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Hi i’m new here.
I’m getting treated for Lyme and co-infections for more than 5 years now. When I started treatment I was completely bedbound in a dark room 24/7 and not able to walk, talk, eat by myself (i was tube-fed), watch TV or shower. Treatment was really hard, but finally I’m making progress and at the moment I’m feeling better than I’ve felt in years. My LLMD said the Lyme is not active at the moment and 6 months ago we stopped the antibiotics. A month ago I went to my LLMD and we did some testing. My test results show my C3a and C4a are low. Does anyone know what low levels of C3a and C4a means? My CD57 is also quite low (40).
I’m getting treated for Lyme and co-infections for more than 5 years now. When I started treatment I was completely bedbound in a dark room 24/7 and not able to walk, talk, eat by myself (i was tube-fed), watch TV or shower. Treatment was really hard, but finally I’m making progress and at the moment I’m feeling better than I’ve felt in years. My LLMD said the Lyme is not active at the moment and 6 months ago we stopped the antibiotics. A month ago I went to my LLMD and we did some testing. My test results show my C3a and C4a are low. Does anyone know what low levels of C3a and C4a means? My CD57 is also quite low (40).