CAUK founder Ian Stuart is raising awareness
CAUK founder Ian Stuart is attending this year’s British NeuroVascular Group (BNVG) Meeting in Cardiff today raising awareness of #cavernoma CAUK & the CARE Study.
March 29, 2022
CAUK founder Ian Stuart is attending this year’s British NeuroVascular Group (BNVG) Meeting in Cardiff today raising awareness of #cavernoma CAUK & the CARE Study.
We sit down with the founder of popular, hero-inspired clothing company, Scamp & Dude, to talk about how shock diagnosis of cavernoma and emergency brain surgery has transformed her life, both personally and professionally.
Member Matt talks about his wife, Emma, and son, Ollie, and their cavernomas.
Our member John Conway provides a diary of events that lead him to brain surgery and the removal of his cavernoma.
Sveta suffered a big brain bleed in 2017 leaving her with balance and coordination issues, and paresis of several of the muscles on the right side of her face and body. Her cavernoma journey has led her to become a visual coach, helping people who have the same issues are her.
Our member Sara, 23 years old, from Spain shares their cavernoma story.
In this video, Kath Charles shares her #RareDisease story just before the four year anniversary of her diagnosis with brainstem cavernoma“It’s the greatest gift I’ve
Dani shares her story of cavernoma for Cavernoma Awareness Month My name is Dani and I am 28 years old. I live in Edinburgh, but
Our member Melissa shares her cavernoma story for Cavernoma Awareness Month
Our member Jade shares her cavernoma story for Cavernoma Awareness Month
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