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Happy Holidays from LymeBrave!

I remember Christmas of 2012 clearly. I had just been diagnosed with Lyme disease and Babesia that past May and endured what would prove to be the hardest summer of my life. Although I was beginning to see improvement with treatment, the victories seemed few and far between. I was still sleeping twenty hours a day, still feeling the muscle aches and bone pain that bore little relief, still experiencing any number of the dozens of symptoms I complained to my doctor about on a monthly basis.

I still wasn't well.

I stayed at my parents over the holiday that year because I couldn't drive the fifteen minutes to their house. I dragged myself to the dining room, ate a few bites of our traditional dinner, then collapsed back onto the couch. It seemed like my body and spirit were at war with one another. On the one hand, it felt like my body was in decay. On the other hand, I was so grateful to be surrounded by those I loved most, celebrating a holiday that has always been dear to me. I can admit now what I didn't want to face then: There were times over the course of those two days when I wondered if it would be the last holiday I would spend with them, and I wanted to make it count.

I wanted those memories to last.

Fast forward five years. A few short months of remission, one relapse, a reinfection, and two new co-infections later, and everything feels so different. I'm still sick, that is undeniable. But the darkness that once enveloped me--the one that had me clinging to this holiday because I was questioning my future--has been replaced with light, with joy, with hope.

That is what time gives us. That is its greatest gift. Hope. Strength. Courage to appreciate the present and look forward to the future.

Wherever you stand in your battle with Lyme disease, I hope you are able to find some peace and joy in the season. I hope you are able to see the strength in yourself--how much courage it takes to survive this disease every single day. I hope you are able to feel how much love and support you have in this community, that there are people on your side, fighting with you in spirit.

More importantly, I hope that you are able to recognize that there is a light inside of you that this disease can never take from you.Enjoy this holiday with your loved ones. Make those beautiful memories. Keep that fighting spirit alive.

You are meant to be here.

Resources National Suicide Prevention Lifeline

Patients with Lyme Disease and other tick-borne infections are at risk of suicide due to the documented psychological manifestations of Lyme and accompanying decrease in quality of life. If you or someone you love is suffering from depression and/or suicidal ideation, please contact your physician immediately or call the National Suicide Prevention Lifeline (1-800-273-TALK).

Mental Health & Illness: Lyme Disease

​A collection of articles by top Lyme physician Dr. Robert Bransfield as published in the Lyme Alliance Newsletter. These articles focus on how Lyme affects mental health as evidenced in neuropsychiatric symptoms that manifest themselves as familiarly-labeled psychiatric disorders, specifically in the late or chronic stage of the disease. Read his Neuropsychiatric Assessment of Lyme Disease to learn more.

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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 & Crisis Lifeline

 

1-800-273-TALK

(1-800-273-8255)

OR

988

Disclaimer

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.

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