Dr Poppy Budworth
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poppybudworth.bsky.social
Dr Poppy Budworth
@poppybudworth.bsky.social
400 followers 800 following 26 posts
Social researcher interested in disability, youth, belonging, and everyday life 📖 coffee and cat lover 🐈‍⬛ all views my own ☕️
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poppybudworth.bsky.social
Yes, we definitely will! 🫶🏻
August 29, 2025 at 11:13 AM
poppybudworth.bsky.social
Thanks so much for sharing, it’s great to see that the asynchronous ways to be involved in the #StitchAssemblyRGS25 has to the potential to make #Creativity and academic conferences more accessible..?

We hope you enjoy stitching and the rest of the RGS! 🧵
August 28, 2025 at 7:09 PM
poppybudworth.bsky.social
Thanks so much for sharing Tilly. It was great to meet you and chat today, and we are glad you enjoyed the session!
August 28, 2025 at 7:06 PM
Reposted by Dr Poppy Budworth
tillyrobinsonmiles.bsky.social
My output inspired by what I believe the vision & values of my work in creating a #GoodFoodNation to 'build a long table not a higher wall'

A table with people connecting and eating around it together. A space of equity.
August 28, 2025 at 11:30 AM
poppybudworth.bsky.social
Here’s the link to download the PDF versions of the toolkits: getyourbellyout.org.uk/poppy/

Thanks @getyourbellyout.bsky.social 🎉
GetYourBellyOut supporting research
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getyourbellyout.org.uk
August 28, 2025 at 6:50 PM
poppybudworth.bsky.social
This project was funded by @nwssdtp.bsky.social

The toolkits will be FREE to download soon - but if you’d like an early PDF copy, just drop me an email:

poppy.budworth@manchester.ac.uk 📩
August 28, 2025 at 6:32 PM
poppybudworth.bsky.social
Both toolkits were shaped by the experiences + feedback of 14 young people in the UK who live with (or lived with) an ileostomy or colostomy.

Huge thanks to everyone who generously shared their time + insights 💜
August 28, 2025 at 6:32 PM
poppybudworth.bsky.social
🟣 What I Wish YOU Knew
A toolkit for friends, family, healthcare professionals + the public - helping build better understanding of life with an ostomy.
Infographic titled “What I Wish YOU Knew …about life with an ostomy.” It explains key facts about living with an ostomy, alongside illustrations. 1. What is an ileostomy or colostomy? Illustration of a person changing an ostomy bag, with text bubble: “My ostomy does not smell. Most ostomy bags have deodorising technology.” Text explains that a bowel ostomy (or stoma) is a surgically formed opening on the stomach; people wear a bag to collect poo. An ileostomy comes from the small intestine, a colostomy from the large intestine. 2. Why do people have an ostomy? Illustration of a stoma. Text explains people may need surgery for conditions such as IBD, Hirschsprung’s Disease, bowel cancer, NEC, FAP, and more. Surgery can be permanent or temporary. Note: people of all ages, genders, and ethnicities can have a stoma. 3. Do people with an ostomy have fulfilling relationships? Illustration of two people holding hands. Text says people with an ostomy can have the same positive relationships as anyone else, including friendships, family bonds, sex, and intimacy. 4. Does language matter? Illustration of two people. One has a shirt that says: “My stoma is NOT a ‘worst case scenario.’” Text explains language matters: avoid negative assumptions, and remember many people with a stoma live full, happy lives. Note: not all disabilities are visible, and there are many valid reasons someone may use a disabled toilet. Footer credits: Researcher Dr. Poppy Budworth, collaborator Victoria Marie from GetYourBellyOut, artwork by Lucy Harman, funded by NWSSDTP and The University of Manchester.
August 28, 2025 at 6:32 PM
poppybudworth.bsky.social
🟣 What I Wish I Knew
A toolkit for people with a newly formed ostomy - includes advice + practical tips from young people who live with an ileostomy or colostomy themselves.
(Part 1 – “What I Wish I Knew …about life with an ostomy,” sections 1–4): Infographic explaining practical advice for people with a new ostomy. 1. Everyone’s stoma looks and behaves differently. Illustration of a person lifting their shirt to show a stoma. Text explains that stomas can change in appearance; keeping photos and a food diary can help. Diet is trial and error, and hydration is important. Extra tip: electrolyte drinks and rehydration solutions help with dehydration. 2. There are lots of products I can try. Illustration of three ostomy bags in different colours. Text explains people can try different products and bags until they find what’s comfortable, with help from a stoma nurse or suppliers. 3. I carry the essentials when I go out. Illustration of a bag labelled “Stoma Bag Essentials” with supplies inside. Text explains carrying spare supplies and clothes reduces worry. Suggestions: keep kits at school, work, or in the car (but avoid heat). Have smaller bags for day trips and larger ones for longer trips. 4. There are different ways I can empty my stoma bag. Illustration of a person kneeling, standing, and sitting while emptying a bag into the toilet. Text explains techniques vary by context and clothing. Extra tip: you can use a larger capacity bag for travel or situations where toilets are hard to access. Part 2 – “What I Wish I Knew …about life with an ostomy,” sections 5–8): Continuation of the infographic with more tips for life with an ostomy. 5. Accessibility tools make my life easier when on the go. Illustration of a blue “Just Can’t Wait!” card. Text explains people can order cards that explain they need urgent toilet access, and Radar keys to unlock disabled toilets in the UK. 6. There are ways to manage an increase in my daily tasks. Illustration of a weekly pill organiser. Text explains that bag changes and supplies can be managed with planning. Tips: order supplies in advance, set reminders, and ask your GP about prescription timings. People in England with a stoma are often entitled to free prescriptions. 7. I can continue with my hobbies and the activities that make me happy. Illustrations of a person in swimwear with a stoma and a person rock climbing. Text explains people with an ostomy can enjoy hobbies like swimming, climbing, running, singing, travelling, and more. Extra tip: physical activity is safe with the right adaptations; speak to healthcare providers or trainers. 8. Online communities are a place to connect with people like me. Illustration of a phone showing a community page. Text explains online groups like GetYourBellyOut are safe spaces to share experiences, ask questions, and connect. Platforms include Facebook, Instagram, TikTok, Reddit, and more. Footer credits: Researcher Dr. Poppy Budworth, collaborator Victoria Marie (GetYourBellyOut), artwork by Lucy Harman, funded by NWSSDTP and The University of Manchester.
August 28, 2025 at 6:32 PM
poppybudworth.bsky.social
If only you were at the RGS Conference @alackof.bsky.social (Kate, I’m Dave’s daughter in law!)
August 28, 2025 at 1:48 PM
poppybudworth.bsky.social
Thanks for sharing and for being part of the session, Kate!
August 28, 2025 at 1:40 PM
Reposted by Dr Poppy Budworth
tillyrobinsonmiles.bsky.social
#StitchAssemblyRGS25 ❤️
August 28, 2025 at 11:31 AM