As 2024 ends, we’re so grateful for your support in improving the lives of those with #EpidermolysisBullosa. Here’s to another year of hope and progress! 🎉✨ Check out our blog for highlights: https://t.co/kXFf88Pfqj
Today kicks off #EBAwarenessWeek! Big thanks to Mayor Mike Savage for proclaiming Oct 25–31 as EB Awareness Week in Halifax. Nothing says support like posing while someone rocks last year’s pic of you! 😄💙 Let’s make a difference together! 🦋#EpidermolysisBullosa#WeFightEB
Announcing our 2024 #debraBenefit Jouni Uitto Impact Award Honoree: Dr. Anna Bruckner of @ChildrensColo! 💫 Join us in celebrating Dr. Bruckner's outstanding contributions to the #EpidermolysisBullosa Community on Oct 26 at @SoFiStadium in LA!
The 2024 #debraCareConference was unforgettable, and it's all thanks to YOU —our amazing EB warriors, families, researchers, and advocates! 🎉 A heartfelt thank you to our sponsors, speakers, volunteers, and attendees. #DCC2024
The 2024 #debraCareConference was unforgettable, and it's all thanks to YOU —our amazing EB warriors, families, researchers, and advocates! 🎉 A heartfelt thank you to our sponsors, speakers, volunteers, and attendees. #DCC2024
In the more severe cases of #EpidermolysisBullosa , >75% of the body may be covered in open wounds, leaving individuals susceptible to life-threatening infections. How can you tell if a wound is infected? 🔍 Learn more athttps://pulse.ly/vqzu5sldxo
February 29th is Rare Disease Day. Rare Disease Day raises awareness and generates change for 300 million people worldwide living with a rare disease. Thank you, @MikeSavageHFX for proclaiming February 29, 2024 Rare Disease Day in Halifax #RareDiseaseDay#EpidermolysisBullosa
This is the time when I ask you to do one https://t.co/HVzW64sGjY RT or social media post to help boost awareness.
If you have before, my thanks, if not, pick one (I know there are A LOT) & have at it. Shout outs are as good as donating! Lets help #FeedTheNeed
Thanks, kids! -Andy
Having loose joints, or hypermobility, contributes to the impaired walking ability seen in children with epidermolysis bullosa, per a study. https://t.co/KzSRMZr3yn
Today I was out visiting a @lockviewhigh co-op student with @hfxgov - Transformation & Innovation. Mckenna has been gathering raw data for lots of cool projects, learning Microsoft tool tips, & assisting her mentors with data collection for city planner reports. #DataAnalytics
Nutrition is a priority for those with #EpidermolysisBullosa as it promotes growth and development, provides nutrients for wound healing, strengthens the immune system to fight infection, and more. 🥑🍗
➡️ https://t.co/77jDwGxWZt
What an awesome afternoon of music from three talented singers n the release of Sarah Bradford (red) debut single Naive. Watch for the video story on The Laker website n socials #EastHants@CarletonHalifax@mattdagley
Repost from @ebresearch: We are heartbroken by the devastating news of the passing of EB community leader, Deanna Molinaro. Deanna was a fierce advocate, brilliant artist, and incredible person who we were blessed to work with and get to know over the years.
Singer Sarah Bradford from #EastHants will release her debut single this Sunday at @CarletonHalifax. #FallRiverNS (The Laker News will be there covering it)
https://t.co/BjSu19lXt9
Skin infections are particularly problematic for those with #EpidermolysisBullosa because they decrease our body’s ability to heal wounds.
Dr. Marissa Perman of CHOP offers guidance on treating skin infections in EB in her EB Connect video talk.
➡️ https://t.co/sNKNhu3nLO
"Along with his extraordinary wife @jillvedder77, they helped cofound @EBResearch which hosted a major EB conference & the benefit shows here in Seattle. Together their work ethos is pure synergy bringing hope, awareness & funding for EB research." @eddievedder