Gardasil: Destroyed and Abandoned#android#Ipad#retweet

By Lidia from Donegal, Ireland

Gardasil: Destroyed by the vaccine; abandoned by the medical profession

I am 16 years old. For me, everything started a few days after I received the HPV vaccine, Gardasil. I woke up one day choking and unable to breathe. I felt like I was going to pass out so my parents took me to a hospital. I was stabilized, kept overnight and sent home, just like that. No tests, no medications, no explanations as to what could have caused the problem. This was only the beginning.

First it was just trouble with breathing, nausea, and feeling faint. Every doctor I saw dismissed me with, “Well, you’re breathing now.”

Then it progressed to choking, hyperventilating, panic attacks and soon enough I was getting panic attacks every day, sometimes as many as four times a day.

Then the depression came. This is going to be hard to talk about, as it still triggers a lot of anxiety and depression in me, but I will try my best to tell as much as I can.

Going to psychologists and psychiatrists didn’t help at all. All they ever told me was to “take a relaxing bath,” “light some nice smelling candles” and “go out with friends”. I tried all those things. I tried every single thing they told me to try and yet none of it worked. Still, they didn’t seem to care about that and kept telling me to try the same things again and again.

Many times I’ve been told to “think about all the people that have it worse than me” and many times people laughed after I expressed my thoughts or feelings about a certain topic.

The psychologists were late to every appointment and talked about everything with a passive attitude as if I was exaggerating and making everything up.

One of the doctors at a hospital told my parents the reason all this was happening to me was because I’m “troubled.” She said it even though I was in the room.

Another doctor stood by my hospital bed as I screamed and cried in pain because of back spasms and watched me for about ten minutes before simply walking away. I didn’t receive any help that time, no painkillers, nothing. I just stayed in my bed until the spasms passed.

A few months later Dad and I went to the same doctor for a check-up.  As he flipped casually through my medical file he said “I don’t have any record of pain written down here from that time” and shrugged his shoulders.

Another doctor, a substitute for one of my psychologists, was somehow convinced that my parents were abusing me regardless of the fact that I told him that wasn’t the case every time we met for an appointment.

Every doctor we went to dismissed us and tried to get rid of us.

Overall, I just felt useless, hopeless, and broken. I felt guilty – like all that was happening was my fault somehow. When I didn’t feel like crying my eyes out, I felt completely nothing and sat still, staring off into space.

The amount of times I imagined myself dying is terrifying. I was scared of myself. I was scared that I would lose control and start screaming and breaking everything around me from all the pain, terror and anger. Yes, I was angry – I was really angry! Angry that my feelings were so easily dismissed, as if they were something you can pick up, explore for a little while and toy with a little, before being thrown in the trash.

When it comes to physical symptoms…there were a lot. There still are, they still come back every so often.

There were hallucinations of a girl named Trillion who hit me. There were episodes where my body would switch itself off and I’d be left unable to move, speak, swallow, blink and yet still able to feel and hear everything around me. That could last from ten minutes to eight hours. My legs would become paralyzed, for periods lasting from thirty minutes to four days.

I couldn’t go out at all, unless I wanted to risk an anxiety attack so bad I would have to return home within half an hour of being out of the house. Being around people made me anxious, it still does.

Once I felt so bad, so depressed, and so angry that I cut into my arm with a needle. I regretted doing that instantly. I still get an urge to do it, though it’s faint.

I genuinely had to force myself to want to live. I wanted to disappear. I wanted all of the symptoms to stop.

Now without a doubt, I can say that I am a lot better. I have been taking homeopathy remedies for a few months. They have helped more than all of the anti-depressants I was prescribed for two years.

Perhaps soon I can leave Gardasil and the past behind me. Maybe I can have a normal life after all.

Article compliments of www.SaneVax.org

Lidia, thank you for writing your story. You are a brave girl. 

It is hard to hear that you are sixteen and enduring this trial at this time of your life.

You have been let down by many in the medical field, I am sorry for this.  This is not the way anyone should be treated, let alone at your age. I am amazed at how strong you are. 

The good news is that you can help guide others through sharing this story.  

There are also health practitioners that have listened to the quiet guidance within and have found ways to heal, at different levels, those who have been injured.  If you contact any of the physicians in the links below, I think you will find them to be far more understanding and helpful than your previous experiences.  I can’t say enough about these practitioners.

Sane Vax has a Medical listing and this is a link to my Featured doctors, who have experstise in working with individuals who have encountered vaccine injuries.  Distance is not an issue with many of them.  Just feel free to send them an email.

I would love to hear how things go.  I am a big fan of homeopathy and am happy to hear you have found some remedies that are working out well for you.

Remember to keep your Creator at the helm and you will have all the guidance you will ever need.  

Just know that many of us are praying and cheering you on from all around the world.

Here’s a little artistic clip that I hope takes your mind off things for awhile. 

your friend, jen

 

I want my daughter’s life back the way it was before Gardasil#android#iPad#retweet

By Ann Fitzpatrick from Carlow, Republic of Ireland

GardasilI Impact

My daughter turned 15 in February of 2015. Once she had lots of friends and participated in many activities  both in school and at home.  She did Irish dancing from 4 years of age, played football for her parish and county, and was awarded 2nd place in the world handwriting competition. She was great in school. In short, she was healthy, active and happy.

All of that changed shortly after she got her first injection of the HPV vaccine, Gardasil in October 2012.

By November she started having seizures. Since then she has had chest pains, vision problems, non-epileptic seizures, low blood pressure,  inflammation of the stomach and small bowel, reflux, is very tired and has no energy.  She has a pulse rate that can go up to 216 just walking 10 feet, or 178 sitting down. She has been told so many things by doctors in the last 2 1/2 years that she does not even want to go near them anymore

In April 2013, due to the number of seizures she was having at school, she was told by the school administration that she wouldn’t be allowed to attend anymore ‘for health and safety reasons’. They said that she should be home-schooled instead. So my daughter went to the papers and told her story.  She let people know that she wanted to go to school and that they could not stop her. She is now in Junior Cert year but has only got 5 hours a week of home schooling.

I have reported the HPV vaccine connection in every hospital Carol has been in over the last two-and-a-half years. I reported the connection to the HSE and Medical Council.

I was told by an American neurologist that was over Carol that if Gardasil did not cause her new seizures, it contributed to them.

All I have heard from other doctors is that she is a complicated case. Even at the start of her seizures, one Doctor in Kilkenny said he would not like to take her on. Then we had other doctors trying to make out it was all in her head who then sent her to people who told her they could not help her.

In my opinion it’s them that need help. They need to open their eyes and see what the health system has done to a child. Two and a half years and  still they have no answers.

No words can express how I feel about all of this. I just want my daughter’s life back the way it was before she got this injection. I want the support of our health system. I want them to do whatever tests and treatments necessary to help her recover her normal life.

Read this article in French here.

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

Ann and Carol, I am amazed by your fortitude and determination.  I am glad that you are getting your story out.  It will undoubtedly help others.

It is a shame that Carol has not been more assisted and supported by her school and doctors. 

I hope and pray that doors will open and she will have all the support she requires in those areas.

Here is a link to doctors that have experience treating in this area. Featured Doctors

I am so grateful that you have a connection to www.SaneVax.org They are kind and experts in this area.

Hang in there and pray every day.  The Lord will hear your prayers and guide you all along the way.

Here is a little musical gift.  I hope it lifts your hearts.

your friend, jen

 

Gardasil Survivors in Ireland Launch Support Group#android#iPad#retweet

Are Gardasil and other HPV vaccines causing the greatest epidemic of 'conversion disorder' the world has ever seen?

Members of ten families from all over the country came together to share experiences and express their exasperation at the inability of health authorities to recognise the pattern of serious adverse reactions being suffered by children who, up until receiving the Gardasil injection, enjoyed an active healthy lifestyle. One of the main complaints raised at the meeting was that the information provided by the HSE (as part of the ‘informed consent’ process) is extremely misleading, particularly with regard to how safe the vaccine is.

A high incidence of serious reactions have been reported in the U.S ever since Gardasil was released there in 2006. Even the drug manufacturer’s own clinical trials reveal a 1 in 40 (2.5%) incidence of a serious adverse reaction*, yet Irish parents are still told by the HSE that Gardasil is ‘very safe’.

Although its cancer-preventing properties have never been proven, the HSE insists that the benefits of Gardasil outweigh the risks and even claim that it has been ‘fully tested’. This is despite the limited safety testing that took place as a result of this “life-saving vaccine” being fast-tracked through the regulatory approval process. HSE did not inform parents that Gardasil contains genetically engineered non-human recombinant DNA, the effects of which are unknown and unpredictable when injected into a human host.

The types of long term debilitating health conditions reported by Irish parents have in many cases meant that the girls are unable to continue their education in school. Because of the nature of the chronic illnesses, Irish doctors and consultants are unable to offer any effective treatment. With 1 or 2 rare exceptions, medical professionals dismiss these serious reactions as unrelated to Gardasil and merely coincidental. When tests come back negative, parents are often told that their girls simply have psychological/psychosomatic problems.

The group also launched the website www.Regret.ie, where parents can read first-hand accounts from Irish victims and their families. The site is a focal point for raising awareness among other parents whose daughters have yet to receive the injection, with the schools vaccination program set to resume in September.

The group can be contacted at Support@Regret.ie

According to Catherine Weitbrecht, spokesperson for R.E.G.R.E.T.,

Since the the group was formed, 4 new parents with daughters injured by Gardasil have come forward via the website to join our group. 2 of these stories are particularly horrendous. One is so depressed she has to be watched 24/7;  the other has a bleeding disorder so bad that she could literally bleed to death if she has a small accident. The third girl had POTS and the fourth has seizures.

It seems Gardasil and other HPV vaccines are causing the greatest epidemic of ’conversion disorder’ the world has ever seen.

*According to the FDA a serious adverse event must fit one of the following criteria: death, life-threatening, hospitalization, disability or permanent damage, congenital abnormality/birth defect, or the requirement to intervene to prevent permanent impairment.

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

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