Hey friends!
if you aren’t familiar with my medical history,
i want to touch on why this is so important to me.
AVM’s like mine are already considered very rare, hereditary, and prenatal, essentially meaning it’s passed down and present at birth. With that said there’s very little research and understanding about the complexity of them, and brain aneurysms alike, and it was just my luck upon my cranioplasty it was discovered that i grew another one in a different region in my brain. There’s no real explanation for this and i want to one day be able to help as many other people as i can overcome challenges like this and ideally one day there’s enough research and technology to not only understand, but to be proactive and diffuse it before it ever becomes a big deal.
thank you for your support!
