Cavernoma Scotland's (CAVS) goal is to raise awareness of Cavernoma, offer help and support, raise funds and go beyond the condition by including other health organisations who experience similar symptoms with us. This will enable CAVS to support a wider network of people.
Cavernoma Scotland, Cavernoma & Me
Welcome to Cavernoma Scotland, which is about Cavernoma Scotland, Cavernoma & Me – Kirsten, founder of Cavernoma Scotland. This video explains why I created Cavernoma Scotland. Having been in the position myself where I was in so much discomfort because of pain and banging headaches from a cavernoma. Cavernoma is classed as a rare condition, so much so, medics need to Google it before treating the patient! As its rare, there is not much information out there on the condition. It is through groups like these that help and support people I explain the condition and symptoms cavernomas causes.
Standing proud for Cavernoma Scotland in a volcano called Stefanos🌋 Making a stand for Cavernoma Scotland and maybe the first person to have Cavernomas?? ( The Volcano Stefanos🌋, in NISSIKOSS GREECE 🇬🇷)