Epclusa Ruined My Life (Page 3)
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Has anyone experienced severe anxiety, constant crawling feeling in body after epclusa treatment. Its like my brain and body aren't working right anymore? I had terrible side effects. Finished in January, now it's June and feels like I'm still taking the poison.

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Re: Chris (# 267)

Really understand what your saying I also did epclusa ,I could never get a straight answer from epclusa people ,I think it has damaged me big time ,in fact think I felt better pre treatment ,very worried about covid after taking epclusa my immune system isn't good take care ok ,

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Hi Barbara ,hope your condition has improved these days ,I found one old message of yours and your were not going very well with epclusa ,I was the same restless led body jerks I still get puffy feet ankles heaps different infections ,I don't think I feel much different these days ,I had no support from Gilead or other people. Where are you? I'm in Australia ,only person who helped me a bit was lady called Kathleen from U.S. I wonder what happened to her as I havnt heard anything for a few years , do you remember her? Now I'm really scared with covid about as since doing epclusa I have weak lungs COPD asthma .I'm in 60s really don't feel strong enough to put up with a virus.anyway hope you survived .

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Re: Emmy (# 265)

This stuff is an immune suppressant. In other word it kill your immune system. DAA switch of T-cells. You never get better. You think you are better at times then bam, back. Look it up, all the same thing. Hep-c is not a virus as I thought. It is elevated levels of things in you that the body produces. Every thing about viruses are false fraud. Not saying can't get ill but how is it people who drink get it by drinking? It's because the drink causes damage, not because it something you catch. Fraud.

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Re: Emmy (# 265)

Sorry to hear that !the time does pass, it's been a few yrs for me, can't say I feel much different, but who knows maybe I would have got sick if no treatment was done, I didn't get any support at all, just same old line "oh we've never heard of that happening before" I'm in Australia where are you.? Good luck any ?s

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Re: Kathleen (# 17)

Hey I’m on my 2nd bottle massive side effects I feel like I’m dying daily my sanity is holding on by A strong massive weight loss no appetite aches pains rash sores bruises brain fog memory problems the list goes on ??

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Re: Lou (# 259)

Sorry just read couple of my messages I meant to send to covid vaccine not epclusa sorry

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Re: Davoe (# 70)

I've been on the med for 5 days feel brain fog no energy. Lots of anxiety and headaches. I feel like a I can hardly move I'm afraid it has upset my sober life too. I hope I wake up refreshed not like last 5 days

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Had it 2017. Was OK at first but missed 11 weeks. On the last week I felt too poisoned to take it. Spent 2 years waking up with swollen fingers, then seizures from flourescent light, then bad electromagnetic hypersensitivity. It took to 2022 and still learning what they did to us. I spent 8 months on a mattress hidden in corner of lounge as a bedroom full of static wall sheets on floor and everything. I got bad. I never went back in the room then I grounded with wire that I put though vent in ground. Bad headache but felt better so I slept with an anti static wrist band around my ankle, hiding and living on a mattress. My body got so weak I had to stay laying down. I had strength to do some quick exercises but no normal strength in spine, legs, arms - all weak. I could not even sit in a chair, I had to lay down. I thought this was it for me, near death, could not do anything. Just on phone laying there with bed rash on elbows because I spent all time on elbows on phone.

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Absolutely! I’ve had this horrible restlessness in my legs with a buzzing feeling. it causes me to cry out “Please go away please go away“ when it gets really bad. I’ve also been getting this unnatural feeling in my lower stomach and have bad diarrhea that is a yellow orange color (Sorry to sound gross). My hands and feet feel clammy sometimes. I have other less prominent symptoms that I can’t think of at the moment (bigger symptoms overshadow the smaller ones I guess).

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Re: Kathleen (# 248)

All best wishes for new year ,hope everything improves for you ????had my booster shot yesterday ,bit of sore arm so far ok .short of breath this morning probley side effect all the best to you and family ,I'm really tired been awake seems like days ,

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Re: Kathleen (# 10)

Hope this finds you my friend or maybe a friend of yours can contact me.

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Re: Skpp930 (# 7)

Hope you are feeling better now days ,it's been a few yrs since I did treatment ,still got unwanted things going on ,puffy feet Edema nausea ect,I had Astrazeneca recently send to have made everything worse ,I don't think I should have had vaccine Astrazeneca I'm 68,with immune system not so good thanks to epclusa hope you are ok ,I'm in Australia.

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Re: Verwon (# 1)

Hello Verwon, I am a bit concerned about Kathleen ,on this Epclusa Poste,she was in ill health,she was a regular on this Poste and a friend.thankyou

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Re: Elizabethgrace (# 226)

Hi I read your message mths ago. I finished Epclusa 3 yrs ago now have numerous problems. I was wondering if you decided to do the treatment and how you are feeling? There's another lady named Kathleen I communicate with through this site from California. I have not heard from her, she has been very ill since taking Epclusa treatment. I'm very worried about her. Maybe somebody else on this site may have heard if she is ok. Anyway hope all is well with you. Happy new year.

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Re: Kathleen (# 251)

I hope this finds you and you are ok??

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Re: Kathleen (# 251)

K,how are you? Are you ok ? I can understand you not feeling up to texting,I'm often same ,Xmas is tiring for us ,just bit worried about you,what this Epclusa treatment has done to too many people is criminal in my opinion.

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Re: Kathleen (# 246)

Best wishes and prayers Kathleen from your auzzie mate Lou

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Re: Kathleen (# 251)

Hi ,hope everything is ok where you are ,and that the Colcry helped a bit with your arthritis ,IV been having a few problems with skin infections that take forever to heal so sick of antibiotics ended up in hospital for a few days had a couple of injections of penicillin seemed to fix ,IV been trying to find out if many older people suffer immune damage after the so called wonder med Epclusa,I think it is more common then they want released to people in case they miss out on a few dollars,I don't know if it's me or the air con but my coughing an shortness of breath seems worse lately plus heat and humidity has been bad,it's all pretty scary now covid 19 seems to be infecting few more people lately,really doesn't feel like Xmas much,this year,I see where Trump is still whinging ,I hope the best for you and son for Xmas with not too much pain,must be nice to have Xmas when it's cool instead of this heat .

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Re: Elizabethgrace (# 226)

Hi,just wondering if you ended up doing Epclusa as I did 3 yrs ago, hope you are going ok, IV got health issues but all the experts say is it's probably from having virus for so long, I'm really sick of trying to get any facts out of liver clinic,IV had no support since they started me on Epclusa, take care

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Re: Lou (# 250)

Hi lou, Dr put me on a med called Colcrys. It is for arthritis. It is only taken for four days. Today is day three and it isn't working. My hands, fingers and wrists hurt so deep I cry. EPCLUSA is the think that has started all of these issues.

I have told doctors about my epclusa issues and they just look at me. Their employers get kick backs. They won't say anything. Sorry it is so hot there. It's been wonderfully cold here. My wrists hurting so will close this saying you are on my mind a lot.

Take care mate

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