Jaime Holland
@prettyrottenguts.bsky.social
Professional loudmouth (public speaker) with a crush on public policy. I also write, edit, and manage projects for humans in the healthcare and chronic disease space.
Reposted by Jaime Holland
If you wonder why men *obsessed* with the United States having more children are kidnapping children and sending them to other countries, those children were the incorrect color.
April 28, 2025 at 2:29 PM
If you wonder why men *obsessed* with the United States having more children are kidnapping children and sending them to other countries, those children were the incorrect color.
It’s been a month, if you haven’t listened to us yet give it a go. #inflammatoryboweldisease
🌱 As parents w/IBD, we're doing our best! We want to focus on things we can control, because guilt isn't productive! On About IBD Podcast Episode 167, Jaime Holland (@prettyrottenguts.bsky.social) and I give tips on managing fatigue, stress, & guilt! Listen in a podcast app or at bit.ly/AIBD167 #IBD
How to Thrive as a Parent with IBD – About IBD Podcast Episode 167
Amber hands over hosting duties to Jamie Holland, a patient advocate with Crohn's disease. They discuss their personal experiences with …
bit.ly
March 14, 2025 at 7:51 PM
It’s been a month, if you haven’t listened to us yet give it a go. #inflammatoryboweldisease
Reposted by Jaime Holland
🌼 For #AboutIBDPodcast 167, I passed the hosting job to Jaime Holland (@prettyrottenguts.bsky.social)! 😮 I answer questions from the community about choosing j-pouch surgery and how it intersected with fertility, pregnancy, and parenthood! Listen on any podcast app or at bit.ly/AIBD167! 🎧
January 29, 2025 at 3:35 PM
🌼 For #AboutIBDPodcast 167, I passed the hosting job to Jaime Holland (@prettyrottenguts.bsky.social)! 😮 I answer questions from the community about choosing j-pouch surgery and how it intersected with fertility, pregnancy, and parenthood! Listen on any podcast app or at bit.ly/AIBD167! 🎧
Reposted by Jaime Holland
how life feels when I open social media
January 22, 2025 at 7:16 PM
how life feels when I open social media
First lawsuits filed over today, Jan 20, Executive Orders (EO). For a refresh an EO is a memo from POTUS for departments to act on without Congress. But Congress could circumvent an EO by halting or slowing funding, or passing legislation. A lawsuit for could also be filed to prove unconstitutional.
ACLU and other advocates sue Trump over executive order ending birthright citizenship. (scroll down to story). apnews.com/live/trump-i...
Live updates: Trump issues pardons for Jan. 6 rioters and signs more executive orders
President-elect Donald Trump was sworn in as the 47th President with his wife Melania by his side. He pledged in his inaugural address to “completely and totally reverse” Joe Biden’s policies. He's ex...
apnews.com
January 21, 2025 at 5:21 AM
First lawsuits filed over today, Jan 20, Executive Orders (EO). For a refresh an EO is a memo from POTUS for departments to act on without Congress. But Congress could circumvent an EO by halting or slowing funding, or passing legislation. A lawsuit for could also be filed to prove unconstitutional.
I guess this is my first official post on BlueSky. ¯\_(ツ)_/¯ Yep, chose a panda. IYKYK.
a panda bear is waving at the camera and smiling .
ALT: a panda bear is waving at the camera and smiling .
media.tenor.com
January 21, 2025 at 3:54 AM
I guess this is my first official post on BlueSky. ¯\_(ツ)_/¯ Yep, chose a panda. IYKYK.
Reposted by Jaime Holland
Hello BlueSky! I’m Aaron. Came over from Twitter.
I live with #CrohnsDisease and an ultra-rare genetic bone disease called #hypophosphatasia.
I have been advocating for these diseases for a long time. I also have a background in #science and love to talk about that! #chronicillness
I live with #CrohnsDisease and an ultra-rare genetic bone disease called #hypophosphatasia.
I have been advocating for these diseases for a long time. I also have a background in #science and love to talk about that! #chronicillness
November 15, 2024 at 4:19 PM
Hello BlueSky! I’m Aaron. Came over from Twitter.
I live with #CrohnsDisease and an ultra-rare genetic bone disease called #hypophosphatasia.
I have been advocating for these diseases for a long time. I also have a background in #science and love to talk about that! #chronicillness
I live with #CrohnsDisease and an ultra-rare genetic bone disease called #hypophosphatasia.
I have been advocating for these diseases for a long time. I also have a background in #science and love to talk about that! #chronicillness