I have Cerebral Small Vessel Disease - so far caused loss of balance

Im gonna check it out thank you so much and please keep in touch

Google Prevention and management of Cerebral Small Vessel Disease. It is the most current info I have found so far. Good luck

Thank you for your input so much of my husbands problems are listed as small vessel diease of the brain and poly neruophathy ill defined which i take that as meaning they dont have a clue whats wrong so frustrating

Thats what we were told that it is down deep in the brain nothing can be down

I have the bigger on the left frontal lobe, but when I had the MRI done the doctor told me that I have in 6 in total so the bigger one is to deep into my brain, can't do surgery.

that's frustrating.

I wonder too...... So many of these things are similar...

On a day to day basis he doesnt spend to much time on his feet because his balance is bad and since he sits all the time he tires easy when hes on his feet he doesnt talk to me about how he feels other than to say when hes on his feet he feels like hes swaying even if he doesnt look like he is he gets agitated easily

Im niot sure what the malfirmation are my husband has white matter disease his motor skills have been affected the most i guess most of the doctors we've seen are ok they dont offer us mush advice it seems like you have to figure things out for yourself

Hello Bellisima,
I was recently diagnosed with a cerebral cavernous malformation in the right temporal lobe. I had what I thought were migraines for years. I've blacked out too but I imagine they were actually small seizures. I go into Mayo Monday to have it checked out better. I'm really anxious to see what they have to say.
Where are your cavernous malformations? Do you like your doctors. How are you feeling on a day to day basis?