Category: Seizures
I want my daughter’s life back the way it was before Gardasil#android#iPad#retweet
By Ann Fitzpatrick from Carlow, Republic of Ireland
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
Maine Doctors Testify That They Are Unqualified To Vaccinate Patients#android#iPad#retweet
By Ginger Taylor
So I wrote this bill…
Last summer a reporter I had never heard of from the Portland Press Herald called me about vaccine stuff. I started with my standard, “First of all I am not anti-vaccine. I vaccinated my children and one of them got hurt…” thing. Then he interviewed me for an hour and I got to discuss all the corruption problems at length. Seemed like an OK interview. But as is the reality of our world, the hack, Joe Lawlor, turned out to be a poor man’s Mnookin, and “Ginger Taylor, an anti–vaccineadvocate from Brunswick…” Cut to two weeks later and look who is sitting on a dais with Paul Offit at the National Press Club being held out as an example of exactly how to journalize right on vaccination. After writing ONE story on vaccination. (Lawler is the new Offiteer on the beat… will he soar like Seth “I hate my mother’ Mnookin to teach science journalism at MIT or become he head of a media strategy group serving Eli Lilly and GSK like Trine “Cupcake” Tsouderos … stay tuned and find out.)
There have been half a dozen propaganda pieces by Lawlor since then, all working to get people excited about the HUGE new opportunity we have to get rid of measles in Maine by restricting vaccine exemptions. Well, I mean, there hasn’t been a measles case in Maine in 18 years, so we are not so much trying to get rid of Measles as much as we hope that removing the rights of parents will help us achieve negative measles in Maine. That way if we still get a few cases of measles, we can still have no measles. You have to stay hyper vigilant, you know. Measles is only a tea cup ride away…
Gardasil: When will our nightmare end?#android#iPad#retweet
By Martin, County Meath, Republic of Ireland
My daughter, Abbey, was a healthy happy 13 year old when she started secondary school. On the 22nd September 2014 she received her Gardasil vaccine along with the Tdap vaccine in school. She had an adverse reaction straight away. For over an hour, she was left lying on a mat on the floor while the rest of the girls were being vaccinated.
During this time she had seizure-like jerking, rolling eyes, blurred vision, headache, nausea etc. Eventually after an hour and twenty minutes we were called to the school to pick her up. No ambulance was called. The school administrators were not informed this episode had happened until the next day.
When I arrived at the school and asked why an ambulance wasn’t called,I was told I was OVERREACTING and this would wear off.
The next day, her mother and I thought Abbey was suffering withdrawals. Little did we know our nightmare was only getting started.
Two days after the vaccine Abbey returned to school but took another seizure and was taken by ambulance to Drogheda hospital A&E and admitted for six days.
After loads of blood tests, an MRI, and a lot of scratching of heads she was sent home with no diagnosis and no medication. We were told we would learn to adjust our lives and live with the situation.
Six months later, we are still waiting to see a neurologist.
At the moment, Abbey is not attending school because of her illness. Every day is a struggle thanks to Gardasil. Most days she simply wishes all this would be fixed and she can get back to school.
There has been no help offered from either the school or the health service!!
The vision problems, chest pains and stroke like symptoms continue!! The doctors keep suggesting BEHAVIOURAL problems and panic attacks but we have known our child for 13 years. She has never had any type of behavioural problems as the doctors are trying to suggest.
We have shortened this story a good bit so as not to bore the readers but our nightmare is now over 6 months long…….we can only speculate as to how much longer we must endure.
This article in it’s entirety, is complements of http://sanevax.org
Martin, Abbey and mom,
I am speechless and so sorry you have endured this. What kind of people would treat anyone like this, let alone a child? It’s time for our school, government and health officials to wake-up. No more.
Our youth are the best asset this world has to offer.
The last thing Abbey needs is to have someone tell her this is all in her head. Treat the source, right.
You all are really strong and please know there are many, many wonderful people cheering you on across the world.
Fortunately, you know of Sanevax.org. They have helped many youth and their families to locate doctors with expertise in this area. I also have practitioners within my Featured Doctors section as well. I hope you find a healing source soon and know that you are never alone in this.
Below is a clip that I hope lifts your spirits. Pray always.
God bless, and remember even with all the chaos, and this can be especially hard to do, remember this phrase:
A light heart lives long.
Your friend, jen