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Lyme Awareness Month, Day Sixteen: A Letter To My Chronic Lyme Disease

May is Lyme Awareness Month--a month dedicated to educating the public on all facets of Lyme disease and other tick-borne illnesses. We thank all of the patients, advocates, and Lyme organizations for their dedication in helping to spread the word and save lives. Here at LymeBrave Foundation, we're taking an unfiltered look at what it's like living with this chronic illness by opening up our journals and sharing the highs and lows of life with Lyme. Join us for our 2018 awareness campaign by helping to #shareyourstory. Contact us to find out how!

 

 

 

 

Editor's Note: The following was originally posted on Cassidy's personal blog, dated October 2016. Check out her profile below to learn more of her Lyme disease story.

 

 

Dear Lyme,

 

We’ve been together for over six years now and there are some things I’d like to say to you.

 

First, I’d like to thank you for taking my life and turning it completely upside down. Thank you for taking away my adolescence and making me grow up way ahead of schedule. Thank you for making me quit my sports, school, and many other activities because you get to dictate my life. I was put up against the harshness of politics, medicine, and money before I’ve even had to face my first college exams because of you. Thank you for giving me no control over my body--giving me the shakes, taking my breath away, giving me nausea, and refusing to let me rest. You’ve made me come face to face with the fact that my life won’t turn out like the fairytale I’d dreamed up, and I now know that that’s the real world. But sometimes, I wish you weren’t so generous.

 

Thank you for making it easy for me to tell who truly cares about me and who doesn’t. You also introduced me to my best friends and my “Lymie” family, and without you I would have never met them. You’ve showed me how strong I am, and for that I actually am grateful. You’ve taken my life and turned it upside down, sideways, diagonal, in every way imaginable.  We met when I was fourteen. Who knows, we may have crossed paths years before that.

 

I’ve come to the realization that we will be together for the rest of my life, but I will no longer let you control me.

 

Sincerely,

 

Cassidy Colbert

 


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Will you show the world you're LymeBrave and join us for our Lyme Awareness Month campaign? Contact us at info@lymebravefoundation.org to find out how you can help#shareyourstory!

 

 

 

 

Cassidy Colbert has been battling chronic Lyme disease for over six years. She now dedicates her time to advocating so no one else feels the burden of this horrible disease.

Want to know more about Cassidy? Find her on social media!

 

Instagram: Lyssaandlymie
Youtube: Lyssaandlymie
Twitter: CassidyMaree30
Blog: thelymediary.wordpress.com

 

 

 

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Become a contributor to the Being LymeBrave Blog by submitting your essay to: info@lymebravefoundation.org!

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© 2018  LymeBrave Foundation, Inc.

LymeBrave Foundation, Inc. is an education and support services 501(c)(3) non-profit organization created by patients, for patients. The material found herein is for informational purposes only and is not a substitute for the medical services or advice of professionals. While we aim to provide emotional support resources to patients and caregivers, LymeBrave Foundation, Inc. makes no representation of warranties with respect to the context of the information herein. LymeBrave Foundation, Inc. is not liable for any damages, including the health and wellbeing of individuals, arising herefrom. LymeBrave Foundation, Inc. is not responsible for third-party content, nor does it recommend or endorse third-party content.

Crisis Lifeline

Lyme patients are at-risk of suicide due to the accompanying decrease in quality of life. If you or someone you love is suffering from depression or suicidal ideation, contact your physician immediately or call the
National Suicide Prevention Lifeline

 

1-800-273-TALK
(1-800-273-8255)

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