Epclusa Side Effects (Page 5)
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Hello. I am 16 months post epclusa and feel worse than when I started. I was a server for over 40 years. Full of energy. Then hep c happened. I had epclysa for 12 weeks. Now I am in bed most of the tune from no energy. My ears are ringing. I feel deflated. Anyone else feel like this? My hep c nurse waived off my complaints.

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Re: Kathleen (# 57)

Hi Kathleen ,hope you are ok and enjoyed Xmas as much as possible and new year is a important for us and many others,it's very hard to enjoy anything with this horrible covid risk ,the numbers here are getting out of control,yet some people insist on going out ,watching sport our gov won't do anything they just want to make $$ don't care about people. I'm having trouble with our messages don't think I'm getting messages thru wish I had better address , happy NY.

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Re: Kathleen (# 54)

Xmas was quite this year ,I'm basically a hermit these days ,can't risk catching a virus or flu ,kinda use to not seeing people these days ,hope my posted getting thru.

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Re: Kathleen (# 58)

Hi Kathleen hope you are going ok ,I havnt received any replies lately I'm wondering maybe I'm doing something wrong with my phone on line maybe! Oh well I will keep trying ,hope your app with eye dr was alright ,

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Re: Kathleen (# 54)

Hope eye dr appointment went ok for you !

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Re: Kathleen (# 54)

Best wishes and prayers to you and family in these extra strange days ,the gov over here didn't want to miss out making$ any longer ,so opened up all borders now it's all backfired on them virus now out of control ,our prime minister is a crawler , always a lap dog to U.S. people over here don't trust him ,now his trying to tell china what to do ,anyway just take care ok maybe next year be good for us.!!

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Re: Anna (# 69)

Anna hope your condition improves, this virus is bad news ,one thing for sure we won't be going out all the best from Australia

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Re: Lou (# 68)

Very mild year. Minnesota is beautiful.
Prayers for you.??

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Re: Lou (# 67)

In US. I am bedridden

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Re: Sunshyne (# 65)

We all deserve apology for all the crap theve put us thru, take care ! MN is it good place ??

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Re: Anna (# 66)

Anna sorry that you have had similar effects ,what part of world are you ? I think it's time we started getting some kind of action on these people there's a lot of really good people suffering , with not Evan apology just lies.take care, a lot of people have had a hard enough life already we didn't deserve crap and lied.

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Yes this is devastating I was a healthy person no liver issues shouid have been left alone this is not living I hope someone gets them

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Re: Lou (# 63)

I am in Northern MN.
It's not a miracle drug. ??
Like the Jab. Not to be trusted.????

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Re: Kathleen (# 57)

Hi just heard ashow on radio talking about the new strain of covid and how contagious it is,have to be very lucky not to catch it ,And I don't go out much maybe once a week if possible, having COPD plus vitD deficient the cortasteroids I have to take make me I'll.terrible news the tornado in USA! That's one thing we don't get as yet tornadoes.good luck

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Re: Sunshyne (# 61)

Sunshyne ,I finished Epclusa about 3 yrs ago I thought I was doing the right thing ,got rid of virus but stuffed up my immune system as well, before I did treatment I didn't feel too bad, now I have had infections lung problems Edema nausea ,I made the mistake of listening to the so called experts now my life is crap much better before treatment ,like why would they wanna help us! Besides $$$ they never have wanted to help before ,what part of the world are you from.

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Re: Kathleen (# 57)

Hi Kathleen sorry to hear about immune system arthritis, it does not sound good, how do find the vit D? I'm taking capsule supplement my dr said take 4 a day, yet the nurse said that's too much, so I'm trying to take 3 I just hope they work so that my vit D gets built up a bit as my immune system has no t been normal since epclusa, my dr can't tell me if maybe AstraZeneca vacc may have affected me, I felt like I had covid after 2nd shot, our stupid government is opening up all the borders and stopping any restrictions just before Xmas, I'm sure it's because they want to make money over holiday season, I can't understand why when the new strain is getting bad in other countries, I had a bit of a breathing episode other day, I thought about going to hospital but then I heard hospital isn't the safest place when immune is low, I really hope the dr can help you tomorrow, good luck, pity I can't send you my email address. Take care of yourself Kathleen, a talk might be good for you, your wisdom might help others I think.

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Re: Lou (# 51)

Don't do the drug if your not sick. But dont drink any alcohol.
You can live a long life and die with the hep c. But die from a heart attack.
My husband was living fine with the hep. Strong & healthy.
Read back I'll n how fast it took him.
He would have never done but he trusted his dr.
And they paid most to make it seem like he we on a lottery.
Shameful what it's doing to people.

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Re: Kathleen (# 54)

Praying for you. ??

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Re: Lou (# 1)

It took my husband's life. He had no cancer in blood or CT.
Started Harvoni was clear week 5. They kept him on for 12 weeks. He died 8 weeks later to the day of start (5months). With liver, pancreas and adrenal cancer.
Harvoni killed a strong healthy 235# Pipe fitter
In 5 months. At 160#
Shame on the drug companies and the profit over people.
You'll see what will happen to those who dont get the jab.
Look at Australia.
It's all about profit, control and kill off the sick.

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Re: Lou (# 56)

Been on vit d for many years now. Also calcium every Saturday.
Never felt this way until epclusa.
Yes it killed her c but was never informed ay what cost to my body.

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Re: Lou (# 56)

So good to hear from you again Lou.
I was diagnosed with immune system arthritis last year. Started steroids and another drug . Now my eyes are so sensitive to light that I finally see a doctor tomorrow. None of these things happened until epclusa.
I dont know how they get away with doing us like this?
I'm so glad you are hanging in there with me.
I have been asked to do a talk about Epclus at a center here.
I am considering doing so. Will let you know..
Take care lou

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