHTING TO GET THE WORD OUT! I will go to whatever lengths I must to prove to the WORLD what is happening to our children is unethical and needs to STOP!!

Blessings to all!

This article in it’s entirety, is compliments of www.SaneVax.org

Shannon and Leah, it was hard to read through the piled on adversity you have been through.  You are strong women, and have endured this time amazingly well.

I am so glad you have located SaneVax, they are angels, and have expertise in healing from vaccine injuries.

I have a Featured Doctors menu option as well, with doctors that have experience in this area. I hope the tide has turned and things only improve for you from here.

I chose the following artistic piece for you being it hits on the depth of pain you must endure at times, and the reminder that, “Whoever saves one life saves the world entire.”  A great man was given a gold ring with that phrase engraved on the inside for his generous, and courageous acts as seen in the film, “Schindler’s List”.

For you to take the time, with all you face each day, to reach out, and to save other teens from the tragedy of the Gardasil/Cervarix vaccines is touching. I am certain that you will save another in this effort.

I hope your testimonies travel far, and that Leah, you receive all the care that you need.

You will be stronger from this, and I believe you can receive miracles in many different ways.

Being that you are putting your trust in God, you will never be alone and he will guide your every step.  God bless, your friend, jen.

 

Awake at 3 a.m.? Try this quick and easy trick to fall back asleep#insomnia#iPad#android

By Dr Flannery

Do you often wake up at 3 a.m., your mind racing with thoughts, and you can’t fall back asleep? Try this crazy sounding but highly effective tip: Eat something! Make sure it’s not something sweet but instead something with protein and fat, such as nut butter, a bit of hard boiled egg, or some meat. Make sure to keep some food next to your bed with a glass of water so you don’t wake yourself up too much by going to the kitchen. You won’t feel hungry and most likely won’t feel like eating, but do it anyway as an experiment. Chances are you will fall right back to sleep. Why?

If things go according to plan you don’t bolt awake at 3 a.m. While you’re sound asleep you’re brain is hard at work and needs plenty of fuel. It is forming memories, clearing out old cells, regenerating — all while you’re fasting, having gone hours without eating. In order to give the brain the energy it needs, the body gradually raises cortisol, an adrenal hormone. Cortisol triggers the release or synthesis of glucose to fuel the brain during the nightlong fast and you sleep through the night.

That’s if things are working right. If you suffer with chronically low blood sugar then you are one of those people who is likely to bolt awake at 3 or 4 a.m. People with low blood sugar will have difficulty making enough cortisol to sustain the brain during the night. To compensate and keep the brain going, the body then releases “fight-or-flight” adrenal hormones. These adrenal hormones raise blood sugar back to a safer level to give the brain fuel. Unfortunately, they also raise stress, which can cause anxiety or panic in the middle of the night. This explains why you wake up at 3 or 4 a.m. with a racing mind, an infinite to-do list, in a panic, or some other stress-addled state.

Things you can do during the day to avoid waking up at 3 a.m.

Although a few bites of food may help you fall back asleep, it’s better to prevent that anxious wake up call in the first place. If low blood sugar has you waking up every morning at 3 a.m. try the following tips:

  • Always eat breakfast, even if you don’t feel like it, and avoid sugary, high-carbohydrate foods with breakfast. Low blood sugar will cause you to wake up with no appetite. You may even feel nauseous. Eat anyway, you need to break the nightlong fast and stabilize your blood sugar.
  • During the day eat frequently enough so blood sugar does not crash.
  • Avoid sweets and starchy foods (breads, pasta, rice, potatoes, etc.) and adopt a lower-carbohydrate diet. People with low blood sugar symptoms typically eat too many sweets and starchy foods as well as frequently skip meals. Eat enough protein and healthy fats to sustain your energy.

Ask my office about nutritional compounds that can help you manage your blood sugar better and sleep through the night.

Post in it’s entirety, is compliments of www.drflannery.com

Why your doctor can’t help you#iBelieve#ASD#repost

Some good insight, that puts things in perspective from one of our, Featured Doctors.

You notice you’re feeling worse and worse. You suffer from chronic fatigue, pain, digestion issues, depression, anxiety, insomnia …. the list goes on. Yet when you go to your doctor, you’re told your lab tests are fine, it’s just age, or perhaps you need an antidepressant. If you press for more tests or keep returning with complaints, you’re labeled a problem patient or told it’s all in your head.

Unfortunately, this happens to untold numbers of people each year. When you can barely muster the energy to get through life’s daily tasks and you have long since abandoned your hobbies, sports, or time with friends, hitting a brick wall at the doctor’s office can fill you with despair.

It isn’t that your doctor is an uncaring person, he or she simply works in a paradigm that is woefully outdated when it comes to the exploding incidences of chronic and inflammatory conditions today. There are instances when conventional medicine is like a miracle, but for the one in five people suffering from autoimmune disease (a disease in which the immune system attacks and destroys tissue in the body or brain), and countless others suffering from undiagnosed autoimmunity, chronic inflammation, severe pain, environmentally induced illnesses, food sensitivities, chronic viral, bacterial, or parasitic infections, brain chemistry imbalances, hormonal imbalances, hair loss, unexplained weight gain, and more — being told your lab tests are fine and you simply need an antidepressant can feel like a kick in the groin.

Medical schools don’t teach nutrition

Medical doctors receive very little nutritional training despite an ever growing body of evidence linking diet with the explosion of chronic diseases today. We know, for instance, that the high blood sugar that comes from eating standard American fare can ultimately lead to diabetes, Alzheimer’s, or heart disease.

The standard approach to autoimmune disease, the occurrence rate of which far surpasses that of cancer and heart disease combined, is to wait until its advanced enough to either surgically remove the affected tissue or administer severe immune-suppressing drugs.

Gluten intolerance is still overlooked by many doctors. Standard testing for gluten sensitivity and celiac disease is limited and outdated, missing countless positive diagnoses. This despite the growing body of evidence that links gluten with autoimmune and neurological conditions. Other dietary proteins can also provoke severe immune reactions, something many doctors are not aware of unless it’s a classical food allergy (which is a different beast than a food sensitivity).

Doctors are constrained by their medical education, which has yet to catch up with modern illnesses. Liability insurance, health insurance, peer pressure, lack of time, and other factors often keep them from investing in the education required to help the millions of people suffering from “mystery” symptoms which, when you look at the science, are not always that mysterious.

Functional medicine for chronic symptoms and illness

Fortunately, functional medicine specializes in using nutritional, botanical, and nutraceutical approaches to manage chronic, inflammatory, and autoimmune conditions. We keep up with the latest science and the latest lab testing, which is integral to unraveling chronic symptoms and conditions. If you’ve hit a dead end with your medical provider, ask our office how functional medicine can help you regain your energy, vitality, and well-being.

This post in it’s entirety, is compliments of www.drflannery.com

 

 

Dr. Kory Branham – Featured Doctor#Vaccines#ASD#Health

I have been pleased to find Dr. Kory Branham.  Upon moving to the Salt Lake City, Utah area, I wanted to find a physician that matches the type of healing I find most beneficial for my family and I. He has aided many individuals, and families, and I am fortunate to benefit from his tried and tested techniques. Dr. Branham’s practice has much to offer, whether you are interested in strengthening your immune system or healing from vaccine damages.

Thank you, Dr. Branham for all the good that you do.

I approach immune challenges from a whole body standpoint. I use Applied Kinesiology (manual muscle testing), to tune into each individual body, to determine the organs that are the weakest and identify the factors contributing to the weakness ranging from infections to heavy metals and chemical toxicities, to food allergies, to emotional challenges, to inherited weaknesses.

I use remedies ranging from herbs, flower remedies, vitamins and minerals to structural, spinal and cranial adjusting to emotional release techniques to homeopathic acute and constitutional remedies. Often times the immune system which is a complex of the thymus gland, the spleen, and the lymphatic system is damaged or inhibited by food allergens, or low-grade persistent infections ranging from yeast to viruses, to parasites.

Other organs being depleted will also impact the immune system including low or high adrenal or low thyroid function. It is well known that chronic depression, anxiety or bitterness can suppress the immune system and lead to illness. This is true “Holistic healing,” assessing all factors and then identifying which ones are the priority to address for each individual person.

Some of the most common immune support supplements are zinc, selenium, vitamin C, B vitamins, Reishi and astragalus mushrooms, antibiotic herbs like oregano, and goldenseal and thymus and spleen glandular extracts.

Which, in regard to vaccinations, I use homeopathic test vials for the different vaccines to assess if the body is stressed by them, and specifically which glands or tissues are stressed, then I identify the appropriate remedy or treatments to heal that stressed tissue.

On average about 1/3 of all weaknesses are identified as having emotional components. A big part of what I do is to bring awareness to these issues and help the patient release this energy.

Another hidden factor creating a lot of immune stress is hidden food allergies or sensitivities which can be assessed using Applied Kinesiology.

Dr. Branham’s Practice – Premier Wellness Utah

BIO

Dr. Kory Branham

Dr. Branham was born in St. George, Utah in 1955.
At six months of age, his family moved to northern Wisconsin where he grew up and attended high school.
His exposure to natural healing methods began early as his mother opened a health foods store in their home in Wisconsin in the 1960’s. Also from a young age he was exposed to Chiropractic adjustments by his father who had attended McCoy Chiropractic Institute in Seattle, Washington, but was drafted into the Army during the Korean War before finishing school.
At age 19, Dr. Branham served a mission for the LDS church in both Toronto, Canada and Sao Paulo, Brazil. On his return, he attended undergraduate school at BYU and then did his Chiropractic studies at the National College of Chiropractic in Lombard, Illinois. He graduated Magna Cum Laude in 1980 and began his career first in Texas then in Detroit, Michigan where he spent three years working for Dr. George Goodheart.
Dr. Goodheart was the founder of Applied Kinesiology, which is a diagnostic technique using manual muscle testing to evaluate the body. Through “AK”, a practitioner can quickly evaluate and integrate many different kinds of natural therapy and apply it to the patient very specifically. Dr. Branham became certified as a Diplomat of the International College of Applied Kinesiology and has become a master of this technique.
In addition to this technique Dr. Branham has studied and integrated many other healing modalities into his practice including craniosacral therapy, trigger-point release techniques, Neuro-Emotional Technique(“NET”), diversified adjusting, and functional medicine which utilizes functional hair, blood, and stool analysis to diagnose the patient.
Dr. Branham moved to Utah and began practice here in 1986. Initially attracted to the mountains and snow for the climbing and skiing he met his wife Julie here and has made it his home. He currently resides in Alpine, Utah where he and his wife are raising four children and running a Yoga studio.
In addition to his busy practice and family life, Dr. Branham enjoys a variety of outdoor activities including skiing, snowboarding, road and mountain biking, running barefoot, sailplane and airplane flying and windsurfing.
He is continually learning and experiencing new things and his philosophy in life and for his patients is to improve and maximize the quality of life for all so we can each have the most enjoyment and fulfillment of our time here on earth.