GARDASIL Vaccine Warning

I have always been put off to many of the vaccines they are coming up with. I am a proponent of researching and reading on ANY Vaccine in DEPTH before you even consider it, even for a child. We just vaccinate because we are told we have to. We dont, and even to get into school you dont. There are waivers.

Anyways I read a story on Gardasil the other day off Yahoo, from there I read about others who have died as a result, teenage girls. There is now talk of this vaccine being given to boys also.

DONT

READ! Do your research!

That girl is still alive…. but this girl didnt make it… Jenny Tetlock

http://shine.yahoo.com/channel/parenting/did-gardasil-kill-jenny-tetlock-494571/

When did Jenny start showing symptoms or signs that something was wrong?

Barbara: In May 2007, Jenny came home from school one day having tripped over a hurdle in P.E. class. It was 1 and a half feet high. All the other kids cleared it easily. A few days later, she tripped again on the same hurdle and fell on her knee. She hurt it badly, and stayed home for a few days. Then she developed a limp that never went away. With some degenerative neurological diseases, you can lose as much as 40% of your motor neurons before you even begin to show weakness. That may have happened to Jenny.

We thought it would get better, but when it didn’t, we went back to her pediatrician. We thought, perhaps her legs were different lengths. But no, the doctor said things were fine and gave her strengthening exercises. A month or two went by and we didn’t see any improvement. The pediatrician suggested sports therapy. We went to Children’s Hospital in Oakland and started several months of physical therapy in August 2007.

In October 2007, things weren’t getting better. She then went to a pediatric neurologist, who started tests. In December 2007, we took her to another specialist at Children’s Hospital in Philadelphia, PA. He immediately started treatment for multifocal motor neuropathy. Jenny received IVIG (intravenous immunoglobulin). We went home and followed up with a specialist at UCSF. The treatment wasn’t working. She was getting weaker. By that time, she was falling too much and went from crutches to a walker. She started taking steroids. That didn’t seem to work either. We still didn’t know what the problem was, and we hoped the Philadelphia doctor was correct in his diagnosis. He thought she’d eventually recover in 9-10 months after extensive treatment.

In January 2008, we took Jenny to Children’s Hospital in Stanford. The Stanford doctor immediately put her in the hospital to do testing, imaging, biopsies, and more. We stayed there for two weeks, but the treatments didn’t seem to help. After being home for a few weeks, we went back for a few more weeks. Meanwhile, Jenny was losing her ability to hold herself up. She tried going back to school with an electric scooter, but it was just too hard. She couldn’t even write or take notes. She stayed home with a tutor. We were going to the hospital and seeing many different doctors to figure out what was going on. Jenny started new treatments — chemotherapy in March 2008. We didn’t see any improvement at that point either.

Around April, we noticed that her breathing was compromised. Her FVC (forced vital capacity) was about half of what it should be. Eventually she needed help with breathing, so she went on a noninvasive ventilator. She was also given a feeding tube.

In June/July 2008, we tried to figure out how to adapt with life at home. We had nursing help. Jenny was losing her ability to turn over in bed. I slept with her and turned her whenever she wanted, trying to keep her happy and comfortable. By now, she was in bed most of the time. We had two goals. One was to find a cure, and the other was to maintain her quality of life. We wanted to keep her busy, happy, and distracted. Friends, family, and specialists came by. We had wonderful friends helping us look for other children who were similar to Jenny. We set up a website. We reached out to doctors all over the world to find treatments, experimental drugs, and medications. We tried so many things. Sometimes we thought she was getting better. Maybe the disease was slowing down or even reversing. Then she’d get a little worse, and we knew we were wrong.

In August/September 2008, school started. We got a tutor for her and overnight nursing help. Jenny had physical and occupational therapy several times a week. She was using the noninvasive ventilator around the clock. She also had a computer to help her communicate. We weren’t making a lot of progress, although we kept thinking we might be. Christmas was a low point. She felt miserable. There was nausea from the medications and treatments, air in her stomach from the ventilator, and other types of pain. We worked hard to keep her feeling as good as possible.

Her birthday came on January 12th, 2009. At that point, we felt like there was actually some strengthening in her hands. She was getting more control. Then in early March, she started having trouble breathing — despite the noninvasive ventilator. We took her to the hospital and brought her home. But things got worse. On March 9th, 2009, we took her to UCSF. She was losing her voice and her breath was very labored. She died on March 15th, 2009.

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