Gardasil: An experience no child should have to go through#android#iPad#retweet

By Tara Gramza, Phoenix AZ

Gardasil changed my life.

I am a labor and delivery nurse at Scottsdale Osborn, and studying to become a nurse practitioner. My daughter was born on December 6, 1999. She was approximately 14 years, and 2 months old when she first suffered an adverse reaction to a vaccine.

J.G. was a happy, very healthy, normal, teenage girl. All that changed when the doctor in her pediatrics office recommended she receive Gardasil as prevention against cervical cancer.

As a mother and an informed registered nurse, I was confident in the vaccination and willing to allow J.G. to be vaccinated. On January 7, 2012, J.G. received her first dose of Gardasil at East Valley Pediatrics in Arizona. She progressed normally over the next few months, showing no apparent signs of an adverse reaction to the vaccination.

On July 26, 2012, J.G. received the second shot of Gardasil at East Valley Pediatrics in Arizona. She again progressed normally, still showing no apparent signs of adverse reaction.

On January 23, 2013, J.G. received her third and final injection of Gardasil at East Valley Pediatrics.

By March of 2013, I noticed that J.G. was bruising relatively easily, but thought she was a normal teen with maybe a low iron deficiency. After all, she was growing normally and she had just started menstruating. However, J.G. had never bruised like this before, and I had never seen the bruises shaped like this before. I was concerned, but chalked it up to her being an active, growing teenager. Being a nurse, I did not see any reason for immediate concern.

However, my concern increased in July of 2013 during a vacation to Hawaii. J.G. was playing like a normal kid would and was pushed off the boat, hitting her hip against the side.

The next day, the bruise that developed looked like she had been hit super hard, almost as if someone had taken a baseball bat to her hip. I remember asking her, “How hard did you hit the boat?”

She replied, “Not that hard, I guess it’s low iron like you suggest.”

Despite my nursing background, I still did not think anything was seriously wrong.

Ultimately, at the end of January of 2014, J.G. and I went to see her primary care doctor, Dr. Chapman, for a well-child check-up. We reported to her that J.G. was bruising a lot and had been for months. We thought she needed her iron level checked.

Dr. Chapman sent her for labs. That afternoon, we had her labs drawn.

I wish one could be un-injected.

The next morning, we received a phone call. Dr. Chapman told us J.G.’s platelets were low (I believe at 23k), and she needed to see a hematology doctor A.S.A.P.

I picked up J.G. from school and kept her home until her appointment in 2 days. When we arrived to the office at Phoenix Children’s Hospital, they took more blood samples, 14 tubes, I believe, to double-check the labs and verify the diagnosis. She was again low – at approximately 24k platelets. They then asked how long we had noticed symptoms, and if we had seen bloody noses or spots on her skin. She had not at this time, just bruising.

Phoenix Children’s Hospital decided to refer J.G. to a rheumatologist named Dr. Ede and have her follow up with Dr. Shah, the hematologist. The plan was to send her labs and watch her to see what her body will do.

Dr. Ede told us during our appointment that J.G. did not meet the guidelines for Lupus, and her urine was negative for any indication of kidney damage that is present with kids with Lupus.

He did tell us that her labs were positive for something called Anti-phospholipid antibodies. This meant she was at high risk for clots. He wanted to follow her case, but felt she was not going to be a Lupus patient. He also asked that her labs be run again prior to any treatment for low platelets, such as Immunoglobulin therapy (“IGG”) to recheck the ANA and Double Stranded DNA.

J.G. was diagnosed on February 11, 2014, with immune thrombocytopenic purpura, ITP.

Dr. Shah told us J.G. would probably remain in the 30k platelet range for a few months, and would likely need intervention therapy such as IGG, Rituximab, or steroids.

The antiphospholipid issue was explained as being a possible positive as an auto immune response. The physicians could not say for sure which autoimmune condition came first, antiphospholipid antibody syndrome or thrombocytopenia.

They also said her labs were all negative for virus or other causes of ITP, and decided it was more likely a chronic immune thrombocytopenia. For several months, J.G. did stay at around 35K platelets.

Then, in May of 2014, J.G. experienced a seriously heavy period, nose bleeds twice in one day that would not stop, and little red dots all over her arms and legs. We took her to the Phoenix Children’s Hospital urgent care and they found J.G.’s platelets were 14K. (Note: a normal platelet count ranges from 150,000 to 450,000)

Gardasil took more than it gave me.

Dr. Williams, a hematologist with Dr. Shah, began seeing J.G. They told us to come back in the morning first thing for her first round of IGG. She was admitted all day for the infusion. They ran her blood for labs that Dr. Ede requested and started the infusion. These labs showed her ANA and double stranded DNA were both negative now. Dr. Ede decided to continue to follow her case, but did not need to see her anymore, because she does not meet the guidelines for Lupus.

J.G. came back to Phoenix Children’s Hospital for labs again to check her platelets a few days later. Her levels were around 75K. However, they quickly fell to 10K again, and she was then admitted again for another dose of IGG. Her levels rose again to 100k then fell down again to 23K.

Dr. Williams decided it would be best to start her on a medication called Rituximab to try to reverse the effects of her immune system’s response by resetting her B cells that cause her body to mark her platelets for destruction.

That night, J.G. started with bleeding of the nose again, small red marks all over her body, including her bottom, and heavy, irregular menstrual bleeding. She went to urgent care again and was told she had a 4k platelet count. The physician on call reported to the hematologist who then decided to admit her again for a high dose of steroids known as dexamethasone.

She took a super high dose of steroids for a few days to try to give her a boost while the Rituximab did its job. The steroids made J.G. very ill, with a stomach ache, headache, and racing heart. She gained some weight, too. She started the infusions of Rituximab, which is given in 4 doses for 4 weeks.

J.G. was admitted outpatient all day for those infusions and tolerated it well. She was to continue the lower dose steroids for several weeks so her platelet levels would stay above 25k. She did remain around 30K for many weeks. Then in August of 2014, her platelets jumped to over 150k. She was doing great and responding well to the treatment. She was removed from steroids. She officially completed Rituximab on June 24, 2014, and had a complete response with normal platelet count since July of 2014.

We have spent numerous hours and dollars fighting J.G.’s illness, all brought about by the Gardasil vaccination.

Worse yet, J.G. has lost her teenage years due to her debilitating condition, and cannot live a normal life. The fear of bruising and her potentially low platelet count dominates her mind wherever she goes.

J.G. continues to remain in remission, and continues to be seen by Dr. Williams every few months. During her last visit in January of 2015, her labs were rerun to show a negative DNA and slightly positive ANA and positive antiphospholipid antibodies.

Dr. Williams has said he thinks that the antiphospholipid antibodies and ANA should go away in time. However, she is still at a high risk for chronic ITP due to her age, her history of bruising post-vaccination, and the presence of other antibodies.

Her labs have continued to remain positive and her court expert Dr. Shoenfeld thinks she will remain APS positive for life. It will never go away. She will have high clot risk and the risk of return of blood related disorders and high pregnancy risk. Unfortunately it won’t go away. But so far so good. She’s still healthy.

No child should have to go through what my daughter has experienced.

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

Tara and J.G., my heart aches for what you have been through.  I am so sorry you have been through such a trauma and live with the anxiety brought on by an unnecessary shot.

A terrible crime by the pharmaceutical industry and government agencies that allow it.

I am so happy you are maintaining well at this time.  Sounds like a lot of hoops and tests to get to this point.

You have no doubt been guided and blessed.

Stick with the guidance of the Lord and he will continue to carry you when you need it.

J.G. you are a brave girl and so positive. 

Always let the Lord be your constant guide and you will always have the best possible response.

Thank you for sharing your story.  Just know that another girl will be able to avoid what you have been through because of it.

There are physicians with expertise in healing from Gardasil/Cervarix/Silgard injuries.

Here is a Featured Doctors link and Sane Vax has wonderful doctors listed at their site as well.

I wish you all the best on the this journey.

 Fair thee well.  your friend, jen

There’s some boys that want to sing a little song to you.  🙂

Blackmail and the Medical Vaccine Exemption#android#iPad#retweet

 

By Barbara Loe Fisher

Vaccine risks for you or your child can range from zero to 100 percent depending upon the genes you were born with; your microbiome DNA; the environment you live in; your age and health at the time of vaccination, and the type and how many vaccines you get. 1 2

Vaccines are not safe or effective for everyone because we are not all the same and we do not all respond the same way to pharmaceutical products like vaccines. 3 4

Our response to infectious diseases and the risk for complications can also vary, depending upon our genes, environment, and age and health at the time of infection. 5 That is why malnourished, vitamin deficient children living in impoverished environments, for example, are at higher risk for complications from gastrointestinal, respiratory and other childhood infections. 6 7 8

The doctor or nurse giving vaccines to you or your child does not know whether the odds will be in your favor. You may get vaccinated and have no reaction or your immune system and brain function could be severely compromised. 9 10 The scientific literature is clear…

Continue to the Article Here

http://www.nvic.org

Mold and BioToxin Illness#android#retweet#iPad

Hear what one of our sharp Featured Doctors has to say in the following clip. She is joined by other physicians that have had success worth studying further.

Dr. Dashore, having spoken at some of the biggest Lyme conferences, has now turned some of her attention to an equally formidable foe, mold. This is a huge problem all over the world, but particularly in the Northeast of the United States, where we have the combination of lots of precipitation and old wooden houses.

In this podcast you will learn

  • The new data on the scourge of mold on chronic disease
  • The common symptoms associated with mold toxicity
  • Best testing, protocols and tips for adding mold strategies to your practice

http://functionalforum.com

March 2015 Settlements in Vaccine Court: 117 Vaccine Injuries and Deaths#android#iPad#retweet

by Brian Shilhavy
Health Impact News Editor

The Depart of Justice issues a report on vaccine injuries and deaths every quarter to the Advisory Commission on Childhood Vaccines (click on “Meeting Book PDF – 11 MB” and start reading at page 51.). This March 5, 2015 report states that there were 117 cases for vaccine injuries and deaths compensated from 11/16/2014 to 2/15/2015.

92 of the settlements were listed in the report, giving the name of the vaccines, the injury, and the amount of time the case was pending before settlement. Five of those settlements were for deaths linked to vaccines, with three deaths related to the flu shot. 73 of the 92 settlements were for injuries and deaths due to the flu shot, and the majority of flu shot injuries were for Guillain-Barré Syndrome.

These quarterly reports on vaccine injuries and death settlements from the U.S. vaccine court are seldom, if ever, reported in the mainstream media. We report them here at Health Impact News. Here is the March 5, 2015 report…

Continue to the Article Here

http://healthimpactnews.com

Managing Mitochondrial Dysfunction#autoimmune#cdcwhistleblower#asd

I am pleased to share this recent article written by one of our Featured Doctors, Dr. Jodie Dashore.  A doctor that is leading the way in accurate diagnosis and in treating the root cause of illness. You can read a short segment below. 

The “powerhouse” of the cell and its implications for children with autism and other chronic conditions.

Managing Mitochondrial Dysfunction

clip_image002

Dr. Jodie A. Dashore OTD, MS (Neurology), OTR/L, SIC, NDTC, TLPC, BOMC

Board Certified Doctor of Occupational Therapy

Member International Lyme and Associated Diseases Society

Clinical Director

11 Burlington Drive, Marlboro, NJ 07746

Phone: 732 772 1989; Fax 732 333 4526

While Mitochondrial Disorders (MD) are known

to be genetic in origin, over the last few years

research has also looked into identifying epi-genetic

triggers like vaccination, emotional trauma, etc.

Studies show that MD can be a predominant genetic

complication in many children diagnosed with autism

spectrum disorders (ASD).

On the other hand, there has been increasing evidence and recognition of “acquired” mitochondrial dysfunction

(not a full-blown disorder) in children with chronic and/or autoimmune conditions like autism, ADHD, ADD,

SPD, Lyme Disease and PANDAS with several environmental, immunological, infectious, and inflammatory

factors playing a role. Studies show that substantial percentages of these patients dis-play several peripheral

markers of mitochondrial energy metabolism dysfunction…What are Mitochondria…

Managing Mitochondrial Dysfunction

BIO

 

Dr. Jodie A. Dashore OTD, MS(Pediatric Neurology),HHP.

Clinical Director

Integrative Neuro-Sensory Associates, LLC

Marlboro, New Jersey. USA.

Member International Lyme and Associated Diseases Society (ILADS)

Member North American Association of Homeopaths

Member American Association of Drugless Physicians

Office 732 772-1989

Dr. Dashore completed her specialization in Neurology in 1991 from King Edward Memorial Hospital and Medical school in Bombay, India.  In 1992, she went on to complete research collaboration on Stroke and Cognitive deficits and working as a consultant for the NHS in London. Subsequently she immigrated to the United States to earn her Doctorate in Occupational Therapy- Evidence Based Medicine and Neurology from Rocky Mountain University in 2004. She went on to complete her Post- Doctoral dissertation in Sensory Integration from University of Southern California.

Dr. Dashore is currently a Board Certified Doctor of Occupational Therapy, specializing in Neurology. Dr. Dashore is also Board Certified in Sensory Integration, Holistic and Energy Medicine and Homotoxicology. She has obtained additional training in the areas of Tick Borne Diseases, Nutrigenomics, Herbalism, and Neuro -Immune Syndromes. She is currently training to be a Board Certified Herbalist.

She is an esteemed member of the International Lyme and Associated Diseases Society (ILADS), and The North American Association of Homeopaths (NASH). She has trained intensively and continues to stay current and mentored by Dr. Charles Ray Jones, MD, and Dr. Dietrich Klinghardt, MD, PhD. Dr. Dashore is the founder and Medical Director of Integrative Neuro-Sensory Associates, LLC , a functional medicine and Sensory Integration practice in Marlboro, NJ. She works with children and adults from across the country with  Autism, Lyme Disease, PANDAS, Methylation Dysfunction, Mitochondrial Disorders, IBS, chronic fatigue, Neuro- Degenerative Diseases, Allergies, Autoimmune Disease, and more.

www.mysptc.com/#

 

How Does Healthy Look? Simple!การมีสุขภาพที่ดีจะรู้ได้อย่างไร? ง่ายนิดเดียว!#Health#retweet#สุขภาพ ที่ดี

I recently spent a couple of weeks visiting with Derek and Indy.  I have known them to be very health-oriented, and well over the years.  To see their daily lifestyle up close was very unique, and I would like to share some of the best points with you. 

Their routine is very simple, and greatly benefits them day in and, day out. They share a blog picture into their life in the link below. There is a Thai translation included as well.

Derek and Indy’s Healthy Lifestyle

To find out more, you can visit: www.indyslifestyle.com

เมื่อเร็วๆนี้ ดิฉันได้มีโอกาสเยี่ยม เดเรคและอินดี้ เป็นเวลาหลายสัปดาห์ ทำให้ดิฉันได้เรียนรู้ว่า พวกเค้าทั้งสองเป็นผู้ที่รักการดูแลสุขภาพให้มีสุขภาพแข็งแรงสมบูรณ์ มาเป็นเวลานานหลายปีแล้ว จากการที่ดิฉันได้เห็นการใช้ชีวิตประจำวันของพวกเค้าซึ่งมีสิ่งที่พิเศษน่าสนใจอย่างมาก และทำให้ดิฉันอยากแบ่งปันสิ่งสำคัญและน่าสนใจนี้กับพวกคุณด้วย

กิจวัตรประจำวันของพวกเค้าเป็นวิธีที่ง่ายไม่ยุ่งยาก และเป็นประโยชน์อย่างยิ่งต่อพวกเค้าในทุกๆวัน พวกเค้าแบ่งปันเกี่ยวกับชีวิตประจำวันและรูปภาพของพวกเค้าไว้ในเว็ปลิงก์ด้านล่าง และในเว็ปลิงก์มีทั้งสองภาษาไทยและภาษาอังกฤษด้วย

ไลฟ์สไตล์เพื่อสุขภาพของเดเรคและอินดี้

หาข้อมูลเพิ่มเข้าไปได้ที่

www.indyslifestyle.com

Is “silent” autoimmunity causing your mysterious symptoms?#iBelieve#autoimmune#follow

Insightful article from one of our functional featured doctors

Autoimmune disease has become frighteningly common today. This degenerative condition, which can affect any tissue in the body or brain, happens when the immune system attacks and destroys the body as if it were a foreign invader. Chances are either you or someone you know has an autoimmune disease. Some of the more commonly known autoimmune diseases include Hashimoto’s hypothyroidism, multiple sclerosis, lupus, rheumatoid arthritis, type 1 diabetes, celiac disease, and psoriasis.

Although the statistics for autoimmune disease are alarming enough — it affects one in five people, the majority of them women — these numbers do not tell the whole story. The truth is the autoimmune process typically is underway long before the tissue damage is advanced enough for it to be diagnosed as a “disease.”

In fact, some people go an entire lifetime suffering from the symptoms of an autoimmune reaction that never progresses to the disease stage. This is because tissue damage and symptoms have to be quite severe or life threatening before conventional medicine can offer remedies in the way of steroids, chemotherapy drugs, or surgical removal.

This means untold numbers of people suffer from autoimmune reactions that cause symptoms but are not advanced enough to be diagnosed as disease. This creates confusion and frustration for the suffering patient.

For instance, someone with an autoimmune reaction to the pancreas may struggle with keeping her blood sugar stable despite eating a very good diet. This is because she is on the path to possibly developing type 1 diabetes. It’s estimated 10 percent of those with type 2 diabetes, a lifestyle-induced condition, also have pancreatic autoimmunity and thus markers for type 1 diabetes autoimmunity. Another example is autoimmunity that causes hypothyroidism — Hashimoto’s hypothyroidism. Patients are given thyroid hormone in ever increasing doses but are not instructed on how to dampen or halt the autoimmune attack on the thyroid gland.

People can also have symptoms that suggest multiple sclerosis, arthritis, brain disorders (depression, anxiety, loss of balance, loss of memory, etc.), poor adrenal function, irritable bowel, and others because their immune system is attacking the glands or tissues associated with those symptoms. However, the tissue destruction is not advanced enough to be labeled as a disease and hence medicine has little or nothing to offer.

Fortunately, functional medicine shines in this arena. Specialized lab testing can determine whether autoimmunity is affecting a number of different tissues. Testing can identify (or rule out) the source of chronic, mysterious, and undiagnosable symptoms, such as chronic fatigue, chronic pain, declining brain function, gastrointestinal issues, hair loss, weight gain or weight loss, and more.

This information can validate patients who have long been dismissed or belittled by their doctors for “making things up.” Testing can also uncover autoimmune reactions that are not causing any symptoms. For instance, a person may be producing antibodies (an autoimmune marker) to the sheaths that coat the nerves. In its progressed stage, this becomes multiple sclerosis. Knowing this kind of information can give you more incentive to avoid inflammatory foods and pursue other lifestyle choices that may lower your risk of that silent autoimmune reaction becoming a disease.

In functional medicine we use a variety of strategies to dampen autoimmunity and relieve symptoms. These strategies include an anti-inflammatory diet that removes foods to which you are sensitive and stabilizes blood sugar, minimizing your exposure to toxic chemicals and metals, adopting lifestyle habits that minimize stress and maximize well being (socializing, exercise, play time, laughter, etc.), and the use of natural compounds that dampen inflammation and support the balance of immunity, stress, gut health, and blood sugar.

Ask my office for more information.

drflannery.com

HPV vaccines are NOT good for everyone#Vaccines#HPV#iBelieve

HPV vaccines are NOT good for everyone

By Mara Mexia, Mexico City

HPV Vaccines were not good for me.

I ask you to please read Yael Leycegui’s story. She is my daughter and one of the unfortunate girls who suffered a severe reaction to the HPV vaccine, Gardasil. I write because only one side of the HPV vaccine story is mentioned before you receive the injections in my country, and many others. You only hear how wonderful it is because it could prevent cervical cancer. There is little mention of potential side effects. When they are mentioned, you are told the vast majority of them are minor.

I write asking for your help to alert the population to the fact that side effects associated with HPV vaccines pose a serious threat to some girls. My daughter was obviously one of them. ­I wish we would have been warned.

Our bitter experience:

On February 28, more than a year ago, my 12 year old daughter was injected with her third dose of Gardasil. Four days later Yael could no longer move her arm on side where the shot was given. Her arm was swollen and very painful. We went to the doctor and he told me that it was a rare reaction and she was prescribed cortisone. The problem continued in spite of the cortisone. After 15 days, pain appeared on the other arm and the leg.

In March, my daughter could no longer eat by herself because she did not have enough strength to lift a glass or close her hand around the silverware. By April, she was suffering with terrible and disabling pain throughout her body. She needed a wheelchair to get around and was totally dependant on her family.

In order to rule out disorders like Lupus, Autoimmune Reactions, Arthritis, Guillain Barre Syndrome, and others, my daughter was subjected to diagnostic tests of all kinds including a Lumbar Puncture, EEG, resonances, hair follicle test for metal exposure, and an Electromyography … all of them were very shocking.

She went through all of these just to find everything was normal and had no abnormal results except for a high concentration of aluminum. Everything else came back normal. She was diagnosed a “probable adverse reaction to the HPV vaccine”.

Before Gardasil, my daughter was a healthy, happy and active girl, and outstanding at school. She used to go swimming, running, cycling, skating, dancing, etc.

Now, a little over a year later, Yael is not capable of attending school because of the incapacitating pain. There are still days when she needs help to get out of bed and go to the restroom or take a bath. Sitting and writing prove really hard for her. Sometimes, she goes out for a walk out of the house and has to come back with us carrying her.

In October, I was told that she had Fibromyalgia so I took her to a well-known doctor who has been treating this disease for years, DOCTOR MANUEL MARTINEZ LAVÍN. He is considered an authority on the condition.

He told me that my daughter does not have Fibromyalgia, that it all looks very related to the vaccine ….

Then, I started looking on the internet and finally found an association of people who have been affected by HPV vaccines in Spain, the AAVP. I decided to make contact. It turns out there are more cases like my daughter, that doctors ignore. The doctors say that the vaccines carry risk, yet they do not warn parents so they can make an informed decision prior to administering the vaccine.

Some say adversely affected girls are just statistically insignificant – that serious reactions are extremely rare. I am here to say, ”My daughter is not simply a statistic, nor is her life insignificant. Gardasil was NOT good for my daughter. ”

There are about a hundred strains of the HPV virus and the vaccine given to Yael only contains four. My daughter was affected and her life ruined by a “protection” against two strains of a virus that may or may not have caused cervical cancer for her and two strains that cause genital warts.

In any case, the condition(s) could be readily detected and easily treated without subjecting her to the risks involved with HPV vaccines. Risks that no one warned us about.

As it turns out, there are girls similarly affected all around the world – Colombia, Spain, Argentina, Mexico, Denmark, just to name a few. Girls who are going through the same thing as my daughter. Girls who have been misdiagnosed, ignored, or told they have psychiatric disorders or that their families are inventing their problems. This is not acceptable!

Girls around the world are crying for help

I hope you can help me do something. I hope you are among the few people who have the courage to help get the truth out there. Every parent in the world must act in solidarity.

HPV vaccines are very dangerous for some people. They have not been proven to be effective because they haven’t prevented any cases of cervical cancer this far.  Who knows whether or not they will in the future.

What I do know is HPV vaccines have caused untold pain, disability and death to many healthy girls around the world. Japan and India have already stopped recommending them. In France and Spain there are already many cases filed in court seeking justice for the injured and their families.

Please, help make parents aware of the potential risks. Parents have a right to make the decision to vaccinate their girls or not, but only after being properly informed.

My daughter is not an isolated case. Simply do an internet search for “HPV vaccine adverse reactions”.

PLEASE Share our story – give other girls a chance; a chance my daughter never had. Don’t allow other girls to suffer like my daughter has. Help our voices to be heard around the world.

Article in it’s entirety is compliments of SaneVax.org

Maria, I am so sorry that you, Yael and your surrounding family have experienced such a horrific trial.  I am glad that Yael has such a tremendous, and supportive mother.  You are shining a light of truth that will spread far and wide.  Thank you for sharing your story so that others can avoid the medical/pharmaceutical crimes taking place.

Yes, Yael is Significant, and the immense risks of the HPV vaccine should have been disclosed so that she had a choice.  As you can see from your research, the HPV vaccine has not prevented one case of cervical cancer. 

I hope your family receives plenty of support at this time, and thank heavens you have heard of SaneVax.org.  They have contacts the world over that are experts in healing from the damages of this vaccine. Here are some contacts I have as well.  Distance is not a problem.   Blog Featured Doctors

May God be with you.  Miracles do exist today.

Below is a clip of a talented group with a gifted solo vocalist.  I hope their music can lift your hearts, and help you take your mind off the pain for awhile.  Your friend and sister in truth, jen  🙂