#LymeWarrior
Ren partnered with Project Lyme for "Project Lab Coat" at NYFW to raise funds and awareness

As a survivor misdiagnosed for six years, he used his Sick Boi platform and FOX 5 interviews to spotlight chronic illness.

Wanna collaborate towards a cure?

Join 👇
projectlyme.org
#lymewarrior #fashion
Ren | Lyme Disease Awareness - Fox 5 NY
YouTube video by RenMakesStuff
youtu.be
September 23, 2026 at 1:56 PM
#LymeAwareness #LDAM #LymeWarrior
Mai- Monat der Lyme-Borreliose! Die Petition zur ICD-11 (WHO) braucht Unterstützung. Internationale Unterschriften ausdrücklich erlaubt!
D verzögert diesen Fortschritt! Bitte unterzeichnen Sie bis zum 11. Mai 2026. epetitionen.bundestag.de/content/peti...
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May 8, 2026 at 6:45 PM
#LymeAwareness #LDAM #LymeWarrior
May = Lyme Disease Awareness Month! German ICD-11 (WHO) petition needs your help. International signatures are welcome!
However, Germany is delaying this progress! Please sign the petition (by May 11, 2026, at the latest). epetitionen.bundestag.de/content/peti...
May 8, 2026 at 6:41 PM
Earlier this month Therapeutic Coach Samantha Quemby joined Morven-May MacCallum on LDUK Connect.

An edited recording of this session is now available for those who were unable to attend.

lymediseaseuk.com/healing-your...

#Lyme #lymewarrior #lymedisease #lymeadvocate #lymeawareness
March 10, 2026 at 2:38 PM
I’m still fighting. 3 years of Lyme but progressively worse since June. Mine manifests with extraordinary chronic pain. Then we are all watching our country fall apart daily. My soul can’t breathe. I want to breathe… #lymedisease #lymewarrior
January 16, 2026 at 4:51 AM
Breathe deep in fresh air when you can all the way into your belly. It will help with brain energy and clearing your mind even for a moment. Then it helps you detox harmful things from your body. Just breathe. #sanskrit #lymewarrior
November 2, 2025 at 1:54 PM
And I forgot the #LymeWarrior so I have to go back. And I want to change pic to something current. It wasn’t hard at all.
June 23, 2025 at 7:12 PM
Were you dismissed like my first Lyme disease patients? Share your story below. #LymeDisease #LymeAwareness #ChronicLyme #LymeDoctor #LymeWarrior #TickBorneIllness #MedicalJourney #PatientStory #case #explainer #lymephysician
May 22, 2025 at 11:05 PM
In honor of May also being #LymeDiseaseAwarenessMonth here is a video discussing common misconceptions about testing and diagnosis. #Lyme #lymedisease #lymewarrior #LymeDiseaseAwareness #factsyoudidntknow #DidYouKnow

igenex.com

youtube.com/shorts/LJ7x4...
May is Lyme Disease Awareness Month.
YouTube video by Talia Smith - Finding Vulneraries
youtube.com
May 15, 2025 at 12:51 PM
Today and every day, we celebrate the incredible strength, love, and resilience of all moms—especially those fighting for the health of their children.
Happy Mother’s Day from all of us at the LivLyme Foundation. Thank you for never giving up. 💚💐

#MothersDay #LymeMoms #LivLyme #LymeWarrior #Thanku
May 11, 2025 at 2:27 PM
May is #LymeDisease Awareness Month. Visit Johns Hopkins Lyme Disease Research Center. Learn the truth about one of the fastest growing epidemics in the world. Support them. Subscribe to their newsletter. #LymeWarrior #LymeDiseaseAwareness www.hopkinslyme.org/about-the-ce...
About the Center : Johns Hopkins Medicine Lyme Disease Research Center
The Johns Hopkins Medicine Lyme Disease Research Center was established in 2015 under the direction of John Aucott, MD. Our clinical research team sees patients at Johns Hopkins at Green […]
www.hopkinslyme.org
April 30, 2025 at 1:20 PM
My partner once again made me a key lime pie for my (not key) lyme anniversary (9 years today)

It was scrumptious 🤤

#LymeDisease #lyme #LymeWarrior #FuckLyme #LymeAnniversary #KeyLimePie
April 26, 2025 at 3:29 AM
Beautiful day, Kira and I are enjoying a little bit of sunshine. It's sad that a primary thing on my mind, as I enjoy a few minutes of outdoors, is whether or not we're picking up ticks. #LymeDisease #LymeWarrior #DogsOfBlueSky #ItalianGreyhound
April 24, 2025 at 3:32 PM
Johns Hopkins Lyme Disease Research Center. Here is their current newsletter issue, in PDF format. Visit them at hopkinslyme [dot] org. #ChronicLyme #LymeDisease #LymeWarrior #LymeDiseaseResearch #JohnsHopkins

www.hopkinslyme.org/wp-content/u...
www.hopkinslyme.org
April 23, 2025 at 3:33 PM
Love and light to anyone feeling alone or trapped.

I have survived things I could’ve never imagined.

You have, too, I bet.

Now is our time to thrive in ways we’ve never imagined—

at least not yet.

#lymewarrior
March 16, 2025 at 5:19 PM
"Many of the epidemiologists at the CDC in Fort Collins, working on tick-borne diseases were just fired. "

#lymedisease #lymewarrior #chroniclyme

www.lymedisease.org/cdc-budget-c...
CDC budget cuts affect Lyme disease research at Fort Collins | LymeDisease.org
In a February 20 Facebook post, Dr. Richard Horowitz relates: "Many of the epidemiologists at the CDC in Fort Collins, working on tick-borne diseases were
www.lymedisease.org
February 22, 2025 at 8:53 PM
February 11, 2025 at 3:25 PM
Mmm, breakfast

These are all the meds (all supplements) I take with breakfast every day. None of these fight lyme, but almost all are because of lyme

#ThatChronicIllnessLife #ChronicIllness #LymeDisease #Lyme #disabilitysky #disabledsky #lymesky #ThatLymeLife #medicine #LymeEducation #LymeWarrior
January 30, 2025 at 8:02 PM
Ran out of room but wanted to include #LymeDisease #LymeWarrior #lymesky and #FuckLyme
January 26, 2025 at 9:08 PM
I'm currently doing an unusual, RNA based lyme treatment instead of antibiotics (like I've done for the last 8.5 years)

Today was IV #3

I really hope these work

#LymeWarrior #lyme #LymeDisease #FuckLyme #disabled #disability #ChronicallyIll #DisablitiySky #LymeSky
January 14, 2025 at 12:27 AM
🌿 Your story matters!

Are you a Lyme disease patient or caregiver? Sharing your journey could raise awareness, support others, and inspire change.

💚 Submit your story here:

👉 lymediseaseuk.com/contact-us/s...

#LymeDiseaseAwareness #ShareYourStory #LymeWarrior
January 12, 2025 at 5:55 PM
I desperately want my life back. I’m a shell of the person I once was.

I’m holding onto every glimpse of hope that I’ll finally heal.

#lymedisease #lymeawareness #lymewarrior #MECFS #CIRS #mentalhealth #PTSD #anxiety #chronicillness #hope
January 2, 2025 at 1:13 AM
I now fully understand why patients of #lymedisease use the term #lymewarrior.

It feels like my body is legit trying to take me out and I’m not even close to being on the #Lyme protocol yet. My body was too sensitive for the gentle treatment, so now we move to what they give children.
December 27, 2024 at 8:59 PM