3 weeks ago I was treated in Albany

I had great support from family and friends

had 2 jugular veins opened  no stent needed

felt not pain or discomfort

noticed better energy,my body not so heavy, walking straighter with my walker

this week feel a bit sluggish,feet feel heavy,bladdar acting up

my neck feels tight

what should I expect in the next 3 months

has anybody had their ups and downs after CCSVI treatment

I told my family and friends I'm doing great

don't want to disappoint them or myself

CCSVI was the greatest experience, it's worth it and would do it again

do I need a physiotherapist

I do walk around my house more