Posts in A Story
Featured Artist Arielle Coree, Shares Soulful Words For The Healing Heart: A Collection of Poetry and Soul Musings for Those on a Healing Journey

Within these pages you will find the unfiltered and spirit filled words of my soul. Some of these were written in the depths of depression while others were written to capture the fleeting moments of hope, light and empowerment. Some are directly related to my personal healing journey with Lyme and others are simply a tribute to life in this world as a soulful and highly sensitive woman with dreams larger than the Universe itself. There is no right or wrong way to experience this collection of thoughts.

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The Burden That Blooms: Heart-led Thoughts From the Partner of Someone With Lyme Disease

This isn’t a stance we normally take. This isn’t a perspective that that I’m used to standing in. This isn’t the road I normally walk down when going to share with you a new voice. This isn’t what I’m used to and I’m quite certain it’s exactly what’s needed.

When things aren’t going well, I get caught up in my own thoughts. I retreat. I try and piece together “next steps” that seem somewhat logical and straightforward, only to be adjusted time and time again. Illness, it’s a funny thing, and sometime a selfish thing, as I don’t often think about what those around me must be feeling. Of how they are needing to process. Are they wanting to retreat? Are they also terrified? How are they going to deal with this? How are they going to get through this, too?

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Lyme Isn't a Crutch. It's a Catalyst.

I was diagnosed January of 2014 after my immune system plummeted when I came down with the Epstein barr virus (mono). It was devastating and relieving news all at the same time. I contracted it around the age of ten when I was living in the woods of NJ. For over a decade I was in and out of doctor’s offices running tests and looking for answers. When the tests results came in positive it gave me something to treat, something to work on. Before, I was discouraged and frustrated, shooting in the dark with strict diets, supplements, and palliative measures. I finally knew what my body was screaming at me so desperately trying to communicate. On the outside I look healthy, but on the inside I feel like my body is failing me and at 22 years old that is not acceptable. I have my entire life ahead of me and I will not let this disease change how I live.

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Alexandra Noll

Lyme Disease was honestly just a name for the myriad of problems I had been dealing with since early adolescence. Chronic illness was nothing new; I watched my grandmother slowly slip away from a combination of medical mysteries that included Crohn’s Disease, ankylosing spondylitis, and many others. As a kid, I battled constant headaches and seasonal allergies that worsened after my family moved from Massachusetts to Texas.

I remember having a lot of growing pains and being tired. I never wanted to run around like the other children my age. In 2010, my headaches worsened. My best friend recommended that I try a gluten-free diet, which miraculously cured the problem. I always managed to pick up weird things, like a staph infection on my face after a week of backpacking.

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Laura Ehlers

I was diagnosed with Lyme Disease in early 2013, after ten years of searching for an answer to my chronic migraines which turned into chemical sensitivities, mold sensitivities and neurological symptoms. My health became drastically worse about one month after I married my husband, when I moved into his home- a brand new starter house. You may not be aware that new building materials are highly toxic and give off chemicals such as formaldehyde in the form of a gas. Some people with strong bodies have no noticeable problems with this, but I was not one of those people. My body was so damaged from the Lyme Disease I did not yet know I had, that the chemical off gassing triggered downward spiral. We barely had a newlywed stage and jumped right into "in sickness and in health". The saddest part of this experience for me has been fighting for better health instead of being able to immerse myself into my marriage right away. I'm not able to work full time, because the stress of being mentally "on" for forty hours a week is too much for my adrenals to handle.

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Keri Fisher

Question: Letting go. In the process of being diagnosed with Lyme Disease, what things have you had to sacrifice and let go of? And how do you cope and adjust to this new way of life?

Keri: Letting go is very hard, especially because I really loved my extremely active and on-the-go life, and I miss it. By the age of 26 I had traveled to over 20 countries, lived abroad twice, and earned two college degrees. I find myself saying “before I got sick I did this...” “when I was healthy I was very...” so that type of language and thought implies that I can’t be myself or be who I am because of my symptoms and how this disease has plagued my brain. Besides the stress and pain of being sick, we are sick with bacterias that our government denies and doesn’t even know how to test for or treat! Now that I am out of my brain fog and have my short-term memory back, I adjust and cope by practicing non-attachment from yoga, realize that every moment, emotion, and body ache is fleeting, and I tell myself and my body how much I love them.

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