When the goals of deworming programs will shift from morbidity control to transmission interruption and elimination, diagnostics will play a critical role. I am very proud to be part of this challenge. Check out: sciencefiguredout.be/drop-blood-fig… UGent VetMed FWO Ethiopian Public Health Institute

Find someone who will be your strength when you need it most. 💚 #rideoutlyme #powerthru2cure #strongertogether #lyme #lymewarrior #lymedontkillmyvibe #soulcycle #paloalto #lajolla #manhattanbeach #losangeles #boston #wellesley #nyc #cycling #charityride

Politicians know that reducing the #pain medicines of the sick & #disabled is not reducing #opioid deaths. They were never the cause, that’s ILLEGAL drug use. So, they are literally sacrificing patients for politics. “We were surprised that pain..causes.. sciencedaily.com/releases/2016/…

January to March 2020, a total of 581, 599 so half a million people people died due to ..... alcohol! There’s a reason opioid deaths include ILLEGAL DRUG USE & span 19 years (1999-2018), there just aren’t that many deaths from legal prescriptions so they can’t justify torture.

The feds (#CDC) & others who have kept #lymeDisease medicine from advancing & have ensured millions to go undiagnosed while becoming very sick, immune compromised, & disabled (1/2)-you have no idea who you have turned us into: Survivors. We will eventually be writing the history.

And the rest 💚 #lyme #lymedisease #lymediseaseawareness #lymewarrior #chronicillness #chroniclyme #spoonie #lymelife #invisibleillness #lymedontkillmyvibe #lymefighter #lymeawareness #chronicfatigue #chronicpain #lymesucks #chroniclymedisease #lymetreatment #lymie #bartonella

Is today a good day or a bad day? 💚💚 #LymeAwareness #LymeDiseaseAwareness #LymeNow #lymesymptoms #lymewarrior #lymelife #chroniclymedisease #lymetreatment #lymesucks #lymediseasesucks #lyme #lymestrong #lymesurvivor #chronicpain #yolandahadid #spoonie #lymedontkillmyvibe

We are an international Consortium of Experts in #NTDs, with a focus on helminth diseases 🪱: #STHelminthiasis, #strongyloidiasis, #schistosomiasis, #echinococcosis, #taeniasis, #neurocysticercosis and porcine #cysticercosis 👇🏾

#TheQuietEpidemic is NOW STREAMING on AppleTV, Prime Video, and Vimeo On Demand! Right in time for #LymeDiseaseAwarenessMonth. Please share this news far and wide. Thank you all for your continued support. You are not alone, and your story matters!

The worst thing was when I was gaslit, called a hypochondriac, & sent to a psychiatrist for anxiety & depression. Told the ID Dr's "I'm depressed bcuz I'm SICK, not SICK bcuz I'm depressed." 20 yrs for dx. #chronicillness #chronicpain #CFSME #autoimmune

From our upcoming video podcast. I want to know what’s so funny. They all seem to be in on some inside joke. Here you have a primary care doctor, who actually wants opioids to be illegal so he doesn’t have to deal with “these patients.” #stigma #medicallyabandoned #pain

“I’m tired of being tired…tired of being in #pain. I’m tired of having to budget my limited supply of energy. I’m tired of always having to say no. I’m tired of my brain not being able to find the words…I’m tired of no one understanding.” buff.ly/3oMTemV #chronicillness

Princess, The Tower I'm just tired of not having the life I once made #ChronicPain stole that life just left me to deal with #pain of all sorts 😞😔

Proud to be publishing this book with my daughter! Based on the journal she kept during the worst years of her #Lyme disease experience.

Nicole Nicole Malachowski says that everything that she needed to be a good fighter pilot--such as discipline, focus, commitment, determination, and confidence--are the traits and the characteristics she needed to survive the worst depths of her illness. lymedisease.org/podcast-nicole…

Here is another thing used against pain Pts. You’re never allowed to miss an appointment. It doesn’t matter if you’re sick which makes no sense considering they’re literally chronic illness patients.

💚Hmmmm...should I be offended people don't quite fully understand? Or should I connect with YOU, the people who know exactly what this sentence means and refrain from beating my head against a wall? Source: PA Lyme Resource Network

When doctors said "It's all in your head," we said, "It's all in the research." For over 35 years, we've been standing with Lyme patients when no one else would. Stand with us now by becoming a member today: lymedisease.org/members/join-s…

Repost if you feel the same.

Do you remember when you joined X? I do! #MyXAnniversary