A Day in the Life of a Lyme Disease Patient

A Day in the Life of a Lyme Disease Patient

Something I find fascinating about life with Lyme Disease is that it looks different for each person. Each person uses different treatment protocols. Our routines change regularly as we add or take away various forms of treatment.

Some of us Lyme Disease patients work outside the home while others are not able to work. I’ve experienced many forms of working while treating Lyme. At some points, I worked full time. Other times, I did work for a full time job from home when I wasn’t well enough to be in the office. During the worst months with Lyme, I was mostly bedridden,homebound, and unable to work. Now I work part time and also do some other work from home.

I decided to document a day of my life while treating Chronic Lyme Disease to give you a glimpse into my life.

This particular day was off to a later, slower start after being unable to get quality sleep during the night. This was one of the more productive days. In the past, before making more progress with my health, I wasn’t able to do much reading or work on the computer. Now, on the better days, I’m able to do a lot more. Each day is different. Some days I exercise. Other days I need more time in bed. Some days I’m alone all day. Other days, my fiancé, Jonathan comes over. This is an average day in my life as I treat Lyme Disease and work on writing/blogging projects.

Lyme Disease - A Day in the Life

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Here’s a day in the life of a blogger who is treating Lyme Disease:

A few minutes after Noon

– Wake up, put a spoonful of coconut oil in my mouth to begin oil pulling.

– Go to my favorite big comfy chair in the office to pray and read my Bible. I’m currently studying Job and also using this Bible commentary.

12:30 p.m.

– Spit out oil and rinse mouth, make a mug of warm lemon water and prepare herbal tinctures.

– Go back to Bible study while drinking lemon water.

12:55 p.m.

– Rinse out mouth from lemon water, take herbal tinctures and other supplements.

– Do a few tasks around the kitchen.

– Make a breakfast protein shake. This time it was Chocolate Vegan Shakeology, but other times I use this kind of chocolate bone broth protein along with almond milk, spinach, moringa, frozen blueberries, and ice.

1:30 p.m.

– Sit down on the couch to drink the protein shake and work on the computer. Do various blog tasks and connect with my friends from Hope*Writers.

2:00 p.m.

– Get up to take more supplements, put Ylang Ylang essential oil in the diffuser, and grab the heating pad.

– Back to the couch to spend more time online replying to emails, checking social media, and creating a few images for Pinterest.

3:20 p.m.

– It’s time for a coffee enema! Eek. For some, the idea of coffee enemas is completely overwhelming, but I have found them to be really helpful for my healing journey. I use this enema kit and this kind of special enema coffee.

4:15 p.m.

– After getting everything ready for and performing the enema, showering, getting ready for the day, and cleaning up enema supplies, I’m exhausted! So I make more warm lemon water and this time add a little sea salt to it. Then I drink bone broth while I rest on the couch.

A Day in the Life of a Chronic Illness Blogger

5:00 p.m.

– My fiancé, Jonathan, comes over and we review Ephesians 4 and 5 before we drive a few blocks to church for a premarital counseling session with our pastor.

5:30 p.m.

– Premarital counseling session.

6:30 p.m.

– Drive back to my house where we eat leftover lentil potato soup that I cooked the other night. Take supplements with dinner.

– When we’re done eating, we talk about life, our relationship, and some misunderstandings we had previously been working through. Life with the anxiety of Lyme Disease can put a strain on relationships, so we are constantly learning how to cope, go to the Lord about our struggles, and genuinely trust each other. Tears are shed on my end, but we end the conversation feeling happy and content!

8:00 p.m.

– Jonathan and I play Dominion – our favorite game!

9:30 p.m.

– Jonathan leaves and I catch up on Voxer messages from Hope*Writers and then check social media while using the heating pad.

– Eat a snack/meal and begin to draft a blog post.

11:10 p.m.

– Eat another snack.

– Just sit and rest for a while.

– Do a couple rounds of DNRS to retrain my brain.

12:30 a.m.

– Take bedtime supplements and go to bed.

So that’s a day in the life of a Lyme Disease patient who is also a chronic illness blogger. :)

 

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  1. The story of my battle with chronic Lyme Disease
  2. Practical application questions and scripture to bring hope
  3. Encouragement for your journey
  4. Personal prayer support at any time!
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Emily Lofgren’s heart beats for authenticity. She craves true connection where we can be real about our struggles and find hope together. Emily became a Christian in college and since then has had a passion for writing in a way that helps others encounter life. Grab your free copy of her eBook Finding Hope Through the Fog.

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2 thoughts on “A Day in the Life of a Lyme Disease Patient

  1. This made me feel better. I should write my own post about a day in the life of a chronic illness special needs mom blogger with two crazy dogs! I made myself tired just writing that.

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