A Quote by Yolanda Hadid
The Lyme disease had so severely affected my brain functioning that it was extremely hard for me to think, form sentences, and stay focused.
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I'm the only one in - of my siblings, my mom and my family - that hasn't been affected by Lyme disease. It's been really hard for me because I'm the only one that doesn't really understand it.
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.
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.
My life is raw, authentic, and focused on giving back to the journey God has given me; I want to leave this earth a better place with answers and education on Lyme and invisible chronic disease.
Courtney Love gave me advice on how to stay focused. She told me I have a lot of positivity and I have a lot of light and to just stay on that path, because it's easy to become affected by the negativity.
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.
I had the idea of 'Live From Daryl's House' way before I contracted Lyme disease.
It's hard to edit. It's hard to stay focused. And yet, we know we'll only do our best work if we stay focused. And so, you know, the hardest decisions we made are all the things not to work on, frankly.
Lyme has brought me to my knees; this disease is a silent killer and does not have a face.
But if the brain is not like a computer, then what is it like? What kind of model can we form in regard to its functioning? I believe there's only one answer to that question, and perhaps it will disturb you: there is no model of the brain, nor will there ever be. That's because the brain, as the constructor of all models, transcends all models. The brain's uniqueness stems from the fact that nowhere in the known universe is there anything even remotely resembling it.
Talking to a drunk person was like talking to an extremely happy, severely brain-damaged three-year-old.
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 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.
I've just learned that you can't take this game for granted. You have to stay professional and stay focused and stay prepared to produce and continue to work hard. Nothing's given.
Stay away from those who would hang around you and drink and do drugs. Drugs are not the answer, because you have to remain focused. There is a lot to be had within music, but you have to stay focused.
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