Title: Epilepsy Book Covers & Genre Categories: Mis(h)adra by Iasmin Omar Ata (Graphic Novel) The ABC Murders by Agatha Christie (Murder Mystery) Tall All of Us by Natalie Leif (YA Horror) (Inclusive Pride Flag badge added to image to indicate queer intersectionality) When You Reach Me by Rebecca Stead (Middle Grade) The Gentleman's Guide to Vice and Virtue by Mackenzie Lee (Historical Romance) (Inclusive Pride Flag badge added to image to indicate queer intersectionality) Talking to Alaska by Anna Woltz (Middle Grade) The Match by Sarah Adams (Contemporary Romance) Bondrac Studios logo at bottom of image.

Title: Oligo/Rheumatoid Arthritis Book Covers & Genre Categories: Time and Time Again by Chatham Greenfield (YA Romance) (Inclusive Pride Flag badge added to image to indicate queer intersectionality) Errant Gods by Erick Henry Vick (Dark Fantasy) Cursed by Karol Ruth Silverstein (Contemporary Teen) The First Move by Jenny Ireland (YA Romance) Sick Kids Love by Hannah Moskowitz (YA Romance) Cursed Cocktails by S A Rowland (Cozy Romantasy) (Inclusive Pride Flag badge added to image to indicate queer intersectionality) BonDrac Studios logo at bottom of image.

TItle: Osteogenesis Imperfecta Book Covers & Genre Categories: Handle With Care by Jodi Picoult (Contemporary Fiction) Hummingbird by Natalie Lloyd (Middle Grade) House of Glass by Susan Fletcher (Gothic Historical Fiction) BonDrac Studios logo at bottom of image.

Title: Tuberculosis Book Covers & Genre Categories: Extraordinary Means by Robyn Schneider (Teen Romance) The Dark Circle by Linda Grant (Historical Fiction) The Magic Mountain by Thomas Mann (Historical Fiction) With Every Breath by Elizabeth Camden (Historical Fiction) Under the Wide and Starry Sky by Nancy Horan (Historical Fiction) BonDrac Studios logo at bottom of image.

💬 Is there a rare disease you wish had some representation in the fiction world?

#rarediseaseawareness #rarediseaseday #sicklit #representationmatters #bookstoread #raiseawareness #1in10

tr.ee/qo6dDM

1in10 - The Ehlers-Danlos Support UK 1 in 10 diagnosed. 10 in 10 deserve care. Only 1 in 10 people with Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD) are diagnosed in primary care. Recent research found that on...

📢 “1 in 10 diagnosed. 10 in 10 deserve care.”
Too many are being missed. Join us this May to raise awareness and push for better access to diagnosis and care.
👉 www.ehlers-danlos.org/1in10

#1in10 #EDSAwarenessMonth #HSDAwarenessMonth #TeamZebra

#Endometriosis has floored me for an entire week. wtf body?

#endo #endometriosis #womenshealth #1in10 #chronicillness #painflare

1 in 10 diagnosed.10 in 10 deserve care.
This needs to increase across the UK. Too many are missed, misdiagnosed, or left without support.

👉 Join the campaign www.ehlers-danlos.org/1in10
#1in10 #EDSAwarenessMonth #HSDAwarenessMonth #TeamZebra #EhlersDanlosSyndrome #HypermobilitySpectrumDisorder

The clock's hands spin wrong,
Dates and times all #mix and fade,
World in disarray.

⏰😵‍💫

#WSS366 #Mix #Senryu #PoetrySky #MicroPoem #Dyscalculia #1in10 #SpLD #MathsAnxiety #NeuroDivergent #Dyslexia #Numbers

Wednesday 3/26 is international #PurpleDay2025 for #epilepsyawareness 💜💜
#1in10 people will experience a #seizure in their lifetime.
#1in26 will develop #epilepsy.
Epilepsy is more prevalent than autism, Parkinson's, and cerebral palsy COMBINED.
Please show your support by wearing purple Wednesday!

While this new treatment option in England is positive news for giving people options, it’s import to note it’s not a ‘magic bullet’. It’s vital we continue to look for non-hormonal treatments like with the Edinburgh EXPPECT team and whole-body and lifestyle studies like ours! #1in10 #endometriosis

What is Endometriosis? Endometriosis affects 1 in 10 women and those assigned female at birth, causing severe pain, fatigue, and fertility challenges. Despite its impact, it often goes undiagnosed for years. 💛 Share this to spread the word. #EndoAwareness #1in10 #Endometriosis

March is Endometriosis Awareness Month 💛
Endometriosis isn’t “just bad cramps.” Chronic pain, exhaustion, and medical dismissal. For me, it means pain that steals my days, fatigue that drains me, and the fear of never finding relief. Awareness matters. You’re not alone. 💛 #1in10

It's Endometriosis Action Month coming up in just a couple of days. The theme for 2025 is #EndometriosisExplained

Here are some ways you can be a part of it this year, from our friends at EndometriosisUK buff.ly/3QBv5tN #1in10 #ENDO1000

My adhered ovary just won't give me a break #endo #1in10

A group of 7 women stand in a lab, all wearing white lab coats and looking happy.

The ENDO1000 lab team welcomed our colleagues in Development and Alumni, (who help us out with fundraising and donations) to the lab yesterday! It's great to be able to share what each team is doing and stay connected for our cause!
Thanks for coming by! #1in10 #TalkEndo #Endometriosis

The Traitors' Elen has opened up about her stage 4 endometriosis Like too many women, she had to fight for years to be heard

1 in 10 women have endometriosis. Even this might be an underestimate due to the delay in diagnosis. It's no surprise that more women are speaking out about their experience with it. It's vital that we continue to #TalkEndo https://buff.ly/3CXAAj2
#1in10 #Traitors #Endometriosis

Now that we've selected our app developer, it's time to brainstorm ideas! We kicked things off with our first focus group last week. We'll be working with different groups of users over the development of the app to ensure it's user friendly and asking the right questions! #endometriosis #1in10

A group of 10 women, including Black, Asian, and white women, and a man take a group photograph in a restaurant. They stand or sit smiling in front of a wooden table which has several ENDO1000 branded cups and two poster boards on it.

It was an absolute pleasure to meet up with some of our southerly ambassadors in London last night to meet in person and get inspired for next steps. We’re excited to keep pushing the ENDO1000 project towards our goal of raising £1M to fund this crucial research #endometriosis #1in10 #talkendo

Several items of ENDO1000 branded items, including stickers in tattoo aftercare packs, a charity collection pot, a pen, a pin badge, a large sticker, and a reusable coffee cup are placed together on a dark surface against a white wall in an ENDO1000 supporter’s tattoo shop

Last week we sent some goodies to a long time supporter to help her raise money for us. A huge thanks to Claire for her efforts! If you’d like to know more about how you can raise money for our vital research project, head to www.endo1000.com/donate/
#endometriosis #1in10 #womenshealth #talkendo

On a plain red background, the ENDO1000 logo in white at the top, the text "We're taking a break, see you in 2025!" in navy writing, and navy splatter effect across the bottom.

The team are taking a break for the festive period. We’re really proud of what we’ve achieved so far with the ENDO1000 project, and we can’t wait to come back rested and ready to go in January 2025.
Wishing everyone a restful end of year!
#endometriosis #1in10

‘Medical misogyny’ condemns women to years of gynaecological pain, MPs told Damning parliamentary report blames lack of education by healthcare workers and ‘pervasive stigma’ for poor care

Some much needed recognition of the medical misogyny and dismissal that is all too common for endometriosis sufferers
👏👏👏 #talkendo #endometriosis #1in10

www.theguardian.com/society/2024...

Waiting for my second surgery endo surgery ✨ Do me a favour if you’re reading this and don’t know what endometriosis is: look it up and read about it. Chances are you or someone you love suffers from it #1in10.