Lyme and a Coconut

chronic lyme disease with a taste of nut

Stemming from Hope

I’d like to preface this blog post by saying the opinions expressed are mine alone. If you have lyme disease and are considering treatment, please see a lyme literate doctor … Continue reading

June 21, 2017 · Leave a comment

When You Change from Lowercase to Upper

I started out writing about my journey to an LLMD. That was certainly noteworthy. Especially the appointments. The antibiotics regimen. The herxheimer reactions. Learning new information about detoxing and how … Continue reading

June 10, 2017 · Leave a comment

Should the Ocean Hit Me

I went on a major field trip today. Walmart. Woohoo! It was really quite the momentous day because I had just gotten a walker thanks to our local thrift store … Continue reading

October 9, 2016 · Leave a comment

A Bee a Day Keeps the Spirochetes Away

Man, I’ve promised you updates eons ago, didn’t I.Well, this is going to be a l-o-n-g blog post so get comfy. I’ve missed you; what can I say. Honestly, things … Continue reading

March 12, 2016 · 4 Comments

A Banner Day: My 4th LLMD Appointment, a Neuro-feud, and a Floating Cat

October 26th, I went to see Dr. W for my check-in. I already knew it would be a banner appointment because Dr. W had gone to the ILADS conference in … Continue reading

November 1, 2015 · Leave a comment

The Air Above and the Water Below

There are a few reasons why someone writing a lyme blog would not write or update in a long time. The reasons are, in my opinion, as follows: They have … Continue reading

October 19, 2015 · Leave a comment

The Horrible Sitcom: Babs & Bart

One, two, three, four, five, six, seven, eight Schemeel, schlemazel,  Hasenfeff Inc Yes, ladies and gents, it’s like a bad sitcom (except “Laverne & Shirley” was a great, classic sitcom!): Bart & … Continue reading

September 7, 2015 · Leave a comment

Lots of Puh-Tewies and a Popdizzy (Just Another Saturday)

Another Saturday night. Another Saturday night in my bedroom herxing “to high heaven,” as my lymie mentor says. She says if I’m herxing to high heaven then that means the … Continue reading

August 29, 2015 · 1 Comment

Wiggin Out at Wal-Mart (and other wiggins)

Shhh… please read this quietly. I can’t write a long post like I normally do. I can’t even stare at this screen too long. I had to write an update, … Continue reading

August 26, 2015 · Leave a comment

Saturday in the Park

Saturday, what a day. Not the 4th of July. My past two Saturdays have not been a picnic in the park. The good thing is that I’ve found a blog that … Continue reading

August 9, 2015 · Leave a comment
Follow Lyme and a Coconut on WordPress.com

Enter your email address to subscribe to this blog and receive notifications of new posts by email.

Join 596 other subscribers

Categories

Invisible Illness Awareness

One Year of Bee Venom Therapy

December 18, 2016
1 year of Bee Venom Therapy!
WIM

A Literary Magazine that gives platform to writers and artists with invisible illness.

LifeLoveLyme

Staying grounded while recovering from Lyme disease

Bloody Lymey

A Blog About Living with Lyme Disease

Lyme, Arizona, and me

My journey in getting treatment for Lyme Disease

The Daily Advocate By Painspeaks

Advocacy is FREE and its never-ending ripples spread awareness for all worthy causes!

The Lymie Limey

A Lyme Disease Blog from Bruce county ontario

lauraslymerecovery

Recovery from Lyme Disease, chronic pain, and fatigue

From Lyme to Life

How the light gets in.

chronicallyhoping

My Journey With Bee Venom Therapy