DEBRA Bathgate

12/08/2026

Did you know your DEBRA membership gives you access to Wisdom, a wellbeing platform packed with practical support for both parents and children?

From calming children's meditations to expert advice on school challenges, parental rights, family wellbeing and mental health, Wisdom offers resources to help your family navigate everyday life with confidence. 💙

🎧 Children's wellbeing resources, including guided meditations
📚 Expert articles and support for parents and families
🩵 Tools to support emotional wellbeing at home and beyond

Whether you're looking for advice, reassurance, or a moment of calm, Wisdom is there whenever you need it.

📲 Find out more and sign up today: https://bit.ly/4qW3wLq

All DEBRA members have access to the Wisdom Wellbeing assistance programme. It gives you free, confidential access to expert support, plus a host of other wellbeing resources and benefits.

12/08/2026

🥾 Take your support one step further with the Edinburgh Kiltwalk! 💙

If you support us by shopping, donating or volunteering at DEBRA Bathgate, why not take that support one step further and join at the Edinburgh Kiltwalk on 13th September?

Choose the distance that's right for you:

✅ The Mighty Stride – 21 miles
✅ The Big Stroll – 11 miles
✅ The Wee Wander – 4.5 miles (perfect for families and even dogs!)

Every step you take and every pound you raise will help DEBRA provide care and support for people living with epidermolysis bullosa (EB), a painful genetic skin condition, and fund research into future treatments.

When you join , you'll receive a DEBRA t-shirt, fundraising materials and support from our team all the way to the finish line.

💙 As a local supporter of our shop, we'd love to see you representing our community at this fantastic event.

📅 Edinburgh Kiltwalk – 13 September
💰 Raise whatever you can for DEBRA

Find out more and sign up today: https://www.debra.org.uk/product/the-kiltwalk-2/?gad_source=1&gad_campaignid=22557552945&gclid=Cj0KCQjwm8bTBhDWARIsAC9Hi8nkOJfmA8R1OJzDJ_oQVXWZxKc-dLx0choT_RcfRYgjbcUxEGQTeJMaAnKrEALw_wcB

11/08/2026

🔥 This summer's been warm, but are you ready to take the heat up a notch?

Every step across the embers will help make a difference for people living with EB. Join at our Derby Firewalk this October, challenge yourself, and support a community facing the daily pain of butterfly skin. 💙🦋

The best part?

There's no training required, and it's a fantastic challenge to take on with friends, family or colleagues. Gather a team, cheer each other on, and make an unforgettable evening of it!

Ready to take the first step? 👉 https://bit.ly/4vYEOfR

Take on our DEBRA Firewalk Challenge and raise vital funds to support people living with EB.

10/08/2026

We need your pre-loved furniture 🛋️

It’s easy and FREE to donate! Just complete our quick online form and one of our team will be in touch to book your collection: https://www.debra.org.uk/shop/furniture-collection/

Every item you donate will help change the lives of people living with butterfly skin so thank you 💙

09/08/2026

🔬 Research blog: Helping JEB skin cells to strengthen themselves🔬

Dr Svitlana Kurinna, at The University of Manchester, is working on a DEBRA‑funded project exploring whether we can strengthen skin by targeting the molecules that control how cells attach to each other and their surroundings.

💬 “What excites me most is combining biology with physics-based technologies to directly measure how cells stick. Using advanced tools such as atomic force microscopy, we can measure the forces that hold a single skin cell in place.”

Read Svitlana's blog now: https://bit.ly/4b3VF9B

Using advanced tools such as atomic force microscopy, we can measure the forces that hold a single skin cell in place.

08/08/2026

💙 Could your story help raise awareness of EB?

Every experience is unique, and by sharing your story, you can help others better understand what it's like to live with epidermolysis bullosa.

If you'd like to get involved, we'd love to hear from you.

🔗 Complete the form: https://bit.ly/4f4tSbr

07/08/2026

When DEBRA member Ciara's son Ralph was born with EB earlier this year, she became determined to help drive change for the EB community.

She's launched a petition calling for greater support and funding for EB research.

As a key funder of EB research, DEBRA UK is committed to driving progress towards effective treatments. We rely on fundraising to support this work, and additional funding from government and other organisations could help accelerate research and bring life-changing treatments closer for people living with EB.

🩵 Support Ciara's petition here: https://bit.ly/3Tq869J

Increase dedicated, ring-fenced Government funding for research into rare skin conditions, including all forms of Epidermolysis Bullosa (EB), to accelerate the development of effective treatments and support UK clinical trials.

06/08/2026

🌟 We're coming back to Northern Ireland! 🌟

Last year's Northern Ireland Members Connect event was so special, we just had to do it again. 💙

At our Belfast event, 19 members came together to share experiences, make new connections and, for some, meet another person living with EB for the very first time. Watching friendships form and seeing members realise they are not alone was incredibly powerful.

Now we're excited to be returning this October for another opportunity to connect with the EB community in a welcoming and supportive environment!

Whether you've attended a DEBRA event before or are thinking about joining us for the first time, we'd love to welcome you.

📅 Saturday 17th October 2026
📍 Titanic Hotel Belfast
💙 Open to DEBRA members and their families

Spaces are limited, so book your place today: 👉 https://bit.ly/4wokeGE

We can't wait to see you there and create more meaningful connections within the EB community. 💙

06/08/2026

20% off for DEBRA Reward members between 3rd - 9th August only! ✨🛍️

Enjoy 20% off all items – exclusively for members (excludes new goods). Don’t miss out on this fantastic saving! 💙

Not a DEBRA Reward member yet? Simply sign up in-store and start enjoying exclusive member benefits.😊

05/08/2026

Thinking about making or updating your Will?

We know the process can feel overwhelming, which is why we created a free Gifts in Wills Guide to help make it as straightforward as possible.

The guide includes:

✅ Step-by-step support for writing or updating your Will
✅ Information about DEBRA's Free Will Service
✅ Real stories showing how gifts in Wills help support people living with EB and fund life-changing research

Request your free copy today and discover how you could help to of EB: https://bit.ly/46BiQWS

04/08/2026

Did you know that understanding the specific genetic mutation behind EB can help guide future care, monitoring, research opportunities, and even access to certain treatments? 🧬

In our newest blog post, Advanced Nurse Practitioner at Guy's and St Thomas' NHS Foundation Trust, Kati Paalosalo-Harris, explains why genetic testing is so important and how it can empower people with EB to make informed decisions about their health and future.

🔗 Read more: https://bit.ly/4x08mKW

An EB specialist explains why genetic testing matters for epidermolysis bullosa, from diagnosis to treatment options and family planning.

04/08/2026

Feeling a bit blue in Bathgate today due to the change in weather

Open 7 days a week so pop in for s visit any time

03/08/2026

💙 Shop, save, and support people living with EB.

From today (Monday 3rd) until Sunday 9th August, DEBRA Rewards members can enjoy 20% off all donated goods in DEBRA charity shops*.

Every purchase helps raise vital funds to support people living with epidermolysis bullosa (EB) today and fund research to help tomorrow.

If you're not already a DEBRA Rewards member, now's the perfect time to sign up and start enjoying member benefits while supporting a cause that matters. Just ask at the till and become a member in minutes!

📍 Find your nearest shop and start planning your visit: https://bit.ly/3Z1Dz0S

*Excludes new goods.

02/08/2026

🔬 Exciting progress for EB research!

In 2025, DEBRA UK awarded funding to six ground-breaking research projects covering all types of inherited epidermolysis bullosa (EB).

From a major UK clinical trial testing repurposed drugs for EB, to innovative gene therapy, microRNA research and new approaches to tackling pain, these projects bring hope for improved treatments and outcomes for the EB community.

Even more encouragingly, five of the six awards are supporting researchers receiving DEBRA UK funding for the first time, helping to build the next generation of EB experts.

None of this would be possible without the support of our members, fundraisers, researchers and wider community. Thank you for being part of this journey! 💙

👉 Read more about the projects we're funding and the impact they could have for people living with EB: https://bit.ly/4bJqOPK

29/07/2026

Volunteer with us 💙

Give back, meet new people and make a real difference in your community – join our amazing team today ✨

27/07/2026

Christmas has come early at DEBRA UK! 🎄✨

Our brand-new Christmas cards are now in store, so why not get ahead of the festive rush and pick up your favourites today? 💙

15/07/2026

Students get more! 🎓✨

Show your student ID in store to enjoy a little extra off your purchase 💙

01/07/2026

Some of the current stock we have instore today

Pop in or give us a call on 01506 340328

01/07/2026

Beautiful cards for every occasion – just 5 for £5 all July! 🌸

We’ve got lots of lovely new designs in store for all customers, perfect for birthdays, celebrations and everything in between. Pop in, have a browse, and stock up on quality cards for friends and family. 🦋