THE STORY BEHIND THE NAME by lymepoet

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· @lymepoet · (edited)
$1.62
THE STORY BEHIND THE NAME
### WHY LYMEPOET?

https://cdn.pixabay.com/photo/2015/02/01/21/16/chalkboard-620316_960_720.jpg
Image source: [here](https://cdn.pixabay.com/photo/2015/02/01/21/16/chalkboard-620316_960_720.jpg)

Recently I have been asked on few different occasions why I chose @lymepoet as a username. What was the reason behind it or if there was a connection between Lyme disease and me.

Those of you who read my blog regularly must have noticed that the topics of my posts include poetry, health and wellness, travel or  Lyme-related articles.

To answer the question, I will say that **Lyme and poetry are two of the things that describe me the most**. I write poetry and I am a Lyme disease advocate. I even write poetry about Lyme disease. 

### MYSTERIOUS SYMPTOMS

As a chronic Lyme disease sufferer I have seen my health deteriorating to a point where I thought there was no turning back. Lyme stole my best years from me and threw me on a roller-coaster ride that I was not prepared for. It took me a few good years to get back on track.

That’s after I spent two years trying to get a proper diagnosis and seeing over twenty-six specialists who passed me on from one to another, shrugging their shoulders as they were unable to tell me why my health went down the hill so fast. 

### HITTING ROCK BOTTOM

When I was in my late twenties, within less than four months, I went from 154 pounds (70 kg) to 99 pounds (45kg) and I  lost my ability to walk without help. In addition, while I was fighting chronic pain, fatigue and having a wide array of debilitating symptoms (burning under the skin, muscle twitches, electric shocks in the limbs, numbness, migraines,etc.), I plunged into a depression that lasted a few good months. As a bonus, I developed anxiety as well.  I had hit rock bottom when I was supposed to enjoy my best years.

Needless to add the levels of frustration and anger were skyrocketing. You can’t imagine how it feels to have your whole life, your future taken away from you. The perspective of ending up in a wheelchair for the rest of your life is not something that crosses your mind when you are in your twenties!

### INVISIBLE  ILLNESS

Due to my invisible illness and the lack of a real diagnosis, people thought I had become anorexic. I lost a lot of friends on the way because they were not able to see what I was going through and I had no strength or energy left to explain how I felt. I had doctors telling me my symptoms were not real. I never gave up looking for an answer. 


If you are interested in knowing more details about my Lyme journey, you can read them [here](https://a-zlyme.com/my-lyme-journey/).

### GETTING DIAGNOSED

When I finally discovered that I had Lyme, my illness was already at the late stage, which meant the recovery was going to be a slow and lengthy process. I had change my lifestyle completely, make tabula rasa and find new ways to define my so called *normality*. 

I turned into an obedient patient who alternated cocktails of antibiotics with homeopathic remedies just to ensure my liver had a survival chance. I went a gluten- free, sugar-free, yeast-free diet for more than five years. I downsized twice and adopted a minimalist lifestyle.

I had friends and relatives from all over the world bringing me medicine (antibiotics) that I was not able to get within my country. Thanks to Lyme I lost my job, my friends and drained my bank account.

### THE NEW ME

Fast forward a couple of years. I got better and I learnt how to keep my Lyme symptoms under control. I got better at blocking or ignoring the pain and focus on the positive things in my life.

Therefore, I was able to see the silver linings of my condition. Lyme allowed me to reach my real potential, discover the myself and see things in a different light.


A few years ago I finally took a step and became a Lyme advocate. I realized that if I was not going to Lyme-educate the people around me, they won’t know what’s going on with me.

### THE BIRTH OF LYMEPOET NAME

Last year, I started my own awareness campaign for Lyme disease. On my  [A-ZLYME.COM](https://a-zlyme.com/ ) website I wrote about Lyme disease in detail from how to diagnose it to ways of transmission and available treatments. 

https://steemitimages.com/0x0/https://scontent.fymq1-1.fna.fbcdn.net/v/t1.0-9/27332234_1826696574071567_8126326298509791461_n.jpg?oh=1396db57d6cd457a9d90749779857bf6&oe=5ADEC4E0

Some of my Lyme-related articles have been also published by [THE MIGHTY](https://themighty.com/author/lavi-picu/) and then featured by Yahoo. I was glad to see that I got such a wide exposure. What got me thrilled was the fact that my words reached those who needed them. I got messages from people all over the world who suffered from Lyme or had someone close to them affected by this illness. 

The reaction I got from the readers humbled me. It was for the first time when I actually experienced the feeling of a support community. It encouraged me to continue my awareness campaign because I know somewhere around the world, someone needs to hear that he is not alone and that the symptoms he is experimenting are real.

What's the story behind your Steemit username?

https://steemitimages.com/DQmcm8oUzhnpBUPY3j36E9VEh9wVauw843pmtxKSaJf6x3d/20.png***

Here are other  Lyme-related  posts:

[**TOP 10 WORST SYMPTOMS OF LYME DISEASE**](https://steemit.com/health/@lymepoet/top-10-worst-symptoms-of-lyme-disease)

[**WHAT ARE THE SIGNS AND SYMPTOMS OF LYME DISEASE?**](https://steemit.com/steemstem/@lymepoet/what-are-the-signs-and-symptoms-of-lyme-disease)

[**WHAT IS EARLY LYME DISEASE?**](https://steemit.com/science/@lymepoet/what-is-early-lyme-disease)

[**WHY IS LYME DISEASE TOUGH TO DIAGNOSE?**](https://steemit.com/science/@lymepoet/why-lyme-disease-is-tough-to-diagnose)

[**HOW CAN YOU PROTECT YOURSELF AGAINST TICK BITES?**](https://steemit.com/health/@lymepoet/how-can-you-protect-yourself-against-tick-bites)

[**WHAT IS THE LYME DIET**?](https://steemit.com/health/@lymepoet/what-is-the-lyme-diet)

[**LYME PERICARDITIS**](https://steemit.com/health/@lymepoet/lyme-pericarditis-what-lyme-can-do-to-your-heart)

[**HOW I FOUND THE SILVER LINING OF LYME DISEASE**](https://steemit.com/life/@lymepoet/how-i-found-the-silver-lining-of-lyme-disease)

[**THE PAIN OF NOT LOOKING SICK**](https://steemit.com/health/@lymepoet/the-pain-of-not-looking-sick)

[**JOURNEY TO SELF-DISCOVERY**](https://steemit.com/womenspeakout/@lymepoet/journey-to-self-discovery)

[**9 WAYS TO KEEP A RELATIONSHIP GOING WHEN BOTH PARTNERS ARE ILL**](https://steemit.com/health/@lymepoet/9-ways-to-keep-a-relationship-going-when-both-partners-are-ill)

All of the above posts were written by me, as part of my Lyme Disease awareness campaign and were originally published on my personal website [**A-ZLYME.COM**?](https://a-zlyme.com/)

If you would like to learn more about Lyme disease, visit my website [**A-ZLYME.COM**?](https://a-zlyme.com/) where I write weekly Lyme-related articles which I might re-post on Steemit, in order to increase the awareness about this infamous illness.




https://steemitimages.com/DQmcm8oUzhnpBUPY3j36E9VEh9wVauw843pmtxKSaJf6x3d/20.png***

Thank you for reading, I hope you enjoyed it! Feel free to resteemit or upvote it!
Please leave your feedback in the comments, I would love to hear your thoughts!

**@2018 LaviPicu aka The Lyme Poet. All rights reserved.**

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art and flair courtesy of @PegasusPhysics</center>
***

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πŸ‘  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
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vote details (58)
@lilyraabe ·
What an inspiring story, thank you so much for sharing it here--a remarkable thing you’re doing to advocate for raised awareness through this issue. It takes a lot of strength to put your personal experience out on the line like this. Keep being awesome! <3
πŸ‘  
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@lymepoet ·
Lyme needs a lot more exposure. It is a terrible illness and doctors are not taught yet how to recognize it.  Over 300 000 people get sick each year within the U.S. only. And these are those lucky ones who get a positive test result for Lyme. The rest get misdiagnosed and suffer for years, not knowing that their debilitating symptoms are caused by Lyme or the co-infections that come along with it.
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@goldendawne ·
I have an auto-immune disease and it can wreak havoc on a person. Some days are worse than others.
πŸ‘  ,
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@lymepoet ·
I am sorry to hear that you have health issues. I can only wish you to stay strong and take things slowly, one at the time. When you have an auto-immune disease, each day brings a new struggle. Thank you for reading and leaving a comment!
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@derekrichardson ·
Whoa. I'm glad you were finally able to get diagnosed before it got even worse. I'm sure it was very tough. I'm glad you are doing better now. And I think it's great that now you are helping other people with Lyme.
πŸ‘  
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@lymepoet ·
Getting diagnosed with Lyme is very challenging as the tests are unreliable. Also most of the doctors do not look at the whole puzzle. If you don't find a tick on you and you don't develop the specific bull's eye rash (Erithema migrains) for Lyme, doctors will overlook the possibility of being infected with Lyme (Borrelia Burgdorferi) and will not ask you to get tested for Lyme Not everyone develops the specific rash. I didn't!
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@nationall ·
I am a very quiet person
I do not speak much
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@soyrosa ·
It is super important and valuable you are sharing your story wherever and whenever you can. Thank you <3
πŸ‘  
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@lymepoet ·
I learnt the hard way that without telling people what is going on, no one will ever understand. We all have lives and we can't know what happens with someone if he doesn't open up. I was expecting people to see things my way but when that did not happen, I felt awful. It took me some time to understand my approach was wrong.
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@soyrosa ·
I know, I've had to learn too. You're doing great :-)
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@awakentolife ·
Basically, my amazing friend. You are an inspiration to all of us. And, you have taken the best out of a bad hand you have been dealt. Love your positive attitude. It is inspirational. I hope you get better and better as you go along. Wish you all the best. 

Loved this message from you: 

> I got better at blocking or ignoring the pain and focus on the positive things in my life.Therefore, I was able to see the silver linings of my condition. Lyme allowed me to reach my real potential, discover myself and see things in a different light.

Love your name and the story behind it. Maybe I should write a story behind my user name as well. :) 

Thank you for sharing. Have an amazing day. :)
πŸ‘  
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@lymepoet ·
Thank you for taking the time to write to me.  Each day is an inspiration. When you learn not to take things for granted, everything seems better, more beautiful. You enjoy life more and feel happier. 
I am looking forward to reading the story of your username, as I am sure there is a great life-changing story behind it.
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@appiepearl ·
Thank you for sharing your story.   A true inspiration and a fantastic example of taking your life into your own hands and making the best of the life you were given.   You're absolutely beautiful before, after and now!
πŸ‘  
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@lymepoet ·
Thank you! When life gives you lemons, you do a lemonade. I made a Lymonade. ;-)
πŸ‘  
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@appiepearl ·
Love it!   Says a lot about who you are.
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@vegan.niinja ·
Very interesting story, love! And you are making areal change for the people who needs it. Thats so inspiring!
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@lymepoet ·
Thank you for stopping by! People need to learn more about Lyme, because it is spreading like wild fire.
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@felobtc ·
I had the opportunity to see your website before knowing about your story @lymepoet and now I totally understand the reason why your profile had this link. 

You're a real warrior, you're worth all the gold in the world and now thanks to you many people can fight Lyme disease and follow your example 'cause you're inspiration for the world. 

That really comes from the bottom of my heart and I hope you keep supporting everybody as much as you can!
πŸ‘  
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@lymepoet ·
Hi @felobtc! Thank you for commenting and re-blogging this post. Lyme is a global threat. The more people know about it, the better. I do my best to spread more awareness about it, though some days I think it's not enough. I know, we can't change the world within a day. It takes small baby steps, which is what I'm doing.
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@sultnpapper ·
Your story is inspiring and the name is very understandable given your situation. I haven't read any of your other posts yet, the title on this one drew me in. If you don;t mind me asking, is there one particular test that diagnosed it or is it several tests?
I know nothing about the disease other than I know it is transmitted by tics and it wreaks havoc on folks.
πŸ‘  
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@lymepoet ·
Western Blot and Elisa are test used to diagnose Lyme. The problem is that this two-tier testing approach fails to diagnose half of those who undergo the tests. It's a huge controversy about in the medical community.  
The chances of getting a positive test result for Lyme are similar to  winning the lottery, as the labs test only for a small number of strains (less than ten if I remember well) when there are over three hundred of Borrelia strains out in the world. Thus, let's say you get bitten by a tick in Europe or in Asia, and you undergo the test in the states, you will not get a positive result.
Also during the early stage of Lyme, the levels of antibodies are too low for the test to detect and you get a "false negative" result.
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@sultnpapper ·
That explains  a lot and why it sometimes goes undetected I guess.  Good luck with the management of your condition.
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@naquoya ·
I'm sorry to read of your health struggles, and although what I have had is different to what you are going through, I can relate. This particularly caught my attention:

>I lost a lot of friends on the way because they were not able to see what I was going through and I had no strength or energy left to explain how I felt. 

When I first got ill 16 years ago this was my experience. And nobody understands it when it's explained to them. Why would people do that? is usually what I get asked. It's not something that is easy for others to believe and accept. Leaving me usually feeling like perhaps I was the cause of it after all. Whilst I am not happy to read you went through that also, it offered a small amount of reassurance.
πŸ‘  
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@lymepoet ·
" I was the cause of it after all" - I have been there and it hurt like hell. When you are sick, you need help, support, empathy, compassion. The last thing you need is to waste your precious energy on explaining yourself to others or trying to convince them that you are sick. I had to defend myself, convince others that my sickness was real and that I was not crazy. Their ignorance took me to a dark place and because I know how it feels being there, I am trying to help others to avoid it.
Thank you for stopping and leaving a comment!
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@lifeaef ·
You went through a lot, I'll sure be checking your website. Thank you for spreading awareness. I myself have heard a lot of people talking about Lyme disease but it's not that well taught in Medical School. It's portrayed as uncommon infection. 


If you're interested, I recommend you watching this series
> www.youtube.com/watch?v=nW7scUy3e8c&list=PL7muM_3ugIOitPa1CQ-wudS3FuvySZ-13 

and this documentary
https://www.youtube.com/watch?v=OhCd7CyaSWE
πŸ‘  
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@lymepoet ·
Within the past two three years, Lyme gained a bit more popularity, meaning we heard of more cases of people being diagnosed with Lyme. Usually their stories present the same scenario: they all develop mysterious debilitating symptoms and the doctors have no answers for them. Their health goes rapidly down the hill, no one can help them. They even doubt their sanity as doctors tell them the symptoms are "in their head". It's a sad reality that people infected  with Lyme are facing. 
I have tried the MMS years back but in my case it did not do much. I know that for others did wonders. 
Thank you for taking the time to read and comment on this post!
πŸ‘  
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@calumam · (edited)
I'm so glad you spoke about this and I was able to read it. It sounds like you had it pretty rough for a little while and I imagine it would of been very hard to get back onto the horse.

YOU ARE ROCKING IT THOUGH!

Not only did you crush it, you have stood up and made sure others don't suffer as much. I've got a huge amount of respect for you. I have no doubt that you will continue to help thers and change their lives fr the better. It's amazing to know somebody who is changing the world for the better.
πŸ‘  
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@lymepoet ·
Thanks my friend! When I got sick there was not a lot of information available about Lyme. The little I found was scattered on various health forums and it was hard to read and remember where it was. When I created my website I wanted to have everything together in one place, in an easy to read format because I know by experience how difficult it is to read something when you are dealing with vision issues and brain fog. 
I learnt a lot of things along the way and I wanted to share this knowledge with those who need it. Why should they have to pay to learn about something that could be offered for free?
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@calumam ·
I see the struggle. Good work and very admirable.

You're a visionary and a great asset to the people struggling with the disease :)
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@alexdory ·
I also agree with that! You found a vacuum of information and you filled it, just because it's how you are. You will be fine, and will make us aware for the rest of our lives about this! This is what I call a contribution.
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@alexdory ·
Impressive journey. 
Well, let me tell you that we are a sum of our experiences and although I don't believe in fate, I think you are where you are supposed to be. I found a little here and there about how you think about the world and I honestly liked it. I know very little of the disease but I was sure from the first instant I saw your nickname that there must be a connection. We all have our crosses to carry and while here, you don't need to do it alone. We are all here because we are explorers. 
I must say that I was expecting your articles to gather more exposure and worth in terms of rewards, but I guess you must increase your network first. 
Have a wonderful weekend and thanks for writing for us!
πŸ‘  
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@lymepoet ·
Thanks for taking the time to read and comment. I learnt that everything happens for a reason (nothing to do with religion) and that everything will fall into place.
 If I would have not gone through all this, I wouldn't have met some amazing people who helped me grow, discover myself and I would have been who I am today.
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@bigtom13 ·
Thanks for an inspiring look behind the curtain.  

I also have an auto immune disorder, though mine doesn't bite me near as hard as yours does.  I'm glad we don't have Lyme here because I love to rummage around in the places where it'd be common.  

Again, thanks for a wonderful post.
πŸ‘  
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@lymepoet ·
Sorry to hear (better said read) about your health struggle. Thank you for your kind words!
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@thesteemengine ·
Congratulations! This post has been chosen as one of the daily Whistle Stops for The STEEM Engine!

<center>[![](https://ethandsmith.com/wp-content/uploads/2017/12/commentSTEEMengine.jpg)](https://steemit.com/@thesteemengine)</center>

You can see your post's place along the track here: [The Daily Whistle Stops, Issue # 78 (3/19/18)](https://steemit.com/curation/@thesteemengine/the-daily-whistle-stops-issue-78-3-19-18)

The STEEM Engine is an initiative dedicated to promoting meaningful engagement across Steemit. [Find out more about us and join us](https://steemit.com/introduceyourself/@thesteemengine/introducing-the-steem-engine-initiative) today!
πŸ‘  
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vote details (1)
@maverickinvictus ·
Takes such courage to be able to be able to share this and was written so beautifully that it is a shame no one saw this piece. 

I would love to invite you to the promo-mentors group 

You have been scouted by @promo-mentors. We are always on the look out for promising authors.

I would like to invite you to our discord group https://discord.gg/vDPAFqb.

When you are there send me a message if you get lost! (My Discord name is the same as the one here)


<center>https://steemitimages.com/DQmSz9qLgp8NUrUg7UBxDyBKMJJ5cexca3ASox8JptVqTs1/4b.gif</center>
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@lymepoet ·
Thank you for invite! I have heard of the @promo-mentors. I will join the group.
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@crescendoofpeace ·
I can totally relate, having had autoimmune issues for years, and now living in the apparent tick capital of the Appalachians.  

My poor dog has been miserable ALL WINTER with chiggers . . . in winter?  Yup.  Seriously.

I posted a couple of weeks ago with a remedy (that works for me anyway) for tick bites, but once you've got lyme disease, it's not all that helpful.  

And allopathic doctors in the States are the WORST at diagnosis.  My late sister had thyroid issues, and vitiligo was one of the most evident symptoms of the disease, yet she was misdiagnosed for years . . . despite clear evidence they could SEE right in front of them.

If it hadn't been for an accident, when my mom ruptured her spleen going down a flight of wt stairs, she might never have been diagnosed properly.  As it was, an emergency room  doctor called aside a first year resident, and asked him for his assessment, and he correctly diagnosed vitiligo and underlying thyroid disease.  

So a first year resident could call it correctly, but her MD general practitioners had been giving her the runaround for at least five years at that point. Sigh.
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