Gardasil Victims Take Legal Action Against Merck Over Miscarriage, Deadly Reactions

When one Australian woman decided to lead the charge against Gardasil maker Merck after experiencing serious adverse reactions, she soon found another 7 Victorian women with similar intentions and experiences. Naomi Snell, a resident of Melbourne, Australia, suffered an auto-immune and neurological attack after being injected with the HPV shot Gardasil. After reading about a Sydney neurologist who exposed Gardasil as a potential cause of MS-like symptoms, Snell realized that Gardasil could be behind her recent health ailments.

She made a timeline of her declining health using reports from her doctor and physiotherapist. What she found was that the events unfolded right after she had received the Gardasil vaccine. At 28 years of age, Snell lost her ability to walk, suffered from crippling back and neck pain, and experienced convulsions that put her life on hold for 2 years. The health issues started soon after receiving the HPV shot in July 2008.

I never attributed it to my vaccine so I went back for my second and third dose, Ms Snell said. My doctors said I was a case for Dr House. They were baffled.

After launching the class action lawsuit against Merck, 7 Victorian women considered joining the case after experiencing similar reactions to the Gardasil vaccine. One woman linked the Gardasil injection to her miscarriage, which occurred afterwards in her local supermarket.

Gardasil has led to thousands of adverse reactions and even death

Naomi Snell is not the first Gardasil recipient to develop adverse reactions. In fact, many before her have actually died as a result of the Gardasil vaccine.

The Gardasil vaccine has a very questionable timeline, riddled with corruption and devastating side effects. Shockingly, the HPV shot led to 3,589 harmful reactions and 16 deaths between May 2009 and September 2010 alone. Of the 3,589 adverse reactions, many were debilitating. Permanent disability was the result of 213 cases; 25 resulted in the diagnosis of Guillain-Barre Syndrome; there were 789 other “serious” reports according to FDA documents.

Merck of course makes no mention of this in their deceptive advertisements, leading consumers to think that the vaccine is safe.

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