Gardasil: Conversion disorder? I don’t think so!#Vaccines#HPV#Health

By Tamara Toussaint-Brown, Loveland Colorado

Haleigh and Gardasil

Haleigh’s story starts out like many others.  She was always involved in some kind of sports: gymnastics, dance, cross country, track/field, flag football, basketball, softball, plus just doing outdoor activities bike riding, long boarding, hanging out with friends etc…  The family was always involved and enjoyed watching her at any of her events.  She was very happy, though she was always shy and quiet in her classes (her teachers always told us how much they loved her and how respectful she is but wished she would talk more).

The only time she ever went to the doctor was to get immunizations and physicals to play sports and couple of injury visits. Haleigh received her first injection of Gardasil on the 26th of June 2008 and the second on the 24th of September 2009.

She was in 7th grade with her 13th birthday coming up at the end of Jan 2010.  We planned a trip to the “haunted” Stanley Hotel in Estes. I remember earlier in January she was sick and vomiting a couple different times. When she recovered I thought – good, she will be healthy for the trip to the hotel.

While at the ‘haunted’ hotel, she slipped and fell on a small grass hill and broke her wrist.  We all joked about it saying that a ghost pushed her.

During the first weeks of Feb 2010, she started to have stabbing pains in her right side (gallbladder) and more nausea. At first, the doctors thought maybe the pain was from the fall at hotel and prescribed physical therapy and some pain meds.

That didn’t work, so they said she was either having cramps or she was constipated. She was prescribed a soft laxative.  Haleigh knew this was not her problem.

We returned to the office several times, pleading with them to not prescribe any more medications that would simply mask the problem. We knew something was seriously wrong.

They could see from her medical records that we did not visit them previously for anything other than routine visits.  Haleigh explained repeatedly that she was experiencing stabbing pains and nausea all the time.

In April we went in and the doctor actually asked how she was during spring break insinuating that she might have been faking symptoms to avoid school. I said, “As the matter of fact, it is her spring break now and she is miserable.”

I could not believe they just kept trying to medicate her for a UTI (urinary tract infection), cramps and constipation.

After two and half months of watching her suffer rolled in ball crying,  I searched for additional help and found a doctor who ordered a hydascan (special nuclear die test).  This test revealed that her gallbladder was functioning at less than 10% of normal capacity.

Conversion disorder?

Her gallbladder was removed two days before Easter 2010. The surgeon said he had no idea why it was not functioning because it looked to be a healthy gallbladder with no sludge or any defects.

No, she did not fit the profile for a gallbladder issue but we were happy to have the answer and move on.  She would feel better now.  The stabbing pain was gone.  She was affected by foods now that she didn’t have a gallbladder.  We had to spend some time getting used to know what foods she could and could not eat.

In Sept 2010, she started having issues again – back to hospitals and doctor visits. This time we thought it was due to her gallbladder but, the stabbing pain had come back in the lower right side this time.

The doctors said this was because she might have ovarian cysts and sent her to the women’s clinic during the first week of November.  The clinic put her on birth control pills and Vicodin.

By the end of November, Haleigh was in so much pain her family doctor sent us back to the women’s clinic where the doctor said this has nothing to do with cysts.  She felt it was appendicitis and admitted her to the hospital.

The hospital kept her there for two nights and many tests with no explanations forthcoming.  They said she was a ‘mystery’.

The family doctor thought stress was causing her stomach to produce too much acid and said she should take some antacids.

After watching her suffer again with stabbing pain, I started searching for answers with other doctors.  We went to Children’s Hospital and saw a gastroenterologist. The week before Christmas she was back in surgery getting her appendix removed and small cyst that had ruptured on her right ovary.

Again the surgeon stated that the appendix looked healthy.  So now that she has no gallbladder or appendix and she’s on birth control pills to help with cysts. She should be on the up and up now.

Despite all of Haleigh’s mysterious new symptoms, no one considered the possibility of any connection to the Gardasil vaccine. She received her third and final injection on the 9th of March 2011.

Throughout the entire ordeal, her teachers were very understanding and helpful.  They knew Haleigh and felt so bad knowing she was not well.   She desperately wanted to get back into sports.  Running was painful for her now and tiring.  We thought this to be from her surgeries.

Haleigh started gymnastics again just before 9th grade started and injured the lisfranc ligament in her foot.  She was unable to start the softball season in high school because she was in a boot.

The summer before 10th grade she had high school softball practice and began the season.  Right at the start of school she had a first aid class outside and was stung by a bee in the foot.  Haleigh has been stung before and had no allergic reaction, but this time her foot became so swollen she could not get her cleats on for her softball games for a couple of weeks.

Once she was back to practice she was hit in the face with ball while warming up with a teammate. She was unable to play for most of the season because of the concussion, but was back playing by the end of season.

Someday I will have my life back.

After Haleigh’s 16th birthday in January, she experienced pounding headaches and spells of vomiting every day up to 6 times per day for almost 3 months.  We now had a different family doctor.  He ordered many tests to be done all of which came back normal.  Again with the “mystery” illness.  He thought she should try Prilosec. This did not help, so he sent us back to Children’s Hospital to the gastroenterologist.  They did an endoscopy and found that she had bile in her stomach and that her stomach lining was irritated – but could not see why.

She was also having constant headaches that did not go along with GI problems, so we were referred back to the concussion clinic. They stated it was too far past the time of the accident for her conditions to be post-concussion symptoms.

Throughout this time we did all that was asked of us, went wherever they sent us, and submitted to every test they recommended. With no questions asked!

Her doctor would just say, “She’s a mystery, maybe we are just chasing our tails with no answers to be found.”

Now it’s 2014, she has missed lots of school. Her teachers could tell she wasn’t well and were very helpful with her class work.

January and February of this year brought on another bout of nonstop vomiting and headaches.  Back to ER more blood tests and scans – all coming back normal.

Now, doctors are mentioning more and more that she must be under stress which is causing all of her ‘mysterious’ new medical conditions. This of course does not make us happy. We know that depression is not the cause of our daughter’s new health issues.  Having doctors claim it is depression is discouraging and depressing all by itself.

Around the middle of Feb 2014, she began to have some type of small seizures.  I came home from work and found her on the floor, very upset and scared.  She said her heart was racing, then her legs went stiff and she fell to floor shaking.

I called the doctor and they sent us to the emergency room. The ER doctor did CAT scan and blood tests and found everything normal. The doctor stated Haleigh obviously had depression which was causing this to all happen.

At this visit we spoke with the hospital counselor. That is when the light came on for us regarding Gardasil.  I discovered that she had her 2nd HPV shot just 4 months before the Jan 2010 stomach issues.

We followed up with the family doctor and asked if it could be the HPV Vaccine.  His answer was, “I’m looking on the VAERS reports right here and I don’t see anything that shows any side effects reported.”

He said he felt it was “conversion disorder” and wrote it down for me.  He said he wasn’t saying she was crazy or doing it on purpose but that her brain was causing all of this to happen.

I asked him right then, “So, what you are saying is that her brain caused her gallbladder to stop functioning?”

His answer was, “That may have been the root cause for all of this. She should go to a psychiatrist so that she has someone that would listen since she’s been through so many mystery illnesses with no answers.”

He also said that he didn’t want to put her through any more test with no answers; that we were just going in circles.

I asked if there was some test that could be done to at least rule out the possibility that her symptoms might be related to Gardasil.

He replied, “We haven’t got one yet.”

In April 2014, Haleigh got very sick again. This time her throat and face started to swell, so we were told to take her to ER where she tested positive for mono.  She was vomiting every day for two weeks, she also had headache and dizziness.

We now have more of an understanding of what is going on with our Haleigh. Just knowing helps us get through this nightmare ride. We hope to get answers by reaching out.

Here is a list of some of her many symptoms throughout the past 4 years:

  • Nausea
  • Vomiting
  • Headache/stabbing headache
  • stabbing abdominal pain
  • Dizziness
  • chest pain
  • fatigue
  • joint pain
  • shortness of breath
  • Racing heart
  • back pain
  • neck pain
  • skin rash
  • seizure symptoms
  • Black outs
  • foot pain
  • bloating/swelling

Here is a partial list of the medications she was given the last 4 years:

  • Amitriptyline
  • Cephalexin
  • flexeril
  • Keflex
  • Meloxicam
  • Promethazine
  • Compazine
  • Naproxen
  • Prilosec dr
  • Ranitidine
  • Zofran

 

  • Cyproheptadine
  • Prednisone
  • meclizine
  • amoxicillin
  • tramadol
  • imitrex
  • trokendi xr
  • Carafate
  • Sprintec
  • Oxycodone
  • ondansetron

 

Some of these medications were prescribed many times. Had any of them worked at all for her, we would have stop searching for answers. At this point, reaching out to others who are in similar circumstances is our only hope of obtaining any answers. We have no other option.

I hate the fact that I was made to question my daughter. I hate the fact that the medical community tried to convince me this was simply teen hormones and/or stress.

I cannot begin to describe how difficult it has been to watch her suffer so badly and receive nothing but doubt and excuses from the professional medical community. I can only imagine how difficult it has been for Haleigh.

Nevertheless, Haleigh has stayed strong through the whole ordeal.  She has had the support of family, close friends and teachers.  We will all continue to support her and fight to find answers for her.

Haleigh and Tamara, I am so sorry to hear of your plight. What a trial!  Your fortitude, and exactness, through this time, is truly impressive. It is so nice to hear of the wonderful support from your friends, family and teachers.

Thankfully, you have heard about SaneVax.org. No need to lose any time now.  They will have excellent guidance, and please look through the Featured Doctors section of my blog.  There are individuals healing the world over, and probably best to work with a doctor that is familiar, and successful in caring for like conditions.

I hope you like James Taylor and The Dixie Chics.  I like to share a little music to help you take your mind off things for awhile. 

Please know, you are in good hands now, and look ahead to the future.  Your friend, jen  🙂

This article is complements of SaneVax.org

World’s Number One Herbicide Found in Mother’s Breast Milk#Health#GMO#Breastfeeding

 World’s Number One Herbicide Found in Mother’s Breast Milk                          Mother breast feeding her infant

•    Pilot study shows build-up of Glyphosate herbicide in Mothers’ bodies
•    Urine testing shows glyphosate Levels over 10 Times higher than in Europe
•    Initial testing shows Monsanto and Global regulatory bodies are wrong regarding bio-accumulation of Glyphosate, leading to serious public health concerns
•    Testing commissioners urge USDA and EPA to place temporary ban on all use of Glyphosate-based herbicides to protect public health, until further more comprehensive testing of Glyphosate in breast milk is completed.

 Read Entire Article Here

‘Global, Silent Pandemic’: Study Links Common Toxins to Brain Disorders in Children#Vaccines#ADHD#ASD

by
April 5th, 2014

 

kid toxic gas mask pandemic 263x164 Global, Silent Pandemic: Study Links Common Toxins to Brain Disorders in ChildrenYou don’t have to be a doctor or even a parent to notice the increasing number of children shouldering heavy diagnoses. Conditions like ADHD and autism are far more common now than they were just a few decades ago. While some of this could be attributed to Big Pharma’s need for a greater demand (and conventional doctors answering that call in kind), to ignore the potentially disastrous effects of common pesticides, solvents, and other toxins in our world would be remiss.

A new study published in the Lancet Neurology indicates not only could these toxins be having damaging effects on the youngest among us, but their dangers are being shoved under the rug….

Read Entire Article Here

Autism Awareness Month#Autism#ASD#Health

Autism Awareness Month                                                           Lighthouse beaming light ray over stormy clouds

Being this is Autism Awareness month, I decided to take some time to do added research in this area. I was surprised at the material I discovered. To start I have to say, why isn’t insurance covering the speech and behavioral therapies so needed for these children?

There are many parents begging to be heard.  This signaled a recollection of a tune I have heard many, many times over the years.  So often, we look to the authorities for the needed health answers when the ones on the 24 hour front lines have a wealth of valuable information!

One side of the Autism discussion says it’s incurable while the other side shouts that children are healing and being healed.   

Why would groups such as, Autism Speaks and NAAR (National Alliance for Autism Research),  spend so much time and resources on autism genetic research? Last I heard they might consider environmental components as a possibility in relation to Autism for their research.

I found a hope and excitement stemming from parents who are having spectacular results.  Commonalities of healing through biomedical interventions. 

I think if I had a child suffering in this area, I would want to join discussions with TACA , (Talk About Curing Autism).  I would be on the phone with a DAN! Doctor and looking into their conferences. (Defeat Autism Now)

I would be contacting Generation Rescue to find a  Rescue Angel to help me along the path of healing and look into possible grants. I would want to be surrounded with this kind of hope, support and direction.

A great month to donate to Generation Rescue and the Autism Research Institute.

One parent in particular has a site that lends much hope and success stories. Autismrecoveryvideos.org

I read of one family after another that found their way to doctors and research that lends hope and leads to paths of healing.

As I read, across the board, these families lead a hard life.  There is so much behind the scenes that no one sees, and these parents deserve so much love and support.  I hope their lives can be eased in any way possible, and to be able to enjoy any little speck of added affection, and communication with their dear child suffering with autism.  To hope that the many physical symptoms can be healed. A long road, but wouldn’t every little bit be wonderful.

I will continue my research, and share what I come across throughout the month.  On the Featured Doctors menu option are additional doctors with differing methodologies having success in this area as well.  If you haven’t dipped a toe into this life spring of hope then this is a great month to go for a dip.

Autism Awareness Month  – A great month to send our prayers to strengthen our brothers and sisters in this area.  🙂

I came across a quote while researching in the book, Mother Warriors, that really rings true to me.

“Autism is a combination of infections and toxins that can ultimately lead to a neurological breakdown.”

 

 

Is your brain on fire? Brain fog, memory loss, depression, autism, ADHD…#ASD#health#adhd

Is your brain on fire? Brain fog, memory loss, depression, autism, ADHD…

brain on fire

Do you suffer from brain fog — that spacey, detached feeling like your head is in a fish bowl? Do you suffer from depression, or does your child have autism? Are you concerned about Alzheimer’s? These conditions are signs of possible brain inflammation, or a brain “on fire.”…

Read Entire Article Here

Dr. Flannery is one of our Featured Doctors.  If you experience any of the above symptoms, it would behoove you to read further.

Allyson McQuinn – Featured Doctors Week#Vaccines#Autism#ASD

I am thrilled to introduce Dr. Allyson McQuinn as one of this week’s Featured Doctors. Dr. McQuinn and her husband have an advanced homeopathic approach they use called, the Heilkunst Treatment.  This husband and wife team have patients they treat the globe over and know how to better the health and heal children with autism.  You will hear more about the details of their approach in the article below.

If you or a loved one have a child with ASD you will love the following story.  Very heartwarming and thrilling to see the healing that little Alexandre has received.  You can read more about this healing method in her first of ten books titled,  “The Path To Cure; The Whole Art of Healing” (www.thepathtocure.com)  I cannot wait to get my hand on this book.

Thank you Dr. Allyson for taking the time to share this precious story of Alexandre and his family.  We hope to hear more from you in the future.

Alexandre; Out of the Spectrum

I first met Alexandre on Feb. 7th, 2013.  I was invited by his mother to meet him in order to begin his Heilkunst Treatment (literally  the whole art and science for healing and curing) for Autism.  While 80% of my patients are treated by Skype, Facetime, Google Hangouts or phone, this time I had the pleasure of meeting this 5 year old in person.

When I arrived, I was greeted by Alexandre’s mom, Nicole, who also introduced me to her very vivacious and outgoing 3 year old, Zoë.  I was invited into Alexandre’s room, which is where I first observed him playing.  He did not look up to greet me, but continued playing, clearly absorbed with his trains and plastic letters.  I was completely astounded by the back of his head, bent slightly forward, and I listened to him breath in concentration.  Something felt hauntingly familiar; ‘Oh my God, he looked exactly like my own son, Jordan, at this age.’

I felt pummelled in the stomach with primal memories of my Jordan’s spectrum gestures.  I was landsliding head-long, back 17 years into what it felt like to have a child who lived in a vacuum, cut off from me, and the rest of the world.  I slowed my own breathing to match Alexandre’s as the tears threatened to choke my throat.  I very quietly and deliberately brought my leg up under me to sit on his bed.  I took out my notebook to take notes, hoping to distract myself and his mother.

It felt like my whole organizing lens was toggling back and forth between my present to my past.  I was recalling very quickly why, over the last 10 years as a Physician of Natural Medicine, that I’ve mostly referred off babes in the spectrum to my husband and fellow physician, Jeff Korentayer.  I’d been attempting to keep it clean and neat, and avoiding this exact pit of tumultuous feelings, still running riotous at my core.

Thankfully, the very familiar intake form that my Office Manager had asked Nicole to fill out prior, was before me, prompting me to start asking the requisite questions as I also tried to process my own feelings. “What’s Alexandre’s diet like? How much water does he drink?  What are his sleeping patterns? Any nightmares?  Where does he spend his days?  What are his verbal skills? When was he diagnosed?” The list went on as I scribbled notes with fervor.

I wrote down the answers and felt myself relax into Alexandre’s case while also allowing myself to feel what it felt like to never have been asked pertinent questions with regards to my own son’s case early on.  I was told by the medical doctor who’d removed the stool manually from my son’s body under general anesthetic that, “… some boys just suffer from extreme gut issues.  We don’t know what causes it, so the best we can do is manage it with drugs and diet.”  At that point, all those years ago, the terror of being trapped without a diagnosis still brings up fear and anger.  The host of alternative practitioners that we consulted offered the same nebulous non-answers, albeit their prescriptions were “more natural,” they’re results impotent.

As I watched Alexandre, I noticed how he loved to place the plastic letters in no particular order, but when Zoë came closer, he would body check her while grunting from his throat with his primal, non-verbalized dissent.  At this point, Nicole was describing how when Alexandre was 2, she was entirely in denial with regards to his developmental milestones even when he never crawled as a baby.  If he got excited, he’d express himself through pinching, biting, or pulling hair.  I recalled these same feelings in me those many years ago when Jordan did not speak, rocking back and forth in a corner instead.

As Nicole described his diet of pizza, fries, and chicken nuggets, I did not judge her in any way, as my own son would literally have starved himself of any food if I did not comply with his wishes.  Watermelon and raw carrots were the only fruit and vegetable that he would eat at the time.  When I tried making chicken fingers from scratch with almond meal instead of flour, they were launched across the room to hit the wall with a resounding “pwouff,” and then sliding down to lay lifeless on the floor; his anger and my anger intertwined.

In addition to Alexandre’s “ASD”, he’d suffered bouts of ear pain, eczema, a marked hearing deficit, sinus issues, and a chronic cough.  I went back to my office to formulate his medicines, knowing I was armed with the arsenal that would launch this babe out of the spectrum efficiently and quickly using the principles of Heilkunst Medicine.  I prepared his Emotional Support Dropper with homeopathic remedies and flower essences that would help to stabilize him constitutionally, while also stripping the excess.  In addition, I also made up his Drainage and Organ Support Dropper to begin the process of detoxing his physical body from toxins and heavy metals, while also supporting his organs and lymphatic system.  This enabled me to set the stage for clearing each issue from his timeline of traumas, including the the use of antibiotics, a car accident, running into a busy street from daycare, his boosters, vaccinations, and birth.

After these events, I knew that I would have access to his Genetic Miasms based on the law of the succession of forces.  Every individual has these in their cellular memory based on a few thousand years of human evolution, layered like a geological dig.  It’s just a matter of which ones predominate, throwing up unwanted symptoms.  Buried in each one of us is the predisposition for skin afflictions (Psora), bronchial complaints (Tuberculinum), heart disease (Medhorrinum), cancer, joint/tendon issues, and autism (Syphilis).  These Genetic Miasms (there are 8 all together), unfortunately, never go away unless cured on the basis of natural law, “like cures like”.  Vaccinations can trigger some of them, or all of them, to start wreaking havoc.

Over 15 years ago, the same Heilkunst medical path, with few variances, was followed for my son, Jordan, who was cured within the year of his own spectrum issues.  Today, at almost 20, he is a trampoline acrobat and Parkour Instructor, as well as a Bowen Practitioner (soft tissue modality) with his own growing practice.  No one, meeting him, would ever suspect he’d ever been in the spectrum.  I’m so thankful for the principles of Heilkunst Medicine or he’d never have realized his essential self.  So many children have now been cured by these foundational principles by the just over one hundred Practitioners world-wide.

Source:  See also http://amzn.to/1hGYdpb

Six months ago, and six months into treatment, Nicole cited, “What brought me to see Allyson is my beautiful, non verbal autistic 5 year old son, Alexandre. I needed to figure this out! I was not settling for what we were dealing with at the time. We still have leaps and bounds to go, but he is growing, I can see light bulbs turning on left and right and he is here with us so much more than he used to be!

We started our journey in early February, he has been a trooper with everything I’ve thrown at him. He asks for his drops if I haven’t given them at the appropriate time, if we’re due for an appointment, his body tells us! Simply amazing. He is now speaking at the rate of a 2 year old, repeating everything and now using small sentences! It’s a start and I’m aching for more!”

Fast forward to March 2014, one full year into treatment, and here is Nicole’s testimonial:

“One year into this journey and my son is a different person, he still has a delay in verbal communication, however, he knows how to get his point across and mimics almost every word that leaves my lips.  Just this morning I was trying to get them into the car to leave for daycare, I told him to “get in the car” in a bit of a demanding tone, he repeated using a very similar influx in his tone.  I beamed and was high fiving myself and him in my head.

I still ache for more!

Being the non-confrontational person I am, I avoid conversations of vaccines and different therapies, that others have a huge opinion on.  That said, I do not hide the treatment plan that we’ve discovered through Ally.  I run a blog and facebook page named “The LeBlanc’s vs Autism”, on this page, I do share some of our treatment plan and the great success that we have had through it.
Alexandre has received all vaccines that the doctors suggest his tender 6 year old body is “supposed” to,  Zoë however will not.  I do not regret the choices I have made, I wish I had known the truth about allopathic medicine before I vaccinated the crap out of my babies.  I thought I was protecting them, and this is what happened.

I still am not sure if the vaccines caused his Autism, but I do know that since we have gone to see Ally, our world has changed.  He still has a limited diet, but he loves water more than any other beverage, and he is open to have a sprig of broccoli on his plate now and then.  We’ve grown together, I have changed, he has changed and Zoë is now on board with her own droppers and paper hearts.  I know without a doubt that I am helping my family and keeping them safe and protected without causing an ounce of pain.

Thank you Ally for coming into our lives.  We genuinely love you and how much you have taught us.”

At this juncture, a year and one month later, Alexandre has many words in his vocabulary and continues to progress on all levels of his cognition.  He interacts well with other children and his family members and his grandparents and relatives have written notes to me acknowledging his leaps and gains with regards to becoming a more engaged and communicative child.  Alexandre is just halfway through his first round of Genetic Miasms.  I’m just imagining where he’ll be in another few months!

Bio:

Allyson McQuinn, DHHP, JAOH, is a Physician of Heilkunst Medicine in international practice.  She is the author of 10 books, including her 1st book, “The Path To Cure; The Whole Art of Healing” (www.thepathtocure.com), which is about her son Jordan’s departure from the Autism Spectrum.  Allyson’s husband, Jeff Korentayer, specializes in the treatment of vaccine damaged individuals, also using the principles of Heilkunst Medicine.  Both of them regularly provide patients with homeopathic remedies for the flu and immunizations for children and world travellers, prescribing most anything patients seek on the sound basis of homoprophylaxis with 99% efficacy (without causing an ounce of harm) over the last 12 years.
Alexandre; Out of the Spectrum

 

Have HPV vaccines caused a global epidemic of psychosomatic disorders?#Vaccines#World#Family

By Norma Erickson

 promoting only safe, affordable, necessary and effective vaccines and vaccination practicesMass hysteria, conversion disorder, psychogenic illness, Munchausen by proxy, fabricated illness – all are terms familiar to those who experience new medical conditions after using the HPV vaccines, Gardasil and Cervarix. Countless people have been told that their new and mysterious symptoms are psychosomatic because doctors are unable to discover what is causing their symptoms.

 Do health authorities truly expect people to believe there is a global epidemic of psychosomatic disorders that just ‘happened’ to begin shortly after the implementation of HPV vaccination programs?

 Why is it that families with daughters and sons who experience new medical conditions after taking Gardasil or Cervarix can visit every kind of medical specialist available without discovering the cause of their child’s symptoms?

 Part of the problem could be that while studying to become doctors, people are taught that vaccine injuries are so rare that they will probably never see one during their entire career.

 Part of the problem could be that vaccine injuries exhibit such a broad range of symptoms that it is difficult to determine whether the symptoms are the result of illness or injury.

 Part of the problem could be there is no diagnostic criteria established for vaccine injuries. Therefore, physicians have no idea what to look for in order to determine if the symptoms are a result of HPV vaccine administration or not.

 Then again, Dr. Mark Flannery may have hit the nail on the head in a recent article he wrote for www.vaccinationwaivers.com, in which he stated:

 

“It is not uncommon for me to encounter a condition I have never seen before as I treat so many people who have been to practitioner after practitioner seeking answers for their obscure health condition. I see patients being dismissed by the medical field because they cannot find a diagnosis.

In the medical field it is all about the diagnosis. In order to get paid or reimbursed by insurance there has to be a diagnosis. In order to determine medical treatment there has to be a diagnosis. If there is no diagnosis to be found then there must not be a problem or the problem is in the head (made up).”

 

So basically, if it’s not ‘in the book,’ it doesn’t exist except for in the mind?

 Another typical example of the callous disregard for the suffering of those who experience adverse events after Gardasil or Cervarix was expressed by Dr. Yutaka Ohno, of Keio University, who has stated publicly:

 

“It is impossible to find physical causes for the alleged and presumed adverse reactions at those vaccinated girls, so we cannot help concluding that their so-called adverse reactions are the mere consequences of psychosomatic reactions.  The government should provide counselling to the girls so that they may be freed from their psychosomatic reactions.”

 

This is a prime example of the attitude being exhibited worldwide when it comes to the thousands of families impacted by serious adverse events after HPV vaccine administration. Forget trying to treat their ailments; let’s free them from their psychosis.

 Where does this leave those unfortunate families whose children are suffering after HPV vaccinations? It doesn’t matter to them that vaccine injuries are supposed to be rare – Their children are suffering and the world does not seem to care.

 Society has failed these families. No one will dispute the fact that vaccine injuries can and do happen. It truly does not matter how rare vaccine injuries are, or are not. What matters is people are suffering needlessly.

 The time has come to find out why some people suffer such severe side effects and why.

 A diagnostic criteria must be established for vaccine injuries so medical professionals know what to look for.

 It is time for medical professionals to find cures for the vaccine injured – it is time to choose science over psychosis.