... hep C. Does anyone else have this? I am interested in knowing about other people's experience with it. How did your symptoms present/ progress? Did they go away during hep c treatment? The information I've found on the internet is very clinical, and the pictures scare me a little bit.. Thanks and good luck to everyone
Each person is effected differently. Symptoms depend on: Hep C type, Condition of Liver, Other effected organs, esophagus , pancreas ect. that could be effected directly from the liver... This blood disease and the liver will kick out toxins ANY way it can to get out... So, on that note, if and when you have any I'd be more than happy to tell you my experiences and what I have and what I am going through because this is my second attempt trying to cure this nasty disease... Keep your eye on the prize!
I am under the 4th week of hcv treatment with epclusa. I was diagnosed hcv in 1994 and with cryoglobulimia in 2009 but only had 2 episodes of hand/joint pains . The last one has lasted over 10 months and very severe. The specialist has got me on the epclusa treatment for hcv and also aiming to treat / resolve my joint pains which is believe related to the cryoglobulimia. They can not say what the outcome will be. I can advice to exercise, yoga and pilates helps me. I will keep posting any outcones at the end of treatment approx. october 17. All the best.
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