Welcome to Life with Lyme #19 - 3.5.17. On this episode, we discuss the emotional roller coaster that occurs when you get a diagnosis. Thank you very much for listening.

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Hello and happy holidays! Tonight, we return from a very long absence. In this episode, we discuss the holiday season through the eyes of someone battling chronic illness and what some of those hardships are like. We also discuss what we are hoping for this coming year and end the episode with a beautiful song from our friends in Chemtrail for you to relax to and enjoy! #Lyme #LymeDisease #LifeWithLyme #Podcast #PodernFamily #LymeIsReal

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Welcome to Life with Lyme, Episode 17, on March 10th, 2016! This episode, we address the sometimes infuriating ways people criticize and talk to the disabled. We also discuss the possible pitfalls of celebrity-worship in the Lyme community. Thank you so much for listening!

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In this episode we discuss neurological Lyme Disease and the difficulties that come with it as well as various other topics including the upcoming Mayday Protest.

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In this episode, we discuss the short film we recently released online called, "The Lyme Wars," new developments in Lyme disease research, what's happening in Lyme news, and we address, in more detail, the situation regarding Rick's Lyme disease article and Yolanda Foster. Thank you for listening! Please comment and share! 

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Hello, good people! In this episode, we talk about the National Guidelines Clearinghouse including the ILADS guidelines on their website, celebrities with Lyme, the Under Our Skin movies, sauna and yoga treatment, and a lot more. Thanks for listening!

Welcome to Life with Lyme. This episode, Sarah and Rick discuss toxic relationships and their effects on Lyme patients. Thanks for listening!

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Here it is! Life with Lyme, recorded at the Mayday protest on May 1st, 2015. We had all sorts of conversations in front of the IDSA building with people who came from all over the country. Thanks for listening!

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In tonight's episode, we discuss everything from the Lyme Disease Challenge to the upcoming protest at the IDSA building in Arlington, Virginia! We close with a song from artist, Ishaan Reyna, called, "I Won't Give Up," dedicated to his mother who has Lyme Disease. Thanks for listening!

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In this episode, we talk about the IDSA, eating with Lyme, recent Lyme related news articles, there is a somewhat impromptu interview with Rick, the writer of Chronic Lyme: A New Era of Ignorance recently published by the Pontiac Tribune, and a whole lot more! Thank you for listening! 

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In this episode, we talk about irresponsible journalism and misrepresentation of Chronic Lyme in the media.

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In this episode, we talk about new laws, new antibiotics, artists in the lyme community, and more! We close with a beautiful song from fellow lymie, Bekah, called "The Beach." Thanks for listening!

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In this episode, we talk about what it's like to be sick during the holidays and the latest in Lyme news.

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The first half of this episode addresses the issue of misinformation about Lyme disease in the mainstream media. But most importantly, this episode is dedicated to a friend of mine who recently committed suicide. I hope talking about this prominent issue in the Lyme community will help someone, anyone, out there listening.

The second half of the episode is dedicated to this topic, my honest feelings on it coming from a patient's point of view.  Apologies and a bit of a forewarning, I break down a bit towards the end and Rick is nice enough to finish with reading the piece I intended to share. Something I wrote to my friend years ago, apropos to the subject matter, and hopefully something others can find some help in hearing.

Thank you to Tylan for allowing me to conclude the episode with a beautiful song for Heather. Tylan was one of her favorite musicians, you can find more of her work here tylanmusic.com and here patreon.com/tylanmusic.

Also mentioned in this episode is a fundraiser by Ross Anderson which you can learn more about here: http://www.gofundme.com/cm8v4k

Thank you all for listening. Take care of yourselves.

In this episode, I address topics brought up by listeners such as what to do when your'e feeling extra crappy, ways to try to get loved ones to understand what it's like to live with lyme, and I also talk about the upcoming IDSA conference and more!

Thank you for listening!

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To end Lyme Disease Awareness Month, we collected interviews from protesters at the rally held at the IDSA building in Arlington, VA. Stories of hope, suffering, and strength. We finish out this special episode with a song by singer/songwriter, and fellow Lymie, Alisa Turner, written during some of her hardest moments with the disease. Thank you all for sharing your time and your stories.

In this episode, I bring up some topics suggested by listeners, including why there isn't more public awareness, what we wish people close to us knew about having Lyme, and the May Day Protest that I was about to attend.

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What do you do when you get bit by a tick? Where do you go, and how do you know what the right steps are? I have a discussion with my friend Alexander Rhodes about his recent tick bite and some of the complications people have in getting accurate care. Please keep in mind I am not a medical professional, and if you believe you are ill please seek proper medical care.

It's the start of Lyme Disease Awareness month, and the official start of the new Life with Lyme podcast, too!  I'm Sarah, and I've had chronic Lyme for over a decade. This podcast will hopefully shed some light on what it's like, both personally, as well as what is going on in the medical community with this misunderstood illness. But before all that, this is my introduction. Enjoy!