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Post Info TOPIC: dermatitis, thyroid, and RA post treatment?


Guru

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RE: dermatitis, thyroid, and RA post treatment?
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Hi Meghan,

Glad to hear life is improving. I'm getting my Rheumatoid Factor done tomorrow as I've got a lot of joint pain and stiffness ( at EOT + 11.5w). Good luck for the future.



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Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm



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I am getting better...not nearly as much dermatitis and joint stiffness is subdued but still there.  I tested negative for RA so hoping it goes away...its been 9 months since treatment now.  :)



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geno 1a, mother & brother also hep c +...mom got a blood transfusion and passed it along.  Started tx with incivik 11/23/11 and brother started 2/8/2012.  Both of us und. at 4,8,12 and me at 24.  I am going 36 wks and brother is going 48 weeks.



Guru

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I read somewhere that Interferon can activate auto immune disorders, I have Fibromyalgia that is also one of the things the virus is known to activate and interferon can make worse. It might help to read some of the people treated for cancer with interferon on the internet, as I read some of them were having simialr experiences. Past that I can't suggest anything else as I have never had interferon. Good luck with recovery. Hugs x



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Genotype: 3b

VL.�over 15, 000 000

Failed TX 2014: Interferon/Riba.

Cured using Sof/Dak combination.

I can eat cake again! <3 



Guru

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keep us posted how it goes! i got joint aches, since quite possibly, hcv infection...now during tx it's getting worse, anxious what will be post tx...

best



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GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




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Almost 6 months post treatment.  Cleared virus but yes, Being tested for RA.  Stiff, stiff, still.  Joint aches which I never had before.  Funky things.  Youre not alone. Keep me posted on what you find out.  My hep PA said it had nothing to do with treatment.  Went to my primary care guy.  He says OF COURSE it does.  We'll hang in there!



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Debra

 

Geno type 1a1b

Began Peg/Rib 4/16/2012  

Began Victrelis May 14, 2012            4 week and 8 week labs undectable

12 weeks und. 16 weeks und. Week 17 Cut peg, added Neopogen 5+months und.!



Guru

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Hey Meghan
6 months post and I am doing pretty good. I have noticed some achiness in my joints mostly the knees. My thyroid is now back to the normal range--it was given me fits for awhile. But I had hypothyroidism before tx. Hope it gets settled for you--pesky thyroid can cause some issues. I have actually started sleeping better than I have in years. Hope you are doing well otherwise.

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Diagnosed 1996 genotype 1b VL alot tx starting 12/23/11 Victrelis UND week 8!!! 28 weeks of tx

Completed tx 7/6/12--still UND!!!!



Guru

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Hi Meghan,

Sorry for the late reply, I usually look at the "Chatbox" on the left of the screen for new postings; sometimes they get "buried" by newer ones.        I still have occasional  joint pain and muscle soreness on and off; also still have what I call "lesions" on various spots of my skin, which erupt  from time-to-time and are itchy & scaley.  My NP charecterizes these skin lesions as looking alot like Psoriasis, suggesting  ongoing side effects of interferon, which has caused other issues (my right optic nerve) with my body.  

Other post tx issues that I experience are:   a weird crawly feeling on my skin, mostly up around my head and neck, but also occurs on torso and legs as well.   In addition, a bit of anxiety and difficulty staying asleep have been my main tribulation; I'll be ever-so-thankful to get back to 'normal' on these last 2 issues.

Take care,

Tim



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"hrsetrdr"=Tim

Treatment halted on Aug.8,2012 due to vision problem.  6 month post tx labs

Aug.2013 SVR

Be strong when you are weak, brave when you are scared, and humble when you are victorious.
- Unknown

 

 



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Hey, I am 7 months post treatment now and still am having dermatitis on neck, ears, eyelid, and scalp.  I have RA like symptoms in my hands....they are stiff when I wake up.  Also, My TSH is very high but T3 and T4 normal.  All of these together make me think its autoimmune or still side effects of the interferon....although it has been 7 months since tx.  Anyone else experiencing these symptoms?  They may be totally unrelated but I am just curious. :)

Thanks,

Meghan



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geno 1a, mother & brother also hep c +...mom got a blood transfusion and passed it along.  Started tx with incivik 11/23/11 and brother started 2/8/2012.  Both of us und. at 4,8,12 and me at 24.  I am going 36 wks and brother is going 48 weeks.

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