Welcome to Connect, @maria7521,

I moved your message and combined it with this existing discussion on cavernoma. I did this as I saw that you had also posted in this group, and thought it would be beneficial for you to be introduced to the many members who have discussed much of what you are experiencing.
If you click on VIEW & REPLY in your email notification, you will see the whole discussion and can join in, meet, and participate with other members talking about their or their loved ones' experiences.

We have several members talking about cavernoma – please meet @ees1 @jeans @bellisima @jc2buds @nancye3 @brenda68 @pegorr – and you may also be interested in joining these discussions:
– Meningioma and Cavernoma https://connect.mayoclinic.org/discussion/meningioma-and-cavernoma/
– Cavernoma https://connect.mayoclinic.org/discussion/cavernoma/

While we wait for members to join in, here's some information from the Angioma Alliance, about what to expect after surgery:
http://www.angiomaalliance.org/pages.aspx?content=82&id=73

@maria7521, have you seen a doctor for your symptoms after surgery?