Story
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<h1 style="margin-top: 0px; margin-right: 0px; margin-bottom: 0.6em; margin-left: 0px; outline-width: 0px; outline-style: initial; outline-color: initial; font-weight: bold; font-style: normal; font-size: 22px; font-family: inherit; vertical-align: baseline; color: inherit; padding: 0px; border: 0px initial initial;"><strong style="outline-width: 0px; outline-style: initial; outline-color: initial; font-weight: bold; font-style: inherit; font-size: 22px; font-family: inherit; vertical-align: baseline; padding: 0px; margin: 0px; border: 0px initial initial;"><em style="outline-width: 0px; outline-style: initial; outline-color: initial; font-weight: inherit; font-style: italic; font-size: 22px; font-family: inherit; vertical-align: baseline; padding: 0px; margin: 0px; border: 0px initial initial;">“Imagine the symptoms of autism, cerebral palsy, Parkinson’s, epilepsy, and anxiety disorders…all in one little girl.” -RSRT.org</em></strong></h1>
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<p>Did you know that Rett Syndrome (1 in 15,000) has no government funding and no drug company funding? No celebrities Tweeting our cause or walking the red carpet at an event to raise awareness. </p>
<p>But there's hope...we're THIIIIIS close to a cure/treatment to this very new, very young brain disease that has made itself at home in our family. </p>
<p>So on Sept 11th, Grace & I are walking the 5k ADIDAS Women's Challenge, London to stand with our sisters and find a cure. It WILL happen in Grace's lifetime. Please help me.</p>
<p><strong>Visit <a href="http://www.graceforrett.com" target="_blank">www.GraceForRett.com</a> to learn more about our Gracie.</strong></p>