Posts tagged postthepeople
Giving Back with Dedication + Love: How Ethel Takes on the Obstacles of Living with a Chronic Illness

From curiosity about someone else's illness, to the discovery of her own, Ethel is determined to create a life for herself more than the limitations that this disease can bring; a life where raising awareness for Lyme Disease is in the forefront of her will to keep moving forward. To keep motivating herself and others to pursue dreams and goals that may seem impossible when facing such daunting obstacles. 

This Is Ethel's Story...

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No Matter the Odds: Kaitlin Child's Choice To Live a Life More Than Lyme

Meet Kaitlin.

A determined, resilient, hard working, brave, courageous, and honest woman, who has taken the obstacles that this disease as placed in front of her, and turned them into every reason to live her life to the fullest. 

At thirteen years old, Kaitlin's life was packed full of hospital visits, unanswered questions, and a diagnoses that changed everything; Late Stage Lyme Disease was about the only answer she was given to her seemingly never ending list of questions, and it was an answer that would continue to haunt her for the years that followed, limiting her to a life that was so far from the one she wanted. A life that was scattered with fear, doubt, and an overwhelming sense that this thing, this thing was never going to go away.

This is her story...

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Megan's Two Year "Lyme-iversary"

Two Year "Lyme-iversary"

Written By: Megan (Salo) Breimeier

Today is April 15, 2016 and it is my 2 year “Lyme-iversary.” When I think of the word anniversary, I automatically think of a celebration, a great milestone, an exciting day, but today is just a typical day of the life I’ve been living for the past 2 years. I was diagnosed with Lyme disease on April 15, 2014, after almost 1 year of being passed around from doctor to doctor and enduring countless tests. Despite significant brain fog, I remember the moment clearly. I was driving home from work on a sunny day with the sun roof open. I had reduced to working part time due to a rapid decline in my health. I probably wasn’t safe to drive at the time, nor should I have been checking my phone. I remember seeing a message from my new doctor in Seattle. My heart started beating faster. This was it, the moment I was waiting for, my last resort, my last strand of hope. As I listened to the message, a smile came across my face when I heard that I tested positive for Lyme disease. I finally had an answer, I wasn’t crazy, and my persistence in finding out what was wrong with me had paid off. I could now tell people that I had a diagnosis, it will all make sense, and they will understand.

Little did I know what was in store for me. I quickly learned that this was going to be a very long battle and that Lyme disease comes with an endless list of symptoms, judgment, controversy, and a mountain of insecurities...

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