A Quote by Ally Hilfiger

I believe I got Lyme disease for a reason and if that is to help bring awareness, that is my mission and I will do the best that I can to do that. — © Ally Hilfiger
I believe I got Lyme disease for a reason and if that is to help bring awareness, that is my mission and I will do the best that I can to do that.
In 2013, after a challenging two years of long-term IV antibiotics and six weeks at a clinic in florida, I received the 'Star Light' award from the Lyme Research Alliance for my advocacy and strength to light the way of Lyme disease awareness.
The Centers for Disease Control and Prevention has established highly specific criteria for the diagnosis of Lyme disease: an acknowledged tick bite, the appearance of a bull's-eye rash, and, for those who don't live in a region where Lyme is common, laboratory evidence of infection.
Lyme disease is very debilitating. Being from the East Coast I know Lyme disease is quite common and may lay dormant and may produce flu-like symptoms, as well as neurological issues.
Lyme disease has become a fast epidemic worldwide. I am determined to help find a cure and figure out a way to share knowledge with the millions of people struggling with this debilitating disease.
I saw a video on YouTube of a girl who had very similar reactions to late-stage Lyme disease as I did. And I thought it was crazy. And when I saw her basically have a seizure on camera that looked very much like my seizure I felt, "Oh my god. That's me." And so it was really important to me, and I said to Sini, 'We have to find some way to not just talk about Lyme disease, but to show it.
Speaking out about multiple sclerosis to others who may be dealing with this disease is actually helpful to me as well as, I hope, to others. It builds community, helps bring awareness to MS, and strengthens the MS movement that will ultimately lead to the end of this disease.
I believe everybody has a mission and my mission was to bring children in - that wanted to be in a body that was nutritionally balanced, meditative, emotionally stable, because I believe it has a lot to do with how the child develops.
I believe that illness has led me to a life of gratitude, so I consider Lyme disease at this point in my life to be a blessing in disguise.
I have late-stage Lyme disease. I was misdiagnosed for many, many years and told I had lupus, MS, Crohn's disease, even degenerative arthritis. And finally in 2010, I got the correct diagnosis, because on the last Le Tigre tour, I was having several seizures a day and at times not being able to brush my own teeth.
The only reason I ever shared my health journey with the world was because I felt it to be my duty to sufferers that are bed-ridden and dying because there has yet to be found a proper diagnostic test for Lyme Disease in this country.
I believe evidence is overwhelming that chronic Lyme is a terrible, overwhelming disease, and we need to find ways to treat this. To say otherwise is an inaccurate and unscientific opinion.
I will continue to work in Congress to support Lyme disease research and education through funding for the National Institutes of Health and the CDC.
I will continue to pave the way and share my health journey with the world until I find a cure and proper diagnostic testing for this silent killer called Lyme disease.
In the 21st Century I believe the mission of the United Nations will be defined by a new, more profound, awareness of the sanctity and dignity of every human life, regardless of race or religion.
In the 21st century, I believe the mission of the United Nations will be defined by a new, more profound awareness of the sanctity and dignity of every human life, regardless of race or religion.
We believe that this time of transition will make for a more dynamic Revolution Church, and will help us focus and expand our scope and mission.
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