Pete Caruso
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petecaruso.bsky.social
Pete Caruso
@petecaruso.bsky.social
Interested in research and awareness of invisible chronic illnesses: ME, Long COVID, Post Vaccine injury, POTS, Sjogrens, and Lyme.

Pfp: A man wearing a green face mask
Banner: Colorful MEmes from patient-led Long COVID and ME awareness
“We already have a division at NIH devoted to study Long COVID and figure out cures...creating a CDC agency for vaccine injuries and also Lyme disease…more and more people are suffering from these diseases” - RFK Jr.

Chris Cuomo didn't ask about the Long COVID Recover cuts announced this week.
March 28, 2025 at 4:21 PM
The @wecrunchme report "The Future is a Policy Choice" shows that #LongCOVID and #MECFS are significantly underfunded, compared to other major diseases. This information needs to be shared to inform policy makers.
January 29, 2025 at 5:04 AM
The @wecrunchme report shows that #LongCovid has the same disease burden of Type I and Type II diabetes, yet it's considerably underfunded.

Download and share "The Future is a Policy Choice" in the
drive.google.com/file/d/17fgU...
January 29, 2025 at 5:04 AM
Gaslit by subreddit moderators, Who You Gonna Call?

#GreatestMEdicalScandal
#JohnVsJonVsME
December 31, 2024 at 8:53 PM
For recent followers, I’m an Aerospace engineer (permanently paused) to take care of my spouse with moderate M.E. I use my spoons to promote Long COVID, M.E. research and clean air prevention measures. I follow patient-let awareness campaigns and try to provide creativity to the campaign. 🧵
November 18, 2024 at 7:48 PM
Main takeaways:
- Specific IgG antibodies from people can develop Long Covid symptoms in mice
- IgG antibodies transfer specific symptoms of subsets of patients
- A mouse model of LC can support development of treatments
- More evidence of biomarkers for subtypes
June 2, 2024 at 4:19 PM
I support every Long Covid and ME awareness event with a song. The Unite to Fight Long Covid and ME/CFS community driven conference is May 15-16.
May 7, 2024 at 2:08 AM
If link to draft agenda doesn’t work, screenshots are shown below.
December 2, 2023 at 9:02 AM
Similar story.   Debra's parents are 89, shower every day, meet friends socially, and leave the house 4 times a week - all things that she can only do once every 10-14 days.   For this reason, 40 is the new 90.  We need to speed up treatments.   
#LongCovid
#MECFS
October 30, 2023 at 7:49 PM
Fall has finally arrived in the Southeast.
October 25, 2023 at 4:38 AM
Same beach, two weeks ago.
October 15, 2023 at 6:41 PM
October 15, 2023 at 6:38 PM
#Sjogrens disease activity was reduced using the ESSDAI: European League Against Rheumatism Sjögren’s Syndrome Disease Activity Index and the ESSPRI: European Alliance of Associations for Rheumatology SS patient Reported Index.
October 13, 2023 at 5:25 AM
The #sjogrens study compared a significantly enhanced stem cell group to placebo group for saliva production. Graph shows increasing UWS: unstimulated whole saliva; SWS: Stimulated whole saliva; and LF: lacrimal flow.
October 13, 2023 at 5:21 AM
The people living with the condition are the experts.
October 6, 2023 at 3:56 PM