I’m 66 and have had Hep C over 40 years. I’m now cured with Epclusa and 3 months post treatment. I’ve had severe fatigue and anxiety issues for 40 years. I’ve read Hep C has been found in the brain. It seems the direct acting antivirals do not break the blood brain barrier. Does that mean Epclusa cannot eliminate the virus within my nervous system and brain? I’m thinking I’ll have to live with my symptoms if that’s the case.
Has anyone with severe fatigue gotten better after treatment?