Honeychick Homestead

Homestead, Health, and Happiness


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Cosmo Mom’s Lyme Story

One neat thing about starting a blog is I’ve been introduced to some new, and informative blogs. I found Brandi’s blog, Cosmo Mom with a Twist of Lyme shortly after I starting blogging. Her Lyme story highlights how much “Lyme denial” exists in the medical field. It’s disturbing that she knew she had been bitten, and still had several doctors tell her she couldn’t possibly have Lyme Disease.

She was diagnosed in 2011 and continues to be treated for Lyme and co-infections. Her blog has lots of information about Lyme Disease, and great stories about her family. She recently wrote about running her first 5K! I would appreciate if you took the time to read her story, and her blog.

Here’s Brandi’s Lyme Story


 


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The “Fun” of Traveling While Treating Lyme

 

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This picture is everything “Lyme related” I needed to pack for our trip. I felt compelled to share this, not because I’m complaining butI hope it will encourage EVERYONE to be vigilant about protecting yourself from ticks.

I don’t want anyone to ever have to deal with any of this! Believe me, you don’t want to experience this mess. Tick population is expected to increase as global warming intensifies, more ticks = more Lyme Disease. If you do get bit, see a Lyme Literate doctor immediately. They will treat you correctly and minimize the chance of developing last stage Lyme Disease.

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Angeli VanLaanen’s Lyme Story

In honor of Lyme Disease Awareness month, I’m sharing Angeli Vanlaanen’s recent Facebook post. She competed the Sochi Winter Olympics, and is an inspiration to me! Her story was featured in a short (9 min) documentary, that’s worth watching. Share to help spread awareness about Lyme Disease! Don’t forget to protect yourself and your loved ones while enjoying the great outdoors! Here’s her post from Facebook.

November 2009. While driving the support vehicle for#CycleForACause, a road biking trip/fundraiser along Highway 101, I received the call from my doctor about test results. A call that changed my life forever. Self portrait on the Oregon coast from the day I was diagnosed with Lyme Disease.
May is #LymeDiseaseAwareness month. Help spread the word by educating your family and community. Knowledge is power and If caught early #LymeDisease can be treated more effectively.

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Take Action!

LymeLight Foundation  provides grants to help kids and young adults fund their treatment for Lyme Disease. Thank you for reading my post!