Here’s an informational brochure I made to educate people and spread awareness about eosinophilic gastritis, a rare disease that currently has no known cure.

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@eosinophil-hate-blog
Here’s an informational brochure I made to educate people and spread awareness about eosinophilic gastritis, a rare disease that currently has no known cure.
when I was a kid and P.E. teachers would make the class do stretches I always thought I was just better at stretching than everyone else in my class bc I could bend over and touch the ground with my palms while everyone else struggled to touch their toes. turns out I have clinically hypermobile joints
when I was a kid and P.E. teachers would make the class do stretches I always thought I was just better at stretching than everyone else in my class bc I could bend over and touch the ground with my palms while everyone else struggled to touch their toes. turns out I have clinically hypermobile joints
eosinophilic hate blog i return to seek your solace. i was the one mutual with eosinophilic gastroenteritis/colitis on here and twt from like 2018 and now in the big 2026 my gastro consultant thinks i have fucking EOE!!!!!! of all things!!!!!! i hate my baka life!!!! i hope u r well
Damn that is rough :( I'm sorry to hear that, and I hope your gastro is helpful and you're able to figure out a treatment that works for you
hate that I immediately did the mental image equivalent of the pointing wojak when I saw eosinophilic esophagitis mentioned in a product description
hate that I immediately did the mental image equivalent of the pointing wojak when I saw eosinophilic esophagitis mentioned in a product description
Eosinophilic esophagitis haver here
Fuck eosinophils they scarred my fucking Tube
I'm pouring one out for your Tube, since it's not like we could drink it anyway. Cheers!
I feel like I should post something for Rare Disease Day, but I don't really know what to say. I was diagnosed with eosinophilic gastritis in 2017. After nearly a decade of living like this, I don't really have any more basic awareness-raising things to say that I haven't already said before. So I guess all I really have to say today is that one annual day for raising basic awareness is great, but the disease doesn't end at midnight, and neither should advocacy, especially advocacy around more in-depth education that goes beyond the 101 level given to people who are just now finding out about these things for the first time.
"we were hoping to see you at The Event :("
buddy you did everything you could to make The Event as inaccessible for me as possible
look at this point I fully expect doctors to not be familar with rare diseases, but until last week I did expect them to at least know what kidneys are
This week is National Eosinophil Awareness Week!
I'm passing along this email from the founder of the CURED (Campaign Urging Research for Eosinophilic Disease) Foundation:
"CURED Foundation Appeals to Our Community: Stand Together to Secure the Future of Rare Disease Research!
NIH pulled funding for eosinophilic diseases research
Dear CURED Families, Professionals, and Advocates,
We are reaching out today with an urgent plea for action. In an alarming and unforeseen move, the National Institutes of Health (NIH) has withdrawn the 5-year renewal application for the Consortium of Eosinophilic Gastrointestinal Disease Researchers (CEGIR), the only federally funded research and clinical care network for EGID patients in the United States.
This withdrawal was not due to scientific merit but rather a minor administrative item that had not previously been addressed.
Regrettably, the CEGIR is not alone. The Frontiers in Congenital Disorders of Glycosylation Consortium (FCDGC) has suffered the same fate, further jeopardizing progress in rare disease research.
Thousands of rare disease families are now at risk. The implications are staggering:
Clinical studies and trials face indefinite delays or cancellations.
Families may lose access to EGID specialists at NIH-supported centers.
Pioneering diagnostic and therapeutic research risks grinding to a halt.
The centralized infrastructure for EGID studies in the U.S. is in danger of collapse.
Without intervention, this could be the beginning of widespread setbacks for rare disease programs.
NIH contacts have informed us that all appeals have been exhausted, with this decision being imposed “from the top down.” If we fail to act now, a dangerous national precedent could take hold, threatening rare disease research everywhere.
We need your help urgently: Call all four of the Rare Disease Congressional Caucus Co-Chairs… Tell them we need the CEGIR and FCDGC applications reinstated and reviewed at the April 22, 2025, NIH Final Scientific Review meeting
· Rep. Gus Bilirakis (R-FL): 202-225-5755
· Rep. Doris Matsui (D-CA): 202-225-7163
· Sen. Roger Wicker (R-MS): 202-224-6253
· Sen. Amy Klobuchar (D-MN): 202-224-3244
Contact your member of Congress… Find them here
Ask them to urge NIH Director Dr. Jay Bhattacharya to reinstate the application before April 22nd.
Share this Alert Widely… Reshare on social media, forward this newsletter, and activate your personal and professional networks. We need loud, fast, unified support.
Families & Professionals: Are You Willing to Speak with the Media?
We are gathering personal stories and professional perspectives for national coverage. If you have:
· Participated in a CEGIR trial or study
· Traveled to a CEGIR site between 2015–2024
· Worked closely to provide care and research support to families
Please email us at: Ellyn or Shay
This week is critical. Please don’t wait.
We know this is difficult news to process. But we are NOT giving up. We are fighting not just for CEGIR, but for the future of rare disease research across the country.
Please stand with us. The clock is ticking.
In unity and urgency,
Ellyn Kodroff President and Founder, CURED On behalf of CURED & our rare disease partners at FCDGC"
Happy Rare Disease Day to those who celebrate